TECHNICAL FIELD
THIS INVENTION relates to biocatalytic reactions, and more particularly to the use of enantiomer selective hydrolases to obtain optically active epoxides and vicinal diols
BACKGROUND
Optically active epoxides and vicinal diols are versatile fine chemical intermediates for use in the production of Pharmaceuticals, agrochemicals, ferro-electric liquid crystals and flavours and fragrances Epoxides are highly reactive electrophiles because of the strain inherent in the three-mem be red ring and the elect ronegativity of the oxygen. Epoxides react readily with various O-, N-, S-, and C-nucleophiles, acids, bases, reducing and oxidizing agents, allowing the production to bifunctional molecules Vicinal diols, employed as their highly reactive cyclic sulfites and sulfates, act like epoxide-like synthons with a broad range of nucleophiles The possibility of double nucleophihc displacement reactions with amidines and azide, allow access to dihydroimidazole derivatives, aziridines, diamines and diazides. Since enantiopure epoxides and vicinal diols can stereospecifically be interconverted, they can be regarded as synthetic equivalents.
Optically active 2,2-disubstituted epoxides (TDE) and 2-substituted-1,2-diols (DVD) have considerable synthetic potential, since these compounds constitute highly flexible molecular scaffolds which can be converted to valuable optically active tertiary alcohols, a-methylamino acids and ct-hydroxy-a-methyl carboxylic acids {Steinreiber et al. 2000)
Epoxide hydrolases (EC 3.3 2.3) are hydrolytic enzymes that convert epoxides to vicinal diols by ring-opening of the epoxide with water. Epoxide hydrolases are present in mammals, plants, insects and microorganisms.
SUMMARY
The invention is based in part on the surprising discovery by the inventors that certain microorganisms express epoxide hydrolases with high enantioselectivity. The microorganisms of the invention selectively hydrolyse 2,2-disubstituted epoxides or selectively form 2-substituted-1,2-diols and their genomes encode polypeptides having highly enantioselective epoxide hydrolase activity.
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More specifically, the invention provides a process for obtaining an optically active epoxide and/ or an optically active vicinal diol, which process includes the steps of providing an enantiomeric mixture of a 2,2-disubstituted epoxide (TDE), creating a reaction mixture by adding to the enantiomeric mixture a polypeptide, or a functional fragment thereof, having enantioselective 2,2-disubstituted epoxide hydrolase activity, the polypeptide being a polypeptide encoded by a gene of a yeast cell; incubating the reaction mixture, and recovering from the reaction mixture- (a) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol (DVD); (b) an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide, or (c) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol and an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide.
Another aspect of the invention is a process for obtaining an optically active epoxide and/or an optically active vicinal diol, which process includes the steps of providing an enantiomeric mixture of a 2,2-disubstituted epoxide, creating a reaction mixture by adding to the enantiomeric mixture a cell comprising a nucleic acid encoding, and capable of expressing, a polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity, the polypeptide being a polypeptide encoded by a gene of a yeast cell; incubating the reaction mixture; and recovering from the reaction mixture: (a) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol, (b) an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide, or (c) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol and an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide.
The following embodiments apply to both of the above processes. The cell can be a yeast cell The polypeptide can be encoded by an endogenous gene of the cell or the cell can be a recombinant cell, the polypeptide being encoded by a nucleic acid sequence with which the cell is transformed The nucleic acid sequence can be an exogenous nucleic acid sequence, a heterologous nucleic acid sequence, or a homologous nucleic acid sequence. The polypeptide can be a full-length yeast epoxide hydrolase or a functional fragment of a full length yeast epoxide hydrolase.
Moreover both processes can be carried out at a pH from 5 to 10 They can be carried out at a temperature of 0°C to 70 °C In the processes, the concentration of the 2,2-disubstituted epoxide can be at least equal to the solubility of the 2,2-disubstituted epoxide in water.
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In both processes, the 2,2-disubstituted epoxide of the enantiomeric mixture can be a compound of the general formula (I) and the vicinal diol produced by the process is a compound of the general formula (II),

wherein:
R1 and R2 are, independently of each other, selected from the group consisting of a variably substituted straight-chain or branched alkyl group, a variably substituted straight-cham or branched alkenyl group, a variably substituted straight-chain or branched alkynyl group, a variably substituted cycloalkyl group as well as cycloalkenyl groups, a variably substituted aryl group, a variably substituted aryl alkyl group, a variably substituted heterocyclic group, a variably substituted straight-chain or branched alkoxy group, a variably substituted straight-chain or branched alkenyloxy group, a variably substituted aryloxy group, a variably substituted aryl alkyloxy group, a variably substituted alkylthio group, a variably substituted alkoxycarbonyl group, a variably substituted straight chain or branched alkylamino or alkenyl ammo group, a variably substituted arylamino or arylalkylamino group, a variably substituted carbamoyl group, a variably substituted acyl group, and a functional group; or wherein R1 and R2, together as a whole unit are a carbocycle with 5-7 atoms or a heterocycle with 5 to 7 carbon atoms.
Moreover, in the processes, the enantiomeric mixture can be a racemic mixture or a mixture of any ratio of amounts of the enantiomers. The processes can include adding to the reaction mixture water and at least one water-immiscible solvent, including, for example, toluene, 1,1,2-tnchlorotrifluoroethane, methyl tert-butyl ether, methyl isobutyl ketone, dibutyl-o-phtalate, aliphatic alcohols containing 6 to 9 carbon atoms or aliphatic hydrocarbons containing 6 to 16 carbon atoms Alternatively, or in addition, the processes can include adding to the reaction mixture water and at least one water-miscible organic solvent, for example, acetone, methanol, ethanol, propanol, isopropanol, acetonitnle, dimethylsulfoxide, A/,A/-dimethylformamide, or N-methylpyrrolidine. In addition, or alternatively, one or more surfactants, one or more cyclodextrins, or one or more phase-transfer catalysts can be added to the reaction mixtures. Both processes can include stopping the reaction when one
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enantiomer of the epoxide and/or vicinal diol is in excess compared to the other enantiomer of the epoxide and/or vicinal diol. Furthermore, the processes can include recovering continuously during the reaction the optically active epoxide and/or the optically active vicinal diol produced by the reaction directly from the reaction mixture.
In both processes the yeast cell can be of one of the following exemplary genera Arxula, Brettanomyces, Bullera, Bulleromyces, Candida, Cryptococcus, Debaryomyces, Dekkera, Exophtala, Geotrichum, Hormonema, Issatchenkla, Kluyveromyces, Lipomyces, Mastigomyces, Myxozyma, Pichia, Rhodospondium, Rhodotorula, Spondiobolus, Sporobolomyces, Trichosporon, Wingea, or Yarrowta.
Moreover, in the processes, the yeast cell can be of one of the following exemplary species: Arxula ademmvorans, Arxula terrestns, Brettanomyces bruxellensis, Brettanomyces naardenensis, Brettanomyces anomalus, Brettanomyces species (e g.NCYC 3151J, Bullera dendrophila, Bulleromyces albus, Candida albicans, Candida fabiann, Candida plabrata, Candida haemulomi, Candida intermedia, Candida magnoliaeCandida parapsilosis, Candida rugosa, Candida tenuis, Candida tropicalis, Candida famata, Candida kruisei, Candida sp (new) rel to C. sorbophila, Cryptococcus albidus, Cryptococcus amylolentus, Cryptococcus bhutanensis, Cryptococcus curvatus, Cryptococcus gastricus, Cryptococcus humicola, Cryptococcus hungancus, Cryptococcus laurentii, Cryptococcus luteolus, Cryptococcus macerans, Cryptococcus podzoticus, Cryptococcus terreus, Cryptococcus macerans, Debaryomyces hansenii, Dekkera anomala, Exophiala dermatitidis, Geotrichum species (e.g UOFS Y-0111), Hormonema species (e.g. NCYC 3171), Issatchenkia occidentals, Kluyveromyces marxianus, Lipomyces species (e.g.UOFS Y-2159), Lipomyces tetrasporus, Mastigomyces philipporn, Myxozyma melibiosi, Pichia anomala, Pichia fmlandica, Pichia guillermondu, Pichia haplophila, Rhodospondium lusitaniae, Rhodosporidtum paludigenum, Rhodospondium sphaerocarpum, Rhodospondium toruloides, Rhodospondium paludigenum, Rhodotorula araucanae, Rhodotorula glutims, Rhodotorula minuta, Rhodotorula minuta var minuta, Rhodotorula mucilaginosa, Rhodotorula philyla, Rhodotorula rubra, Rhodotorula species (eg. UOFS Y-2042), Rhodotorula species (e.g. UOFS Y-0448), Rhodotorula species (e.g NCYC 3193), Rhodotorula species (e.g. UOFS Y-0139), Rhodotorula secies (e.g. UOFS Y-0560), Rhodotorula aurantiaca, Rhodotorula species (e.g. NCYC 3224), Rhodotorula sp "mucilaginosa", Sporidiobolus salmonicolor, Sporobolomyces holsaticus, Sporobolomyces roseus, Sporobolomyces tsugae, Tnchosporon beigeln, Trichosporon cutaneum var cutaneum, Tnchosporon delbrueckii, Trichosporon jirovecii, Trichosporon mucoides, Trichosporon ovoides, Trichosporon
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puilulans, Tnchosporon species (e.g. UOFS Y-0861), Tnchosporon species (e.g. UOFS Y-1615), Tnchosporon species (e.g. UOFS Y-0451), Tnchosporon species (e.g NCYC 3212), Tnchosporon species (eg UOFS Y-0449;, Tnchosporon species (e.g NCYC 3211), Tnchosporon species (e.g UOFS Y-2113), Tnchosporon species (eg NCYC 3210), Tnchosporon monihiforme, Tnchosporon montevideense, Wmgea robertsiae, or Yarrowia iipolytica
The yeast cell can also be of any of the other genera, species, or strains disclosed herein.
Another aspect of the invention is a method for producing a polypeptide, which process includes the steps of: providing a cell comprising a nucleic acid encoding and capable of expressing a polypeptide that has enantioselective 2,2-disubstituted epoxide hydrolase activity, culturing the cell; and recovering the polypeptide from the culture. Recovering the polypeptide from the culture includes, for example, recovering it from the medium in which the cell was cultured or recovering it from the cell per se The cell can be a yeast cell. The polypeptide can be encoded by an endogenous gene of the cell or the cell can be a recombinant cell, the polypeptide being encoded by a nucleic acid sequence with which the cell is transformed. The nucleic acid sequence can be an exogenous nucleic acid sequence, a heterologous nucleic acid sequence, or a homologous nucleic acid sequence The polypeptide can be a full-length yeast epoxide hydrolase or a functional fragment of a full-length yeast epoxide hydrolase. The cell can be of any of the yeast genera, species, or strains disclosed herein or any recombinant cell disclosed herein.
The invention also features a crude or pure enzyme preparation which includes an isolated polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity - The polypeptide can be one encoded by any of the yeast genera, species, or strains disclosed herein or one encoded by a recombinant cell.
In another aspect, the invention features a substantially pure culture of cells, a substantial number of which comprise a nucleic acid encoding, and are capable of expressing, a polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity. The cells can be recombinant cells or cells of any of the yeast genera, species, or strains disclosed herein
Another embodiment of the invention is an isolated cell, the cell comprising a nucleic acid encoding a polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity, the cell being capable of expressing the polypeptide The cell can be any of those disclosed
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herein
The invention also features an isolated DNA that includes (a) a nucleic acid sequence that encodes a polypeptide that has enantioselective 2,2 disubstituted epoxide hydrolase activity and that hybridizes under highly stringent conditions to the complement of a sequence that can be SEQ ID NO 8, 9, 10, 11, 12, 13, or 14; or (b) the complement of the nucleic acid sequence. The nucleic acid sequence can encode a polypeptide that includes an amino acid sequence that can be SEQ ID NO 1, 2, 3, 4, 5, 6, or 7 The nucleic acid sequence can be, for example, one of those with SEQ ID NOs" 8, 9, 10, 11, 12, 13, or 14
Also provided by the invention is an isolated DNA that includes (a) a nucleic acid sequence that is at least 55% identical to a sequence that can be SEQ ID NO: 8, 9, 10, 11, 12, 13, or 14; or (b) the complement of the nucleic acid sequence, the nucleic acid sequence encoding a polypeptide that has enantioselective 2,2-disubstituted epoxide hydrolase activity.
Another aspect of the invention is an isolated DNA that includes, (a) a nucleic acid sequence that encodes a polypeptide consisting of an ammo acid sequence that is at least 55% identical to a sequence that can be SEQ ID NOs- 1,2,3, 4, 5, 6, or 7, or (b) the complement of the nucleic acid sequence, -the polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity.
Also included are vectors (e.g., those tn which the coding sequence is operably linked to a transcnptional regulatory element) containing any of the above DNAs and cells (eg., eukaryotic or prokaryotic cells) containing such vectors
Also provided by the invention is an isolated polypeptide encoded by any of the above DNAs. The polypeptide can include an amino acid sequence that is at least 55% identical to SEQ ID NOs: 1, 2, 3, 4, 5, 6 or 7, the polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity. The polypeptide can also include: (a) a sequence that can be SEQ ID NO: 1, 2, 3, 4, 5, 6, or 7, or a functional fragment of the sequence; or (b) the sequence of (a), but with no more than five conservative substitutions, the polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity
In another embodiment the invention features an isolated antibody (e g., a polyclonal or a monoclonal antibody) that binds to any of the above-described polypeptides.
The term "exogenous" as used herein with reference to nucleic acid and a particular host cell
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refers to any nucleic acid that does not occur in (and cannot be obtained from) that particular cell as found in nature Thus, a non-naturally-occurring nucleic acid is considered to be exogenous to a host cell once introduced into the host cell. It is important to note that non-naturally-occurring nucleic acids can contain nucleic acid subsequences or fragments of nucleic acid sequences that are found in nature provided the nucleic acid as a whole does not exist in nature. For example, a nucleic acid molecule containing a genomic DNA sequence within an expression vector is non-natu rally-occurring nucleic acid, and thus is exogenous to a host cell once introduced into the host cell, since that nucleic acid molecule as a whole (genomic DNA plus vector DNA) does not exist in nature Thus, any vector, autonomously replicating plasmid, or virus (e g., retrovirus, adenovirus, or herpes virus) that as a whole does not exist in nature is considered to be non-naturally-occurring nucleic acid. It follows that genomic DNA fragments produced by PCR or restriction endonuclease treatment as well as cDNAs are considered to be non-naturally-occurring nucleic acid since they exist as separate molecules not found in nature It also follows that any nucleic acid containing a promoter sequence and polypeptide-encoding sequence (e.g , cDNA or genomic DNA) in an arrangement not found in nature is non-naturally-occurring nucleic acid. Nucleic acid that is naturally-occurring can be exogenous to a particular cell. For example, an entire chromosome isolated from a cell of yeast x is an exogenous nucleic acid with respect to a cell of yeast y once that chromosome is introduced into a cell of yeast y It will be clear from the above that "exogenous" nucleic acids can be "homologous" or "heterologous" nucleic acids. As used herein, "homologous" nucleic acids are those that are derived from a cell of the same species as the host cell and "heterologous" nucleic acids are those that are derived from a species other than that of the host cell.
In contrast, the term "endogenous" as used herein with reference to nucleic acids or genes and a particular cell refers to any nucleic acid or gene that does occur in (and can be obtained from) that particular cell as found in nature
The alkyl group can be a straight chain or branched alkyl group with 1 to 12 carbon atoms The alkyl group can be selected from the group consisting of. methyl-; ethyl-; propyl-; isopropyl-; butyl-; isobutyl-; s-buty!-; t-butyl-; pent-1-yl-; pent-2-yl-; pent-3-yl-; 2-methylbut-1 -yl-; 3-methylbut-1-yl-; 2-methylbut-2-yl-; 3-methylbut-2-yl-, hex-1-yl-; hex-2-yl-, hex-3-yl-, 1-methylpent-1-y!-; 2-methylpent-1-yl-; 3-methylpent-1-yl-; 2-methylpent-2-yl-; 3-methylpent-2-yl-, 4-methylpent-2-yl-; 2-methylpent-3-yl-, 3-methylpent-3-yl-, 2-ethylbut-1-yl-, hept-1-yl-; hept-2-yl-; hept-3-yl-, hept-4-yl-; 1-methylhex-1-yl-, 2-methylhex-1-yl-, 3-methylhex-1-yl-, 4-methylhex-1-yl-, 5-methylhex-1-yl-, 2-methylhex-2-yl-, 3-methylhex-2-yl-; 4-rn ethyl hex-2-yl-;
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5-methylhex-2-yh 2-methylhex-3-yl-; 3-methylhex-3-yl-, 4-methylhex-3-yl-; 5-methylhex-3-yl-; 2-methylhex-4-yl-; 1,1-dimethylpent-1-yl-; 1,2-dimethylpent-1-yl-, 1,3-dimethylpenM-yl-, 1,4-dimethylpent-1-yl-; 2,2-dimethylpent-1-yl-; 2,3-dimethylpent-1-yl-, 2,4-dimethylpenM-yl-, 2,5-dimethylpent-1-yl-, 3,3-dimethylpent-1-yl-, 3,4-dimethylpent-1-yl-, 3,5-dimethylpent-1-yl-, 4,4-dimethylpent-1-yl-, 4,5-dimethylpent-1-yl-; 5,5-dimethylpent-1-yl-; 2,2-dimethylpent-2-yl-; 2,3-dimethylpent-2-yl-, 2,4-dimethylpent-2-yl-; 3,3-dimethylpent-2-yl-; 3,4-dimethylpent-2-yl-; 212-dimethylpent-3-yl-; 2,3-dimethylpent-3-yl-; 2,4-dimethylpent-3-yl-; 2,2-dimethylpenM-yl-, 2-ethylpent-1-yl-, 3-ethylpenM-yl-; 1,1,2-tnmethylbut-i-yl-, 1,2,2-tnmethylbut-1-yl-, 1,2,3-trimethylbut-1-yl-; 2,2,3-trimethylbut-1-y!-; 2,3,3-trimethylbut-1-yl-; 2,3,3-but-2-yl-; 2-isopropylbut-1-yl-; 2-isopropylbut-^-yl-, oct-1-yl-, oct-2-yl-, oct-3-yl-; oct-4-yl-; 2-methylhept-1-yl-; 3-methylhept-1-yl-; 4-methy1hept-1-yl-, 5-methylhept-1-yl-, 6-methylhept-1-yl~, 2-methylhept-2-yl-; 3-methylhept-2-yl-; 4-methylhept-2-yl-; 5-methylhept-2-yl-; 6-methylhept-2-yl-; 2-methylhept-3-yl-; 3-methylhept-3-yl-; 4-methylhept-3-yl-; 5-methylhept-3-yl-; 6-methylhept-3-yl-, 2-methylhept-4-yl-; 3-methylhept-4-yl-, 4-methylhept-4-yl-, 2,2-dimethylhex-1-yl-; 2,3-dimethylhex-1-yl-; 2,4-dimethylhex-1-yl-, 2,5-dimethylhex-1-yl-, 3,3-dimethylhex-1-yl-, 3,4-dimethylhex-1-yl-, 3,5-dimethylhex-1-yl-, 4,4-dimethylhex-1-yl-; 4,5-dimethylhex-1-yl-; 5,5-dimethylhex-1-yh 2,3-dimethylhex-2-yls 2,4-dimethylhex-2-yl-; 2,5-dimethylhex-2-yl-; 3,3-dimethylhex-2-yl-, 3,4-dimethylhex-2-yls 3,5-dimethylhex-2-yl-; 4,4-dimethylhex-2-yl-; 4,5-dimethylhex-2-yl-; 5,5-dimethylhex-2-yl-; 2,2-dimethylhex-3-yl-, 2,3-dimethylhex-3-yl-, 2,4-dimethylhex-3-yl-; 2,5-dimethylhex-3-y!-; 3,3-dimethylhex-3-yl-; 3,4-dimethylhex-3-yl-, 3,5-dimethylhex-3-yl-; 4,4-dimethylhex-3-yl-; 4,5-dimethylhex-3-yl-, 5,5-dimethylhex-3-yl-; 2,2,3-trimethylpent-1~yl-, 2,2r4'-trimethylpent-1-yl-; 2,3,3-trimethylpent-i-yl-, 2,3,4-tnmethylpent-1-yl-, 3,3,4-trimethy!pent-1-yI~; 3,4,4-trimethylpent-1-yl-, 2,4,4-trimethylpent-i-yl-; 2,3,3-tnmethylpent-2-yl-, 2,3,4-tnmethylpent-2-yl-; 3,3,4-trimethylpent-2-yl-; 3,4,4-trimethylpent-2-yl-; 2,4,4-trimethylpent-2-yl-; 2,2,3-tnmethylpent-3-yl-; 2-methyl-3-ethylpen-1 -. yl-; 3-ethy!-3-methylpent-1-yl-, 3-ethyl-4-methylpent-1-yI-; (3-methylhex-3-yl)methyl-; (4-methylhex-3-yl)methyl-; (5-methy!hex-3-yl)methyl-; (2-methylhex-2-yl)methyl-; 2-methyl-3-ethylpent-2-yl-; 3-ethyl-3-methylpent-2-yl-; 3-ethyl-4-methy1pent-2-yl-, 2-methyl-2-ethylpent-3-yl-; 2-methyl-3-ethylpent-3-yl-, 2,2,3,3-tetramethylbut-1-yl-, 2-ethyl-3,3-dimethylbut-2-yl-; 2-isopropyl-3-methylbut-2-yl-; (3-ethylpent-3-yl)methyl-; (2,3-dimethylpent-3-yl)methyl-; (2,4-dimethylpent-3-yl)methyl-, non-1-yl-; non-2-yl-; non-3-yl-; non-4-yl-; non-5-yl-; 2-methyloct-1-yl; 3-methyloct-1-yl-, 4-methylocM-yl-, 5-methyloct-1-yl-; 6-methyloct-1-yl-, 7-methyloct-1-yl-; 2-methyloct-2-yl, 3-methyl oct-2-yl-; 4-methyl oct-2-yl-; 5-methyloct-2-yl-; 6-methyloct-2-yl-, 7-methyloct-2-yl-; 2-methyloct-3-yl; -3-methyloct-3-y!-; 4-methyloct-3-y!-; 5-methyloct-3-yl-; 6-methyloct-3-yl-; 7-methyIoct-3-y!-, 2-methyloct-4-yl, 3-methyloct-4-yl-, 4-methyloct-4-yl-; 5-methyloct-4-yl-; 6-methyloct-4-yl-, 7-methyloct-4-yl-, 2,2-dimethylhept-1-yl-; 2,3-
9

dimethylhept-1-yl-; 2,4-dimethylhept-1-yl-; 2,5-dimethylhept-i-yK 2,6-dimethylhept-1-yl-; 3,3-dimethylhept-1-yh 3,4-dimethylhepM-yl-; 3,5-dimethylhept-1-yl-; 3,6-dimethylhepM-yl-, 4,4-dimethylhept-1-yl-; 4,5-dimethyfhept-1-yl-, 4,6-dimethylhept-1-yl-, 5,5-dimethylhept-1-yl-, 5,6-dimethylhept-1-yl-; 6,6-dimethylhept-1-yl-, 2,3-dimethylhept-2-yI-, 2,4-dimethylhept-2-yl-; 2,5-dimethylhept-2-yl-; 2,6-dimethylhept-2-yl-, 3,3-dimethylhept-2-yl-, 3,4-dimethylhept-2-yl-, 3,5-dimethylhept-2-yl-; 3,6-dimethylhept-2-yI-, 4,4-dimethylHept-2-yl-, 4,5-dimethylhept-2-yi-; 4,6-dimethylhept-2-yl-, 5,5-dimethylhept-2-yl-, 5,6-dimethylhept-2-yl-, 6,6-dimethylhept-2-yl-, 2,2-dimethylhept-3-yl-; 2,3-dimethylhept-3-yl-; 2,4-dimethylhept-3-y!-; 2,5-dimethylhept-3-yl-; 2,6-dimethylhept-3-yl-; 3,4-dimethylhept-3-yl-; 3,5-dimethyihept-3-yl-, 3,6-dimethylhept-3-yl-, 4,4-dimethylhept-3-yl-; 4,5-dimethylhept-3-yl-, 4,6-dimethylhept-3-yl-, 5,5-dimethylhept-3-yl-; 5,6-dimethylhept-3-yl-; 6,6-dimethylhept-3-yl-, 3-ethylhept-1-yl-, 3-ethylhept-1-yl-; 4-ethylhept-1-yl-; 3-ethylhept-2-yl-, 4-ethylhept-2-yl-, 5-ethylhept-2-yl-, 3-ethylhept-3-yl-; 4-ethylhept-3-yl-; 5-ethylhept~3-yl-, 3-ethylhept-4-y!-, 4-ethylhept-4-yl-; 2,2,3-trimethylhex-1-yl-; 2,2,4-trimethylhex-1-yl-, 2,2,5-trimethylhex-1-yi-; 2,3,3-trimethylhex-1-yl-, 2,3,4-trimethylhex-1-yl-, 2,3,5-trimethylhex-1-yl-, 2,4,4-tnmethylhex-1-yl-; 2,4,5-trimethylhex-1-yl-, 2,5,5-tnmethylhex-1-yl-, 3,3,4-tnmethylhex-1-yl-, 3,3,5-trimethylhex-i-y!-, 4,4,5-trimethylhex-1-yl-, 4,5,5-trimethylhex-1-yl-; 2,3,3-tnmethylhex-2-yl-; 2,3,4-tnmethylhex-2-yl-, 2,3,5-trimethylhex-2-yl-, 2,4,4-trimethyihex-2-yl-; 2,4,5-tnm6thylhex-2-yl-; 2,5,5-tnmethylhex-2-yl-; 3,3,4-trimethylhex-2-yl-, 3,3,5-trimethylhex-2-yl-; 3,4,4-trimethylhex-2-yl-; 3,4,5-tnmethylhex-2-yl-; 3,5,5-trimethylhex-2-yl-; 4,4,5-trimethylhex-2-yl-; 4,5,5-trimethylhex-2-yl-; 2,2,3-trimethylhex-3-yl-, 2,2,4-tnmethylhex-3-yl-; 2,2,5-trimethy!hex-3-yl-; 2,3,4-trimethylhex-3-y!-; 2,3,5-trimethylhex-3-yl-; 2,4,4-trimethylhex-3-yl-, 2,4,5-trimethylhex-3-yl-, 2,5,5-trimethylhex-3-yl-, 4,4,5-trimethylhex-3-yI-, 4,5,5-trimethylhex-3-yl-; (2-methylhex-3-yl)methyl-; 3-ethyl-2-methylhex-1-yl-; 3-ethyl-3-methylhex-1-yl-; 3-ethyl-4-methylhex-1-yl-, 3-ethyl-5-methylhex-1-yl-; 4-ethyl-2-methylhex-1-yl-; 4-ethyl-3-methylhex-1-yl-; 4-ethyl-4-methylhex-1-yl-; 4-ethyl-5-methylhex-1-yl-; {2-methylhex-1-yl)methyl-, (3-methylhex-1-yl)methyl-; (4-methylhex-1-yl)methyl-, (5-methylhex-1-yl)methyl-; (6-methylhex-1-yl)methyl-; 3-isopropylhex-1-yl-; 4-ethyl-5-methylhex-1-yl-; 3-ethyl-3-methylhex-2-yl-, 3-ethyl-4-methylhex-2-yl-, 3-ethyl-5-methylhex-2-yl-; 4-ethyl-2-methylhex-2-yl-; 4-ethyl-3-methylhex-2-yl-; 4-ethyl-4-methylhex-2-yl-; 4-ethyl-5-methylhex-2-yl-; 3-isopropylhex-2-yl-; 4-ethyl-5-methylhex-2-yl-, 3-ethyl-2-methylhex-3-yl-; 3-ethyl-4-methylhex-3-yl-; 3-ethyl-5-m ethyl hex-3-yl-; 4-ethyl-2-methylhex-3-yl-, 4-ethyl-3-methy!hex-3-yl-; 4-ethyl-4-methylhex-3-yl-; 4-ethyl-5-methylhex-3-yl-; 4-isopropylhex-1-yl-; 2,2,3,3-tetramethylpent-1-yl-, 2,2,3,4-tetramethylpent-1-yl-, 2,2,4,4-tetramethylpent-1-yl-, 2,3,3,4-tetramethylpent-1-yl-; 2,3,4,4-tetramethylpent-1-yl-, 2,3,4,4-tetramethylpent-1-yl-; 3,3,4,4-tetramethylpent-1-yl-, 2,3,3,4-tetramethylpent-2-yl-, 2,3,4,4-tetramethy!pent-2-yl-; 2,3,4,4-tetramethylpent-2-yl-, 3,3,4,4-tetramethylpent-2-yl-; 2,2,3,4-tetramethylpent-3-yl-; 2,2,4,4-
10

