DESCRIPTION

A BACTERIUM PRODUCING A PRODUCT OF A REACTION CATALYZED BY A PROTEIN HAVING 2-OXOGLUTARATE-DEPENDENT ENZYME ACTIVITY AND A METHOD FOR MANUFACTURING THE PRODUCT

Technical field
The present invention relates to the microbiological industry, and specifically to a method for manufacturing a product of a reaction catalyzed by a protein having 2-oxoglutarate-dependent enzyme activity such as 4-hydroxyrL-isoleucine or a salt thereof using a bacterium transformed with a DNA fragment containing a gene coding for a protein having 2-oxoglutarate-dependent enzyme such as L-isoleucine dioxygenase activity. This bacterium has also been modified to have enhanced expression of a gene coding for an L-isoleucine transporter, and has the ability to produce (2S,3R,4S)-4-hydroxy-L-isoleucine.

Background art
4-hydroxy-L-isoleucine is an amino acid which can be extracted and purified from fenugreek seeds (Trigonellafoenum-graecum L. leguminosae). 4-hydroxy-L-isoleucine displays an insulinotropic activity, which is of great interest because of its stimulating effect which is clearly dependent on the plasma glucose concentration in the medium. This effect has been demonstrated both in isolated perfused rat pancreas and human pancreatic islets (Sauvaire, Y et al. Diabetes, 47: 206-210, (1998)). Such a glucose dependency has not been confirmed for sulfonylurea (Drucker, D. J., Diabetes 47:159-169, (1998)), which is the only insulinotropic drug currently used to treat type II diabetes [or non-insuiin-dependent diabetes (NIDD) mellitus (NIDDM)], and as a consequence, hypoglycemia is still a common undesirable side effect of sulfonylurea treatment (Jackson, J., and Bessler, R. Drugs, 22:211-245; 295-320, (1981); Jennings, A. et al. Diabetes Care, 12: 203-208, (1989)). Methods for improving tolerance to glucose is also known (Am. J. Physiol. Endocrinol., Vol. 287, E463-E471,2004). This glucometabolism enhancement activity, and its potential application to pharmaceuticals and health foods, have been previously reported (Japanese Patent Application Laid-Open No. Hei 6-157302, US2007-000463A1).

4-hydroxy-L-isoleucine is only found in plants, and due to its particular insulinotropic action, might be considered a novel secretagogue with potential applications for the treatment of type II diabetes, since this is a disease characterized by defective insulin secretion associated with various degrees of insulin resistance (Broca, C. et al. Am. J. Physiol. 277 (Endocrinol. Metab. 40): E617-E623, (1999)).

Oxidizing iron, ascorbic acid, 2-oxygIutaric acid, and oxygen-dependent isoleucine by utilizing dioxygenase activity in fenugreek extract has been reported as a method for manufacturing 4-hydro3xy-L-isoleucine (Phytochemistry, Vol. 44, No. 4, pp. 563-566,1997). However, this method is unsatisfactory for the manufacturing of 4-hydroxy-L-isoleucine because the activity of the enzyme is inhibited by the substrate at isoleucine concentrations of 20 mM and above. Furthermore, the enzyme has not been identified, is derived from plant extracts, is not readily obtained in large quantities, and is unstable.

An efficient eight-step synthesis of optically pure (2S,3R,4S)-4-hydroxyisoieucine with 39% overall yield has been disclosed. The key steps of this synthesis involve the biotransformation of ethyl 2-methylacetoacetate to ethyl (2S,3S)-2-methyl-3-hydroxy-butanoate with Geotrichum candidum and an asymmetric Strecker synthesis (Wang, Q. et al, Eur. J. Org. Chem., 834-839 (2002)).

A short six-step chemoenzymatic synthesis of (2S,3R,4S)-4-hydroxyisoleucine with total control of stereochemistry, the last step being the enzymatic resolution by hydrolysis of a N-phenylacetyl lactone derivative using the commercially available penicillin acylase G immobilized on Eupergit C(E-PAC), has also been disclosed (RoUand-Fulcrand, V. et al, J. Org. Chem., 873-877 (2004)).

But currently, there have been no reports of producing (2S,3R,4S)-4-hydroxy-L-isoleucine by using a bacterium transformed with a DNA fragment containing a gene coding for a protein having L-isoleucine dioxygenase activity; wherein the bacterium is also modified to have enhanced expression of a gene coding for L-isoleucine transporter; and has the ability to produce (2S,3R,4S)-4-hydroxy-L-isoIeucine.

Besides (2S,3R,4S)-4-hydroxy-L-isoleucine, products which are produced by reactions catalyzed by proteins having 2-oxoglutarate-dependent enzyme activity, and which are industrially important are known. However, there have been no reports of systems for efficiently producing the products by using the proteins having 2-oxoglutarate-dependent enzyme activity.