tetramethylpent-3-yl-, 2,3,4,4-tetramethylpent-3-yl-, 2,3,4,4-tetramethylpent-3-yl-; (3-ethylhex-3-yl)methyh (4-ethylhex-3-yl)methyh (5-methylhept-3-yl)methyl-; 2,4-dimethyl-3-ethylpent-1-yl-, 3,4-dimethyl-3-ethylpent-1-yl-; 4,4-dimethyl-3-ethytpent-1-yl-, 2-ethyl-2-methylhex-1-yl-, 3-ethyl-2-methylhex-1-yl-; 4-ethyl-2-methylhex-1-yl-, 2-ethyl-3-methylhex-1-yl-; 2-ethyl-4-methylhex-1-yl-; 3-ethyl-3-methylhex-1-y!-, 3-ethyl-4-methylhex-1-yl-, 3-ethyl-5-methylhex-1-yl-, 4-ethyl-3-methylhex-1-yl-; 4-ethyl-4-methylhex-1-yl-; 4-ethyl-5-methylhex-1-yl-; and the like from dec-1-yl-; dec-2-yl-, dec-3-yl-; dec-4-yl-; dec-5-yl-, dec-6-yl-; undec-1-yl-; undec-2-yl-, undec-3-yl-; undec-4-yl-, undec-5-yl-, undec-6-yl-, undec-7-yl-; dodec-1-yl; dodec-2-yl; dodec-3-yl, dodec-4-yl; dodec-5-yl, dodec-6-yl groups. Preferably, the alkyl group is a straight chain or branched alkyl group with 1 to 8 carbon atoms.
The alkenyl group can be a straight chain or branched alkenyl group having 2-12 carbon atoms. The alkenyl group can be selected from the group consisting of vinyl-; allyl-; a-methallyl-, p-methallyl-, 1-propenyl-, isopropenyl-; 1-butenyl-, 2-butenyl-; 3-butenyl, 1-buten-2-yl-, 1-buten-3-yl-, 1-methyl-1-propenyl-, 2-methyl-1-propenyl-; 1-pentenyl-; 2-pentenyl-; 3-pentenyl-, 4-pentenyl-, 1-penten-2-yl-; 1-penten-3-yl-; 2-methyl-1-butenyl-; 1-hexenyl-; 2-hexenyl-; 3-hexenyl-, 4-hexenyl-, 5-hexenyl-; 1 -heptenyl-, 2-heptenyl-; 3-heptenyl-; 4-heptenyl-, 5-heptenyl-, 6-heptenyl-; 1-octenyl-; 2-octenyl-, 3-octenyl-; 4-octenyl-, 5-octenyl-; 6-octenyl-, 7-octenyl-, 1-nonenyl-, 2-nonenyl-; 3-nonenyl-; 4-nonenyl-, 5-nonenyl-, 6-nonenyl-; 7-nonenyl-; 8-nonenyl-; 1-decenyl-; 2-decenyl-; 3-decenyl-; 4-decenyl-; 5-decenyl-; 6-decenyl-; 7-decenyl-; 8-decenyl-; 9-decenyl-, 1-undecenyl; 2-undecenyl; 3-undecen'yl; 4-undecenyl; 5-undecenyl; 6-undecenyl; 7-undecenyl; 8-undecenyl, 9-undecenyl; 10-undecenyl; 1-dodecenyl, 2-dodecenyl; 3-dodecenyl; 4-dodecenyl; 5-dodecenyl, 6-dodecenyl; 7-dodecenyl, 8-dodecenyl; 9-dodecenyl; 10-dodecenyl, 11-dodecenyl groups; and related branched isomers Preferably, the group is a straight chain or branched alkenyl group with 2 to 8 carbon atoms.
The alkynyl group can a straight chain or branched alkynyl group having 2-12 carbon atoms. The alkynyl group can be selected from the group consisting of. ethynyl-; 1-propynyl-; 2-propynyl-; 1-butynyl-; 2-butynyl-; 3-butynyl-; 1-pentynyl-; 2-pentynyl-, 3-pentynyl-; 4-pentynyl-, 1-hexynyl-; 2-hexynyl-, 3-hexynyl-; 4-hexynyl-; 5-hexynyl-; 1-heptynyl-, 2-heptynyl-; 3-heptynyl-; 4-heptynyl-, 5-heptynyl-, 6-heptynyl-; 1-octynyl-; 2-octynyl-; 3-octynyl-; 4-octynyl-; 5-octynyl-; 6-octynyl-; 7-octynyl-; 1-nonynyl-; 2-nonynyl-; 3-nonynyl-; 4-nonynyl-; 5-nonynyl-; 6-nonynyl-; 7-nonynyl-; 8-nonynyl-; 1-decynyl-; 2-decynyl-; 3-decynyl-, 4-decynyl-, 5-decynyl-, 6-decynyl-, 7-decynyl-; 8-decynyt-, 9-decynyl-, 1-undecynyl-; 2-undecynyl-; 3-undecynyl-; 4-undecynyl-, 5-undecynyl-, 6-undecyny!-; 7-undecynyI-; 8-undecynyl-; 9-
11

undecynyl-, 10-undecynyh 1-dodecynyl-, 2-dodecynyl-, 3-dodecynyl-; 4-dodecynyl-; 5-dodecynyl-, 6-dodecynyl-; 7-dodecynyl-, 8-dodecynyl-, 9-dodecynyl-, 10-dodecynyh 11-dodecynyl- groups, and related branched isomers Preferably, the alkynyl group is a straight chain or branched alkenyl group with 2 to 8 carbon atoms
The cycloalkyl group can be cycloalkyl groups with 3 to 10 carbon atoms The cycloalkyl group can be selected from the group consisting of cyclopropyl-; cyclobutyl-, cyclopentyl-; cyclohexyl-; cycloheptyl-, and cyclooctyl- groups. These groups can be variably substituted at any position(s) around the ring. Preferably, the cycloalky! group is a cycloalkyl group with 5 to 7 carbon atoms.
The cycloalkenyl group can be cycloalkenyl groups with 3 to 10 carbon atoms The cycloalkenyl group can be selected from the group consisting of cyclobuteny!-, cyclopentenyl-; cyclohexenyl-, cycloheptenyh and cyclooctenyl- groups that can variably be substituted at any position(s) around the ring Preferably, the cycloalkenyl group is a cycloalkenyl group with 5 to 7 carbon atoms
The aryl group can be selected from the group consisting of phenyl; biphenyl; naphtyl; anthracenyl groups; and the like Preferably, the aryl group is a phenyl group.
The aryl alkyl group can be a group with 7 to 18 carbons The aryl alkyl group can be selected from the group consisting of: benzyl-, 1-methylbenzyl-; 2-phenylethyl-; 3-phenylpropyl-; 4-phenylbutyh 5-phenylpentyl-; 6-phenylhexyl-, 1-naphtylmethyl; and 2-(1-naphtyl)-ethyl groups; and the like. Preferably, the aryl alkyl group is an aryl alkyl group with 7 to 12 carbon atoms.
The heterocyclic group can include 5- to 10-membered heterocychc groups containing nitrogen, oxygen, or sulfur, The heterocyclic ring can be fused with a cyclic or aromatic ring having 3 to 7 carbon atoms such as benzene, cyclopropyl; cyclobutane; cyclopentane, and cyclohexane ring systems. Preferably, the heterocyclic ring has 5 or 6 carbon atoms. The heterocyclic ring can be selected from the group consisting of furyl-; dihydrofuranyl-; tetrahydrofuranyl-, dioxolanyl-, oxazolyl-; dihydrooxazolyl-; oxazolidinyl-; isoxazolyl-, dihydroisoxazolyl-, isoxazohdinyl-, oxathiolanyl-; thienyl-, tetrahydrothienyl-; dithiolanyl-; thiazolyl-, dihydrothiazolyl-; thiazohdinyl-, isothiazolyl-; dihydroisothiazolyl-; isothiazolidinyh pyrrolyl-; dihydropyrrolyl-; pyrrolidinyl-; pyrazolyl-; dihydropyrazolyl-; pyrazolidinyl-; imidazolyls dihydroimidazolyl-; imidazolidin/l-, triazolyl-; dihydrotriazolyl-; triazolidinyl-,
12

tetrazolyl-; dihydrotetrazolyl-, tetrazolidinyl-; pyridyl-; dihydropyridyl-, piperidinyl-, morpholinyl-, dioxanyl-; oxathianyl-, trioxanyl-; thiomorphoiinyl-; pyridazinyl-, dihydropyridazinyl-, tetra hydro pyridazinyl-; hexahydropyndazinyl-, pyrimidmyl-; dthydropynmadinyl-; tetrahydropyrimadinyl-, hexahydropynmadinyl-; pyrazinyl-; piperazinyl-, pyranyl-; dihydropyranyl-, tetrahydropyranyl-; thiopyranyl-, dihydrothiopyranyl-; tetrahydrothiopyranyl-, dithianyl-, purinyl-, pyrimidinyl-, pyrrolizinyl-, pyrrolizidinyl; indolyl-, dihydrotndolyl-; isoindolyl-; mdolizinyl-, indolizidtnyh quinolyl-, dihydroquinolyl-; tetrahydroquinolyl-; isoquinolyl-, dihydroquinolyl-, tetrahydroquinolyl-; quinolizmyl-, quinolizidmyl-, phenanthrolinyl-, chromenyl-, chromanyl-; isochromenyl-, isochromanyl-, benzofuranyl-; and carbazolyl- groups; and the like.
The alkoxy group can be a straight chain or branched alkoxy group having 2-12 carbon atoms such as methoxy, ethoxy; propyloxy; isopropyloxy; butyloxy; isobutyloxy; tert-butyloxy; pentyloxy, hexyloxy, heptyloxy; or octyloxy.
The alkenyloxy group can be a straight chain or branched alkenyloxy group having 2-12 carbon atoms. The alkenyloxy group can be selected from the group consisting of: ethynyloxy-; 1-propynyloxy-; 2-propynyloxy-, 1-butynyloxy-; 2-butynyloxy-; 3-butynyloxy-, 1-pentyny!oxy-, 2-pentynyloxy-; 3-pentynyloxy-, 4-pentynyloxy-, 1-hexynyloxy-; 2-hexynyloxy-, 3-hexynyloxy-, 4-hexynyloxy-, 5-hexynyloxy-; 1-heptynyloxy-; 2-heptynyloxy-, 3-heptynyloxy-; 4-heptynyloxy-; 5-heptynyloxy-, 6-heptynyloxy-, 1-octynyloxy-; 2-octynyloxy-; 3-octynyloxy-, 4-octyny!oxy-; 5-octynyloxy-; 6-octynyloxy-; 7-octynyloxy-; 1-nonynyloxy-; 2-nonynyloxy-, 3-nonynyl-oxy-; 4-nonynyloxy-; 5-nonynyloxy-; 6-nonynyloxy-; 7-nonynyloxy-, 8-nonynyloxy-; 1-decynyloxy-; 2-decynyloxy-; 3-decynyloxy-, 4-decynyloxy-, 5-decynyloxy-; 6-decynyloxy-; 7-decynyloxy-; 8-decynyloxy-; 9-decynyloxy-, 1-undecynyloxy-, 2-undecynyloxy-; 3-undecynyloxy-; 4-undecynyloxy-, 5-undecynyloxy-, 6-undecynyloxy-; 7-undecynyloxy-; 8-undecynyloxy-; 9-undecynyloxy-, 10-undecynyloxy-; 1-dodecynyloxy-, 2-dodecynyloxy-; 3-dodecynyloxy-; 4-dodecynyloxy-; 5-dodecyny!oxy-; 6-dodecynyloxy-, 7-dodecynyloxy-, 8-dodecynyloxy-, 9-dodecynyloxy-, 10-dodecynyloxy-; and 11-dodecynyloxy- groups; and related branched isomers. Preferably, the alkenyloxy group is a straight chain or branched alkenyloxy groups with 2 to 8 carbon atoms
The aryloxy group can be an aryloxy group, such as a phenoxy or naphtyloxy group (e.g.: phenoxy; 2-methylphenoxy; 3-methylphenoxy, 4-methylphenoxy; 2-allylphenoxy, 2-chloro phenoxy; 3-chlorophenoxy, 4-chloro phenoxy; 4-methoxy phenoxy, 2-allyloxyphenoxy, naphtyloxy; and the like). The group can optionally be substituted with an alkyl or alkenyl or
13

alkoxy group having 1 to 4 carbon atoms or halogens.
The aryl alkyloxy group can be benzyloxy or 2-phenylethyloxy.
The alkylamino group can be a straight chain or branched alkylamino group having 2-12 carbon atoms such as. methylamino, ethylamino; propylamino; isopropylamino; butylamino; isobutylamino; tert-butylamino, pentylammo; hexylamino; heptylamino, or octylammo
The alkenyl amino group can be a straight chain or branched alkenylamino group having 2-12 carbon atoms. The alkenyl ammo group can be selected from the group consisting of: ethynylamino-; 1-propynylamino-, 2-propynylamino-, 1-butynylamino-; 2-butynylamino-; 3-butynylammo-, 1-pentynylamino-; 2-pentynytamino-, 3-pentynylamino-, 4-pentynylamino-; 1-hexynylammo-, 2-hexyny!amino-, 3-hexynylamino-; 4-hexynylammo-; 5-hexynylammo-, 1-heptynylamino-, 2-heptynylamino-; 3-heptynylamino-; 4-heptynylamino-, 5-heptynylamino-; 6-heptynylamino-, 1-octynylamino-; 2-octynylamino-, 3-octynylamino-; 4-octynylamino-; 5-octynylamino-; 6-octynylamino-, 7-octynylamino-, 1-nonynylamino-, 2-nonynylammo-; 3-nonynyl-amino; 4-nonynylammo-; 5-nonynylammo-, 6-nonynylamino-, 7-nonynylamino-; 8-nonynylamino-; 1-decynylamino-;' 2-decynylamino-; 3-decynylamino-; 4-decynylamino-; 5-' decynylammo-, 6-decynylamino-; 7-decynylamino-( 8-decynylammo-, 9-decynylamino-; 1-undecynylamino-; 2-undecynylamino-; 3-undecynylamino-, 4-undecynylamino-; 5-undecynylamino-; 6-undecynylamino-; 7-undecynylamino-, 8-undecynylamino-; 9-undecynylamino-, 10-undecynylamino-, 1 -dodecynylamino-; 2-dodecynylamino-, 3-dodecynylamino-; 4-dodecynylammo-; 5-dodecynylamino-; 6-dodecynylamino-; 7-dodecynylamino-, 8-dodecynylamino-; 9-dodecynylamino-, 10-dodecynylamino-; and 11-dodecynylamino- groups; and related branched isomers. Preferably, the alkenyl ammo group is a straight chain or branched alkenylamino group with 2 to 8 carbon atoms
The arylamino group can be an arylamino group such as a phenylamino or naphtylammo group, optionally substituted with an alkyl or alkenyl or alkoxy group having 1 to 4 carbon atoms, or halogens. The arylamino group can be selected from the group consisting of. phenylamino, 2-methylphenylammo, 3-methylphenylamino, 4- methylphenylammo, 2-allylphenylamino; 2-chlorophenylamino; 3-chlorophenylamim, 4-chlorophenylamino; 4-methoxyphenylamino, 2-ally!oxyphenylamino; naphtylamino, and the like.
The arylalkylamino group can be benzylamino or 2-phenylethylamino.
14

The alkylthio group can be an alkylthio group having 1 to 8 carbon atoms The alkyithio group can be selected from the group consisting of methylthio; ethyithio, propylthio, butylthio; isobutylthio; and pentylthio
The aikenylthio group can be a straight chain or branched alkenytthio group having 1 to 8 carbon atoms The alkenytthio group can be selected from the group consisting of: ethynylthio-; 1-propynylthio-, 2-propynylthio-, 1-butynylthio-; 2-butynyIthio-; 3-butynyithio-, 1-pentynylathio-, 2-pentynylthio-; 3-pentynylthio-, 4-pentynylthio-; 1-hexynylthio-, 2-hexynylthio-; 3-hexynyIthio-; 4-hexynylthio-; 5-hexynylthio-, and the like.
The arylrthfo group can be an aikenylthio group having 1 to 8 carbon atoms such as a phenylthio or naphtyJthio group, which can optionally be substituted with an alkyl or alkenyl or alkoxy group having 1 to 4 carbon atoms; and also halogens, e.g • phenylthio; 2-methylphenylthio; 3-methylphenyIthio, 4- methylphenylthio, 2-aIIytphenyithio; 2-chlorophenylthio, 3-chlorophenylammi; 4-chlorophenylthio; 4-methoxyphenylthio; 2-allyloxyphenylthio, naphtylthio, and the like.
The arylalkylthio group can be an aikenylthio group having 1 to 8 carbon atoms such as a benzylthio- group or a 2-phenylethylthio-group
The alkoxycarbonyl group can be' methoxycarbonyl, ethoxycarbonyl, or the like.
The substituted or unsubstituted carbamoyl group can be; carbamoyl; rnethylcarbamoyl, dimethylcarbamoyl; diethylcarbamoyl; or the like
The acyl group can be an acyl group with 1 to 8 carbon atoms such as: formyl, acetyl; propionyl; or benzoyl groups; or the like
The alkyl, alkenyl, alkynyl, cycfoalkyl, aryl, aryf alkyl, heteroeyclic, alkoxy, alkenyloxy, aryloxy, aryl alkyloxy, alkytamino, alkenylarnino, aryJamirso, aryialkylamino, alkylthio, aikenylthio, aryithio, arylalkylthio, alkoxycarbonyl, substituted and unsubstituted carbamoyl and acyi groyps mentioned above can optionally be substituted Examples of substityents include: halogens (F; Cl, Br, I), hydroxyl groups, mercapto groups, carboxylates; nitre groups, cyano groups; substituted or unsubstituted amino groups {including arrtino, methylamino, dimethylamino, ethylamino, diethylamino, and various protected amines such as tert-butoxycarbonyl- and arylsulfonamido groups), alkoxy groups (having 1 to 8 carbon
15

atoms such as methoxy, ethoxy, propyloxy, isopropyloxy, butyloxy, isobutyloxy, tert-butyloxy, pentyloxy, hexyloxy, heptyloxy or octyloxy), alkenyloxy groups (having 2 to 8 carbon atoms such as a vinyloxy, allyloxy; 3-butenyloxy or 5-hexenyloxy), aryloxy groups (such as a phenoxy or naphtyloxy group which can be optionally substituted with an alky! or alkenyl or alkoxy group having 1 to 4 carbon atoms; and also halogens, e g., phenoxy, 2-methylphenoxy, 3-methylphenoxy, 4-m ethyl phenoxy, 2-allylphenoxy, 2-chlorophenoxy, 3-chlorophenoxy, 4-chlorophenoxy, 4-rnethoxyphenoxy, 2-allyloxyphenoxy, naphtyloxy, and the like); aryl alkyloxy groups (e g., benzyloxy and 2-phenylethyloxy); alkylthio groups (having 1 to 8 carbon atoms such as rhethylthio, ethytthio, propylthio, butylthio, isobutylthio, pentylthio), alkoxycarbonyl groups (e.g methoxycarbonyl, ethoxycarbonyl, and the like), substituted or unsubstituted carbamoyl group (e g carbamoyl, methylcarbamoyl, dimethylcarbamoyl, diethylcarbamoyl and the like), acyl groups (with 1 to 8 carbon atoms such as formyl, acetyl, propionyl, or benzoyl groups), and others.
The above-mentioned cycloalkyl, cycloalkenyl, aryl, aryl alkyl, heterocyclic, alkoxy, alkenyloxy, aryloxy, aryl alkyloxy, alkylthio, and alkoxycarbonyl groups can also be substituted with alkyl groups having 1 to 5 carbon atoms, alkenyl groups with 2 to 5 carbon atoms, or haloalkyl groups with 1 to 5 carbon atoms in addition to the substituents specified above.
The number of substituents can be one or more than one. The substituents can be the same or different.
The RT and R2 groups can be each, independently of each other, be a functional group. The functional group is selected from the group consisting of. halo, pseudohalo, hydroxyl, variably substituted mercapto, variably substituted sulfinyl, variably substituted sulfonyl, carboxylates, variably substituted amino, variably substituted amido, variably substituted ureido, variably substituted carbamoyl, and variably substituted urethano Pseudohalo is nitro, cyano, azido, cyanato, isocyanato, or isothiocyanato.
R1 and R2 together can also be present as a saturated or unsaturated optionally substituted carbocycle or a heterocycle having 5 to 12 carbon atoms, such as cyclopentane, cyclohexane; cyclohexene; cyclohexadiene; cycloheptane, cyclooctane; cyclononane, or cyclodecane
As used herein, a "variably substituted" group is a group that is unsubstituted or is
16

substituted with one or more, in another embodiment one to five, in another embodiment one, two or three, substituents
"Polypeptide" and "protein" are used interchangeably and mean any peptide-linked chain of amino acids, regardless of length or post-translational modification The invention also features yeast derived enantioselective 2,2-disubstituted epoxide hydrolase (YEDH) polypeptides with conservative substitutions. Conservative substitutions typically include substitutions within the following groups: glycine and alanine; valine, isoleucine, and leucine, aspartic acid and glutamic acid, asparagine, glutamine, serine and threonme, lysine, histidme and argmine, and phenylalanine and tyrosine
The term "isolated" polypeptide or peptide fragment, as used herein, refers to a polypeptide or a peptide fragment which either has no naturally-occurring counterpart or has been separated or purified from components which naturally accompany it, e g , microorganism cellular components such as yeast cell cellular components Typically, the polypeptide or peptide fragment is considered "isolated" when it is at least 70%, by dry weight, free from the proteins and other naturally-occurring organic molecules with which it is naturally associated. Preferably, a preparation of a polypeptide (or peptide fragment thereof) of the invention is at least 80%, more preferably at least 90%, and most preferably at least 99%, by dry weight, the polypeptide (or the peptide fragment thereof), respectively, of the invention. Thus, for example, a preparation of polypeptide x is at least 80%, more preferably at least 90%, and most preferably at least 99%, by dry weight, polypeptide x. Since a polypeptide that is chemically synthesized is, by its nature, separated from the components that naturally accompany it, the synthetic polypeptide is "isolated."
An isolated polypeptide (or peptide fragment) of the invention can be obtained, for example, by: extraction from a natural source (e g , from yeast cells), expression of a recombinant nucleic acid encoding the polypepttde; or chemical synthesis A polypeptide that is produced in a cellular system different from the source from which it naturally originates is "isolated," because it will necessarily be free of components which naturally accompany it The degree of isolation or purity can be measured by any appropriate method, e g., column chromatography, polyacrylamide gel electrophoresis, or HPLC analysis.
An "isolated DNA" is either (1) a DNA that contains sequence not identical to that of any naturally occurring sequence, or. (2), in the context of a DNA with a naturally-occurring sequence (e.g., a cDNA or genomic DNA), a DNA free of at least one of the genes that flank
17

the gene containing the DNA of interest in the genome of the organism in which the gene containing the DNA of interest naturally occurs. The term therefore includes a recombinant DNA incorporated into a vector, into an autonomously replicating plasmid or virus, or into the genomic DNA of a prokaryote or eukaryote The term also includes a separate molecule such as' a cDNA (e.g., SEQ ID NOs 8, 9, 10, 11, 12, 13, or 14) where the corresponding genomic DNA has introns and therefore a different sequence; a genomic fragment that lacks at least one of the flanking genes, a fragment of cDNA or genomic DNA produced by polymerase chain reaction (PCR) and that lacks at least one of the flanking genes; a restriction fragment that lacks at least one of the flanking genes; a DNA encoding a non-naturally occurring protein such as a fusion protein, mutein, or fragment of a given protein, and a nucleic acid which is a degenerate variant of a cDNA or a naturally occurring nucleic acid. In addition, it includes a recombirtant nucleotide sequence that is part of a hybrid gene, i.e., a gene encoding a non-naturally occurring fusion protein. Also included is a recombinant DNA that includes a portion of SEQ ID NOs: 8-14 It will be apparent from the foregoing that isolated DNA does not mean a DNA present among hundreds to millions of other DNA molecules within, for example, cDNA or genomic DNA libraries or genomic DNA restriction digests in, for example, a restriction digest reaction mixture or an electrophoretic gel slice.
As used herein, a "functional fragment" of a YEDH polypeptide is a fragment of the polypeptide that is shorter than the full-length polypeptide and has at least 20% (e.g., at least. 30%, 40%; 50%; 60%; 70%; 80%, 90%; 95%; 98%; 99%; 100%, or more) of the ability of the full-length polypeptide to enantioselectively hydrolyse a TDE of interest. Fragments of interest can be made by either recombinant, synthetic, or proteolytic digestive methods and tested for their ability to enantioselectively hydrolyse a TDE.
As used herein, "operably linked" means incorporated into a genetic construct so that an expression control sequence effectively controls expression of a coding sequence of interest.
Unless otherwise defined, all technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention pertains. In case of conflict, the present document, including definitions, will control Preferred methods and materials are described below, although methods and materials similar or equivalent to those described herein can be used in the practice or testing of the present invention All publications, patent applications, patents and other references
18

mentioned herein are incorporated by reference in their entirety. The materials, methods, and examples disclosed herein are illustrative only and not intended to be limiting
Other features and advantages of the invention, e.g., TDE and DVD substantially enriched for one optical enantiomer, will be apparent from the following description, from the drawings and from the claims.
The details of one or more embodiments of the invention are set forth in the accompanying drawings and the description below Other features, objects, and advantages of the invention will be apparent from the description and drawings, and from the claims.
DESCRIPTION OF DRAWINGS
Fig. 1 is schematic depiction of the reactions catalyzed by YEDH using racemic mixtures of two exemplary 2,2-disubstituted epoxides (of general formula (I)) and resulting in optically active epoxides and vicinal diols
Figs. 2A to 10B are line graphs showing the hydrolysis of (±)-2-methyl-1,2-e poxy heptane by the indicated yeast strains to produce optically active (S)-2-methyl-1,2-epoxyheptane and/or (R)-2-methyl-1,2-heptanediol. The A panel in each figure is a line graph showing the change in concentrations of the epoxide and diol enantiomers with time and the B panel in each figure is a line graph showing the enantiomeric excess of the epoxide and diol at different conversions.
Figs. 11A and 11B are line graphs showing the hydrolysis of (±)-2-methyl-1,2-epoxyheptane by the indicated yeast strain to produce optically active (R)-2-methyl-1,2-epoxyheptane and/or (S)-2-methyl-1,2-heptanediol. The A and B panels are as indicated for Figs. 2A to
10B
Figs. 12A and 12B are line graphs snowing the hydrolysis of (±)-2-methy|-3-phenyl-1,2-epoxypropane by the indicated yeast strain to produce optically active (S)-2-methyl-3-phenyl-1,2-epoxypropane and/or {R)-2-methyl-3-phenyl-1,2-propanediol. The A and B panels are as indicated for Figs. 2A to 10B
Figs 13A to 14B are line graphs showing the hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by the indicated yeast strains to produce optically active (R)-2-methyl-3-phenyl-1,2-e poxy propane and/or (S)-2-methyl-3-phenyl-1,2-propanediol The A and B panels are as indicated for Figs. 2A to 10B.
Fig. 15 is a line graph showing the hydrolysis of <±)-2-methyl-3-phenyl-1,2-epoxypropane by the indicated yeast cultivated in a 10 I fermenterto produce optically active (S)- 2-methyl-3-phenyl-1,2-epoxypropane and/or (R)-2--methyl-3-phenyl-1,2-propanediol. The graph shows
19

the change in concentrations of the epoxide and diol enantiomers with time
Figs 16, 17, and 18 are line graphs showing the hydrolysis of (±)-2-methyl-3-phenyl-1,2-
epoxypropane by yeast host strains transformed with vectors expressing YEDH from
selected wild type yeast strains to produce optically active (S)- 2-methyl-3-phenyl-1,2-
epoxypropane and/or (R)-2-methyl-3-phenyl-1,2-propanediol. The graphs show the change
in concentrations of the epoxide and diol enantiomers with time.
Figs. 19A and 19B are line graphs showing the hydrolysis of (±)-2-methyt-3-phenyl-1,2-
epoxypropane using whole cells (Fig. 19 A) and a crude enzyme preparation (Fig 19B)
obtained from the host Yarrowia lipolytica expressing the epoxide hydrolase derived from
Rhodotorula araucariae NCYC 3183 {YL 25 TsA). This experiment demonstrates that whole
cells or enzyme preparations can be used to catalyze the reactions.
Fig. 20 is a restriction map of the pYLHmA (plNA1291) expression vector The positions of
the hp4d promoter and LIP2 terminator and of unique restriction sites available for the
insertion of coding sequences are indicated.
Fig 21 is a restriction map of the pYLTsA (plNA3313) expression vector The positions of
the TEF promoter and LIP2 terminator and of unique restriction sites available for the
insertion of coding sequences are indicated.
Fig. 22 is a depiction of the amino acid sequence (SEQ ID NO 1) of a YEDH polypeptide
encoded by cDNA derived from a Rhodospondium toruloides strain (assigned accession no
NCYC 3181)
Fig 23 is a depiction of the amino acid sequence (SEQ ID NO 2) of a YEDH polypeptide
encoded by cDNA derived from a Rhodospondium toruloides strain (assigned identification
no. UOFSY-0471).
Fig. 24 is a depiction of the amino acid sequence (SEQ ID NO:3) of a YEDH polypeptide
encoded by cDNA derived from a Rhodotorula araucariae strain (assigned accession no.
NCYC 3183).
Fig 25 is a depiction of the amino acid sequence (SEQ ID NO.4) of a YEDH polypeptide
encoded by cDNA derived from a Cryptococcus curvatus strain (assigned accession no.
NCYC 3158).
Fig. 26 is a depiction of the ammo acid sequence (SEQ ID NO.5) of a YEDH polypeptide
encoded by cDNA derived from a Rhodospondium paludigenum (assigned accession no.
NCYC 3179)
Fig. 27 is a depiction of the ammo acid sequence (SEQ ID NO 6) of a YEDH polypeptide
encoded by cDNA derived from a Debaromyces hansenu (assigned accession no. NCYC
3167).
Fig. 28 is a depiction of the partial ammo acid sequence (SEQ ID NO'7) of a YEDH
20

polypeptide encoded by cDNA derived from a Rhodotorula minuta var. mmuta (assigned accession no. UOFS Y-0835)
Fig. 29 is a depiction of the nucleotide sequence (SEQ ID NO:8) of a YEDH polypeptide-encoding cDNA derived from a Rhodospondium toruloides strain (assigned accession no. NCYC3181).
Fig 30 is a depiction of the nucleotide sequence (SEQ ID NO 9) of a YEDH polypeptide-encoding cDNA derived from a Rhodospondium toruloides strain (assigned identification no. UOFSY-0471).
Fig. 31 is a depiction of the nucleotide sequence (SEQ ID NO.10) of a YEDH polypeptide-encoding cDNA derived from a Rhodotorula araucanae strain (assigned accession no. NCYC3183)
Fig. 32 is a depiction of the nucleotide sequence (SEQ ID NO 11) of a YEDH polypeptide-encoding cDNA derived from a Cryptococcus curvatus strain (assigned accession no. NCYC 3158).
Fig. 33 is a depiction of the nucleotide sequence (SEQ ID NO:12) of a YEDH polypeptide-encoding cDNA derived from a Rhodospondium paludigenum (assigned accession no NCYC 3179)
Fig. 34 is a depiction of the nucleotide sequence (SEQ ID NO 13) of a YEDH polypeptide-encoding cDNA derived from a Debaromyces hansenn (assigned accession no. NCYC 3167).
Fig. 35 is a depiction of the partial nucleotide sequence (SEQ ID NO:14) of a YEDH polypeptide-encoding cDNA derived from a Rhodotorula minuta var minuta (assigned accession no. UOFS Y-0835).
Fig. 36 is a table showing the homology at the amino acid level of the YEDH polypeptides with SEQ ID NOs: 1-6.
Fig 37 is a table showing the homology at the nucleotide level of YEDH-encoding cDNA molecules with SEQ ID NOs- 8-13
Fig. 38 is a depiction of the ammo acid sequences of eight enantioselective epoxide hydrolases aligned for maximum homology Also shown are consensus amino acids The sequences labeled #1, #46, #25, CarO54, and #692 correspond to SEQ ID NOs. 1-5 and the sequences labeled #23, Jen46-2 and # 777 correspond to enantioselective hydrolases catalyzing the hydrolysis of non-TDE epoxides . The consensus catalytic triad is composed .of a nucleophile, an acid and a base, the positions of which are indicated by N, A and B, respectively "HGXP" represents the region of the oxy-anion hole of the enzyme. "sxNxss" represents the genetic motif found in a/p-hydrolase fold enzymes. = homology, = identity of 75-100%; = identity of 50-75%;. = gap).
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DETAILED DESCRIPTION
Various aspects of the invention are described below. Nucleic Acid Molecules
The YEDH nucleic acid molecules of the invention can be cDNA, genomic DNA, synthetic DNA, or RNA, and can be double-stranded or single-stranded (i e , either a sense or an antisense strand) Segments of these molecules are also considered within the scope of the invention, and can be produced by, for example, the polymerase chain reaction (PCR) or generated by treatment with one or more restriction endonucleases A ribonucleic acid {RNA) molecule can be produced by in vitro transcription. Preferably, the nucleic acid molecules encode polypeptides that, regardless of length, are soluble under normal physiological conditions.
The nucleic acid molecules of the invention can contain naturally occurring sequences, or sequences that differ from those that occur naturally, but, due to the degeneracy of the genetic code, encode the same polypeptide (for example, one the polypeptides with SEQ ID NOS1 - 7). In addition, these nucleic acid molecules are not limited to coding sequences, e.g., they can include some or all of the non-coding sequences that lie upstream or downstream from a coding sequence.
The nucleic acid molecules of the invention can be synthesized (for example, by phosphoramidite-based synthesis) or obtained from a biological cell, such as the cell of a eukaryote (e.g., a mammal such as human or a mouse or a yeast such as any of the genera, species, and strains of yeast disclosed herein) or a prokarote (e.g., a bacterium such as Escherichia coli) The nucleic acids can be those of a yeast such as any of the genera, species, and strains of yeast disclosed herein. Combinations or modifications of the nucleotides within these types of nucleic acids are also encompassed.
In addition, the isolated nucleic acid molecules of the invention encompass segments that are not found as such in the natural state. Thus, the invention encompasses recombinant nucleic acid molecules (for example, isolated nucleic acid molecules encoding the
22

polypeptides of SEQ ID NOs 1- 7) incorporated into a vector (for example, a piasmid or viral vector) or into the genome of a heterologous cell (or the genome of a homologous cell, at a position other than the natural chromosomal location). Recombinant nucleic acid molecules and uses thereof are discussed further below
Techniques associated with detection or regulation of genes are well known to skilled artisans. Such techniques can be used, for example, to test for expression of a YEDH gene in a test cell (e g. a yeast cell) of interest
A YEDH family gene or protein can be identified based on its similarity to the relevant YEDH gene or protein, respectively. For example, the identification can be based on sequence ' identity. The invention features isolated nucleic acid molecules which are, or are at least 50% (e.g , at least 55%, 60%; 65%, 75%, 85%, 95%; 98%, or 99%) identical to: (a) a nucleic acid molecule that encodes the polypeptide of SEQ ID NOs: 1-7; (b) the nucleotide sequence of SEQ ID NOs: 8-14, (c) a nucleic acid molecule which includes a segment of at least 15 (e g , at least: 20; 25, 30; 35; 40; 50; 60; 80; 100, 125, 150, 175, 200; 250; 300; 350, 400; 500, 600; 700, 800; 900, 1,000; 1,100; 1,200; 1,220, 1,225; 1,228; 1,230; 1,231, 1,232; 1,233; 1,234, 1,235; or 1,236) nucleotides of SEQ ID NOs 8-14; (d) a nucleic acid molecule encoding any of the polypeptides or fragments thereof disclosed below; and (e) the complement of any of the above1 nucleic acid molecules The complements of the above molecules can be full-length complements or segment complements containing a segment of at least 15 (e.g., at least: 20, 25; 30, 35; 40, 50; 60; 80, 100; 125; 150; 175; 200; 250, 300; 350; 400, 500; 600; 700; 800, 900; 1,000, 1,100; 1,200, 1,220; 1,225; 1,228, 1,230; 1,231; 1,232; 1,233;' 1,234; 1,235, or 1,236) consecutive nucleotides complementary to any of the above nucleic acid molecules Identity can be over the full-length of SEQ ID NOs" 8-14 or over one or more contiguous or non-contiguous segments
The determination of percent identity between two sequences is accomplished using the mathematical algorithm of Karlin and Altschul, Proc Natl Acad. Sci. USA 90, 5873-5877, 1993. Such an algorithm is incorporated into the BLASTN and BLASTP programs of Altschul et al (1990) J. Mol Biol 215, 403-410. BLAST nucleotide searches are performed with the BLASTN program, score = 100, wordlength = 12, to obtain nucleotide sequences homologous to YEDH-encoding nucleic acids BLAST protein searches are performed with the BLASTP program, score = 50, wordlength = 3, to obtain amino acid sequences homologous to the YEDH polypeptide. To obtain gapped alignments for comparative purposes, Gapped BLAST is utilized as described in Altschul et al. (1997) Nucleic Acids
23

Res 25, 3389-3402 When utilizing BLAST and Gapped BLAST programs, the default parameters of the respective programs (e g , XBLAST and NBLAST) are used
Hybridization can also be used as a measure of homology between two nucleic acid sequences A YEDH-encoding nucleic acid sequence, or a portion thereof, can be used as a hybridization probe according to standard hybridization techniques The hybridization of a YEDH probe to DNA or RNA from a test source (e.g., a mammalian cell) is an indication of the presence of YEDH DNA or RNA in the test source Hybridization conditions are known to those skilled in the art and can be found in Current Protocols in Molecular Biology, John Wiley & Sons, N.Y., 6 3.1-6.3.6, 1991 Moderate hybridization conditions are defined as equivalent to hybridization in 2X sodium chloride/sodium citrate (SSC) at 30°C, followed by a wash in 1 X SSC, 0 1% SDS at 50°C Highly stringent conditions are defined as equivalent to hybridization in 6X sodium chloride/sodium citrate (SSC) at 45°C, followed by a wash in 0.2 X SSC, 0.1% SDS at 65°C
The invention also encompasses, (a) vectors (see below) that contain any of the foregoing YEDH coding sequences (including coding sequence segments) and/or their complements (that is, "antisense" sequences); (b) expression vectors that contain any of the foregoing YEDH coding sequences (including coding sequence segments) operably linked to one or more transcriptional and/or translational regulatory elements (TRE, examples of which are given below) necessary to direct expression of the coding sequences; (c) expression vectors encoding, in addition to a YEDH polypeptide (or a fragment thereof), a sequence unrelated to YEDH, such as a reporter, a marker, or a signal peptide fused to YEDH, and (d) genetically engineered host cells (see below) that contain any of the foregoing expression vectors and thereby express the nucleic acid molecules of the invention.
Recombinant nucleic acid molecules can contain a sequence encoding a YEDH polypeptide or a YEDH polypeptide having an heterologous signal sequence. The full length ,YEDH polypeptide, or a fragment thereof, can be fused to such heterologous signal sequences or to additional polypeptides, as described below. Similarly, the nucleic acid molecules of the invention can encode the mature form of a YEDH or a form that includes an exogenous polypeptide that facilitates secretion.
The TRE referred to above and further described below include but are not limited to inducible and non-inducible promoters, enhancers, operators and other elements that are known to those skilled in the art and that drive or otherwise regulate gene expression. Such
24

regulatory elements include but are not limited to the cytomegalovirus hCMV immediate early gene, the early or late promoters of SV40 adenovirus, the lac system, the trp system, the TAC system, the TRC system, the major operator and promoter regions of phage A, the control regions of fd coat protein, the promoter for 3-phosphoglycerate kinase, the promoters of acid phosphatase, and the promoters of the yeast a-mating factors. Other useful TRE are listed in the examples below
Similarly, the nucleic acid can form part of a hybrid gene encoding additional polypeptide sequences, for example, a sequence that functions as a marker or reporter. Examples of marker and reporter genes include ß-lactamase, chloramphenicol acetyltransferase (CAT), adenosine deaminase (ADA), aminoglycoside phosphotransferase (neor, G418r), dihydrofolate reductase (DHFR), hygromycin-B-phosphotransferase (HPH), thymidine kinase (TK), lacZ (encoding (3-galactosidase), and xanthine guanine phosphoribosyltransferase (XGPRT), and green, blue, or yellow fluorescent protein As with many of the standard procedures associated with the practice of the invention, skilled artisans will be aware of additional useful reagents, for example, additional sequences that can serve the function of a marker or reporter. Generally, the hybrid polypeptide will include a first portion and a second portion; the first portion being a YEDH polypeptide (or any of YEDH fragments described below) and the second portion being, for example, the reporter described above or an Ig heavy chain constant region or part of an Ig heavy chain constant region, e.g., the CH2 and CH3 domains of lgG2a heavy chain. Other hybrids could include an antigenic tag or a poly-His tag to facilitate purification
The expression systems that carVbe used for purposes of the invention include, but are not limited to, microorganisms such as yeasts (e.g. any of the genera, species or strains listed herein) or bacteria (for example, E colt and B subtilis) transformed with recombinant bactertophage DNA, plasmid DNA, or cosmid DNA expression vectors containing the nucleic acid molecules of the invention; yeast (for example, Saccharomyces, Kluyveromyces, Hansenula, Pichia, Yarrowia, Arxula, Candida, and other genera, species, and strains listed herein) transformed with recombinant yeast expression vectors containing the nucleic acid molecule of the invention; insect cell systems infected with recombinant virus expression vectors (for example, baculovirus) containing the nucleic acid molecule of the invention; plant cell systems infected with recombinant virus expression vectors (for example, cauliflower mosaic virus (CaMV) or tobacco mosaic virus (TMV)) or transformed with recombinant plasmid expression vectors {for example, Ti plasmid) containing a YEDH nucieotide sequence; or mammalian cell systems (for example, COS, CHO, BHK, 293,
25

VERO, HeLa, MDCK, WI38, and N1H 3T3 cells) harboring recombmant expression constructs containing promoters derived from the genome of mammalian cells (for example, the metallothionein promoter) or from mammalian viruses (for example, the adenovirus late promoter and the vaccinia virus 7.5K promoter) Also useful as host cells are primary or secondary cells obtained directly from a mammal and transfected with a plasmid vector or infected with a viral vector.
The invention includes wild-type and recombinant cells including, but not limited to, yeast cells (e.g., any of those disclosed herein) containing any of the above YEDH genes, nucleic acid molecules, and genetic constructs Other cells that can be used as host cells are listed herein. The cells are preferably isolated cells. As used herein, the term "isolated" as applied to a microorganism (e g , a yeast cell) refers to a microorganism which either has no naturally-occurring counterpart {e.g., a recombinant microorganism such as a recombinant yeast) or has been extracted and/or purified from an environment in which it naturally occurs Thus, an "isolated microorganism" does not include one residing in an environment in which it naturally occurs, for example, in the air, outer space, the ground, oceans, lakes, rivers, and streams and the like, ground at the bottom of oceans, lakes, rivers, and streams and the like, snow, ice on top of the ground or in/on oceans lakes, rivers, and streams and the like, man-made structures (e.g , buildings), or in natural hosts (e.g., plant, animal or microbial hosts) of the microorganism, unless the microorganism (or a progenitor of the microorganism) was previously extracted and or purified from an environment in which it naturally occurs and subsequently returned to such an environment or any other environment in which it can survive. An example of an isolated microorganism is one in a substantially pure culture of the microorganism.
Moreover the invention provides a substantially pure culture of a microorganism (e.g., a microbial cell such as a yeast cell. As used herein, a "substantially pure culture" of a microorganism is a culture of that microorganism in which less than about 40% (i.e., less than about : 35%, 30%; 25%, 20%; 15%, 10%, 5%; 2%; 1%; 0.5%; 0 25%; 0.1%; 0.01%; 0 001 %; 0 0001 %; or even less) of the total number of viable microbial cells (bacterial, fungal (including yeast), mycoplasmal, or protozoan cells) in the culture are viable microbial cells other than the microorganism. The term "about" in this context means that the relevant percentage can be 15% percent of the specified percentage above or below the specified percentage. Thus, for example, about 20% can be 17% to 23% Such a culture of microorganisms includes the microorganisms and a growth, storage, or transport medium. Media can be liquid, semi-solid (e g., gelatinous media), or frozen. The culture includes the
26

cells growing in the liquid or in/on the semi-solid medium or being stored or transported in a storage or transport medium, including a frozen storage or transport medium. The cultures are in a culture vessel or storage vessel or substrate (eg,a culture dish, flask, or tube or a storage vial or tube).
The microbial cells of the invention can be stored, for example, as frozen cell suspensions, e.g. in buffer containing a cryoprotectant such as glycerol or sucrose, as lyophilized cells. Alternatively, they can be stored, for example, as dried cell preparations obtained, e g., by fluidised bed drying or spray drying, or any other suitable drying method. Similarly the enzyme preparations can be frozen, lyophilised, or immobilized and stored under appropriate conditions to retain activity
Polypeptides and Polypeptide Fragments
The YEDH polypeptides of the invention include all the YEDH polypeptides and fragments of YEDH polypeptides disclosed herein They can be, for example, the polypeptides with SEQ ID NOs 1-7 and functional fragments of these polypeptides The polypeptides embraced by the invention also include fusion proteins that contain either full-length or a functional fragment of it fused to unrelated amino acid sequence The unrelated sequences can be additional functional domains or signal peptides.
The invention features isolated polypeptides which are, or are at least 50% (e.g., at least: 55%; 60%, 65%; 75%; 85%, 95%, 98%; or 99%) identical to the polypeptides with SEQ ID NOs. 1-7 The identity can be over the full-length of the latter polypeptides or over one or more contiguous or non-contiguous segments.
Fragments of YEDH polypeptides are segments of the full-length YEDH polypeptides that are shorter than full-length YEDH polypeptides. Fragments of YEDH polypeptides can contain 5-410 (eg., 10, 20, 30, 40, 50, 60, 70, 80, 90, 100, 120, 150, 250, 300, 350, 400, 405, 406, 407, 408, or 409) amino acids of SEQ ID NOs:1-7 Fragments of YEDH can be functional fragments or antigenic fragments
The polypeptides can be any of those described above but with not more 50 (e g., not more than 50, 45, 40, 35, 30, 25, 20, 17, 14, 12, 10, nine, eight, seven, six, five, four, three, two, or one) conservative substitution(s). Such substitutions can be made by, for example, site-directed mutagenesis or random mutagenesis of appropriate YEDH coding sequences.
27

"Functional fragments" of a YEDH polypeptide {and, optionally, any of the above-described YEDH polypeptide variants) have at least 20% (e.g., 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 98%, 99%, 100%, or more) of the ability of the full-length, wild-type YEDH polypeptide to enantioselectively hydrolyse a TDE of interest One of skill in the art will be able to predict YEDH functional fragments using his or her own knowledge and information provided herein, e.g., the amino acids alignments in Fig 38 showing highly conserved domains as well and residues required for function of epoxide hydrolase activity.
Fragments of interest can be made either by recombinant, synthetic, or proteolytic digestive methods and tested for their ability to enantioselectively hydrolyse a TDE.
Antigenic fragments of the polypeptides of the invention are fragments that can bind to an antibody. Methods of testing whether a fragment of interest can bind to an antibody are known in the art.
The polypeptides can be purified from natural sources (e g , wild-type or recombinant yeast cells such as any of those described herein) Smaller peptides (e.g , those less than about 100 ammo acids in length) can also be conveniently synthesized by standard chemical means. In addition, both polypeptides and peptides can be produced by standard in vitro recombinant DNA techniques and in vivo transgenesis, using nucleotide sequences encoding the appropriate polypeptides or peptides Methods well-known to those skilled in the art can be.used to construct expression vectors containing relevant coding sequences and appropriate transcriptional/translational control signals. See, for example, the techniques described in Sambrook et a/., Molecular Cloning. A Laboratory Manual (2nd Ed.) [Cold Spring Harbor Laboratory, NY, 1989], and Ausubel et a/., Current Protocols in Molecular Biology [Green Publishing Associates and Wiley Interscience, N.Y , 1989].
Polypeptides and fragments of the invention also include those described above, but modified by the addition, at the amino- and/or carboxyl-terminal ends, of a blocking agent to facilitate survival of the relevant polypeptide. This can be useful in those situations in which the peptide termini tend to be degraded by proteases. Such blocking agents can include, without limitation, additional related or unrelated peptide sequences that can be attached to the amino and/or carboxyl terminal residues of the peptide to be administered. This can be done either chemically during the synthesis of the peptide or by recombinant DNA technology by methods familiar to artisans of average skill.
28