Summary of the invention
An aspect of present invention is to enhance production of a product of a reaction coupled with the formation of succinate from 2-oxoglutarate by a protein having 2-
oxoglutarate-dependent enzyme activity. The product includes compounds in both the free form and a salt form thereof. Another aspect of the present invention is to provide a method for manufacturing the product by a reaction coupled with the formation of succinate from 2-oxoglutarate using a bacterium having 2-oxoglutarate-dependent enzyme activity. This bacterium has been modified to attenuate the expression of a gene coding for oxoglutarate dehydrogenase, preferably modified to attenuate the expression of genes coding for oxoglutarate dehydrogenase and isocitrate lyase, more preferably modified to attenuate the expression of genes coding for oxoglutarate dehydrogenase, isocitrate lyase, and isocitrate dehydrogenase phosphatase.

An aspect of present invention is to enhance production of (2S,3R,4S)-4-hydroxy-L-isoleucine, including both the free form and a salt form thereof This compound may also be referred to as "(2S,3R,4S)-4HIL". Another aspect of the present invention is to provide a method for manufacturing (2S,3R,4S)-4-hydroxy-L-isoleucine or a salt thereof by direct enzymatic hydroxylation of L-isoleucine using a bacterium having L-isoleucine dioxygenase activity. This bacterium preferably over-expresses a gene coding for an L-isoleucine transporter, and has the ability to produce (2S,3R,4S)-4-hydroxy-L-isoleucine.

A bacterium has previously been isolated from nature having a high level of L-isoleucine dioxygenase activity, and a gene was cloned which encodes L-isoleucine dioxygenase. It was found that L-isoleucine dioxygenase may be used in the synthesis of (2S,3R,4S)-4-hydroxy-L-isoleucine.

Another aspect of the present invention includes providing a method for enhanced production of (2S3R,4S)-4-hydroxy-L-isoleucine using a bacterium having L-isoleucine dioxygenase activity. The above object was achieved by finding that a bacterium having L-isoleucine dioxygenase activity produced more (2S,3R,4S)-4-hydroxy-L-isoleucine if the bacterium is modified to overexpress a gene coding for an L-isoleucine transporter.

It is an aspect of the present invention to provide a bacterium transformed with a DNA fragment containing a gene coding for a protein having L-isoleucine dioxygenase activity, wherein said bacterium has been modified to overexpress a gene coding for an L-isoleucine transporter, and wherein said bacterium has the ability to produce (2S,3R,4S)-4-hydroxy-L-isoleucine.

It is a further aspect of the present invention to provide the (2S,3R,4S)-4HIL -producing bacterium as described above, wherein the gene coding for a protein having L-isoleucine dioxygenase activity is selected from the group consisting of:

(a) a DNA comprising the nucleotide sequence of SEQ ID No: 1;

(b) a DNA that hybridizes under stringent conditions with a DNA comprising a nucleotide sequence complementary to the nucleotide sequence of SEQ ID No: 1, and wherein said DNA encodes a protein having L-isoleucine dioxygenase activity;

(c) a DNA comprising a nucleotide sequence that encodes a protein comprising the amino acid sequence of SEQ ID No: 2;

(d) a DNA comprising a nucleotide sequence that encodes a protein comprising an amino acid sequence of SEQ ID NO. 2, except that said amino acid sequence contains a substitution, deletion, insertion, addition, or inversion of one or several amino acid residues, and wherein said protein has L-isoleucine dioxygenase activity; and

a DNA comprising a nucleotide sequence that encodes a protein comprising an amino acid sequence that is at least 98% homologous to the amino acid sequence of SEQ
ID NO: 2, and wherein said protein has L-isoleucine dioxygenase activity.

It is a further aspect of the present invention to provide the (2S,3R,4S)-4HIL-producing bacterium as described above, wherein the bacterium has been modified to enhance the activity of L-isoleucine dioxygenase.

It is a further aspect of the present invention to provide the (2S,3R,4S)-4HIL -producing bacterium as described above, wherein the activity of L-isoleucine dioxygenase is enhanced by increasing the expression of the gene encoding L-isoleucine dioxygenase.
It is a further aspect of the present invention to provide the (2S,3R,4S)-4HIL -producing bacterium as described above, wherein the expression of L-isoleucine dioxygenase is increased by modifying an expression control sequence of the gene encoding L-isoleucine dioxygenase or by increasing the copy number of the gene encoding L-isoleucine dioxygenase.

It is a further aspect of the present invention to provide (2S,3R,4S)-4HIL -producing the bacterium as described above, werein the gene coding for the L-isoleucine transporter is the brnQ gene from Escherichia coli.

It is a further aspect of the present invention to provide the bacterium as described above, wherein the bacterium has additionally been modified to attenuate the expression of genes coding for oxoglutarate dehydrogenase , isocitrate lyase, and isocitrate dehydrogenase phosphatase.

It is a further aspect of the present invention to provide the bacterium as described above, wherein said expression is attenuated by inactivating said genes.
It is a further aspect of the present invention to provide the bacterium as described above, wherein the bacterium has additionally been modified to attenuate the expression of a gene coding for a branched-chain amino-acid aminotransferase.