Alternatively, blocking agents such as pyroglutamic acid or other molecules known in the art can be attached to the amino and/or carboxyl terminal residues, or the amino group at the amino terminus or carboxyl group at the carboxyl terminus can be replaced with a different moiety Likewise, the peptides can be covalently or noncovalently coupled to pharmaceutically acceptable "carrier" proteins prior to administration
Also of interest are peptidomimetic compounds that are designed based upon the amino acid sequences of the functional peptide fragments Peptidomimetic compounds are synthetic compounds having a three-dimensional conformation (i.e., a "peptide motif) that is substantially the same as the three-dimensional conformation of a selected peptide The peptide motif provides the peptidomimetic compound with the ability to enantioselectively hydrolyse a TDE of interest in a manner qualitatively identical to that of the YEDH functional fragment from which the peptidomimetic was derived. Peptidomimetic compounds can have additional characteristics that enhance their therapeutic utility, such as increased cell permeability and prolonged biological half-life
The peptidomimetics typically have a backbone that is partially or completely non-peptide, but with side groups that are identical to the side groups of the ammo acid residues that occur in the peptide on which the peptidomimetic is based. Several-types of chemical bonds, e.g , ester, thioester, thioamide, retroamide, reduced carbonyl, dimethylene and ketomethylene bonds, are known in the art to be generally useful substitutes for peptide bonds in the construction of protease-resistant peptidomimetics
The invention also provides compositions and preparations containing one or more (e.g., two, three, four, five, six, seven, eight, nine, ten, 12, 15, 20, 25, or more) of the above-described polypeptides, polypeptide variants, and polypeptide fragments. The composition or preparation can be, for example a crude cell (e.g., yeast cell) extract or culture supernatant, a crude enzyme preparation, a highly purified enzyme preparation The compositions and preparations .can also contain one or more of a variety of carriers or stabilizers known in the art Carriers and stabilizers are known in the art and include, for example, buffers, such as phosphate, citrate, and other non-organic acids, antioxidants such as ascorbic acid; low molecular weight (less than 10 residues) polypeptides; proteins such as serum albumin, gelatin or immunoglobulins, hydrophilic polymers such polyvinylpyrrolidone; amino acids such as glycine, glutamine, asparagme, argmine, or lysine; monosaccharides, disacchandes, and other carbohydrates including glucose, mannose, or
29

dextrans; chelating agents such as ethyl en ediami net etra acetic acid (EDTA); sugar alcohols such as mannitol, or sorbitol, salt-forming countenons such as sodium; and/or nonionic surfactants such as Tween, and Pluronics
Methods of Producing Optically Active Epoxides and Optically Active Vicinal Diols
The invention provides methods for obtaining enantiopure, or substantially enantiopure, optically active TDE and DVD. ^Enantiopure optically active TDE or DVD preparations are preparations containing one enantiomer of the TDE or DVD and none of the other enantiomer of the TDE or DVD "Substantially enantiopure" optically active TDE or DVD preparations are preparations containing at least 55% (e g , at least' 60%, 70%; 80%; 85%, ,90%; 95%, 97%; 98%, 99%, 99.5%; 99 8%, or 99 9%), relative to the total amount of both TDE or DVD enantiomers, of the particular enantiomer of the TDE or the DVD.
The method involves exposing a TDE enantiomeric mixture to a YEDH polypeptide, e.g., by culturing or incubating the mixtures with an isolated YEDH polypeptide or a cell (wild-type or recombinant) that expresses the polypeptide This exposure can have a variety of outcomes that depend on variables such as, without limitation, the YEDH itself, the chemical nature of the TDE, and, to a lesser extent, the reaction conditions
First, the YEDH polypeptide can catalyse the conversion of only one of the two TDE enantiomers in the mixture to its corresponding DVD enantiomer. Alternatively, it can catalyse the conversion of one of the two TDE enantiomers in the mixture to its corresponding DVD enantiomer at a much more rapid rate than the other TDE enantiomer to its corresponding DVD. YEDH with such selective activity are designated "enantioselective" and catalyse the "classical" kinetic resolution of a mixture of TDE enantiomers Such a YEDH polypeptide can catalyse, for example, the conversion of a (R)-TDE (in the TDE enantiomeric mixture) to its corresponding (R)-DVD. During such a reaction, the concentration of the selected TDE enantiomer decreases, the concentration of the unselected TDE remains constant or decreases at a much slower rate (i.e, the concentration of the unselected TDE increases relative to the concentration of the selected TDE in the mixture); the DVD corresponding to the selected TDE is produced, and,the DVD corresponding to the unselected TDE is not produced or is produced at a much lower rate than that the DVD corresponding to the selected TDE Examples of such reactions include those shown in Figs. 3, 6, 13, and 19. These reactions are of course useful for the enrichment, and hence the production, of a desired TDE enantiomer and/or the production of
30

a desired DVD enantiomer.
In addition, a YEDH polypeptide can catalyse, under certain defined reaction conditions, the conversion of both enantiomers of a TDE to a single DVD Such YEDH hydrolyse each TDE enantiomer with opposite regioselectivity (i e., the attack of water occurs at different carbons of the epoxide ring for each of the TDE enantiomers) and are termed "regiospecific" for each TDE enantiomer. Such YEDH are said to catalyse the "enantioconvergent" hydrolysis of a mixture of TDE enantiomers The YEDH can also have significant selectivity for one enantiomer of the TDE. Where the YEDH has such TDE enantiomeric selectivity, the DVD enantiomer produced has the same ch'irahty as the TDE for which the YEDH polypeptide is selective; for example, if the YEDH polypeptide is selective for an (S)-TDE enantiomer, the DVD enantiomer produced from both TDE enantiomers will be the (S)-DVD enantiomer. Examples of such reactions include those shown in Figs 9 and 11 During these reactions, there is a decrease in the concentrations of both TDE enantiomers (with the concentration of one decreasing faster than the other if the YDEH polypeptide has TDE enantiomeric selectivity) and the production of one DVD enantiomer. Such reactions are particularly useful for the production of a desired DVD enantiomer and, where the YEDH is significantly TDE enantioselective, they can also be useful for the enrichment and hence the production of a particular TDE enantiomer. The degree of the latter enrichment can be enhanced by, for example, stopping a reaction at a time when the concentration of the selected TDE has significantly decreased and that of the unselected TDE enantiomer is still relatively high.
In yet other reaction types, the YEDH polypeptide can catalyse, for example: (a) the conversion of one TDE enantiomer its corresponding DVD enantiomer and the other TDE enantiomer to both DVD enantiomers; or (b) the conversion of both TDE enantiomers to both DVD enantiomers. Naturally, such reactions, if the YEDH polypeptides employed have no enantioselectivity, would not be useful for the production of a desired TDE enantiomer or a desired DVD enantiomer On the other hand, where the YEDH polypeptide has significant selectivity for one TDE enantiomer, the reaction can be used for the production of: (a) the corresponding DVD enantiomer; and (b) the unselected TDE enantiomer. This can be done, as described above, by, e.g., stopping a reaction at a time, or at times, at which the concentration of the desired TDE enantiomer (relative to the total TDE concentration) and/or the concentration of the desired DVD enantiomer (relative to the total DVD concentration) are higher than those of the undesired TDE enantiomer and/or the undesired DVD enantiomer, respectively In situations where a YEDH polypeptide catalyses the conversion of one TDE enantiomer to both DVD enantiomers, advantage can also be taken of the fact
31

that generally the production of one DVD enantiomer (eg., one with the chirality corresponding to that of a selected TDE) is favored over the enantiomer.
A YEDH polypeptide useful for the invention is one that hydrolyses one enantiomer of a TDE, and/or effects the production of one enantiomer of a DVD, with less than 80% (e g., less than: 70%, 60%; 50%; 40%; 30%, 20%, 10%, 5%, 2 5%; 1%; 0 5%; 0 25%, 0,01%, or less), or even none, of the efficiency (as measured by reaction rate) with which it hydrolyses the other TDE enantiomer and/or effects the production of the other DVD enantiomer, respectively.
Useful concentrations of the TDE and conditions of incubation will vary from one YEDH polypeptide to another and from one TDE to another. Given the teachings of the working examples contained herein, one skilled in the art will know how to select working conditions for the production of a desired enantiomer of a desired DVD and/or TDE.
The method can be implemented by, for example, incubating (culturing) the TDE enantiomeric mixtures with a wild-type yeast cell or a recombinant cell (yeast or any other host species listed herein) containing a nucleic acid sequence (e g. a gene, or a recombinant nucleic acid sequence) encoding a YEDH, a crude extract from such cells, a semi-purified preparation of aYEDH polypeptide, or, for example an isolated YEDH polypeptide As used herein, "incubating and "culturing" include growing cells and maintaining them in a resting state
The strain of the yeast cell cari be selected from but are not limited to, the following exemplary genera* Arxula, Brettanomyces, Bullera, Bulleromyces, Candida, Cryptococcus, Debaryomyces, Dekkera, Exophiata, Geotnchum, Hormonema, Issatchenkia, Kluyveromyces, Lipomyces, Mastigomyces, Myxozyma, Pichia, Rhodosporidium, Rhodotorula, Spondiobolus, Sporobolomyces, Tnchosporon, Wtngea, and Yarrowia
Yeast strains innately capable of producing a polypeptide which converts or hydrolyses mixtures of TDE enantiomers to optically active (S)-TDE and/or (R)-DVD include the following exemplary yeast genera and species

Genus Species
Arxula A adeninivorans
Bullera - ;B. dendrophila
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Cryptococcus C albidus
*'C curvatus
C. macerans
C hungancus
C podzolicus
Rhodospondium R paludigenum
R sphaerocarpum
R toruloides
Rhodotorula R araucanae
R aurantiaca
R. giutinis
R species (e g. NCYC 3192, UOFS Y-2042)
Spondiobolus S. salmomcolor
Sporobolomyces : S roseus
s sp. "holsaticus"
s tsugae
Trichosporon T cutaneum var cutaneum
T jirovecn
T moniluforme
T. species (e g. NCYC 3210, NCYC 3211)
Yarrowia Y. lipolytica
Yeast species referred to in the chart above (and the one below) as "species" correspond to strains obtained from a culture collection, the species of which had not at the time of writing been identified.
Yeast strains innately capable of producing a polypeptide that converts or hydrolyses mixtures of epoxides to optically active (R)-epoxides and/or (S)-vicinal diols include the following exemplary genera and species"

Genus Species
Arxula A terrestris
Bullera B. dendrophila
Candida
C. magnoliae C. parapsilosis C rugosa
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C tenuis
C sp (new) nearest C. sorbophila
Cryptococcus C amylolentus
C curvatus
C laurentn
C luteolus
C macerans
Debaryomyces D hansenti
Lipomyces L species
Pichi P finlandica
P. guiliermondii
P haplophila
Rhodotorula R minuta
R mucilaginosa
Sporobolomyces S roseus
S tsugae
Tnchosporon T cutaneum var cutaneum
T. ovoides
Wingea W robertsiae
The yeast strain can be, for example, one selected from Tables 2 and 3 (see below)
Cultivation in bioreactors of wild-type or recombinant yeast strains expressing the polypeptide or fragment thereof having TDE enantioselective epoxide hydrolase activity (with the purpose of preparing yeasts stocks or for the enantioselective preparative methods of the invention) can be carried out under conditions that provide useful biomass and/or enzyme titer yields. Cultivation can be by batch, fed-batch or continuous culture methods. Useful cultivation conditions are dependent on the yeast strain used. General procedures for establishing useful culturing conditions of yeasts, fungi and bacteria in bioreactors are known to those skilled in the art The mixture of epoxides can be added directly to the culture The concentration of the TDE enantiomeric mixture can be at least equal to the solubility of the TDE enantiomeric mixture in the aqueous phase of the reaction mixture The starting amount of epoxide added to the reaction mixture is not critical. The epoxide can be metered out continuously or in batch mode to the reaction mixture. The relative proportions of (R)- and (S)-epoxide in the mixture of enantiomers of the epoxide shown by the general formula (I) is not critical but it is advantageous for commercial purpose to employ a racemic
34

form of the epoxide shown by the general formula (I). The epoxide can be added in a racemic form or as a mixture of enantiomers in different ratios
The amount of the yeast cells, crude yeast cell extract, or partially purified or isolated polypeptide having TDE enantioselective activity added to the reaction depends on the kinetic parameters of the specific reaction and the amount of epoxide that is to be hydrolysed. In the case of product inhibition, it can be advantageous to remove the formed vicinal diol from the reaction mixture or to maintain the concentration of the vicinal diol at levels that allow reasonable reaction rates. Techniques used to enhance enzyme and biomass yields include the identification of useful (or optimal) carbon sources, nitrogen sources, cultivation time, dilution rates (in the case of continuous culture) and feed rates, carbon starvation, addition of trace elements and growth factors to the culture medium, and addition of inducers for example substrates or substrate analogs of the epoxide hydrolases during cultivation. In the case of recombinant hosts, the conditions under which the promoters function for transcription of the gene encoding the polypeptide with epoxide hydrolase activity are taken into account At the end of fermentation (culture), biomass and culture medium can be separated by methods known to one skilled in the art, such as filtration or centnfugation.
The processes are generally performed under mild conditions. For example, the reaction can be carried out at a pH from 5 to 10, preferably from 6 5 to 9, and most preferably from 7 to 8.5. The temperature for hydrolysis can be from 0 to 70 °C, preferably from 0 to 50 °C, most preferably from 4 to 40 °C. It is also known that lowering of the temperature of the reaction can enhance enantioselectivity of an enzyme.
The reaction mixture can contain mixtures of water with at least one water-miscible solvents (e.g., organic water-miscible solvents). Preferably water-miscible solvents are added to the reaction mixture such that epoxide hydrolase activity remains measurable. Water-miscible solvents are preferably organic solvents and can be, for example, acetone, methanol, ethanol, propanol, isopropanol, acetonitnle, dimethylsulfoxide, N.N-dimethylformamide, N-methylpyrolidine, and the like
The reaction mixture can also contain mixtures of water with at least one water-immiscible organic solvent. Examples of water-immiscible solvents that can be used include, for example, toluene, 1,1,2-trichlorotrifluoroethane, methyl tert-butyl ether, methyl isobutyl ketone, dibutyl-o-phtalate, aliphatic alcohols containing 6 to 9 carbon atoms (for example hexanol, octanol), aliphatic hydrocarbons containing 6 to 16 carbon atoms (for example cyclohexane, n-hexane, n -octane, n -decane, n -dodecane, n -tetradecane and n -
35

hexadecane or mixtures of the aforementioned hydrocarbons), and the like Thus, the reaction mixture can include water with at least one water-immiscible organic solvent selected from the group consisting of toluene, 1,1,2-tnchlorotnfluoroethane, methyl tert-butyl ether, methyl isobutyl ketone, dibutyl-o-phtalate, aliphatic alcohols containing 6 to 9 carbon atoms, and aliphatic hydrocarbons containing 6 to 16 carbon.
The reaction mixture can also contain surfactants (for example Tween 80), cyclodextrins or phase-transfer catalysts and the like that can increase, selectively or otherwise, the solubility of the epoxide enantiomers in the reaction mixture.
The reaction mixture can also contain a buffer. Buffers are known in the art and include, for example, phosphate buffers, citrate buffers, TRIS buffers, HEPES buffers, and the like The production of the YEDH polypeptides, including functional fragments, can be, for example, as recited above in the section on Polypeptides and Polypeptide Fragments. Thus they can made by production in a natural host cell, production in a recombinant host cell, or synthetic production. Recombinant production can be carried out in host cells of microbial origin. Preferred yeast host cells are selected from, but are not limited to, the genera Saccharomyces, Kluyveromyces, Hansenula, Pichia, Yarrowia, Arxuia, and Candida. Preferred bacterial host cells include Escherichia coll, Agrobactenum species, Bacillus species and Streptomyces species. Preferred filamentous fungal host cells are selected from the group consisting of the genera Aspergillus, Trichoderma and Fusanum. The production of the polypeptide can be, e.g., intra- or extra- cellular production and can be by, e.g , secretion into the culture medium.
In the fermentation reactions, the polypeptides (including functional fragments) can be immobilized on a solid support or free in solution. Procedures for immobilization of the yeast or preparation thereof include, but are not limited to, adsorption; covalent attachment, cross-linked enzyme aggregates; cross-linked enzyme crystals; entrapment in hydrogels; and entrapment into reverse micelles.
The progress of the reaction can be monitored by standard procedures known to one skilled in the art, which include, for example, gas chromatography or high-pressure liquid chromatography on columns containing chiral stationary phases The vicinal diol formed can be removed from the reaction mixture at one or more stages of the reaction
The reaction can be stopped when one enantiomer of the epoxide and/or vicinal diol is found to be in excess compared to the other enantiomer of the epoxide and/or vicinal diol.
36

Preferably, the reaction is stopped when one enantiomer of an epoxide of general formula (I) and/or vicinal diol of general formula (II) is found to be in an enantiomeric excess of at least 90%. In a more preferred embodiment of the invention, the reaction is stopped when one enantiomer of an epoxide of general formula (I) and/or vicinal of general formula (II) is found to be in an enantiomeric excess of at least 95%. The reaction can be stopped by the separation (for example centrifugation, membrane filtration, precipitation by solvents, and the like) of the yeast, or preparation thereof, and the reaction mixture or by mactivation (for example by heat treatment or addition of salts and/or organic solvents) of the yeast or polypeptide, or preparation thereof. Thus, the reaction can be stopped by, for example, the separation of the catalytic agent from the reactants and products in the mixture, or by ablation or inhibition of the catalytic activity, by techniques known to one skilled in the art.
The optically active epoxides and/or vicinal diols produced by the reaction can be recovered from the reaction mixture, directly or after removal of the yeast, or preparation thereof. Preferably, the process can include continuously recovering the optically active epoxide and/or vicinal diol produced by the reaction directly from the reaction mixture. Methods of removal of the optically active epoxide and/or vicinal diol produced by the reaction include, for example, extraction with an organic solvent (such as hexane, toluene, diethyl ether, petroleum ether, dichloromethane, chloroform, ethyl acetate and the like), vacuum concentration, crystallisation, distillation, membrane separation, column chromatography and the like.
Thus, the present invention provides an efficient process with economical advantages compared to other chemical and biological methods for the production, in high enantiomeric purity, of optically active epoxides of the general formula (I) and vicinal diols of the general formula (II) in the presence of a yeast strain having epoxide hydrolase activity or a polypeptide that is derived from a yeast strain and has such activity
YEDH Antibodies
The invention features antibodies that bind to yeast epoxide hydrolase polypeptides or fragments (e.g., antigenic or functional fragments) of such polypeptides. The polypeptides are preferably yeast epoxide polypeptides with enantioselective activity, and in particular those with meso-epoxide enantioselective activity (i.e ,YEDH), e g., those with SEQ ID NOs' 1, 2, 3, 4, 5, 6 or 7 . The antibodies preferably bind specifically to yeast epoxide hydrolase polypeptides, i.e , not to epoxide hydrolase polypeptides of species other than yeast species.
37

More preferably, they can bind specifically to yeast epoxide polypeptides with enantioselective activity, and in particular to YEDH polypeptides, e.g., those with SEQ ID NOs: 1, 2, 3, 4, 5, 6 or 7.. They can moreover bind specifically to one or more of polypeptides with SEQ ID NOs 1, 2, 3, 4, 5, 6, or 7
Antibodies can be polyclonal or monoclonal antibodies, methods for producing both types of antibody are known in the art The antibodies can be of any class (e g., IgM, IgG, IgA, IgD, or IgE) They are preferably IgG antibodies. Moreover, polyclonal antibodies and monoclonal antibodies can be generated in, or generated from B cells from, animals any number of vertebrate (e.g., mammalian) species, eg., humans, non-human primates (e.g., monkeys, baboons, or chimpanzees), horses, goats, camels, sheep, pigs, bovine animals (e.g., cows, bulls, or oxen), dogs, cats, rabbits, gerbils, hamsters, guinea pigs, rats, mice, birds (such as chickens or turkeys), or fish.
Recombinant antibodies specific for YEDH polypeptides, such as chimeric monoclonal antibodies composed of portions derived from different species and humanized monoclonal antibodies comprising both human and non-human portions, are also encompassed by the invention Such chimeric and humanized monoclonal antibodies can be produced by recombinant DNA techniques known in the art, for example, using methods described in Robinson et al., International Patent Publication PCT/US86/02269; Akira et al, European Patent Application 184,187; Tanigucht, European Patent Application 171,496; Morrison et al, European Patent Application 173,494; Neuberger et al., PCT Application WO 86/01533; Cabilly et al., U.S. Patent No. 4,816,567; Cabilly et al, European Patent Application 125,023; Better et al (1988) Science 240, 1041-43, Liu et al. (1987) J. Immunol 139, 3521-26; Sun et al (1987) PNAS 84, 214-18; Nishimura et al (1987) Cane. Res. 47, 999-1005; Wood et al (1985) Nature 314, 446-49, Shaw et al. (1988) J. Natl. Cancer Inst. 80, 1553-59; Morrison, (1985) Science 229, 1202-07, Oi et al. (1986) BioTechniques 4, 214, Winter, U S. Patent No 5,225,539, Jones et al (1986) Nature 321, 552-25; Veroeyan et al. (1988) Science 239, 1534; and Beidleret al. (1988) J Immunol. 141,4053-60.
Also useful for the invention are antibody fragments and derivatives that contain at least the functional portion of the antigen-binding domain of an antibody that binds to a YEDH polypeptide Antibody fragments that contain the binding domain of the molecule can be generated by known techniques. Such fragments include, but are not limited to: F(ab')2 fragments that can be produced by pepsin digestion of antibody molecules; Fab fragments that can be generated by reducing the disulfide bridges of F(ab')2 fragments, and Fab
38

fragments that can be generated by treating antibody molecules with papain and a reducing agent. See, e g., National Institutes of Health, 1 Current Protocols In Immunology, Coligan et al, ed. 2.8, 2 10 (Wiley Interscience, 1991) Antibody fragments also include Fv fragments, i.e., antibody products in which there are few or no constant region amino acid residues A single chain Fv fragment (scFv) is a single polypeptide chain that includes both the heavy and light chain variable regions of the antibody from which the scFv is derived. Such fragments can be produced, for example, as described in U S. Patent No 4,642,334, which is incorporated herein by reference in its entirety The antibody can be a "humanized" version of a monoclonal antibody originally generated in a different species
The above-described antibodies can be used for a variety of purposes including, but not limited to, YEDH polypeptide purification, detection, and quantitative measurement
The following examples serve to illustrate, not limit, the invention EXAMPLES
Example 1. Materials and Methods
Determination of concentrations and enantiomeric excesses
Quantitative determinations of the compounds and determination of enantiomeric excesses in the reactions described in the Examples below were carried out by gas chromatography. Gas chromatography (GLC) was performed on a Hewlett-Packard 6890 gas chromatograph equipped with FID detector and using H2 as carrier gas Determination of the enantiomeric excesses for 2-methyl-1,2-epoxyheptane and 2-methyl-1,2-heptanediol was performed by GLC using a fused silica p-DEX 225 cyclodextnn capillary column (Supelco) (30 m length, 25 mm ID and 25 um film thickness). The initial temperature of 75°C was maintained for 5.6 minutes, increased at a rate of 8°C per minute to 115°C, and maintained at this temperature for 8 5 minutes. The retention times (min) were as follows: Rt (R)-epoxide = 5.3, R( (S)-epoxide = 5.6, Rt (S)-diol = 17.9 , R( (R)-diol = 18 4 Determination of the enantiomeric excesses of 2-methyl-3-phenyM,2-epoxpropane and 2-methyl-3-phenyl-propanediol was performed by GLC using a fused silica p-DEX 110 cyclodextrin capillary column {Supelco) (30 m length, 25 mm ID and 25 µim film thickness). The initial temperature of 80°C was maintained for 22 minutes, increased at a rate of 4°C per minute to 160°C, and maintained at this temperature for 1 minute. The retention times (mm) were as follows: Rt (S)-epoxide = 31.9, Rt (R)-epoxide = 32 1, R, (S)-diol = 47.7, R, (R)-diol = 48.0. Concentrations of
39

epoxicles and diols were derived from calibration curves obtained from extractions of the epoxide and diol from buffer in the absence of active cells.
Synthesis of rac 2,2-disubstituted epoxides and vicinal diol standards
(a) Synthesis of 2-methyl-1 ,2-epoxyheptane and 2-methyl-1,2-heptanedioi
rac-2-m ethyl-1,2-epoxyheptane was synthesised by direct epoxidation of the corresponding alkene with 3-chloroperbenzoic acid in dry CH2CI2 Yield 50%, 1H-NMR (CDCI3): d = 08-1 0 (t, 3H, J=7 Hz, ?-CH3), 1.25 - 1.30 (s, 3H, -CH3), 1 30 - 1.70 (m, 8H, 4 x CH2), 2.57 -2.65 (dd, 2H, J = 6.8 and 5.5 Hz, -CH2O-). 2-Methyl-1,2-heptanediol was synthesized by acid-catalyzed hydrolysis of (±)2-methyl-1,2-epoxyheptane in THF-H2O (Pedragosa-Moreau et al, 1996) The crude product was purified by silica-gel chromatography (CHCI3/ETOAC 1:1).
(b) Synthesis of 2-methyl-3-phenyl-1,2-epoxpropane and 2-methyl-3-phenyl-propanediol
(i) Synthesis of rac-2-methyl-3-phenyl-1,2-epoxpropane. Methallylbenzene (115.86 g, 0.88 mol) was dissolved in methyl alcohol (460 cm3) containing acetonitnle (82 cm3, 1 58 mo!) and anhydrous potassium carbonate (24.53 g, 0.18 mol) in a one litre round bottomed flask equipped with a magnetic stirrer bar, condenser and pressure-equalising dropping funnel at room temperature. Hydrogen peroxide (35% by mass, 102.2 cm3, 1.05 mol) was then added in a steady stream over about twenty minutes, causing spontaneous boiling of the mixture within thirty minutes of addition commencing The reaction was left to stir, gradually reaching room temperature over the course of an hour. GC analysis indicated that there was only 55% conversion at this stage Further acetonitrile (80 cm3, 1.53 mol) and anhydrous potassium carbonate (24.46 g, 0 18 mol) were added to the mixture, and another portion of hydrogen peroxide (35% by mass, 90 cm3, 0.93 mol) was added as before Conversion had improved to 70-80% typically by this stage. The mixture was placed in a separating funnel, diluted with 400 cm3 of ethyl acetate and the organic component isolated The aqueous phase was washed with a further 200 cm3 portion of ethyl acetate. The combined organic phases were then concentrated to a yellow heterogeneous suspension, dissolved in 200 cm3 of ethyl acetate, washed twice with 50 cm3 saturated aqueous potassium carbonate, and the isolated organic phase dried with magnesium sulphate and concentrated to a clear yellow oil Purification by distillation in vacuo afforded rac-2-methyl-3-phenyl-1,2-epoxypropane (92 88 g, 71%) as a pale yellow oil (bp 73-78 C / 6 mmHg, 95% purity by GC area %). H (200 MHz, CDCI3) 1.33 (3H, br s), 2.65 (1H, d, J 5.0), 2 70 (1H, dd, J 4.8 and 0.6), 2.86 (1H, d, J 14.2), 2 95 (1H, d, J 14.4) and 7.22-7.40 (5H, m).
40