It is a further aspect of the present invention to provide the bacterium as described above, wherein said expression is attenuated by inactivating said gene.
It is a further aspect of the present invention to provide the bacterium as described above, wherein the bacterium belongs to a genus selected from the group consisting of Escherichia, Pseudomonas, Corynebacterium, Arthrobacter, Aspergillus, and Bacillus.
It is a further aspect of the present invention to provide the bacterium as described above, wherein the bacterium is selected from the group consisting of Escherichia coli, Arthrobacter simplex, Corynebacterium glutamicum, Arthrobacter globiformis, Arthrobacter sulfureus, Arthrobacter viscosus, and Bacillus subtilis.
It is a further aspect of the present invention to provide a method for manufacturing (2S,3R,4S)-4-hydroxy-L-isoleucine or a salt thereof, comprising:
cultivating the (2S,3R,4S)-4HIL-roducing bacterium as described above in a culture medium containing L-isoleucine; and
isolating (2S3R,4S)-4-hydroxy-L-isoleucine.
It is a further aspect of the present invention to provide the method as described above, wherein the culture medium contains a carbon source selected from the group consisting of a carbohydrate and a alcohol.
It is a further aspect of the present invention to provide the method as described above, wherein said carbohydrate is glucose and said alcohol is glycerol.
An aspect of present invention is to enhance production of 4-hydroxy-L-proline, including both the free form and a salt form thereof. Another aspect of the present invention is to provide a method for manufacturing 4-hydroxy-L-prolinee or a salt thereof by direct enzymatic hydroxylation of L-proline using a bacterium having L-proline hydroxylase activity.
The present invention is described in detail below.
BRIEF DESCRIPTION OF THE DRAWINGS Figure 1 shows 'shunting' of the TCA cycle in the strain MG1655 (∆sucAB, ∆aceAK,PL,-brnQ)_[pELAC-IDO(Lys, 23)] due to simultaneous oxidation of isoleucine and a-ketoglutarate (2-oxoglutarate).
Figure 2 shows the structure of the recombinant plasmid pET-IlvA. Figure 3 shows the structure of the recombinant plasmid pELAC-IDO(Lys, 23). Figure 4 shows the construction of the E. coli MG1655(PL-brnQ strain. Figure 5 shows the growth of the strains MG1655 and MG1655 (ASMCAB, ∆aceAK, PL.-brnQ) on the M9-salts medium containing glucose or glycerol with or without addition of lysine.

methionine and diaminopimeiate (DAP). Strains were grown in M9-salts medium supplemented with glucose or glycerol and, optionally, lysine, methionine and diaminopimeiate (DAP). Abbreviatios: Strains WT = MG1655; 2d = MG1655 (AsucAB, ∆aceAK, PL-brnQ; Media: A = M9 salts + glucose; B = M9 salts + glucose + (Lys, Met, DAP); C = M9 salts + glycerol; D = M9 salts + glycerol + (Lys, Met, DAP). Figure 6 shows the growth of the strains MG1655 [pELAC-IDO(Lys, 23)] and MG1655 (AsucAB, AaceAK, PL-brnQ) [pELAC-IDO(Lys, 23)] on the M9-salts medium with or without addition of L-isoleucine. Abbreviatios: Strains 1 = MG1655[pELAC-IDO(Lys, 23)]; 2 = MG1655 (A5MCAB, AaceAK, ?L'bmQ) [pELAC-IDO(Lys, 23)]; Media: G = M9 salts + glucose (137 mM); GI = M9 salts + glucose (137 mM) + L-isoleucine (137 mM); Y = M9 salts + glycerol (136 mM); YI = M9 salts + glycerol (136 mM) + L-isoleucine (137 mM).
BEST MODE FOR CARRYING OUT THE INVENTION
1. Bacterium of the present invention
The term "bacterium" as employed in the present specification includes an enzyme-producing bacteria, a mutant, and a genetic recombinant of such bacteria in which the targeted enzymatic activity is present or has been enhanced, and the like.
The term "2-oxoglutarate-dependent enzyme activity" as employed in the present specification refers to an enzymatic activity to catalyze a reaction coupled with the formation of succinate from 2-oxoglutarate.
A number of proteins having 2-oxoglutarate-dependent enzyme activity, such as 2-oxoglutarate-dependent dioxygenases have been reported. The examples thereof include dioxygenases usable for productions of useful products, such as a Pro hydroxylase convening L-Pro to hydroxy-Pro (APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Sept. 1999, p. 4028-4031), ay-butyrobetaine hydroxylase converting y-butyrobetaine to L-Camitine (WO2005/083089). Besides these dioxygenases, a number of dioxygeneases have been reported. For example, refer to: Critical Reviews in Biochemistry and Molecular Biology, 39:21-68,2004 and NATURE CHEMICAL BIOLOGY, 4 NUMBER 3 MARCH: 152-156, 2008. As for the 2-oxoglutarate-dependent dioxygenases described in the reviews, the bacterium has been modified to attenuate the expression of a gene coding for oxoglutarate dehydrogenase (such as AsucAB, AsucA, AsucB), preferably modified to attenuate the expression of genes coding for oxoglutarate dehydrogenase and isocitrate lyase (such as (AsucAB, AsucA, or AsucB) plus AaceA), more preferably modified to attenuate the