(ii) Synthesis of methallylbenzene. An oven-dried apparatus consisting of a three-necked round bottomed flask equipped with a magnetic stirrer bar, two glass stoppers, a 200 cm3 pressure-equalising dropping funnel and a double-sided spiral condenser was cooled to room temperature under nitrogen atmosphere. The flask was charged with magnesium turnings {15 49 g, 0.64 mol) and anhydrous tetrahydrofuran (75 cm3), and cooled to 0 °C in and ice-water bath. Bromobenzene {8 50 cm3, 80.72 mmol) was then carefully layered over the magnesium turnings, and the magnesium scratched with a glass rod to initiate the reaction. An orange patina formed on the scratched surface, along with the gradual evolution of gas bubbles. Stirring was carefully initiated and the cooling bath removed, although external cooling was often re-applied and removed to moderate the course of this exothermic reaction. After ten minutes, additional bromobenzene (58.57 cm3, 80 72 mmol) in anhydrous tetrahydrofuran (225 cm3) was added dropwise to the magnesium mixture over an hour with intermittent cooling. After a further hour, by which time the reaction was at room temperature, methallylchloride (59.90 cm3, 0.61 mol) in anhydrous tetrahydrofuran (100 cm3) was added dropwise to the solution over an hour. A delayed exotherm occurred about twenty minutes after addition began, that could result in reflux of the mixture if left unchecked. This was controlled with cooling to about 15 °C during addition. The reaction was allowed to reach room temperature over two hours, affording a dense white suspension. Addition of 200 cm3 of distilled water and mixing for 30 minutes, followed by phase separation, isolation of the organic phase, drying over magnesium sulphate and concentration in vacuo gave a light brown oil. The procedure was repeated concurrently in a second experiment, and the combined organic residues distilled After a brief forerun, methallylbenzene (125.05 g, 78%) was isolated as a clear oil (bp 61-62 C / 10 mmHg, 95% purity by GC area %). H (200 MHz, CDCI3) 1.72-1.76 (3H, m), 3 39 (2H, br s), 4.78-4.83 (1H, m), 4.84-4.90 (1H, m) and 7.21-7 40 (5H, m)
(in) Synthesis of rac-2-methyl-3-phenyl1,2-propanediol1 A solution of methallylbenzene (20.01 g, 0.15 mol) and N-m ethyl mo rpholine-N-oxide (23 30 g, 0.20 mol) in 7:3 (v/v) acetone.water solution (852 cm3) in a three-necked round bottomed flask was treated with osmium tetroxide (14.1 mg, 55 4 mol), stoppered and stirred at room temperature for seven days The reaction's progress was monitored by gas chromatography After this time, all the acetone was stripped off in vacuo, and the aqueous phase was extracted with ethyl acetate (2 x 200 cm3) The combined organic phases were dried with magnesium sulphate and concentrated to a brown oil This was passed through a plug of silica with ethyl acetate as the mobile phase, affording a yellow oil This was recrystallised from 2% (v/v) ethyl
41

acetate'hexane to yield 2-methyl-3-phenyl-1,2-propanediol (13.53 g, 54%) as colourless needles. H (200 MHz, CDCI3) 1.17 (3H, s), 2 14 (2H, s), 2.80 (1H, d, J 13.2), 2.89 (1H, d, J 13 2), 3 45 (1H, d, J 11 0), 3.53 (1H, d, J 11 0) and 7 20-7 39 (5H, m).
Preparation of frozen yeast cells for screening
Yeast cells were grown at 30°C in 1 L shake-flask cultures containing 200 ml yeast extract/malt extract (YM) mixture (3% yeast extract, 2% malt extract, 1% peptone w/v) supplemented with 1% glucose (w/v) At late stationary phase (48 - 72 h), the cells were harvested by centrifugation (10 000 g, 10 min, 4°C), washed with phosphate buffer (50 mM, pH7 5), pelleted by centrifugation, and frozen in phosphate buffer containing glycerol (20%) at -20°C as 20% (w/v) cell suspensions The cells were stored for several months without significant loss of activity.
Yeast isolate (strain) screening
Epoxide (10 µl of a 1M stock solution in EtOH) was added to a final concentration of 20 mM to 500 µl cell suspension (20% w/v) in phosphate buffer (50 mM, pH 7.5). The reaction mixtures were incubated at 30°C for 2 hours or 5 hours. The reaction mixtures were extracted with EtOAc (300 µl) and centrifuged. Vicinal diol formation was evaluated by TLC (silica gel Merck 60 F254)- Compounds-were visualized by spraying with vanillin/cone. H2SO4 (5g/l). Reaction mixtures that showed substantial diol formation were evaluated for asymmetric hydrolysis of the epoxide by chiral GLC analysis. Some reactions were repeated over longer or shorter times and with more dilute cell suspensions (10%w/v) in order to analyse the reactions at suitable conversions.
General procedure for the hydrolysis of 2.2-disubstituted epoxides
Frozen yeast cells were thawed, washed with phosphate buffer (50 mM, pH 7 5) and resuspended in buffer Cell suspensions (10 ml, 20% or 50% w/v) were placed in 20 ml glass bottles with screw caps fitted with septa The substrate (100 or 250 µl of a 2M (v/v) stock solution in ethanol) was added to final concentrations of 20 mM or 50 mM. The mixtures were agitated on a shaking water bath at 30°C. The course of the bioconversions of epoxides was followed by withdrawing samples (500 µl) at appropriate time intervals. Samples were extracted with 300 µl EtOAc After centrifugation (3000 xg,2 mm), the organic layer was dried over anhydrous MgSO4 and the products analyzed by chiral GLC.
42

Determination of the absolute configuration of residual 2,2-disubstituted epoxides and residual diols
(a) 2-methyl-1,2-epoxyheptane and 2-methyl-1,2-heptanediol
Absolute configurations were deduced from reported elution orders of the epoxide and diol enantiomers on cyclodextrin columns (Mischitz et a/., 1995)
(b) 2-methyl-3-phenyl-1,2-epoxpropane and 2-methyl-3-phenyl-propanediol
Absolute configurations were deduced from reported elution orders of the epoxide and diol enantiomers on cyclodextrin columns and verified by comparison of the optical rotation of the residual epoxide formed during the biohydrolysis of 2-methyl-3-phenyl-1,2-epoxpropane by yeast strain Cryptococcus hungancus UOFS Y-1346 (S)-2-methyl-3-phenyl-1,2-epoxpropane: [a]22D + 5.0 (c 0 25, MeOH) (Orru et al, 1998). Optical rotation was measured on a Perkin-Elmer 341 polarimeter at 589 nm (Na line) in a 1 dm cuvette.
Cultivation of Cryptococcus hunaaricus (UOFS Y-1346) in a 10L fed-batch bioreactor
Cultivation was performed at 25 °C in 15 L Braun Biostat C bioreactors (working volume 10 L) An overpressure of 500 mbar was applied to the reactor. Dissolved oxygen was continuously monitored and maintained at 30% saturation by adjustment of the stirrer speed. Airflow rate was controlled at 5.5 L.min-1 by use of a mass flow meter. pH was automatically maintained at 5 5 ± 0.05 by the addition of 25 % (w/v) NH4OH Excessive foam formation was avoided by the addition of antifoam (Pluriol P 2000).
A Fernbach shake flask inoculum (10 %, v/v) of C hungancus (UOFS Y-1346) was transferred into a 15 I Braun Biostat C bioreactor containing 6 I mixture with the following composition (per litre): citric acid, 2.5 g, yeast extract, 7 g, (NH4)2SO4, 58 g, KH2PO4, 11.3 g; MgSO4.7H2O, 8.2 g; CaCI2 2H2O, 0.88 g; NaCI, 0.1 g, H3PO4, 13 4; vitamin solution, 1.7 ml; trace element solution, 1 ml; antifoam (Pluriol P-2000), 0.5 ml; and glucose, 20 g. Glucose (60 % m/m) was fed to maintain a residual glucose concentration of 5 g/l after the batch phase. Sugar feed was stopped when the sugar uptake rate decreased. Cultivation was continued for 12 hours after the residual glucose concentration was zero. The biomass was harvested by centnfugation and frozen at -20 °C in phosphate buffer pH 7.5 containing 20 % glycerol until use.
Yeast strains
43

Yeast strains with screen numbers donated "AB" or "Car" or "Alf or "Poh" were isolated from soil from specialised ecological niches that were selected based on the inventors' belief that selectivity for specific classes of epoxides in microorganisms can be determined by environmental factors such as terpene-nch environments or highly contaminated soil "AB" and "Alf strains were isolated from Cape Mountain fynbos, an ecological environment unique to South Africa, "Car" strains were isolated from soil under pine trees, and "Poh" strains from soil contaminated by high concentrations of cyanide. It seemed likely that microorganisms existing in these contaminated soils would have developed alternative respiratory mechanisms Nearly all these new isolates displayed activity and selectivity for 2,2-disubstituted epoxides, while only a few of the more than 200 strains from the Yeast Culture Collection that were included in the screening, displayed activity and selectivity for 2,2-disubstituted epoxides Strains belonging to the species Cryptococcus curvatus, Cryptococcus podzohcus, and Cryptococcus laurentll were all obtained from the environment (as described above) and corresponding strains were not either not available from the Yeast Culture Collection or did not display the desired selectivity. Furthermore, the strains from the culture collection that were found to be able to produce optically active epoxides and/or diols from 2,2-disubstituted epoxides belonged in most cases to the same species as those isolated from soil from the selected environments. All new isolates that produced optically active epoxides or vicinal diols during hydrolysis of 2,2-disubstituted epoxides were identified by known biochemical characterisation methods, and most of the isolates were also subjected to molecular identification by sequence analysis of the D1/D2 region of the large subunit rDNA. These new isolates were deposited at the Yeast Culture Collection of the University of the Orange Free State (UOFS) and assigned UOFS numbers Some of the isolates were also deposited at the National Collection of Yeast Cultures (NCYC), Norwich, United Kingdom.
Example II. Cloning and overexpression of wild type yeast epoxide hydrolases in Yarrowia lipolvtica as production host under the control of different promoters
1. Vectors, Strains and Primers (Table 1)
The following features are common to all the E. coli/Y. lipolyttca auto-cloning integrative vectors used'
• LIP2 terminator
• Zeta regions
• Kanamycin resistance for E. coli selection
• mono-copy auto cloning vectors (pINA 1311, pINA 1313, pINA 3313) with a fully
44

functional selection marker gene carry the fully functional ura3d1 allele from the URA3 selection marker gene
• multi-copy auto cloning vectors (pINA 1291, pINA 1293, pINA 3293) with a defective selection marker gene (copy number amplification) carry the defective ura3d4 allele from the URA3 selection marker gene
Table 1. Vectors, strains and primers

Description Cloning sites
Vectors Promoter Selection .marker Targeting sequence Upstream/down streanit Reference/ Origin
pINAl291 (pYLHmA) hp4d ura3d4 none Pml\ (blunt) / BamHl, Kpn\, AvrII Nicaud et at (2002)
pYL3313(1313) (pYLTsA) TEF ura3d1 none Xmn\ (in pro) / ZtomHI, Kpn\, AvrII This study ,
Host Strain Description., iReferenceM* fir:! Origin
Yarrowia hpolytwa Polh MATA, ura3-302, uxpr2-322, axpl-2 (deleted for both extracellular proteases and growth on sucrose) CLIB882
Primers Sequence Specifications
YL-fwd 5'-GGA GTT CTT CGC IDNO:15) CCA C-3S (SEQ amplification of expression casette
YL-rev 5'-GAT CCC CAC CGG (SEQ ID NO:16) AATTG-3' between Not\ sites
pINA-1 5'-CATACAACCACA (SEQIDNO:17) CAC ATC CA-3' PYLHmA fwd primer
pINA-2 5'-TAA ATA GCT TAG ATA CCA CAG-31 pYLTsA/pYLHmA rev primer
45

(SEQIDN0:18)
Pina-3 5'-CTC TCT CTC CTT GTC AAC T-31 (SEQIDNO.19) pYLTsA fwd primer
2. Transform ants (multi-copy and single-copy)

YLTEF/proinoterTLdM t^t°n^YL3313;(13^):(pYLTsA)ap|||p^|jM8
YL 25 TsA Rhodotorula araucanae (NCYC 3183)
YL 46 TsA Rhodospondium toruioides (UOFS Y-0471)
YL 692 TsA Rhodospondium paludigenum (NCYC 3179)
YL 1 TsA Rhodosporidtum toruioides (NCYC 3181)
YL Car 54 TsA Cryptococcus curvatus (NCYC 3158)
in pgg i p ro moter^M ^nf--nn|JA-nQWfnVT.HniA^||^J|^pp|
YL 25 HmA Rhodotorula araucanae (NCYC 3183)
YL46HmA Rhodospondium toruioides (UOFS Y-0471)
YL 692 HmA " Rhodospondium paludigenum (NCYC 3179)
3. Vector preparation
plNA1291 (Fig 20) was obtained from Dr Madzak of Labo de Genetique, INRA, CNRS. This vector was renamed pYLHmA (Yarrowta Lipolytica expression vector, with Hp4d promoter, multi-copy integration selection, Absent secretion signal).
pKOV93 (Fig 21) was prepared by the inventors. This vector was renamed pYLTsA {Yarrowia Ltpolytica expression vector, with TEF promoter, single-copy integration selection, Absent secretion signal)
To prepare the vectors for ligation with an epoxide hydrolase coding sequence (or other insert to be expressed in Y lipolytica), DNA was digested with BamH\ and Avr\4. Insert preparation
Total RIMA was isolated from selected yeast strain cells and messenger RNA (mRNA) was purified from it. The mRNA was used as a template to synthesise complementary DNA
(cDNA) using reverse transcriptase The cDNA was then used as a template for Polymerase
46

Chain Reaction (PCR) using appropriate primers PCR primers were selected by repeated experimentation using multiple test primers for each yeast strain, the sequences of which were based on previously described epoxide hydrolase sequences from a variety of species. The nucteotide sequences of the forward and reverse primers used to generate cDNA coding sequences from mRNA from six different yeast strains with appropriate restriction enzyme recognition sites at their termini are shown below. Restriction enzyme recognition sequences are underlined and the relevant restriction enzymes are shown in parentheses.

Veast Strain Forward primer Reverse primer
Rhodosporidium toruloides GTGGATCCATGGCGACACAC GACCTAGGCTACTTCTCC
NCYC3181 #1 A(SEQ1DNO:20) CACA (SEQIDN0:21)
Rhodosporidium toruloides {BamHl) (Bln\)
UOFS Y-0471 #46
Cryptococcus curvatus NCYC
3158CarO54
Rhodotorula araucariae GATTAATGATCAATGAGCGA GACCTAGGTCACGACGA
NCYC 3183 #25 GCA (SEQ ID NO:22) (Bell) CAG (SEQ ID NO:23)
(BM)
Rhodosporidium paludigenum GTGGATCCATGGCTGCCCA GAGCTAGCTCAGGCCTG
NCYC 3! 79 #692 (SEQ ID NO :24) G(SEQ ID NO:25)
(BamHl) (Nhel)
Debaromyces hansenii NCYC GTGGATCCATGATGCAAGG GACCTAGGCTAAGGATA
3167(#113) (SEQIDNO:26) TT (SEQIDNO:27)
(BamHl) (BM)
Each PCR reaction contained 200 uM dNTPs, 250 nM of each primer, 2 mM of MgCI2, cDNA and 2.5 U of Taq polymerase in a 50 ul reaction volume The PCR profile used was- 95°C for 5 minutes, followed by 30 cycles of: 95°C - 1 min, 50°C - 1 min, 72°C - 2 min, then a final extension of 72°C for 10 minutes The PCR product were purified and digested with the restriction enzymes whose recognition sites are engineered at the end of the primers. The cDNA fragment was cloned into a vector and sequenced for confirmation
Coding seqences to be inserted in either pYLHmA or pYLTsA were prepared with BamHl
47

and Avrll at their termini. The above PCR primers were designed with these restriction sites, unless the sites were also present in the gene to be inserted If this occurred, appropriate compatible restriction enzymes were selected. PCR template DNA was either the insert cloned into a different vector, or cDNA synthesized from the original host organism PCR reactions consisted of 200 µM dNTP's, 250 nM each primer, 1X Taq polymerase buffer, and 2.5 units Taq polymerase per 100 µl reaction. The amplification programme used was: 95°C for 5 minutes, followed by 30 cycles of 95°C for 1 minute, 50°C for 1 minute, followed by a final extension at 72°C for 2 minutes, followed by 72°C for 10 minutes.
PCR products were purified and digested with the relevant restriction enzymes The digested DNA was subsequently repurified and was ready for ligation into the prepared vector
5. Preparation of pYLHmA or pYLTsA constructs
Vector and insert were ligated at pmol end ratios of 3:1 - 10:1 (insert:vector), using commercial T4 DNA Ligase. Ligations were electroporated into any laboratory strain of Eschehchia colt, using the Bio-Rad GenePulser, or equivalent electroporator. Transformants were selected on LM media {10 g/l yeast extract, 10 g/l tryptone, 5 g/l NaCI), supplemented with kanamycin {50 µg/ml). Transformants were selected based on restriction enzyme digests of purified plasmid DNA.
6. Yarrowia lipolytica transformation
6.1.1.Preparation of DNA-method 1
Digestion of the pINA-series of plasmids with Not\ resulted in the release of a bacterial DNA-free expression cassette, containing the ura3d4 (pYLHmA) or the ura3d1 (pYLTsA) marker gene and the promoter-gene-terminator.
Scaled-up quantities of each plasmid were isolated. Not\ was used to restrict the plasmid DNA, and the digested DNA was run on an agarose gel. Not\ digests resulted in generation of the bacterial fragment of the plasmid as a band at 2210 bp, and the expression cassette as a band of 2760 bp + size of insert (pYLHmA) or 2596 bp + size of insert {pYLTsA). The expression cassette fragments were excised from the gel and purified from the agarose The purified fragment was used for transformation of Y lipolyttca Po1h
48

6.1.2.Preparation of DNA - method 2
Primers YL-Fwcl and YL-Rev (Table 1) were used to amplify the expression cassette. PCR reactions consisted of 200 uM dNTP's, 250 pmol each primer, 1X Taq polymerase buffer and 2.5 units Taq poiymerase per 100 ul reaction. The amplification programme used was 95°C for 5 minutes, 30 cycles of 95°C for 1 minute, 50°C for 1 minute, and 72°C for 3 1/2 minutes, followed by a final extension at 72°C for 10 minutes. The PCR product was purified from the PCR reaction mix and used for transformation of Y. lipolytica Po1 h.
6.1.3.Preparation of carrier DNA
DNA from salmon testes was made up as a 10 mg/ml stock in TE (10 mM Tns-HCI, pH 8.0, 1 mM EDTA) and sonicated to result in fragments that ranged from approximately 15 kb to 100 bp, with most fragments in a range of 6 to 10 kb The DNA was denatured by boiling. Aliquots were stored at -20°C.
6.1.4.Transformation of Yarrowia lipolytica with pYLHmA or pYLTsA
An adaptation of the method of Xuan et al (1988) was used for the transformation of V. lipolytica Po1h. The yeast was inoculated into 50 ml YPD (10 g/l yeast extract, 20 g/l peptone, 20 g/l glucose). The culture was incubated at 30°C, 220 rpm until cell densities of 8 x 107 - 2 x 108 cells/ml were reached. The entire culture was harvested, the pellet resuspended in 10 ml TE and reharvested 1 ml TE + 0.1 M LiOAc was used to resuspend the pellet and the culture was incubated at 28°C in a ProBlot Jr (Labnet) hybridisation oven, set at 4 rpm (or similar incubator) for 1 hour Transformation mixes were set up with 0 5-2 µg of transforming DNA + 5 ug of carrier DNA with 100 µl of treated cells
Each mix was set up in a 1 5 ml mtcrofuge tube, and incubated in a 28°C heating block for 30 minutes. 7 volumes of PEG reagent (40% PEG 4,000, 0 1 M LiOAc, 10 mM Tris, 1 mM EDTA, pH 7.5, filter-sterilised) were added to each, mixed carefully and incubated at 28°C for a further 1 hour. The tubes were transferred to a 37°C heating block for 15 minutes, and then the cells were pelleted by centrifugation for 1 minute at 13,000 rpm. The cell pellets were carefully resuspended in 100 µl dH2O The transformations were plated on Y lipolytica selective plates (17 g/l Difco yeast nitrogen base without ammo acids and without (NH4)2SO4, 20 g/l glucose, 4 g/l NH4CI, 2 g/l casamino acids, 300 mg/l leucine) and incubated at 28°C
Colonies which appeared on the selective plates after 3-7 days were transferred onto fresh plates and regrown.
49

6.1.5.Confirmation of integration of pYLHmA or pYLTsA
Colonies that grew on the newly-streaked selective plates were inoculated into 5 ml of YPD medium and grown at 30°C, 200 rpm for 24-48 hours. A small-scale genomic DNA isolation was performed
PCR was performed using this genomic DNA as template, with either plNA-1 and plNA-2 as primers (transformants with pYLHmA), or plNA-3 and plNA-2 (pYLTsA) {Table 1). Each PCR reaction contained 200 µM dNTPs, 250 nM of each primer, 2 mM of MgCI2l genomic DNA and 2 5 U/50ul of Taq polymerase The PCR profile was as described above in this example. These primer sets gave products the size of the inserted genes
Example 111. Selection of yeasts able to produce optically active 2-methvl-1.2-epoxyheptane and 2-methyl-2-heptanediol from (±)-2-methyl-1,2-epoxvheptane
Yeasts were cultivated, harvested and frozen as described above 2,2-disubstituted epoxide 2-methyl-1,2-epoxyheptane was added and the screening was performed as described above. Strains with the highest activities as judged by TLC from diol formation were subjected to chiral GC analysis as described above. The strains with E-values > 2 are depicted as Samples 1-114 (Table 2) E-values were calculated from the followig formulas1

Enantiom
eric excess (ee) (%) = {([R]-[S]) / ([R]+[S])} x 100%, where [R] and [S] represent the concentrations of the R and S enantiomers of the TDE substrate or the DVD product, depending on whether the ee of the substrate or the product is to be calculated.
Notes'
The conversion at appropriate time intervals and ee's of the substrate and product was used
50

to determine E-values calculated from ees and conversion (Equation 1), eep and conversion (Equation 2), and ees and eep (Equation 3) respectively for strains (114) that displayed the most promising enantioselectivities (Table 2) If the degree of conversion can be accurately determined, E-values calculated from all three equations should be the same, provided that the reaction is irreversible and regiospecific (Pedragosa- Moreau et al 1996). In this case, both the epoxide and diol could be extracted very efficiently, and the degree of conversion could be determined with high accuracy If the reaction is not regioselective, E-values are not applicable, since E-values calculated from ees and conversion and from eep and conversion will differ substantially and highly erroneous results will be obtained. If each of the two antipodes of the epoxide is attacked following a different regioselectivity, the ee of the diol will be high, and E-values based on eep and conversion will be higher than those obtained form ees and conversion and from ees and eep. Strains displaying this type of regioselectivity can then be used for the synthesis of diol in high enantiomeric purity, which is difficult to obtain in high yields, from enantioselective but regiospecific reactions. On the other hand, if a catalyst is enantioselective but not regioselective, the ee of the remaining epoxide will be high while the ee of the diol formed will be low, and E-values based on ee5 and conversion will be higher than those obtained from eep and conversion and from ees and eep. Strains displaying this type of regioselectivity can then be used for the synthesis of epoxide in high enantiomeric purity Comparison of E-values calculated from the different equations can thus be used as a qualitative tool to analyse the enantioselectivity and regioselectivity of the reaction and to make appropriate choices of biocatalysts for the synthesis of the desired epoxide or diol enantiomers in high yields and optical purity.
Table 2. Yeast strains that hydrolyse 2-methyl-1,2-epoxyheptane enantioselectively (E > 2)a

Sam pno Scree nno Yeast species Cultur e Collec -tionNr ; Reaction Remaining Epoxide Formed Diol Selectivity
Time (min) Conv (%) E.e. (%) Abs conf E.e. (%) Abs Conf Eb Ed
1 26 9 Arxula adenimvorans NCYC3147 90 3.2 0.7 S 82.5 R 1.6 10.7 10.5
2 69 3 Arxula terrestris NCYC3148 180 17.0 13.3 R 58. 0 S 5.4 4.2' 4.3
43 Bullera dendrophla NCYC3152 180 37.5 46.7 S 82. 6 R 12.7 17.1 16.6
4 66 9 Candida magnoliae NCYC3154 180 17.9 11.7 R 43. 6 S 3.7 2.8 2.9
51

Sam pno Scree nno Yeast species Cultur e Collec -tionNr Reaction Remaining Epoxide Formed Diol Selectivity
Time (mm) Conv (%) E.e. (%) Abs conf Ee. (%) Abs Conf Eb Ec Ed
5 67 7 Candida magnohae UOFS Y-0799 180 28.8 17.4 R 37. 1 S 3.0 2.5 2.6
6 75 1 Candida magnohae UOFS Y-1040 60 18.6 14.4 R 41 S 5.0 2.6 2.8
7 67 8 Candida magnoliae UOFS Y-1297 180 47.4 28.2 R 31. 6 S 2.5 2.5 2.5
8 23 0 Cryptococcus albidus NCYC3156 180 14.7 9.3 S 68.7 R 3.7 6.0 5.9
9 Jen 17 Cryptococcus albidus UOFS Y-0223 - 90 5.2 3.9 S 74. 5 R 6.2 7.1 7.1
10 Jen03 Oyptococcus albidus UOFS Y-0821 90 4.7 2.9 s 30. 5 R 4.0 1.9 1.9
11 375 Cryptococcus amylolentus NCYC3157 90 31.9 43.5 R 91. 8 S 42.0 35.8 36.0
12 Car 054 Cryptococcus curvatus NCYC 3158 10 46.9 54.8 S 48. 2 S 7.3 4.3 4.8
13 37 9 Cryptococcus hungaricus NCYC 3159 90 33.7 32.1 s 55.7 R 6.0 4.6 4.8
14 Jen 12 Cryptococcus laurentu NCYC3160 90 2.6 0.8 R 65. S 1.9 4.9 4.8
15 AB 24 Cryptococcus laurentil NCYC3161 180 71.6 48.0 R 26. 4 S 2.2 3.1 2.6
16 Alf 12 Cryptococcus laurentii UOFS Y-0509 180 34 9 22.0 R 37. 3 s 0.0 2.6 2.7
17 Alf 03 Cryptococcus laurentii UOFS Y-0514 180 56.8 38.3 R 33. 7 s 2.6 3.0 2.9
18 AB 25 Cryptococcus laurentii UOFS Y-1884 180 62.1 43.3 R 30. s 2.5 3.0 3.0
19 AB 26 Cryptococcus laurentii UOFS Y-1885 180 69.0 51.9 R 27. 2 s 2.5 3.0 2.8
20 AB 27 Cryptococcus laurentii UOFSY-1886 180 42.7 26.4 R 37. 6 s 2.7 2.9 2.8
52

Sam pno Scree nno Yeast species Cultur e Collec -tionNr Reaction Remaining Epoxide Formed Diol Selectivity
Time (min) Conv (%) E.e.(%) Abs conf E.e (%) Abs Conf Eb Ec Ed
21 AB 32 Cryptococcus laurentxi UOFS Y-1887 ' 180 59.7 41.9 R 30. 9 S 26 2.9 2.8
22 AB 33 Cryptococcus laurentu UOFS Y-1888 180 53.6 36.9 R 33. 9 S 2.7 2.9 2.8
23 AB 35 Cryptococcus laurentu UOFS Y-1892 180 44.8 35.2 R 46. 4 S 3.5 3.9 3.8
24 Jen 09 Cryptococcus laurentn var laurentii UOFS Y-1349 90 1.2 0.5 R 50. 6 S 2.4 3.1 3.1
25 AB58 Cryptococcus podzolicus NCYC3164 180 38.7 45.4 S 94. 4 R 9.4 64.2 54.7
26 AB53 Cryptococcus podzolicus NCYC3165 180 10.1 6.7 S 84. 4 R 4.3 12.9 12.6
27 AB40 Cryptococcus podzolicus UOFS Y-1881 180 27.7 33.4 s 93. 9 R 20.3 45.3 44.1
28 AB 49 Cryptococcus podzolicus UOFS Y-1882 180 43.0 52.2 s 94. R 9.1 72.2 57.0
29 AB50 Cryptococcus podzolicus UOFS Y-1883 180 50.0 85.5 s 92. 7 R 34.8 88.5 72.1
30 AB 28 Cryptococcus podzolicus UOFS Y-1889 180 34.7 49.7 s 93. 7 R 49.2 50.6 50.5
31 AB34 Cryptococcus podzolicus UOFS Y-1890 180 42.6 66.7 s 90. 1 R 37.6 38.4 38.4
32 AB 36 Cryptococcus podzolicus UOFS Y-1893 180 42.2 58.4 s 93. 7 R 16.1 62.6 55.1
33 AB 52 Cryptococcus podzolicus UOFS Y-1895 180 39.3 41.4 s 94. 4 R 6.8 64.7 52.0
34 AB 37 Cryptococcus podzolicus UOFS Y-1896 180 52.0 70.2 s 89.7 R 9.6 79.1 38.6
35 AB 29 Cryptococcus podzolicus UOFS Y- 180 38 9 57.3 s 94. 0 R 34.6 59.9 58.2
53