expression of genes coding for oxoglutarate dehydrogenase, isocitrate lyase, and isocitrate dehydrogenase phosphatase (such as (∆sucAB, ∆sucA, or ∆sucB) plus ∆aceAK), which is represented by E. coli strain MG1655 (∆sucAB, a∆ceAK) which is described in the below-mentioned Examples, is considered to be a general host for efficiently using 2-oxoglutarate produced from a carbon source such as D-glucose, in 2-oxoglutarate-dependent enzyme reactions.
The present invention will be described by referring to, as an example, an embodiment in which the protein having 2-oxoglutarate-dependent enzyme activity is a protein having L-isoleucine dioxygenase activity and the product of the reaction catalyzed by the protein is (2S,3R,4S)-4-hydroxy-L-isoleucine. However, the present invention is not limited to this embodiment
In the present invention, the term "(2S,3R,4S)-4-hydroxy-L-isoleucine" or "(2S,3R,4S)-4HIL" or "4HIL" refers to a single chemical compound or a mixture of compounds containing (2S,3R,4S)-4-hydroxyisoleucine.
The term "bacterium" as employed in the present specification includes an enzyme-producing bacteria, a mutant, and a genetic recombinant of such bacteria in which the targeted enzymatic activity is present or has been enhanced, and the like.
The L-isoleucine dioxygenase from microbial cells may be abbreviated as IDO.
Screening of environmental microorganisms revealed a unique microbe Bacillus thuringiensis strain 2-e-2, which possesses an activity of catalyzing a reaction in which (2S,3R,4S)-4HIL is directly formed from L-isoleucine, both the free form and a salt form thereof. The novel L-isoleucine dioxygenase was purified from the cultivated microbial cells, and may be abbreviated as IDO(Lys,23).
Furthermore, the N-terminal amino acid sequence of IDO(Lys,23) was determined by purifying dioxygenase derived from of Bacillus thuringiensis strain 2-e-2. Bacillus thuringiensis strain 2-e-2 was named Bacillus thuringiensis AJl 10584 and deposited at the International Patent Organism Depositary, National Institute of Advanced Industrial Science and Technology (Central 6,1-1, Higashi 1-chome, Tsukuba, Ibaraki 305-8566, Japan) on September 27,2006 and given an accession number of PERM BP-10688 imder the provisions of Budapest Treaty.
The DNA encoding IDO(Lys,23) is shown in SEQ ID No: 1. Furthermore, the amino acid sequence of IDO(Lys,23) encoded by the nucleotide sequence of SEQ ID NO: 1 is shown in SEQ ID No: 2. SEQ ID NO: 2 is the amino acid sequence of IDO(Lys,23) encoded by the nucleotide sequence of SEQ ID NO: 1. IDO(Lys,23) of SEQ ID NO: 2 possesses L-isoleucine

dioxygenase activity, and catalyzes the reaction in which (2S,3R,4S)-4HIL shown m the following formula (I) is directly synthesized from one molecule of L-isoleucine.
A DNA that aicodes IDO wWch catalyzes the reaction in which (2S,3R,4S)-4HIL is formed from L-isoleucine is not only the DNA shown in SEQ ID No: 1. This is because there may be differences in nucleotide sequences from each species and strains among Bacillus that form IDO which catalyzes the reaction of producing (2S,3R,4S)-4HIL from L-isoleucine.
The DNA of the present invention not only includes the isolated DNA encoding IDO, but also a DNA in which mutations have been artificially added to the DNA that encodes IDO. This DNA may be isolated from the chromosome of an IDO-producing microorganism. The DNA of the present invention must encode IDO that is able to catalyze the above-described reaction. Methods for artificially adding mutations include typically used methods introducing site-specific mutations described in Method, in Enzymol., 154 (1987).
A DNA that hybridizes under stringent conditions with a DNA having a nucleotide sequence complementary to the nucleotide sequence of SEQ ID No: 1, and encodes a protein having IDO activity is also included in the DNA of the present invention. As used herein, the "stringent conditions" refer to those conditions vmder which a specific hybrid is formed and a non-specific hybrid is not formed. Although it is difficult to numerically express these conditions explicitly, by way of example, those conditions under which DNA molecules having higher homology e.g. preferably 70% or more, more preferably 80% or more, still more preferably 90% or more, and particularly preferably 95% or more homology, hybridize with each other, while DNA molecules having lower homology do not hybridize with each other, or those conditions under which hybridization occurs under typical washing conditions in Southern hybridization, that is, at a salt concentration corresponding to 0.lxSSC and 0.1% SDS at 37°C, preferably O.lxSSC and 0.1% SDS at 60°C, and more preferably O.lxSSC and 0.1% SDS at 65°C. The length of the probe may be suitably selected, depending on the hybridization conditions, and usually varies from 100 bp to 1 kbp. Furthermore, "L-isoleucine dioxygenase activity" may be described as the activity that synthesizes (2S,3R,4S)-4HIL from L-isoleucine. However, when a nucleotide sequence that hybridizes under stringent conditions with a nucleotide sequence complementary to the nucleotide sequence of SEQ ID No: 1, it preferably retains L-isoleucine dioxygenase activity of 10% or more, preferably 30% or more, more preferably 50% or more, and still more preferably 70% or more, of protein having the