Sam pno. Scree n no Yeast species Cultur e Collec -tionNr Reaction Remaining Epoxide Formed Diol Selectivity
Time (min) Conv (%) E.e. (%) Abs conf E.e. (%) Abs Conf Eb Ec Ed
1897
36 AB 41 Cryptococcus podzohcus UOFS Y-1899 180 25.3 27.3 S 93.5 R 12.1 40.7 39.0
37 AB30 Cryptococcuspodzohcus UOFS Y-1904 180 43.2 70.9 S 93. 9 R 61.9 68.1 67.7
38 AB 45 Cryptococcus podzohcus UOFS Y-1906 180 42.6 45.9 S 92. 6 R 6.6 53.6 40.9
39 AB 46 Cryptococcus podzohcus UOFS Y-1907 180 27.8 22 5 s 90. 4 R 4.7 27.8 24.6
40 AB 47 Cryptococcus podzolicus UOFS Y-1908 180 23.2 19.5 s 89. 9 R 5.6 24.4 22.6
41 AB48 Cryptococcus podzohcus UOFSY-1910 180 28.1 24.4 s 88.7 R 7.7 22.0 19.7
42 AB 39 Cryptococcus podzohcus UOFS Y-1912 180 50.4 70.7 s 92. 4 R 11.6 90.1 53.7
43 AB56 Cryptococcus podzohcus UOFS Y-1913 180 42.7 36.5 s 92. 4 R 4.1 52.5 36.3
44 AB 57 Cryptococcus podzohcus UOFS Y-1914 180 46.6 57.6 s 92. 8 R 8.6 66.7 47.8
45 52 0 Pichia finlandica NCYC 3173 180 70.6 79.6 R 30. 8 S 4.4 3.8' 4,1
46 67 6 Pichia haplophila NCYC3176 180 19.1 22.7 R 98. 0 S 64.0 127. 2 126. 6
47 67 3 Pichia haplophila NCYC 3177 60 37.2 40.7 R 53. 7 s 7.9 4.5 4.9
48 28 Pichia haplophila UOFS Y-2136 60 29.9 31.1 R 56. s 8.7 4.5 4.8
49 692 Rhodospondiu m paludigenum NCYC 3179 180 72.9 100. 0 S 36.5 R 17.2 8.4 16.8
50 Alf 01 Rhodospondiu m toruloides NCYC3181 10 98.0 100. 0 S 23. 7 R 4.1 6.5 11.3
54

Sam pno. Scree nno Yeast species Cultur e Collec -tionNr Reaction Remaining Epoxide Formed Diol Selectivity
Time (min) Conv (%) E.e. (%) Abs conf E.e. (%) Abs Conf Eb Ec Ed
51 Car 118 Rhodosporidtu m toruloides NCY0C3182 20 23.5 27.6 S 63. 3 R 23.7 5.4 5.8
52 67 1 Rhodosporidiu m toruloides UO0FS Y-047002 180 52.9 33.2 S 31. 4 R 2.5 2.6 2.6
53 Alf 02 Rhodosporidiu m toruloides UOFS Y-0518 20 46.9 51.0 S 57. 4 R 6.0 6.0 60
54 Car 003 Rhodosporidiu m toruloides UOFS Y-2222 20 31.2 38.0 S 59.5 R 16.3 5.1 5.6
55 Car 006 Rhodosporidiu m toruloides UOFS Y-2223 20 26.1 32.7 S 61.2 R 35.7 5.1 5.7
56 Car 020 Rhodosporidiu m toruloides UOFS Y-2226 20 41.6 44.6 S 57. 1 R 67 5.4 5.6
57 Car 038 Rhodosporidiu m toruloides UOFS Y-2228 20 23.5 28.4 S 63. 6 R 34.1 5.4 5.9
58 Car 052 Rhodosporidiu m toruloides UOFS Y-2230 20 45.9 55.9 S 53. 5 R 8.4 5.1 5.6
59 Car 059 Rhodosporidiu m toruloides UOFS Y-2231 20 37.7 39.3 S 58. 1 R 6.8 5.3 5.5
60 Car 067 Rhodosporidiu m toruloides UOFSY-2236 20 23.3 29.4 S 64.1 R 83.0 5.5 6.1
61 Car 070 Rhodosporidiu m toruloides UOFS Y-2237 60 66.8 100. 0 S 37. 5 R 25.1 4.6 17.3
62 Car 076 Rhodosporidiu m toruloides UOFS Y-2238 60 81.8 100. 0 S 18. R 10.8 3.1 9.4
63 Car 077 Rhodosporidiu m toruloides UOFS Y-2239 60 83.5 100. 0 S 16. 1 R 9.9 2.9 8.7
64 Car 078 Rhodosporidiu m toruloides UOFS' Y-2240 ' 20 27.1 28.6 s 63. 2 R 10.2 5.6 5.8
65 Car Rhodosporidiu UOFS 60 83 9 100. s 15. R 9.7 2.9 8.6
55

Sam pno, Scree nno Yeast species Cultur e Collec -tionNr Reaction Remaining Epoxide Formed Diol Selectivity
Time (min) Conv (%) E.e. (%) Abs conf E.e. (%) Abs Conf Eb Ec Ed
092 m toruloides Y-2241 0 8
66 Car 093 Rhodospondm m toruloides UOFS Y-2242 60 81.9 100. 0 S 18. 1 R 10.7 3.1 9.4
67 Car 094 Rhodosporidm m toruloides UOFS Y-2243 20 22.5 27.7 S 63. 0 R 56.1 5.3 5.7
68 Car 100 Rhodospondm m toruloides UOFS Y-2245 60 66.7 100. 0 S 37. 1 R 25.4 45 17.1
69 Car103 Rhodospondm m toruloides UOFS Y-2246 60 66.5 100. 0 S 37. 2 R 25.7 4.5 17.2
70 Car 108 Rhodospondm m toruloides UOFS Y-2247 60 82.6 100. 0 S 17. 7 R 10.4 3.2 9.3
71 Car 120 Rhodosporidm m toruloides UOFS Y-2249 60 82.5 100. 0 S 17. 5 R 10.4 3.1 9.2
72 Car 121 Rhodospondm m toruloides UOFS Y-2250 60 80.9 100. 0 S 19. 6 R 11.3 3.2 9.9
73 Car 126 Rhodospondiu m toruloides UOFS Y- 2251 20 , 29.3 38.0 S 58 6 R 33.9 4.8 5.5
74 Car 131 Rhodosporidm m toruloides UOFS Y-2252 60 66.0 100. 0 S 37. R 26.7 4.4 17.2
75 Car 134 Rhqdosporidm m toruloides UOFS Y-2253 60 81.9 100. 0 S 18. 1 R 10.7 3.1 9.4
76 Car 142 Rhodospondiu m toruloides UOFS Y-2255 60 71.7 90.0 S 29. R 5.8 3.7 4.9
77 Car 200 Rhodospondiu m toruloides UOFS Y-2256 10 34.8 37.0 S 53. 2 R 7.9 4.3 4.6
78 Car 204 Rhodosporidm m toruloides UOFS Y-2257 60 83.9 100. 0 S 15. 8 R 9.7 2.9 8.6
79 Car Rhodosporidm UOFS 60 63.8 100. S 40. R 31.5 4.6 18.7
56

Sam pno Scree nno Yeast species Cultur e Collec -tionNr Reaction RemainingEpoxide Formed Diol Selectivity
Time (min) Conv(%) E.e. (%) Abs conf E.e. (%) Abs Conf Eb Ec Ed
205 m toruloides Y-2258 0 0
80 Car 209 Rhodospondiu m toruloides UOFS Y-2260 20 14.3 15.5 S 68. 1 R 31.2 5.9 6.1
81 Car 210 Rhodospondiu m toruloides UOFS Y-2261 60 80.7 100. 0 S 19. 1 R 11.4 3.1 9.7
82 46 Rhodospondiu m toruloides UOFS Y-0471 20 11.6 11.0 S 74. 2 R 12.3 7.4 7.5
83 25 Rhodotorula araucanae NCYC3183 180 65.2 57.5 S 3.3.5 R 3.2 3.6 3.4
84 EP 230 Rhodotorula aurantiaca NCYC 3185 180 54.7 46.0 S 51. 9 R 3.4 5.8 4.9
85 50 Rhodotorula glutmis NCYC3186 20 62.2 87.5 S 46. 1 R 8.9 59 7.2
86 68 0 Rhodotorula glutims UOFS Y-0459 20 57.3 75.2 S 51. 5 R 7.7 6.2 6.8
87 71 Rhodotorula glutmis UOFS Y-0489 60 62.5 100. 0 S 377 R 35.3 4.0 17.5
88 Alf 06 Rhodotorula glutmis UOFS Y-0513 20 22.8 28.4 S 64. 0 R 63.9 5.5 6.0
89 Car 022 Rhodotorula glutims UOFS Y-2227 60 - 75.9 100 0 s 26. R 14.5 3..9 12.3
90 Car 060 Rhodotorula glutmis UOFS Y-2232 20 33 9 38.6 s 59. R 10.2 5.2 5.6
91 Car 061 Rhodotorula glutims UOFS Y-2233 60 74.8 100. 0 s 27. 8 R 15.5 4.0 12.9
92 Car 062 Rhodotorula glutmis UOFS Y-2234 20 27.3 31.3 s 61.7 R 14.8 5.3, 5.7
93 Car 066 Rhodotorula glutims UOFS Y-2235 60 77.3 100. 0 s 24. 1 R 13.5 3.6 11.5
94 Car Rhodotorula UOFS 20 42.8 45.3 s 57. R 6.3 55 5.6
57

Sam pno Scree n no Yeast species Cultur e Collec -tionNr Reaction Remaining Epoxide Formed Diol Selectivity
Time (min) Conv (%) E.e. (%) Abs conf E.e. (%) Abs Conf Eb Ec Ed
075 giutims Y-2265 0
95 71 4 Rhodotorula minuta NCYC3187 20 33.3 24.0 R 37 9 S 3.6 2.7 2.8
96 71 2 Rhodotorula minuta UOFS Y-0835 60 46.9 52.7 R 48. 4 S 6.6 43 4.7
97 68 6 Rhodotorula minuta var. minuta NCYC3188 60 30.1 25.8 R 50. 5 S 5.1 3.7 3.9
98 15 8 Rhodotorula sp, "minuta/mucil aginosa" NCYC3194 180 40.1 21.5 R 31. 5 S 2.4 2.3 2.3
99 690 Rhodotorula sp nearest "minuta" UOFS Y-0125 180 49.3 29.5 R 28. 2 S 2.4 2.3 2.3
10 0 17 2 Rhodotorula sp NCYC3192 180 54.9 83.0 S 70. 9 R 13.4 16.0 14.9
10 1 165 Rhodotorula sp - NCYC 3193 180 16.9 133 S 69. 6 R 5.5 6.4 6.4
10 2 24 R]iodotorula sp UOFS Y-2042 180 18.3 17.4 S 83. 2 R 9.3 13.1 12.9
10 29 3 Spondiobolus salmomcolor NCYC3195 90 9.4 8.1 S 61.3 R 8.8 4.4 4.5
10 4 42 Spondiobolus saimonicolor NCYC3196 90 13.2 13.0 S 60.2 R 14.3 4.4 4.6
10 5 28 5 Sporobolomyc es roseus NCYC 3197 90, 44.0 62.0 s 52. 4 R 15.9 4,7 5.9
10 6 69 6 Sporobolomyc es sp "holsaticus" NCYC 3198 180 46.3 39.1 s 45. 2 R 3.8 3.8 3.8
10 7 28 3 Sporobolomyc es tsugae NCYC 3199 90 8.3 6.5 s 18. 7 S 6.4 1.5 1.6
10 8 20 Tnchosporon cutaneum var cutaneum NCYC 3201 180 24.1 15.9 R 61. 7 S 3.5 5.1 4.9
10 9 14 Trichosporon mucoides NCYC3205 180 17.0 8.3 R 3.3 S 2.6 1.1 1.1
11 19 Trichosporon NCYC 180 40.5 27.8 R 41. S 3.1 3.1 3.1
58

Sam pno Scree n no Yeast species Cultur e Collec -tionNr Reaction Remaining Epoxide Formed Diol Selectivity
Time (min) Conv (%) E.e. (%) Abs conf E.e. (%) Abs Conf Eb Ec Ed
0 ovoides 3207 2
11 1 22 5 Tnchosporon sp NCYC3211 180 36 6 21.1 S 37. 4 R 2.6 27 2.7
11 2 39 Winged robertsiae NCYC3228 180 9.3 6.3 R 45. 3 S 4.4 2.8 2.8
11i 71 1 Yarrowia hpolytica NCYC3229 180 8.6 7.5 S 73 5 R 9.8 7.0 7.1
11 4 Jen 48 Yarrowia hpolytica UOFS Y-1700 90 6.5 5.1 S 98. 1 R 7.1 109' 107
a Reaction conditions* 20 mM epoxide, 20 % cells [(w/v), wet weight] in phosphate buffer (50
mM, pH 7.5)
b E calculated from equation 1
c E calculated from equation 2
d E calculated from equation 3
All the yeast strains corresponding to sample 1-114 (Table 2) are kept and maintained at the University of the Orange Free State (UOFS), Department of Microbial, Biochemical and Food Biotechnology, Faculty of Natural and Agricultural Sciences, P.O. Box 339, Bloemfontein 9300, South Africa (Tel +27 51 401 2396, Fax + 27 51 444 3219) and are readily identified by the yeast species and culture collection number as indicated Representative examples of strains belonging to the different species have been deposited under the Budapest Treaty at National Collection of Yeast Cultures (NCYC), Institute of Food Research Norwich Research Park Colney, Norwich NR4 7UA, U K ( Tel: +44-(0)1603-255274 Fax +44-(0)1603-458414 Email. ncyc@bbsrc.ac uk) and are readily identified by the yeast species and culture collection accession number as indicated. The samples deposited with the NCYC are taken from the same deposit maintained by the South African Council for Scientific and Industrial Research (CSIR) since prior to the filing date of this application. The deposits will be maintained without restriction in the NCYC depository for a period of 30 years, or 5 years after the most recent request, or for the effective life of the patent, whichever is longer, and will be replaced if the deposit becomes non-viable during that period Samples of the yeast strains not deposited at NCYC will be made available upon
request on the same basis and conditions of the Budapest Treaty.
59

Example IV. Selection of yeasts that are able to produce optically active 2-methyl-3-phenyl-1.2-epoxypropane and 2-methvl-3-phenvl-1.2-propanediol from (±)-2-methyl-3-phenyl-1.2-epoxypropane
Yeasts were cultivated, harvested and frozen as described above. The 2,2-disubstituted epoxide 2-methyl-3-phenyl-1,2-epbxypropane was added and the screening was performed as described above. Strains with the highest activities as judged by TLC from diol formation were subjected to chiral GC analysis as described above. The strains that were able to produce optically active 2-methyl-3-phenyl-1,2-epoxypropane and 2-methyl-3-phenyl-1,2-propanediol from the racemic epoxide are listed as samples 115-210 in Table 3
Table 3. Yeast strains that hydrolyse 2-methyl-3-phenyl-1,2-epoxypropane enantioselectively

Sampl eNo Screen no Yeast species Culture Collection no. Epoxide ee Diol ee Ea Abs.conf.
(%) (%) Epox Dio1
115 43 Bullera dendrophla NCYC3152 32.2 15.7 1.8 R S
;116- Jen-26 Bullera dendrophla NCYC 3208 21.1 . 20.2 1.8 R S
117 708 Candida rugosa NCYC3155 3.4 26.1 "1.8 R * s
118 POH-29 Candida sp. (new) (C sorbophda) NCYC 3217 6.5 78.5 8.9 R s
119 Jen-2 Cryptococcus albidus NCYC 3156 26.5 93.8 40.2 S R
120 Jen-17 Cryptococcus albidus UOFS Y-0223 21.5 58.6 4.7 S R
121 Jen-3 Cryptococcus albidus UOFSY-0821 100 63.0 38. 8 s R
122' Jen-23 Cryptococcus s-f' amylolentus NCYC 3157 42.2 65.8 \J•7.3 R s
,123 _ Car-14 Cryptococcus curvatus UOFS Y-2225 8.5 34.9 2.2, R s
124 Jen-15 Cryptococcus hungancus NCYC 3159 99.9 172 7.1 S R
125" Jen-12 Cryptococcus laurenth NCYC 3160 5.5 23.7 1.7 R s
126 AB-24 Cryptococcus laurentii NCYC 3161 7.4 15.5 1.5 R s
127_ Alf\03 Cryptococcus laurentii UOFSY-0514 -7.6 20.1 1.6 R s
128 AB-25 Cryptococcus laurentii UOFsV-1884 ' 13 5-14.7 1.4 1 R s T
129 AB-26 Cryptococcus laurentii UOFS Y-1885 'lO 15.2 1 5 R s '
130 AB-27 Cryptococcus laurentii UOFS Y-l 886 8.2 17.5 1.5 R s
131t AB-32 Cryptococcus laurentii UOFS Y-l 887 -.5 . 15.9 1.4 R s_
60

Sampl eNo Screen no Yeast species Culture Collection no. Epoxide ee Diol ee Ea Abs.conf.
(%) (%) Epox Dio 1
132133134 ,135136137 138139140 141 AB-33Jen-9^'Jen-16 BVr2AB-58AB-54 AB-43AB-46AB-56AB-57 Cryptococcus laurentiiCryptococcus laurentii var laurentiiCryptococcus luteolus Cryptococcus macerans ___Cryptococcus podzolicusCryptococcus podzolwus Cryptococcus podzolicusCryptococcus podzolicusCryptococcus podzolicus Cryptococcus podzohcus UOFSY-1888 UOFS Y-1349^NCYC3162 NCYC3213NCYC3164UOFS Y-1900 UOFS Y-1902UOFS Y-1907UOFSY-1913 UOFSY-1914 6.9 1130.1 ,-9.2 4.76.8 6.510.111.1 12.8 16 *28.4t27 4 70.288.22.8 0.894.192.1 96 9 1.5 1181.8 ,6.2,16. 71.1 1.136. 427.273 R RRSs sss s s ss s.,RR RRR R
142 113 Debaryomyces hansenn NCYC3167 4.6 27.4 1.8 R S
143 -144 145 146 147 520 707 702 112 ^ 706 Pichiafinlandica E'h j. Pichia gmllermondii Pichia guillermondn Pichia guillermondn Pichia gudlermondii " I NCYC3173 * NCYC3174 NCYC3175 UOFS Y-0053 UOFS Y-0057 ¦ 8.5 ^4.9 = 1.5 6.2£l ' 79.6 28.3 27.717.3 30" 9.6 1.9 1.8 1.5 1.9 R R R R R s"¦ s s ^ s "
148 149 150 151 152 153 154 155 156 157158 159 Alf 01 Car-118 POH-28 POH-20 POH-38 46 Alf 02 Car-3 Car-6 Car-20Car-3 8 Car-52 Rhodosporidium toruloides ;Rhodospondi urn toruloidesRhodosporidium toruloidesRhodosporidium toruloides Rhodosporidium toruloidesRhodosporidium toruloidesRhodosporidium toruloides Rhodosporidium toruloides Rhodosporidium toruloides Rhodosporidi um toruloidesRhodospon dium toruloidesRhodosporidi um MCYC3181 NCYC3182 NCYC3215 NCYC3216 NCYC3219 UOFSY-0471 UOFSY-0518 UOFS Y-2222 UOFS Y-2223 UOFS Y-2226UOFS Y-2228 UOFS Y-2230 0 5.5 9.1 52 14.6 1.0 1.5 3.5 1.7 3.72.4 5.3 36.9 29.3 15.2 135 11.4 17.6 37.9 25 26.5 24.436.7 27.8 2.2 1.9 1.5 1.4 1.4 1.4 2.3 1.7 1.8 1.72.2 1.9 Ss s s s s s s s ss s R R R R R R R R R RR R
61

Sampl eNo Screen no Yeast species Culture Collection no Epoxide ee Diol ee Ea Abs.conf.
(%) (%) Epox Dio 1
tomloides
160 Car-59 Rhodospondium toruloides UOFSY-2231 0.4 25 1.7 S R
161 Car-67 Rhodosporidi um toruloides UOFS Y-2236 2.7 31.3 2.0 S R
162 Car-70 Rhodosporidtum toruloides UOFS Y-2237 4.8 21.2 1.6 S R
163 Car-76 Rhodosporidtum toruloides UOFS Y-2238 5.9 22.1 1.7 S R
164 Car-77 Rhodospondium toruloides UOFS Y-2239 4.5 22.8 1.7 S R
165 Car-78 Rhodosporidi um toruloides UOFS Y-2240 3.8 29.9 1.9 S R
166 Car-93 Rhodospondium torutoides UOFS Y-2242 30 22.7 1.6 S R
167 Car-94 Rhodospon di um toruloides UOFS Y-2243 4.7 31.8 2.0 S R
168 Car-100 Rhodosporidi um toruloides UOFS Y-2245 4.8 24.3 1.7 S R
169 Car-103 Rhodospondium toruloides UOFS Y-2246 2.1 23.5 1.6 S R
170 Car-108 Rhodosporidi um toruloides UOFS Y-2247 3.8 24.9 1.7 S R
171 Car-120 Rhodospondium toruloides UOFS Y-2249 3.4 27.0 1.8 S R
172 Car-121 Rhodospondium toruloides UOFS Y-2250 5.0 29.6 1.9 S R
173 Car-126 Rhodosporidtum toruloides UOFSY-2251 5.4 18.9 1.5 s R
174 Car-131 Rhodospon dium toruloides UOFS Y-2252 J.J 26.2 1.8 s R
175 Car-134 Rhodospondium toruloides UOFS Y-2253 3.6 23.7 1.7 s R
176 Car-142 Rhodospondium toruloides UOFS Y-2255 5.5 22.4 1.7 S ' R
177 Car-200 Rhodosporidi um toruloides UOFS Y-2256 5.1 8.0 1.2 s R
178 Car-204 Rhodospondium toruloides UOFS Y-2257 3.4 24.3 1.7 s R
179 Car- Rhodospondium UOFS Y-2258 1.9 25.5 1.7 s R
205A toruloides
180 Car-209 Rhodospondium toruloides UOFS Y-2260 6.4 22.0 1 7 s R
181 Car-210 Rhodospon di um UOFS Y-2261 4.6 27.6 1.8 s R
62

Sampl eNo Screen no Yeast species Culture Collection no. Epoxide ee Diol ee Ea Abs.conf.
(%) (%) Epox Dio 1
182 POH-33 toruloides Rhodospondium toruloides NCYC 3218 11.2 10.1 1.4 S R
183 184185186 187 188 189 190 191 192 193 194 195196 197 198199200 201 EP-230 50680713 Alf6 681 Car-22 Car-60 Car-61 Car-62 Car-66 Car-75 714686 712 158690172 24 Rhodotorula aurantiaca Rhodotorula glutimsRhodotorula glutinisRhodotorula glutims Rhodotorula glutims Rhodotorula glutims Rhodotorula glutinis Rhodotorula glutims Rhodotorula glutinis Rhodotorula glutims Rhodotorula glutims Rhodotorula glutims Rhodotorula minuta ""Rhodotorula minuta var minutaRhodotorula minuta var minuta '"Rhodotorulasp. minuta/ mucilaginosaRhodotorula sp nearestminuta """" P Rhodotorula sp Rhodotorula sp NCYC 3185 NCYC3186UOFS Y-0459UOFS Y-0489 UOFSY-0513 UOFS Y-0653 UOFS Y-2227 UOFS Y-2232 UOFS Y-2233 UOFS Y-2234 UOFS Y-2235 UOFS Y-2265 NCYC3187 **NCYC3188 UOFSY-0835-. NCYC3194UOFSY-0125,NCYC3192 UOFS Y-2042 2.4 2.52.68.8 1.0 1 6 2.7 1 7 6.6 4.2 4.0 7.6 ' 99.2 *100 , *-100 16.4,80.1 ,i4.1 11.2 12.2 29.790.336.5 39.7 39.3 14.9 55.2 28.2 27.3 27.7M4.7 513.3 ' 2.415.515.1 78 1 1.3 1.920. 12.3 2.3 23 1.4 3.5 1.9 1.8 1.8 2.0 5.1:25. 84.2^ 1.22 8,1.4 91 S SSS S S S S S S Ss.,R" "R R R,RSs R RRR R R R R R R R R SS.s. s sR R
202 Jen-32 Sporidiobolus salmonicolor NCYC3195 5.4 76.1 7.8 s R
203 204 Jen-29 Jen-28, Sporobolomyces roseus Sporobolomyces tsugae NCYC3197 NCYC3199 3.3 8.8 17 23.9 1.5 1.8 R R S S
205 206 207208209 210 232 20 22 BV-4231 Trichosporon cutaneum var cutaneumTrichosporon cutaneum var, cutaneum^Trichosporon jiroveciiTrichosporon moniliiformeTrichosporon ovoides jw Trichosporon sp NCYC 3202 NCYC3201 NCYC 3204NCYC 3214;NCYC3207 NCYC 3210 32.0 23.8 11.0 5.871 80.3 100 83.276 538.8, 73.7 12. 520012.28.0,2.8 7.1 S R SS,R.,S R S RRc R
63

a E calculated from equation 3
All the yeast strains corresponding to samples 115-210 (Table 3) are kept and maintained at the University of the Orange Free State (UOFS), Department of Microbial, Biochemical and Food Biotechnology, Faculty of Natural and Agricultural Sciences, P O. Box 339, Bloemfontein 9300, South Africa (Tel +27 51 401 2396, Fax + 27 51 444 3219) and are readily identified by the yeast species and culture collection number as indicated. Representative examples of strains belonging to the different species have been deposited under the Budapest Treaty at National Collection of Yeast Cultures (NCYC), Institute of Food Research Norwich Research Park Colney, Norwich NR4 7UA, U.K. (Tel* +44-(0)1603-255274 Fax. +44-(0)1603-458414 Email: ncyc@bbsrc.ac uk) and are readily identified by the yeast species and culture collection accession numbers as indicated The samples deposited with the NCYC are taken from the same deposit maintained by the South African Council for Scientific and Industrial Research (CSIR) since prior to the filing date of this application. The deposits will be maintained without restriction in the NCYC depository for a period of 30 years, or 5 years after the most recent request, or for the effective life of the patent, whichever is longer, and will be replaced if the deposit becomes non-viable during that period. Samples of the yeast strains not deposited at NCYC will be made available upon request on the same basis and conditions of the Budapest Treaty
Three discrepancies were noted in the enantiopreferences for the aliphatic and aromatic epoxides:
1. Bullera dendrophila (NCYC 3152) was screened for both substrates and diplayed
variance in enantiopreference depending on the substitutenf Se/Rd for 2-methyl-1,2-
epoxyheptane and Re/Sd for 2-methyl-3-phenyl-1,2-epoxypropane.
2. Cryptococcus curvatus Car 54 yielded Se/Rd for 2~methyl-1,2-epoxyheptane while
Car 14 gave Re/Sd for 2-methyl-3:phenyl-1,2-epoxypropane.
3 Tnchopsoron cutaneum var cutaneum (NCYC 3201) yielded Re/Sd for both epoxides, while NCYC 3202 yielded Re/Sd for 2-methyl-1,2-epoxyheptane but Se/Rd for 2-methyl-3-phenyl-1,2-epoxypropane.
These discrepancies can be due to the presence of more than one epoxide hydrolase having different activities towards aliphatic and aromatic substrates in these specific strains or to the incorrect classification of the strains One skilled in the art will know how to test for such discrepancies and and to proceed accordingly.
64