amino acid sequence of SEQ ID No: 2 under the conditions of 37°C and pH 8.
Furthermore, a DNA encoding a protein which is substantially identical to the IDO encoded by the DNA of SEQ ID No: 1 is also included in the DNA of the present invention. Namely, the following DNAs are also included in the DNA of the present invention:
(a) a DNA of the nucleotide sequence of SEQ ID No: 1;
(b) a DNA that hybridizes under stringent conditions with a DNA having a nucleotide sequence complementary to the nucleotide sequence of SEQ ID No: 1 and encodes a protein having L-isoleucine dioxygenase activity;
(c) a DNA that encodes a protein of the amino acid sequence of SEQ ID No: 2;
(d) a DNA that encodes a protein having an amino acid sequence that contains a substitution, deletion, insertion, addition or inversion of one or several amino acid residues in the amino acid sequence of SEQ ID No: 2 and having the L-isoleucine dioxygenase activity; and
(e) a DNA that encodes a protein having an amino acid sequence that is at least 70% homologous, preferably at least 80% homologous, more preferably at least 90% homologous and still more preferably at least 95% homologous to the amino acid sequence of SEQ ED N0:2 and has L-isoleucine dioxygenase activity.
Here, "one or several" refers to a number of changes which do not result in significant changes to the 3D structure of the protein, or signficant reduction of the L-isoleucine dioxygenase activity, and more specifically, is in the range of 1 to 78, preferably 1 to 52, more preferably 1 to 26, and still more preferably 1 to 13.
The substitution, deletion, insertion, addition, or inversion of one or several amino acid residues should be conservative mutation(s) so that the activity is maintained. The representative conservative mutation is a conservative substitution. Examples of conservative substitutions include substitution of Ala with Ser or Thr, substitution of Arg with Gin, His or Lys, substitution of Asn with Glu, Gln, Lys, His or Asp, substitution of Asp with Asn, Glu or Gin, substitution of Cys with Ser or Ala, substitution of Gln with Asn, Glu, Lys, His, Asp or Arg, substitution of Glu with Asn, Gln, Lys or Asp, substitution of Gly with Pro , substitution of His with Asn, Lys, Gln, Arg or Tyr, substitution of lle with Leu, Met, Val or Phe, substitution of Leu with He, Met, Val or Phe, substitution of Lys with Asn, Glu, Gln, His or Arg, substitution of Met with He, Leu, Val or Phe , substitution of Phe with Trp, Tyr, Met, He or Leu, substitution of Ser with Thr or Ala, substitution of Thr with Ser or Ala, substitution of Trp with Phe or Tyr, substitution of Tyr with His, Phe or Trp, and substitution of Val with Met, He or Leu.

Furthennore, "L-isoleucine dioxygenase activity" refers to synthesis of the (2S,3R,4S)-4HIL from L-isoleucine described above. However, when the amino acid sequence of SEQ ID No: 2 contains a substitution, deletion, insertion, addition, or inversion of one or several amino acid residues, it preferably retains L-isoleucine dioxygenase activity of 10% or more, preferably 30% or more, more preferably 50% or more, and still more preferably 70% or more, as compared to the protein having the amino acid sequence of SEQ ID No: 2 under conditions of 30 "C and pH 6.0. The L-isoleucine dioxygenase activity of the IDO of the present invention can be measured by analysis of (2S,3R,4S)-4HIL formation from L-isoleucine by using high-performance liquid chromatography (HPLC).
Furthermore, a homologue DNA of SEQ ID NO: 1 can be used as the gene encoding L-isoleucine dioxygenase of present invention. Whether the homologue DNA encodes L-isoleucine dioxygenase or not can be confirmed by measuring L-isoleucine dioxygenase activity of the cell lysate, or cell lysate of the microorganism in which the homologue DNA is overexpressed.
The homologue DNA of SEQ ID NO: 1 can also be prepared from the genome of another Bacillus species, for example. Bacillus cereus. Bacillus weihenstephanensis.
The phrase "a bacterium belonging to the genus Escherichia" means that the bacterium is classified into the genus Escherichia according to the classification known to a person skilled in the art of microbiology. Examples of a bacterium belonging to the genus Escherichia as used in the present invention include, but are not limited to, Escherichia coli (E. coli).
The bacterium beloning to the genus Escherichia that can be used in the present invention is not particularly limited; however, e.g., bacteria described by Neidhardt, F.C. et al. (Escherichia coli and Salmonella typhimurium, American Society for Microbiology, Washington D.C., 1208, Table 1) are encompassed by the present invention.
The phrase "a bacterium belonging to the genus Pseudomonas" means that the bacterium is classified into the genus Pseudomonas according to the classification known to a person skilled in the art of microbiology.
The phrase "a bacterium belonging to the genus Corynebacterium" means that the bacterium is classified into the genus Corynebacterium according to the classification known to a person skilled in the art of microbiology. Examples of a bacterium belonging to the genus Corynebacterium as used in the present invention include, but are not limited to, Corynebacterium glutamicum.
The phrase "a bacterium belonging to the genus Arthrobacter" means that the