Example V. Testing of samples selected from Examples III and IV Exemplary yeast strain samples selected from Table 2 and Table 3 were tested (in this Example as samples 211-223) for their ability to produce optically active epoxides and optically active vicinal diols from 2,2-disubstituted epoxides For each sample, two graphs are provided The first graph (graph A in each figure) shows the change in concentrations of the epoxide and diol enantiomers with time, while the second graph (graph B in each figure) shows the enantiomeric excess of the epoxide and diol at different conversions. The yield of the optically active epoxide or diol that can be obtained at the required enantiomeric purity can be seen from these graphs The TDE that were used to illustrate the use of the different yeast strains to prepare optically active epoxides and vicinal diols from gem-2,2-disubstituted epoxides represented by the general formula (I) is shown in scheme I in (Fig 1)
(a) Samples 211-219. Hydrolysis of (±)-2-methyl-1,2-epoxyheptane by selected
yeasts to produce optically active (S)-2-methyl-1,2-e poxy heptane (1a) and/or (R)-2-
methyl-1,2-heptanediol (1b) (Figs. 2A- 10B).
Hydrolysis of (±)-2-methyl-1,2-epoxyheptane by yeast strains selected from Table 2 was performed as described in Example I to produce (S)-2-methyl-1,2-epoxyheptane and/or (R)-2-methyM ,2-heptanediol.
(b) Sample 220. Hydrolysis of (+)-2-methyl-1,2-epoxyheptane by selected yeasts to
produce optically active (R)-2-methyl-1,2-epoxyheptane and/or (S)-2-methyl-1,2-
heptanediol (Figs. 11A and B).
Hydrolysis of (±)-2-methy1-1,2-epoxyheptane by yeast strains selected from Table »2 was performed as described in Example I to produce (R)-2-methyl-1,2-epoxyheptane and/or (S)-2-methyl-1,2-heptanediol.
(c) Sample 221. Hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxy propane by selected
yeasts to produce optically active (S)-2-methyl-3-phenyl-1,2-epoxypropane and/or (R)-
2-methyl-3-phenyM ,2-propanediol (Figs. 12Aand 12B).
Hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by a yeast strain selected from Table 3 was performed as described in Example I to produce (S)-2-methyl-3-phenyl-1,2-epoxypropane and/or (R)-2-methyl-3-phenyl-1,2-propanediol.
(d) Samples 222 and 223. Hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by
selected yeasts to produce optically active (R)-2-methyl-3-phenyl-1,2-epoxypropane
and/or (S)- 2-methyl-3-phenyl-1,2-propanediol (Figs. 13A to 14B)
65

Hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by yeasts selected from Table 3 was performed as described in Example I to produce (R)-2-methyl-3-phenyl-1,2-epoxypropane and/or (S)-2-methyl-3-phenyl-1,2-propanediol.
Example VI. Hydrolysis of (±)-2-methyl-3-phenyl-1.2-epoxypropane by a yeast cultivated in a 10 L fermenter to produce optically active (S)-2-methyl-3-phenyl-1,2-epoxypropane and/or (R)-2-methvl-3-phenyl-1.2-propanediol
Figs 15A to 15B show hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by a yeast (Sample 224) cultivated in a 10 L fermenter to produce optically active (S)- 2-methyl-3-phenyl-1,2-epoxypropane and/or (R)-2-methyl-3-phenyl-1,2-propanediol.
Example VII. Hydrolysis of (±)-2-methvl-3-phenvl-1,2-epoxypropane by recombinant yeast expression hosts transformed with the epoxide hvdrolase genes from different wild type yeast strains
Figs. 16A to 18B show hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by recombinant yeasts (as samples,225-227) expressing epoxide hydrolases from selected wild type yeast strains to produce optically active (S)- 2-methyl-3-phenyl-1 ,2-epoxypropane and/or (R)-2-methyl-3-phenyl-1,2-propanediol.
(a) Sample 225. Hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by host Yarrowia
iipolytica cells transformed with the epoxide hydrolase coding sequence from Rhodotorula
araucanae (NCYC 3183) (Fig 16). The host strain is Po1h, the vector used was the pINA
1297 zeta-based auto-cloning multicopy vector from which a "yeast cassette" can be purified
and integrated non-homologously into the genome of Po1h. The expression of the epoxide
hydrolase gene is driven by the hp4d promoter The XPR2 secretion signal was replaced by
the LIP2 secretion signal in the vector (See Madzak et al, Journal of Biotechnology 109,
2004) Reaction conditions 50 % (w/v) cell suspension, 50 mM (±)-2-methyl-3-phenyl-1,2-
epoxypropane.
(b) Sample 226. Hydrolysis of (±)-2-methyl-3-phenyM ,2-epoxypropane by host Yarrowia
lipolytica cells transformed with the epoxide hydrolase coding sequence from
Rhodospondium paludigenum (NCYC 3179) (Fig 17) The host strain is Po1h. The
expression of the epoxide hydrolase gene is driven by the constitutive TEF promoter (See
Madzak et a/., Journal of Biotechnology 109, 2004). Reaction conditions. 50% (w/v) cell
suspension, 100 mM (±)-2-methyl-3-phenyl-1,2-epoxypropane
(c) Sample 227. Hydrolysis of (±)-2-methyl-3-phenyl-1,2-epoxypropane by the host
66

Yarrowia lipolytica transformed with the gene from Rhodospondium paludigenum UOFS Y-0482/NCYC 3179 (Fig 18). The host strain is Po1h. The expression of the epoxide hydrotase gene is driven by the hp4d promoter. (See Madzak et a/., Journal of Biotechnology 109, 2004). Reaction conditions- 10 % (w/v) cell suspension, 100 mM (±)-2-methyl-3-phenyl-1,2-epoxypropane.
Example VIM. Hydrolysis of (±)-2-methvl-3-phenvM,2-epoxypropane by a crude enzyme preparation obtained' from the host Yarrowia lipolytica expressing the epoxide hydrolase derived from Rhodotorula araucariae NCYC 3183 (YL 25 TsA)
Figs. 19A and 19B show hydrolysis of {±)-2-methy!-3-phenyl-1,2-epoxypropane by the epoxide hydrolase derived from Rhodotorula araucariae NCYC 3183 (YL 25 TsA) expressed in Yarrowia lipolytica Fig 19A shows hydrolysis by whole cells and Fig. 19B shows hydrolysis by a crude enzyme prepartion obtained from the cells
Example IX. Amino acid sequences of enantioselective epoxide hvdrolase polypeptide for the hydrolysis of ft)-2.2disubstituted epoxides to produce optically active epoxides and/or diols.
The sequences with SEQ ID NOs: 1-5 (Figs 22-26) are examples of ammo acid sequences of enantioselective epoxide hydrolases for the hydrolysis of (±)-2,2 -disubstituted epoxides to produce optically active (S)-epoxides and/or (R)- diols The cDNAs encoding the polypeptides were obtained as described in Example II from the indicated yeast strains. The sequences with SEQ ID NOs.6 and 7 (Figs. 27 and 28) are examples of amino acid sequences of enantioselective epoxide hydrolases for the hydrolysis of (±)-2,2-disubstituted epoxides to produce optically active (R)-epoxides and/or (S)- diols The cDNAs encoding the polypeptides were obtained as described in Example II from the indicated yeast strains.
Example X. Nucleotide sequences of enantioselective epoxide hvdrolase genes for the hydrolysis of (±)-2.2-disubstituted epoxides to produce optically active epoxides and/or diols.
The sequences with SEQ ID NOs. 8-12 (Figs. 29-33) are examples of cDNA sequences encoding enantioselective epoxide hydrolase genes for the hydrolysis of (±)-2,2-disubstituted epoxides to produce optically active (S)-epoxides and/or (R)- diols The cDNAs encoding the polypeptides were obtained as described in Example II from the indicated yeast strains
67

The sequences with SEQ ID NOs 13 and 14 (Fig 34 and 35) are examples of cDNA sequences encoding enantioselective epoxide hydrolase genes for the hydrolysis of (±)-2,2-disubstituted epoxides to produce optically active (R)-epoxides and/or (S)- diols. The cDNAs encoding the polypeptides were obtained as described in Example II from the indicated yeast strains.
Example XI. Homology at the amino acid level of enantioelective epoxide hydolases for the hydrolysis of (±)-2.2-disubstituted epoxides to produce optically active epoxides and/or diols.
Fig. 36 shows the percent homology at the amino acid level of enantioselective epoxide hydrolaseses described in the Example IX Alignments were done using DNAMAN Version 5 2 9 {Lynnon Biosoft) software using the multiple sequence alignment mode (Fast alignment/Quick alignment settings)
Example XII. Homology at nucleotide level of enantioelective epoxide hvdolase cDNA for the hydrolysis of (±)-2.2-disubstituted epoxides to produce optically active epoxides and/or diols.
Fig 37 shows the percent homology at the nucleotide level of cDNAs encoding the enantioselective epoxide hydrolases described in Example X. Alignments were done in DNAMAN Version 5.2 9 (Lynnon Biosoft) software using the multiple sequence alignment mode (Fast alignment/Quick alignment settings)
References cited
Madzak, C, Gaillardin, C, Beckerich, J-M (2004). Heterologous protein expression and
secretion in the non-conventional yeast Yarrowta hpolytica. a review. Journal of
Biotechnology 109. 63-81.
Wlischitz, M.; Kroutil, W.; Wandel, U.; Faber, K. Tetrahedron Asymmetry 1995, 6, 1261-
1272.
Nicaud J-M, Madzak C, Van den Broek P, Gysler C, Duboc P, Niederberger P,
Gaillardin C. (2002) Protein expression and secretion in the yeast Yarrowia hpolytica
FEMS Yeast Research 2, 371-279.
Orru, R.V.A., Mayer, S.» Kroutil, W. and Faber, K. (1998) Chemoenzymatic deracemization
of (±)-2,2-disubstituted oxiranes. Tetrahedron 54. 859-874
68

Pedragosa-Moreau, S., Archelas, A. and Furstoss, R. (1996) Microbiological
Transformations 32 Use of epoxide hydrolase mediated biohydrolysis as a way to
enantiopure epoxides and vicinal diols - Application to substituted styrene oxide derivatives.
Tetrahedron 52: 4593-4606
Steinreiber, A., Osprian, I., Mayer, S.F., Orru, R.V. and Faber, K. (2000) Enantioselective
hydrolysis of functionalized 2,2-disubstituted oxiranes with bacterial epoxide hydrolases
Eur.J Org.Chem 22 3703-3711.
Xuan J-W, Fournier P, Gaillardin C. (1988) Cloning of the LYS5 gene encoding
saccharopine dehydrogenase from the yeast Yarrowia lipolytica by target integration
Current Genetics 14, 15-21
A number of embodiments of the invention have been described. Nevertheless; it will be understood that various modifications may be made without departing from the spirit and scope of the invention. Accordingly, other embodiments are within the scope of the following claims.
69

SEQ. ID. NO. 1
Rhodosvoridium toruloides NCYC 3181 (#1)
Amino acid sequence
ORIGIN
1 MATHTFASPP TRFTVDIPQS ELDELDFRLD KTRWPATEIV PEDGADDPTA FGLGAGPTLP
61 LMKELAKGWR EFDWKKAQDH LNTFEHYTVE IEDLSIHFLH HRSTRPNAVP LILCHGWPGH
121 FGEFLNVIPL LTEPSDPSAQ AFHVVAPSMP GYAWSSPPPS SKWSMPDTAR VFDKLMTGLG
181 YEKYMAQGGD WGSIAARCLG SLHKDHCKAV HLNFLPVFPP VPMWLINPHT LLAWAPRFLV
241 PEKQAARMKR GLAYLEKGSA YYVMQQLTPR TPAYGLTDSP VGLLAWIGEK FEPTIQEASK
301 QAQPTLTRDE LYFTCSLYWF TRSIGTSFLP YSLNPHFTTF LTDSSTTCPT LPCPSTRARS
361 TARQNGTLSV PATSSDQGRA GGRTLCCARE ARRVCRPSQG GVRRHVGEV
SEQ. ID. NO. 2
Rhodosporidium tor uloides UOFS Y-0471 (#46)
Amino acid sequence
ORIGIN
1 MKMATHTFAS PPTRFTVDIP QSELDELHSR LDKTRWPATE IVPEDGTDDP TAFGLGAGPT
61 LPLMKELAKG WREFDWKKAQ DHLNTFEHYM VEIEDLSIHF LHHRSTRPNA VPLILCHGWP
121 GHFGEFLNVI PLLTEPSDPS AQAFHVVAPS MPGYAWSLPP PSSKWNMPDT ARVFDKLMTG
181 LGYEKYMAQG GDWGSIAARC LGSLHKDHCK AVHLNFLPVF PPVPMWLINP HTLLAWAPRF
241 LVPEKQAARM KRGLAYLEKG SAYYVMQQLT PRTPAYGLTD SPVGLLAWIG EKFEPTIQEA
301 SKQAQPTLTR DELYFTCSLY WFTRSIGTSF LPYSLNPHFT TFLTDSKYHL PNFALSLYPG
361 EIYCPAERDA KRTGNLKWIK DAPEGGHFAA LEKPDVFVEH LREAFGVMWE K
SEQ. ID. NO. 3
Rhodotorula araucariae NCYC 3183 (#25)
Amino acid sequence
ORIGIN
1 MSEHSFEAPP QPFTVDFAPH IEDLHRRLDN ARWPTQEIVP VDVSETEHHN AFGLGMGPQL
61 NLMKELANGW RAFDQSALQD HLNSFNNWKV EIEGLSIHFL HHRSTRAGAL PLILCHGWPG
121 GYHEFLHVVQ LLTEPEGADA QAFHLVVPSM PGYAFSSPPP TAKWGMEDTA RVFDKLMTGL
181 GYNKYVAQGG DWGSITARCL GALHKDHCIA VHLNFCPVPP PFPFDQFNPR TLLNWMPRFV
241 ISDQQRAKLE RGLAYLEKGS AYYVMQQLTP RTPAYALNDS PIGLLAWIGE KMIPGINEAS
301 AQPNPTLNRD ALYTTLSLYW FTNSIGTSFL PYSLNPHFST FLTSPRYRLP NFALSSFPGE
361 LFSPTPRDAA RTGVMRWYKE ADDGGHFAAL EKPDVFSQHV REAVKAMLSS
70

SEQ. ID. NO. 4
Crvvtococcus curvatusNCYC 3158 (Car 054)
Amino acid sequence
ORIGIN
1 MATHTFASPP TRFTVDIPQS EVDQLHSRLD KTRWPGTEIV PEDGADDPTA FGLGAGPTLP
61 LMKELAKGWR DFDWKKAQDH LNTFEHYTVE IEDLSIHFLH HRSTRPNAVP LILCHGWPGH
121 FGEFLHVIPL LTEPSDPSAQ AFHVVAPSMP GYAWSSPPPT SKWNMPDTAR VSDKLMNGLG
181 YEKYMAQGGD WGSIAARCLG ALHKDHCKAV HLNFLPVFPP VPMWLINPHT LLAWAPRFLV
241 PEKQAARMKR GLAYLEKGSA YYVMQQLTPR TSAYGLTDSP VGLLAWIGEK FEPTIQEASK
301 QAQPTLTRDE LYFTCSLYWF TRSIGTSFLP YSLNPHFTTF LTDSKYYLPN FALSLYPGEI
361 YCPAERDAKR TGNLKWIKDA PEGGHFAALE KPDVFVDHLR EAFGVMWEK
SEQ. ID. NO.5
Rhodosyoridium patudieenum NCYC 3179 (#692)
Amino acid sequence
ORIGIN
1 MAAHSFTAPP APYNIDFAPQ VNDLHRRLDA ARWPEHDVVP DDVDHGEHGA FGLGAGPSLA
61 LMKELAQEWR GQDQKQLQDH LNSYKNYRVE IEGLNIHFLH YPSSRADAFP LILCHGWPGG
121 YHEFLHVLER LTEPEDQGSR AFHVVVPSMP GYAFSSPPKT AKWGMEDTAR VFDKLMTGLG
181 YAKYAAQGGD WGSITARCLG SLHKENCVAV HLNFCPVPPP FPLNMFNPRT LLDWMPRFVL
241 PDQRRAKIER GVAYIERGSA YYAMQNLTPR TPAYGLNDSP IGLLAWIGEK MIPGIDKAVK
301 HPNATLNREA LFTTLSIYWF TGSIGSSFLP YALNPHFSTF LVSPRHQLPN FALSNFPDEL
361 FTPEERDARR TGNLRWYKDA EDGGHFAALE KPEVFAEHVR EAMGVLLSNQ A
SEQ. ID. NO. 6
Debaromyces hansenii NCYC 3167 (#1131
Amino acid sequence
ORIGIN
1 MMQGQYKIQL RNGVRIFSTF SNYDNHDVFC SGGERKWTRV IFLLHGFPDN NSSYNSVWTV
61 ILDSVPEDEK VLLLAPSMRG YEPSSQGEQC DYKMSDLAGD VSSWIKNISP DGIPVHLVGH
121 DWGAIVAFKT ASMYPEMITS MACLAIPYIT NIRLWEFAWY FPDQIYHSSY MFTMQFGWLY
181 KKRLSDTSSN SYLDGLWRCW SPTWNYTVDE IDSVKRTLQE PGVIDASTAY YRCIANPLNI
241 SNRRWNVDFK KVPTLLLGGE RDGCMNEKLY RLEASKLANN PYVKVKTISN VGHFLHREDP
301 TKVGELITDW FSEYP*
71

SEQ. ID. NO. 7
Rhodotorula minuta var minuta UOFS Y-0835 (#712) Partial Amino acid sequence
ORIGIN
1 HWRFPSI5FH YRSTRPERYS RSFFCHGWPG HFRLSFLNVI PLLTEPSDPS AQAFHVVAPS
61 MPGYAWYSPP PSSKWSMPDT ARVFDKLMTG LGYEKYMAQG GDWGSIAARC LGSLYKDHCK
121 AVHLNFLPVF PPVPMWLINP HTLLAWAPRF LVPEKQAARM KRGLAYLEKG SAYYVMQQLT
181 PRTPAYGLTD SPVGLLAWIG EKFEPTIQEA SKQAQPTLTR DELYFTCSLY WFARSIGTSF
241 LPYSLNPHFT TFLTDSRYHL PNFALSLYPG EIYCPAERDA KRTGNLKWIK DAPEGGHFAA
301 LEKPDVFVEH LREAFGVMWE K
SEQUENCE ID NO 8
Rhodosporidium toruloides NCYC 3181 (#1)
Nucleotide sequence
ORIGIN
1 ATGGCGACAC ACACATTCGC TTCGCCTCCC ACGCGCTTCA CCGTCGACAT CCCACAGTCA
61 GAACTCGACG AACTCGACTT CCGACTCGAC AAGACCCGCT GGCCGGCGAC AGAGATCGTT
121 CCAGAGGATG GGGCGGACGA CCCGACGGCG TTTGGGCTCG GAGCAGGGCC GACGCTGCCG
181 CTCATGAAGG AACTGGCGAA GGGTTGGCGC GAGTTCGACT GGAAGAAGGC GCAGGACCAC
241 CTCAACACCT TTGAGCACTA CACGGTCGAA ATCGAGGACC TCTCCATCCA CTTCCTCCAC
301 CACCGCTCGA CTCGCCCGAA TGCTGTTCCG CTCATCCTCT GCCACGGCTG GCCAGGCCAC
361 TTCGGCGAGT TCCTGAACGT CATACCGCTC TTGACGGAGC CGTCGGACCC GTCCGCCCAG
421 GCGTTCCACG TCGTCGCGCC TTCGATGCCC GGTTATGCTT GGTCTTCGCC TCCTCCGTCC
481 TCCAAGTGGA GCATGCCTGA TACCGCGAGG GTCTTCGACA AGCTCATGAC CGGGCTTGGC
541 TACGAGAAGT ACATGGCGCA GGGCGGAGAC TGGGGCAGCA TCGCTGCTCG CTGCCTTGGA
601 TCGCTTCACA AAGACCACTG CAAAGCCGTC CACCTCAACT TCCTCCCCGT CTTCCCACCC
661 GTCCCGATGT GGCTTATCAA CCCGCACACG CTCCTTGCCT GGGCACCGCG CTTCCTCGTG
721 CCGGAGAAGC AGGCTGCGCG TATGAAGCGC GGGTTGGCGT ACCTTGAGAA GGGCTCCGCC
781 TACTACGTCA TGCAGCAGTT GACGCCTCGC ACGCCTGCGT ACGGCCTGAC CGACAGTCCC
841 GTCGGCTTGC TGGCCTGGAT CGGCGAGAAG TTCGAGCCGA CCATTCAGGA GGCGAGCAAG
901 CAAGCCCAGC CGACCCTGAC TCGCGACGAG CTCTACTTCA CCTGCTCGCT CTACTGGTTC
961 ACCCGCTCAA TCGGCACCTC CTTCCTTCCC TACTCGCTCA ACCCGCACTT CACCACCTTC
1021 CTGACCGACA GCAGGTACCA CCTGCCCAAC TTTGCCCTGT CCCTCTACCC GGGCGAGATC
1081 TACTGCCCGG CAGAACGGGA CGCCAAGCGT ACCGGCAACC TCAAGTGGAT CAAGGACGCG
1141 CCCGATGGAG GACACTTTGC TGCGCTCGAG AAGCCCGATG TGTTTGTCGA GCATCTCAGG
1201 GAGGCGTTTG GCGTCATGTG GGAGAAGTAG
72

SEQUENCE ID NO 9
Rhodosporidium toruloides VOFS Y-0471 (#46)
Nucleotide sequence
ORIGIN
1 ATGGCGACAC ACACATTCGC TTCGCCTCCC ACCCGCTTCA CCGTCGACAT CCCACAGTCG
61 GAACTCGACG AACTTCACTC GCGACTCGAC AAGACCCGCT GGCCGGCGAC AGAGATCGTT
121 CCAGAGGATG GGACGGACGA TCCGACGGCG TTTGGGCTCG GAGCAGGGCC GACGCTGCCG
181 CTCATGAAGG AATTGGCGAA GGGTTGGCGC GAGTTCGACT GGAAAAAGGC GCAGGACCAC
241 CTCAACACCT TCGAGCACTA CATGGTCGAA ATTGAGGACC TCTCGATCCA CTTCCTCCAC
301 CATCGCTCGA CTCGCCCGAA CGCTGTTCCC CTCATCCTCT GCCACGGCTG GCCAGGCCAC
361 TTTGGCGAGT TCCTGAACGT TATCCCGCTC TTGACGGAGC CGTCGGACCC CTCCGCTCAG
421 GCGTTCCACG TCGTCGCCCC TTCGATGCCT GGCTATGCTT GGTCTTTGCC TCCTCCGTCC
481 TCCAAGTGGA ACATGCCTGA CACCGCGAGG GTCTTCGACA AGCTCATGAC CGGGCTTGGC
541 TACGAGAAGT ACATGGCGCA GGGCGGAGAC TGGGGAAGCA TCGCCGCTCG CTGCCTTGGA
601 TCGCTGCACA AGGACCATTG CAAAGCCGTC CACCTCAACT TCCTCCCCGT CTTCCCACCC
661 GTCCCGATGT GGCTTATCAA CCCGCACACG CTCCTTGCCT GGGCACCGCG CTTCCTCGTG
721 CCGGAGAAGC AGGCTGGGCG TATGAAGCGC GGGTTGGCGT ACCTTGAGAA GGGCTCCGCC
781 TACTACGTCA TGCAGCAGTT GACGCCTCGC ACGCCTGCGT ACGGCCTGAC CGACAGTCCC
841 GTCGGCTTGC TGGCCTGGAT CGGCGAGAAG TTCGAGCCGA CCATTCAGGA GGCGAGCAAG
901 CAAGCCCAGC CGACCCTGAC TCGCGACGAG CTCTACTTCA CCTGCTCGCT CTACTGGTTC
961 ACCCGCTCAA TCGGCACCTC CTTCCTTCCC TACTCGCTCA ACCCGCACTT CACCACCTTC
1021 CTGACCGACA GCAAGTACCA CCTGCCCAAC TTTGCCCTCT CGCTTTACCC AGGCGAGATC
1081 TACTGCCCCG CCGAGCGGGA CGCCAAGCGC ACCGGCAACC TCAAGTGGAT CAAGGACGCG
1141 CCTGAGGGAG GACACTTTGC TGCGCTCGAA AAGCCGGATG TGTTTGTCGA GCACCTCAGG
1201 GAGGCGTTTG GCGTCATGTG GGAGAAGTAG
73