bacterium is classified into the genus Arthrobacter according to the classification known to a person skilled in the art of microbiology. Examples of a bacterium belonging to the genus Arthrobacter as used in the present invention include, but are not limited to, Arthrobacter simplex, Arthrobacter globiformis, Arthrobacter sulfureus, and Arthrobacter viscosus.
The phrase "a bacterium belonging to the genus Aspergillus" means that the bacterium is classified into the genus Aspergillus according to the classification known to a person skilled in the art of microbiology.
The phrase "a bacterium belonging to the genus Bacillus" means that the bacterium is classified into the genus Bacillus according to the classification known to a person skilled in the art of microbiology. Examples of a bacterium belonging to the genus Bacillus as used in the present invention include, but are not limited to. Bacillus subtilis.
The brnQ gene from E. coli (synonyms - ECK0395, b0401, hrbA) encodes the branched chain amino acid LIVCS transporter BrnQ (synonyms - B0401, HrbA, LIV-II). The brnQ gene (nucleotides 418815 to 420134; GenBank accession no. NC_000913.2; gi: 16128105) is located between the genephoR and the geneproY on the chromosome of E. coli K-12. The nucleotide sequence of the brnQ gene and the amino acid sequence of the BrnQ protein encoded by the brnQ gene are shown in SEQ ED NO: 3 and SEQ ID NO: 4, respectively.
The sucA gene from E. coli (synonyms - ECK0714, lys, b0726, lys+met) encodes a subunit of the E1(0) component of the oxoglutarate dehydrogenase complex - SucA (synonyms - B0726, Lys). Tne sucA gene (nucleotides 757,929 to 760,730; GenBank accession no. NC_000913.2; gi: 16128105) is located between the gene G6388, partially overlapping with it, and the gene sucB on the chromosome of E. coli K-12. The nucleotide sequence of the sucA gene and the amino acid sequence of the SucA protein encoded by the sucA gene are shown in SEQ ID NO: 5 and SEQ ID NO: 6, respectively.
The sucB gene from E. coli (synonyms - ECK0715, b0727) encodes a subunit of the E2(0) component of the oxoglutarate dehydrogenase complex - SucB (synonym B0727). The sucB gene (nucleotides 760,745 to 761,962; GenBank accession no. NC_000913.2; gi: 16128105) is located between the gene sucA and the gene sucC on the chromosome of E . coli K-12. The nucleotide sequence of the sucB gene and the amino acid sequence of the SucB protein encoded by the sucB gene are shown in SEQ ID NO: 7 and SEQ ID NO: 8, respectively.
The aceA gene from E. coli (synonyms - ECK4007, b4015, icl) encodes a subimit of the isocitrate lyase- AceA (synonym B4015, Id). The aceA gene (nucleotides 4,215,132 to

4,216,436; GenBank accession no. NC_000913.2; gi: 16128105) is located between the gene aceB and the gene aceK on the chromosome of E. coli K-12. The nucleotide sequence of the ace A gene and the amino acid sequence of the AceA protein encoded by the ace A gene are shown in SEQ ID NO: 9 and SEQ ID NO: 10, respectively.
The aceK gene from E. coli (synonyms - ECK4008, b4016) encodes a subunit of the isocitrate dehydrogenase phosphatase- AceK (synonym B4016). The aceK gene (nucleotides 4,216,619 to 4,218,355; GenBank accession no. NC_000913.2; gi: 16128105) is located between the gene aceA and the gene arpA, that is oriented in opposite direction, and partially overlapping with it, on the chromosome of E. coli K-12. The nucleotide sequence of the aceK gene and the amino acid sequence of the AceK protein encoded by the aceK gene are shown in SEQ ID NO: 11 and SEQ ID NO: 12, respectively.
The ilvE gene from E. coli (synonyms - ECK3762, b3770) encodes a subunit of the branched-chain amino-acid aminotransferase- IlvE (synonym B3770). The ilvE gene (nucleotides 3,950,507 to 3,951,436; GenBank accession no. NC_000913.2; gi: 16128105) is located between the gene ilvM and the gene ilvD on the chromosome of £. coli K-12. The nucleotide sequence of the ilvE gene and the amino acid sequence of the IlvE protein encoded by the ilvE gene are shown in SEQ ID NO: 13 and SEQ ID NO: 14, respectively.
Since there may be some differences in DNA sequences between the genera or strains of the Escherichia genus, the brnQ gene with enhanced expression, or the sucA, sucB, aceA, aceK, ilvE genes with attenuated expression are not limited to the genes shown in SEQ ID No: 3, SEQ ID No: 5, SEQ ID No: 7, SEQ ID No: 9, SEQ ID No: 11 and SEQ ID No: 13, but may include genes which are homologous to SEQ ID No: 3, SEQ ID No: 5, SEQ ID No: 7, SEQ ID No: 9, SEQ ID No: 11 and SEQ ID No: 13, but which encode a variant protein of the BrnQ, SucA, SucB, AceA, AceK and IlvE proteins, respectively. The phrase "variant protein" as used in the present mvention means a protein which has changes in the sequence, whether they are deletions, insertions, additions, or substitutions of amino acids, but the activity as the BmQ/SucA/SucB/AceA/AceK/IlvE protein is maintained. The number of changes in the variant protein depends on the position or the type of amino acid residues in the three dimensional structure of the protein. It may be 1 to 30, preferably 1 to 15, and more preferably 1 to 5 in SEQ ID No: 4, SEQ ID No: 6, SEQ ID No: 8, SEQ ID No: 10, SEQ ID No: 12 and SEQ ID No: 14. These changes in the variants can occur in regions of the protein which are not critical for the function of the protein. This is because some amino acids have high homology to one another so the three dimensional structure or activity is not affected by such a change. Therefore, the protein variant encoded by the brnQ/sucA/sucB/aceA/aceK/ilvE

gene may be one which has a homology of not less than 80%, preferably not less than 90%, and most preferably not less than 95%, with respect to the entire amino acid sequence shown inSEQIDNo:4,SEQIDNo:6,SEQIDNo:8,SEQIDNo:10,SEQIDNo:12andSEQ
ID No-14 as long as the activity of the BmQ, SucA, SucB, AceA, AceK and IlvE proteins, respectively, is maintained (prior to inactivation of the sucA/sucB/aceA/aceK/ilvE gene).
Homology between two amino acid sequences can be determined usmg well-knoNvn methods, for example, the computer program BLAST 2.0, which calculates three paraxnetei^:
score, identity and similarity.
Moreover, the brnQ/sucA/sucB/aceA/aceK/ilvE may be a variant which hybridizes under stringent conditions with the nucleotide sequence shown in SEQ ID No: 3/SEQ ID No: 5/SEQIDNo:7/SEQIDNo:9/SEQIDNo: ll/SEQIDNo: 13, or a probe which can be prepared from the nucleotide sequence under stringent conditions, provided that it encodes a functional BmQ/ SucA/SucB/AceA/AceKAlvE protein prior to inactivation. "Stringent conditions" include those under which a specific hybrid, for example, a hybrid having homology of not less than 60%, preferably not less than 70%, more preferably not less than 80%, still more preferably not less than 90%, and most preferably not less than 95%, is formed and a non-specific hybrid, for example, a hybrid having homology lower than the above, is not formed. For example, stringent conditions are exemplified by washing one time or more, preferably two or three times at a salt concentration of 1 *'SSC, 0.1% SDS, preferably 0.1 X SSC, 0.1% SDS at 60 C. Duration of washing depends on the type of membrane used for blotting and, as a rule, should be what is recommended by the manufacturer. For example, the recommended duration of washing for the Hybond™ N+ nylon membrane (Amersham) under stringent conditions is 15 minutes. Preferably, washing may be performed 2 to 3 times. The length of the probe may be suitably selected depending on the hybridization conditions,
and is usually 100 bp to 1 kbp.
The phrase "enhanced expression of the gene" or "overexpression of a gene" meanj that the expression of the gene is higher than that of a non-modified strain, for example, a wild-type strain. Examples of such modification include increasing the copy number of expressed gene per cell, increasing the expression level of the gene, and so forth. The quanti of the copy number of an expressed gene is measured, for example, by restricting the chromosomal DNA followed by Southern blotting using a probe based on the gene sequenc fluorescence in situ hybridization (FISH), and the like. The level of gene expression can be measured by various known methods including Northern blotting, quantitative RT-PCR, an the like. The amount of the protein encoded by the gene can be measured by known metho