SEQUENCE ID NO 10
Rhodotorula araucariae NCYC 3183 (#25)
Nucleotide sequence
ORIGIN
1 ATGAGCGAGC ACAGCTTCGA GGCCCCGCCA CAGCCGTTTA CGGTCGACTT TGCTCCCCAC
61 ATCGAGGATC TCCACCGCCG TCTCGACAAT GCGCGCTGGC CGACGCAAGA GATTGTCCCC
121 GTCGACGTGT CCGAGACGGA GCATCACAAC GCGTTCGGAC TCGGGATGGG CCCGCAGCTC
181 AACCTTATGA AGGAGCTCGC CAACGGCTGG CGCGCGTTCG ACCAGTCGGC GCTCCAGGAC
241 CACCTCAACA GCTTCAACAA CTGGAAGGTC GAGATCGAGG GATTGTCGAT CCACTTCCTC
301 CACCATCGCT CGACGCGCGC CGGCGCTCTC CCGCTCATCC TGTGCCATGG CTGGCCCGGC
361 GGGTACCACG AGTTCCTCCA CGTCGTCCAG CTCCTCACCG AACCAGAGGG GGCGGATGCG
421 CAGGCGTTTC ACCTCGTCGT CCCCTCGATG CCCGGGTACG CCTTCTCGTC TCCGCCGCCG
481 ACGGCCAAGT GGGGCATGGA AGACACTGCA AGGGTTTTTG ACAAGCTCAT GACCGGTTTG
541 GGGTACAACA AGTATGTCGC GCAGGGCGGT GACTGGGGGT CCATCACGGC GCGATGCCTC
601 GGCGCGCTGC ACAAGGACCA CTGCATTGCT GTCCACCTCA ACTTCTGCCC CGTCCCGCCG
661 CCGTTCCCAT TCGACCAGTT CAACCCGCGC ACGCTGCTCA ACTGGATGCC GCGCTTCGTG
721 ATCTCGGACC AGCAGCGTGC GAAGCTCGAG CGTGGGCTGG CGTACCTCGA GAAGGGGTCT
781 GCTTACTATG TCATGCAGCA GCTCACACCG CGTACCCCGG CCTACGCTCT CAATGACAGC
841 CCGATTGGCC TGCTCGCCTG GATTGGCGAA AAGATGATCC CAGGCATCAA CGAGGCGAGC
901 GCGCAGCCGA ACCCGACGCT CAATCGCGAT GCGTTGTACA CCACGCTCTC GCTGTACTGG
961 TTCACCAACT CCATCGGCAC CTCTTTCCTC CCCTACTCGC TTAACCCGCA CTTCAGCACG
1021 TTCCTCACCT CGCCCCGCTA TCGCCTGCCG AACTTTGCGC TGTCTTCCTT CCCGGGCGAG
1081 CTGTTCTCGC CGACGCCGCG CGATGCTGCG AGGACGGGCG TGATGCGCTG GTACAAGGAG
1141 GCGGACGATG GCGGGCACTT TGCGGCGCTC GAGAAGCCCG ATGTGTTCAG CCAGCATGTC
1201 AGGGAGGCAG TCAAGGCCAT GCTGTCGTCG TGA
74

SEQUENCE ID NO II
Crwtacoccus curvatus NCYC 3158 (Car 054)
Nucleotide sequence
ORIGIN
1 ATGGCGACAC ACACATTCGC TTCGCCTCCC ACCCGCTTCA CCGTCGACAT TCCGCAGTCG
61 GAAGTTGACC AACTTCACTC GCGACTCGAT AAGACTCGCT GGCCAGGGAC AGAGATCGTT
121 CCAGAGGATG GGGCGGACGA CCCGACGGCG TTTGGACTCG GAGCAGGACC AACGCTGCCG
181 CTCATGAAGG AACTGGCGAA GGGTTGGCGC GACTTCGACT GGAAGAAGGC GCAGGACCAC
241 CTCAACACCT TCGAGCACTA CACGGTGGAG ATCGAGGACC TCTCGATCCA CTTCCTCCAC
301 CATCGCTCGA CTCGTCCGAA TGCTGTTCCC CTCATCCTCT GCCACGGCTG GCCAGGACAC
361 TTCGGCGAGT TTCTACACGT TATACCACTC TTGACGGAGC CGTCGGACCC GTCCGCTCAG
421 GCGTTTCACG TCGTCGCGCC TTCGATGCCT GGTTATGCTT GGTCTTCGCC TCCTCCTACC
481 XCCAAGTGGA ATATGCCTGA CACCGCAAGG GTGTCCGACA AGCTTATGAA CGGACTCGGC
541 TACGAGAAGT ACATGGCGCA GGGCGGAGAC TGGGGCAGCA TCGCCGCTCG CTGCCTCGGA
601 GCGCTGCACA AAGATCACTG CAAAGCCGTC CACCTCAACT TCCTCCCCGT CTTCCCGCCC
661 GTCCCTATGT GGCTCATCAA CCCACACACA CTCCTCGCAT GGGCTCCGCG CTTCCTTGTG
721 CCGGAGAAGC AGGCTGCGCG CATGAAGCGC GGGTTGGCGT ACCTCGAAAA GGGCTCCGCC
781 TACTACGTCA TGCAGCAATT GACGCCTCGC ACGTCTGCGT ACGGCCTTAC TGACAGTCCC
841 GTCGGCTTGC TGGCCTGGAT CGGCGAGAAG TTTGAGCCGA CCATTCAGGA AGCGAGCAAG
901 CAAGCCCAGC CGACCCTCAC TCGCGACGAG CTCTACTTCA CCTGCTCCTT GTACTGGTTC
961 ACCCGCTCAA TCGGCACCTC CTTCCTGCCC TACTCGCTCA ACCCGCACTT CACGACCTTC
1021 CTGACCGACA GCAAGTATTA CCTGCCCAAT TTTGCCCTCT CCCTGTACCC GGGCGAGATC
1081 TACTGCCCTG CCGAGCGGGA CGCCAAGCGC ACTGGCAACC TCAAGTGGAT CAAGGACGCG
1141 CCTGAGGGAG GACACTTTGC GGCGCTCGAG AAGCCCGACG TGTTTGTCGA CCATCTCAGG
1201 GAGGCATTTG GCGTTATGTG GGAGAAGTAG
75

SEQUENCE ID NO 12
Rhodosvoridium paludisenum NCYC 3179 (#692)
Nucleotide sequence
ORIGIN
1 ATGGCTGCCC ATTCCTTTAC TGCACCTCCT GCACCCTACA ACATCGACTT TGCGCCCCAG
61 GTAAATGACC TGCACCGCCG TCTCGATGCT GCCCGCTGGC CGGAACACGA CGTGGTGCCC
121 GACGATGTGG ATCACGGAGA GCACGGCGCA TTCGGACTCG GCGCTGGTCC CAGCCTCGCC
181 CTCATGAAGG AGCTCGCGCA GGAATGGAGG GGCCAGGACC AGAAGCAGCT GCAGGACCAC
241 CTCAACTCCT ACAAGAACTA TCGCGTCGAG ATCGAGGGTC TCAACATCCA CTTCCTGCAC
301 TACCCGTCGT CTCGCGCCGA TGCGTTCCCG CTCATCCTGT GCCACGGCTG GCCTGGCGGC
361 TACCACGAGT TCCTGCACGT 'CCTAGAGCGC CTCACGGAGC CCGAGGATCA GGGGTCGCGG
421 GCCTTCCATG TCGTCGTGCC TTCCATGCCG GGTTACGCCT TCTCCTCGCC GCCCAAGACG
481 GCAAAATGGG GCATGGAGGA CACGGCTCGC GTGTTCGACA AGCTCATGAC GGGGCTAGGT
541 TACGCCAAGT ATGCGGCCCA AGGCGGTGAC TGGGGGTCTA TCACGGCGCG CTGCCTAGGT
601 TCGCTGCACA AGGAGAACTG CGTCGCTGTC CACCTCAACT TCTGCCCGGT TCCCCCGCCG
661 TTCCCGCTCA ACATGTTCAA CCCGCGCACA CTTCTGGACT GGATGCCTCG CTTTGTCCTG
721 CCTGATCAAC GGCGGGCCAA GATTGAGCGC GGCGTGGCCT ATATCGAGCG CGGCTCTGCC
781 TACTACGCCA TGCAAAACTT GACGCCGCGC ACGCCTGCGT ACGGCTTGAA CGATAGTCCG
841 ATTGGTTTGC TCGCGTGGAT TGGCGAGAAG ATGATTCCGG GCATTGACAA GGCTGTCAAG
901 CATCCGAACG CAACCCTCAA TCGCGAAGCT CTTTTCACGA CACTCTCGAT CTACTGGTTC
961 ACGGGCTCGA TTGGCTCCTC CTTCCTGCCA TACGCTCTCA ACCCGCACTT CTCTACCTTC
1021 CTCGTCTCGC CGCGGCACCA ACTGCCGAAC TTTGCTCTGT CCAACTTTCC CGACGAGCTG
1081 TTCACGCCCG AAGAACGCGA TGCTCGCCGA ACCGGAAACT TGCGGTGGTA CAAGGATGCA
1141 GAGGATGGAG GGCACTTCGC GGCGCTGGAG AAGCCCGAGG TCTTCGCCGA GCACGTAAGG
1201 GAGGCGATGG GGGTCTTGCT GTCGAACCAG GCCTGA
76

SEQUENCE ID NO 13
Debaromvces hansenii NCYC 3167 (#113)
Nucleotide sequence
ORIGIN
1 ATGATGCAAG GTCAATACAA GATTCAACTT CGCAACGGAG TAAGAATATT TTCTACCTTC
61 AGCAATTATG ATAACCACGA TGTATTTTGT AGTGGTGGTG AGCGTAAATG GACTCGAGTT
121 ATATTCCTCC TCCATGGGTT TCCCGATAAT AACAGTTCAT ATAATAGCGT TTGGACAGTG
181 ATATTAGATT CTGTCCCAGA AGATGAAAAG GTATTGTTGC TAGCGCCATC AATGAGAGGT
241 TACGAACCGT CTAGTCAAGG TGAACAATGT GATTATAAGA TGTCAGATCT TGCGGGCGAT
301 GTAAGCTCAT GGATTAAAAA TATTTCACCA GATGGTATTC CAGTACACCT TGTTGGTCAT
361 GATTGGGGAG CGATAGTGGC TTTTAAGACC GCTAGTATGT ACCCTGAGAT GATAACATCA
421 ATGGCTTGTT TGGCCATTCC-ATATATCACC AATATTCGAT TATGGGAGTT TGCATGGTAT
481 TTTCCAGACC AGATTTATCA TTCCAGCTAT ATGTTCACCA TGCAGTTTGG ATGGCTCTAT
541 AAAAAGAGGC TTTCTGATAC GAGTAGCAAC AGTTATTTGG ACGGATTATG GCGCTGCTGG
601 TCTCCGACAT GGAATTATAC CGTAGATGAA ATCGATAGTG TTAAGAGAAC ACTTCAAGAA
661 CCTGGAGTTA TCGATGCATC AACTGCATAC TACAGATGTA TTGCTAACCC CCTAAACATT
721 TCTAATAGGC GCTGGAACGT AGACTTTAAA AAAGTTCCAA CGTTGTTGCT CGGCGGAGAG
781 CGGGATGGGT GCATGAATGA AAAGTTGTAT CGTTTAGAAG CCAGTAAGCT TGCAAATAAT
841 CCATATGTTA AGGTCAAGAC AATTTCAAAT GTCGGGCATT TCTTGCATCG TGAAGACCCT
901 ACAAAAGTTG GTGAATTGAT AACTGACTGG TTCAGTGAAT ATCCTTAG
77

SEQUENCE ID NO 14
Rhodotorula minuta var. minuta UOFS Y-0835 (#712)
Partial Nucleotide sequence
ORIGIN
1 CACTGGCGTT TTCCATCCAT TTCTTTCCAC TACCGCTCGA CTCGCCCCGA ACGCTATTCC
61 CGCTCATTCT TCTGCCACGG CTGGCCAGGC CACTTTCGGT TGAGTTTCTT GAACGTCATA
121 CCGCTCTTAA CGGAGCCGTC GGACCCGTCC GCCCAGGCGT TCCACGTCGT CGCGCCTTCG
181 ATGCCCGGTT ATGCTTGGTA TTCGCCTCCT CCGTCCTCCA AGTGGAGCAT GCCTGATACC
241 GCGAGGGTCT TCGACAAGCT CATGACCGGG CTTGGCTACG AGAAGTACAT GGCGCAGGGC
301 GGAGACTGGG GCAGCATCGC TGCTCGCTGC CTTGGATCGC TGTACAAAGA CCACTGCAAA
361 GCCGTCCACC TCAACTTCCT CCCCGTCTTC CCACCCGTCC CGATGTGGCT TATCAACCCG
421 CACACGCTCC TTGCCTGGGC ACCGCGCTTC CTCGTGCCGG AGAAGCAGGC TGCGCGTATG
481 AAGCGCGGGT TGGCGTACCT TGAGAAGGGC TCCGCCTACT ACGTCATGCA GCAGTTGACG
541 CCTCGCACGC CTGCGTACGG CCTGACCGAC AGTCCCGTCG GCTTGCTGGC CTGGATCGGC
601 GAGAAGTTCG AGCCGACCAT TCAGGAGGCG AGCAAGCAAG CCCAGCCGAC CCTGACTCGC
661 GACGAGCTCT ACTTCACCTG CTCGCTCTAC TGGTTCGCCC GCTCAATCGG CACCTCCTTC
721 CTTCCCTACT CGCTCAACCC GCACTTCACC ACCTTCCTGA CCGACAGCAG GTACCACCTG
781 CCCAACTTTG CCCTGTCCCT CTACCCGGGC GAGATCTACT GCCCGGCAGA ACGGGACGCC
841 AAGCGTACCG GCAACCTCAA GTGgATCAAG GACGCGCCCG AGGGAGGACA CTTTGCTGCG
901 CTCGAGAAGC CCGATGTGTT TGTCGAGCAT CTCAGGGAGG CGTTTGGTGT CATGTGGGAG
961 AAGTAG
78

WE CLAIM:
1 A process for obtaining an optically active epoxide or an optically active vicinal diol, which process includes the steps of:
providing an enantiomeric mixture of a 2,2-disubstituted epoxide,
creating a reaction mixture by adding to the enantiomeric mixture a polypeptide, or a functional fragment thereof, having enantioselective 2,2-disubstituted epoxide hydrolase activity, the polypeptide being a polypeptide encoded by a gene of a yeast cell, incubating the reaction mixture; and
recovering from the reaction mixture, (a) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol; (b) an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide; or (c) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol and an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide.
2. A process for obtaining an optically active epoxide or an optically active vicinal diol,
which process includes the steps of
providing an enantiomeric mixture of a 2,2-disubstituted epoxide,
creating a reaction mixture by adding to the enantiomeric mixture a cell comprising a nucleic acid encoding, and capable of expressing, a polypeptide having enantioselective 2,2-disubstituted epoxide hydrolase activity, the polypeptide being a polypeptide encoded by a gene of a yeast cell; incubating the reaction mixture; and
recovering from the reaction mixture: (a) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol; (b) an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide; or (c) an enantiopure, or a substantially enantiopure, 2,2-disubstituted vicinal diol and an enantiopure, or a substantially enantiopure, 2,2-disubstituted epoxide.
3. The process of claims 1 or 2, wherein the cell is a yeast cell.
4 The process of claims 1 to 3, wherein the polypeptide is encoded by an endogenous ¦ gene of the cell.
5. The process of claims 2 or 3, wherein the cell is a recombinant ceil and the polypeptide is encoded by a nucleic acid sequence with which the cell is transformed.
6 The process of claim 5, wherein the nucleic acid sequence is a heterologous nucleic
acid sequence.
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7 The process of claim 5, wherein the nucleic acid sequence is a homologous nucleic
acid sequence.
8 The process of any of claims 1 to 7, wherein the polypepttde is a full-length yeast
epoxide hydrolase
9 The process of any of claims 1 to 7, wherein the polypeptide is a functional fragment of
yeast epoxide hydrolase.
10 The process of any one of claims 1 to 9, wherein the process is carried out at a pH
from 5 to 10.

11. The process of any one of claims 1 to 10, wherein the process is carried out at a
temperature of 0°C to 70 °C
12. The process of any one of claims 1 to 11, wherein the concentration of the 2,2-
disubstituted epoxide in the reaction matrix is at least equal to the soluble concentration of
the 2,2-disubstituted epoxide in water.
13. The process of any one of claims 1 to 12, wherein the 2,2-disubstituted epoxide of the
enantiomeric mixture is a compound of the general formula (I) and the vicinal diol produced
by the process is a compound of the general formula (II),

wherein
R1 and R2 are, independently of each other, selected from the group consisting of a variably substituted straight-chain or branched alkyl group, a variably substituted straight-chain or branched alkenyl group, a variably substituted straight-chain or branched alkynyl group, a variably substituted cycloalkyl group as well as cycloalkenyl groups, a variably substituted aryl group, a variably substituted aryl alkyl group, a variably substituted heterocyclic group, a
80

variably substituted straight-chain or branched alkoxy group, a variably substituted straight-chain or branched alkenyloxy group, a variably substituted aryloxy group, a variably substituted aryl alkyloxy group, a variably substituted alkylthio group, a variably substituted alkoxycarbonyl group, a variably substituted straight chain or branched alkylamino or alkenyl amino group, a variably substituted arylamino or arylalkyiamino group, a variably substituted carbamoyl group, a variably substituted acyl group, and a functional group; or wherein R1 and R2, together as a whole unit are a carbocycle with 5 to 7 atoms or a heterocycle with 5 to 7 carbon atoms.
14 The process of any of claims 1 to 13, wherein the enantiomeric mixture is a racemic
mixture or a mixture of any ratio of amounts of the enantiomers.
15 The process of any of claims 1 to 14, which process includes adding to the reaction
water and at least one water-immiscible solvent

16. The process of claim 15, wherein the water-immiscible solvent is selected from the
group consisting of toluene, 1,1,2-trichlorotrifluoroethane, methyl tert-butyl ether, methyl
isobutyl ketone, dibutyl-o-phtalate, aliphatic alcohols containing 6 to 9 carbon atoms.and
aliphatic hydrocarbons containing 6 to 16 carbon atoms
17. The process of any of claims 1 to 14, which process includes adding to the reaction
water and at least one water-miscible organic solvent.
18. The process of claim 17, wherein the water-miscible solvent is selected from the group
consisting of acetone, methanol, ethanol, propanol, isopropanol, acetonitnle,
dimethylsulfoxide, N,N-dimethylformamide, and N-methylpyrrolidine
19. The process of any one of claims 1 to 18, which process includes adding to the
reaction mixture at least one reagent selected from the group consisting of one or more
surfactants, one or more cyclodextnns, and one or more phase-transfer catalysts
20. The process of any one of claims 1 to 19, which process includes stopping the reaction
when one enantiomer of the epoxide and/or vicinal diol is in excess compared to the other
enantiomer of the epoxide and/or vicinal diol
21. The process of any one of claims 1 to 20, which process includes recovering
continuously during the reaction the optically active epoxide and/or the optically active vicinal
diol produced by the reaction directly from the reaction mixture.
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22. A process of any of claims 1 to 21, wherein the yeast cell is of a yeast genus selected from the group consisting of Arxula, Brettanomyces, Bultera, Bulleromyces, Candida, Cryptococcus, Debaryomyces, Dekkera, Exophiala, Geotrichum, Hormonema, Issatchenkia, Kluyveromyces, Lipomyces, Mastigomyces, Myxozyma, Pichia, Rhodospondium, Rhodotorula, Spondiobofus, Sporobolomyces, Trichosporon, Wingea, or Yarrowia
23 The process of any of claims 1 to 21, wherein the yeast cell is of a yeast species selected from the group consisting of Arxula adenmivorans, Arxula terrestns, Brettanomyces bruxellensis, Brettanomyces naardenensis, Brettanomyces anomalus, Brettanomyces species (eg.NCYC 3151), Bullera dendrophila, Bulleromyces albus, Candida albicans, Candida fabianll, Candida glabrata, Candida haemulonn, Candida intermedia, Candida magnoiiaeCandida parapsilosis, Candida rugosa, Candida tenuis, Candida tropicalis, Candida famata, Candida kruisel, Candida sp (new) rel to C sorbophila, Cryptococcus albidus, Cryptococcus amylolentus, Cryptococcus bhutanensis, Cryptococcus curvatus, Cryptococcus gastricus, Cryptococcus humicola, Cryptococcus hungaricus, Cryptococcus laurentii, Cryptococcus luteolus, Cryptococcus macerans, Cryptococcus podzohcus, Cryptococcus terreus, Cryptococcus macerans, Debaryomyces hansenn, Dekkera anomala, Exophiala dermatitidis, Geotrichum species (e g. UOFS Y-0111), Hormonema species (e.g. NCYC 3171), Issatchenkia occidentals, Kluyveromyces marxianus, Lipomyces species (e.g UOFS Y-2159), Lipomyces tetrasporus, Mastigomyces philippom, Myxozyma melibiosi, Pichia anomala, Pichia fmlandica, Pichia guillermondn, Pichia haplophila, Rhodospondium lusitaniae, Rhodospondium paludigenum, Rhodospondium sphaerocarpum, Rhodospondium toruloides, Rhodospondium paludigenum, Rhodotorula araucariae, Rhodotorula glutims, Rhodotorula minuta, Rhodotorula minuta var mmuta, Rhodotorula mucilaginosa, Rhodotorula philyla, Rhodotorula rubra, Rhodotorula species (e g. UOFS Y-2042), Rhodotorula species (e.g UOFS Y-0448), Rhodotorula species (eg. NCYC 3193), Rhodotorula species (e.g. UOFS Y-0139), Rhodotorula secies (eg. UOFS Y-0560), Rhodotorula aurantiaca, Rhodotorula species (eg. NCYC 3224), Rhodotorula sp "mucilaginosa", Spondiobolus salmon/color, Sporobolomyces holsaticus, Sporobolomyces roseus, Sporobolomyces tsugae, Trichosporon beigelh, Trichosporon cutaneum var cutaneum, Trichosporon delbrueckn, Trichosporon jirovecn, Trichosporon mucoides, Trichosporon ovoides, Trichosporon pullulans, Trichosporon species (eg. UOFS Y-0861), Trichosporon species (e.g. UOFS Y-1615), Trichosporon species (e.g. UOFS Y-0451), Trichosporon species (e.g. NCYC 3212), Trichosporon species (e.g. UOFS Y-0449), Trichosporon species (e.g. NCYC 3211), Trichosporon species (e.g UOFS Y-2113),
Trichosporon species (eg. NCYC 3210), Trichosporon monilitforme, Trichosporon
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montevideense, Wingea robertsiae, or Yarrowia Itpolytica
24 A method for producing a polypeptide, which process includes the steps of.
providing a cell comprising a nucleic acid encoding and capable of expressing a polypeptide
that has enantioselective 2,2-disubstituted epoxide hydrolase activity,
cultunng the cell, and
recovering the polypeptide from the culture.
25 The method of claim 24, wherein the cell is a yeast cell.
26 The method of claims 24 or 25, wherein the polypeptide is a full-length yeast epoxide
hydroiase.
. 27. The method of any of claims 24 or 25, wherein the polypeptide is a functional fragment of a yeast epoxide hydrolase.
28. The method of any of claims 24-27, wherein the polypeptide is encoded by an
endogenous gene of the cell.
29. The method of claims 22-27, wherein the cell is a recombinant cell and the polypeptide
is encoded by a nucleic acid sequence with which the cell is transformed.

30 The method of claim 29, wherein the nucleic acid sequence is a heterologous nucleic
acid sequence
31 The method of claim 30, wherein the nucleic acid sequence is a homologous nucleic
acid sequence
32 A crude or pure enzyme preparation which includes an isolated polypeptide having
enantioselective 2,2-disubstituted epoxide hydrolase activity.

33. A substantially pure culture of cells, a substantial number of which comprise a nucleic
acid encoding, and are capable of expressing, a polypeptide having enantioselective 2,2-
disubstituted epoxide hydrolase activity.
34. An isolated cell, the cell comprising a nucleic acid encoding a polypeptide having
enantioselective 2,2-disubstituted epoxide hydrolase activity, the cell being capable of
expressing the polypeptide
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35 An isolated DNA comprising
(a) a nucleic acid sequence that encodes a polypeptide that has enantioselective 2,2
. disubstituted epoxide hydrolase activity and that hybridizes under highly stringent conditions
to the complement of a sequence selected from the group consisting of SEQ ID NOs 8, 9, 10, 11, 12, 13, and 14; or
(b) the complement of the nucleic acid sequence
36. The DNA of claim 35, wherein the nucleic acid sequence encodes a polypeptide comprising an amino acid sequence selected from the group consisting of SEQ ID NOs. 1, 2, 3, 4, 5, 6, and 7.
37 The DNA of claim 35, wherein the nucleic acid sequence is selected from the group consisting of SEQ ID NOs. 8, 9, 10, 11, 12, 13, and 14
38 An isolated DNA comprising:
(a) a nucleic acid sequence that is at least 55% identical to a sequence selected from the
group consisting of SEQ ID NOs: 8, 9, 10, 11, 12, 13, and 14; or
(b) the complement of the nucleic acid sequence,
wherein the nucleic acid sequence encodes a polypeptide that has enantioselective 2,2-disubstituted epoxide hydrolase activity
39. An isolated DNA comprising.
(a) a nucleic acid sequence that encodes a polypeptide consisting of an amino acid
sequence that is at least 55% .identical to a sequence selected from the group consisting of
SEQ ID NOs: 1, 2, 3, 4, 5, 6 and 7; or
(b) the complement of the nucleic acid sequence,
wherein the polypeptide has enantioseiective 2,2-disubstituted epoxide hydrolase activity.
40. An isolated polypeptide encoded by the DNA of claims 33-37.
41. An isolated polypeptide comprising an amino acid sequence that is at least 55%
identical to SEQ ID NOs: 1, 2, 3, 4, 5, 6, or 7, the polypeptide having enantioselective 2,2-
disubstituted epoxide hydrolase activity
42. The polypeptide of claim 41, comprising.
(a) a sequence selected from the group consisting of SEQ ID NOs, 1,2,3, 4, 5, 6 and 7, or a
84

functional fragment of the sequence; or
(b) the sequence of (a), but with no more than five conservative substitutions,
wherein the polypeptide has enantioselective 2,2-disubstituted epoxide hydrolase activity
43. An isolated antibody that binds to the polypeptide of any of claims 40-42. 44 The antibody of claim 43, wherein the antibody is polyclonal antibody 45. The antibody of claim 43, wherein the antibody is a monoclonal antibody Dated this 13th day of November 2006

85
The invention provides yeast strains, and polypeptides encoded by genes of such yeast strains, that have enantiospecific 2,2-disubstituted epoxide hydrolase activity. Thejnvention also features nucleic acid molecules encoding such polypeptides, vectors containing such nucleic acid molecules, and cells containing such vectors. Also embraced by the invention are methods for obtaining optically active 2,2-disubstituted vicinal diols and optically active 2,2-disubstituted epoxides.