including SDS-PAGE followed by immunoblotring assay (Western blotting analysis), and the like. Furthermore, wild-type strains that can act as a control include, for example, Escherichia coliK-n.
"Transformation of a bacterium with DNA encoding a protein" means introduction of the DNA into a bacterium, for example, by conventional methods. Transformation of this DNA will result in an increase in expression of the gene encoding the protein(s) of present invention, and will enhance the activity of the protein in the bacterial cell. Methods of transformation include any known methods that have hitherto been reported. For example, a method of treating recipient cells with calcium chloride so as to increase permeability of the cells to DNA has been reported for Escherichia coli K-12 (Mandel, M. and Higa, A., J. Mol. Biol, 53,159 (1970)) may be used-Methods of overexpressing a gene, or enhancing the expression of a gene include increasing the gene copy number. Introducing a gene into a vector that is able to function in a bacterium of the Escherichia genus increases the copy number of the gene. Preferably, low-copy vectors are used. Examples of low-copy vectors include but are not limited to pSC101, pMW118, pMW 119, and the like. The term "low copy vector" is used for vectors, the copy number of which is up to 5 copies per cell.
Enhancement of gene expression may also be achieved by introduction of multiple copies of the gene into a bacterial chromosome by, for example, homologous recombination, Mu integration, or the like. For example, one act of Mu integration allows for introduction of up to 3 copies of the gene into a bacterial chromosome.
Increasing the copy number of a gene can also be achieved by introducing multiple copies of the gene into the chromosomal DNA of the bacterium. In order to mtroduce multiple copies of the gene into a bacterial chromosome, homologous recombination is carried out using a sequence which is present in multiple copies as targets in the chromosomal DNA. Sequences having multiple copies in the chromosomal DNA include, but are not limited to repetitive DNA, or inverted repeats present at the end of a transposable element.
Enhancing gene expression may also be achieved by placing the DNA of the present invention under the control of a potent promoter. For example, the Ptac promoter, the lac promoter, the trp promoter, the trc promoter, the PR, or the PL promoters of lambda phage are all known to be potent promoters. The use of a potent promoter can be combined with multiplication of gene copies.
Alternatively, the effect of a promoter can be enhanced by, for example, introducing a mutation into the promoter to increase the transcription level of a gene located downstream

of the promoter. Furthermore, it is known that substitution of several nucleotides in the spacer between ribosome binding site (RBS) and the start codon, especially the sequences immediately upstream of the start codon, profoundly affect the mRNA translatability.
Moreover, it is also possible to introduce a nucleotide substitution into a promoter region of a gene on the bacterial chromosome, which results in stronger promoter function. The alteration of the expression control sequence can be performed, for example, in the same maimer as the gene substitution using a temperature-sensitive plasmid, as disclosed in International Patent Publication WO 00/18935 and Japanese Patent Application Laid-Open No. 1-215280.
The inventors of the present invention proposed, that attenuating expression of the genes sucA, sucB, ace A and aceK should lead to 'shunting' of the TCA cycle in mutant cells due to simultaneous oxidation of isoleucine and a-ketoglutarate (2-oxoglutarate). This may result in enhanced production of 4HIL. At the same time, simultaneous oxidation of isoleucine and a-ketoglutarate by HX) activity will be the factor necessary for both growth of bacterium and stabilization of the plasmid carrying a gene encoding IDO, In other words, the process of isoleucine hydroxylation will be the necessary for cells growth. In this case, the biotransformation of isoleucine into 4-HIL can be achieved during bacterial cells growth without supplement of any antibiotics. This strategy was achieved by constructing a strain which lacks for succinyl-CoAdue to deletions of sucAB and aceAK genes (Fig. 1, Examples 3 - 5). It is apparent that this principle can be applied to any reactions which are coupled with the formation of succinate from 2-oxoglutarate. It is also apparent that the minimum requirement is attenuating of the expression of the gene coding for oxoglutarate dehydrogenase (such as ∆sucAB, s∆ucA, ∆sucB). Preferably the bacterium is further modified to attenuate the expression of gene coding for isocitrate lyase (such as ∆aceA). More preferably the bacterium is fiirther modified to attenuate modified to attenuate the expression of genes coding for isocitrate lyase, and isocitrate dehydrogenase phosphatase (such as ∆aceAK).
By attenuating the expression of the gene coding for oxoglutarate dehydrogenase, the metabolism of 2-oxoglutarate in cells is suppressed and the supply of 2-oxoglutarate to the 2-oxoglutarate-dependent enzyme is enhanced. The thus-engineered bacterium is a host suitable for conducting 2-oxoglutarate-dependent enzyme reactions. The attenuation of the gene coding for oxoglutarate dehydrogenase increases a 2-oxoglutarate leven in cells and make the supply thereof to a 2-oxoglutarate-dependent enzyme to be efficient. The

oxoglutarate dehydrogenase is the enzyme converting 2-oxoglutarate to succinyl-CoA in the TCA cycle. It is preferably to further combine the attenuation of the gene conding for isocitrate lyase catalyzing the conversion of isocirate to succinate in the glyoxylate cycle, thereby further increasmg the supply of 2-oxoglutarate. By this combination, the pathways from 2-oxoglutarate to succinate in the TCA and glyoxylate cycles are blocked, thereby further increasing the supply of 2-oxoglutarate to the 2-oxoglutarate-dependent enzyme. It is more preferably to further combine the attenuation of the gene coding for isocitrate dehydrogenease phosphatase, thereby suppressing the inactivation of isocitrate dehydrogenase producing 2-oxoglutrate from isocirate. As the branched-chain amino acid aminotransferase deaminate 4HIL (Smimov S.V, et al, FEMS Microbiol Lett;273(l):70-7(2007)), the inventors of the present invention proposed that attenuating expression of the ilvE gene should lead to higher yields of 4HIL due to preventing deamination of 4HIL.
The phrase "bacterium has been modified to attenuate expression the gene" means that the bacterium has been modified in such a way that the modified bacterium contains a reduced amount of the protein encoded by the gene as compared with an unmodified bacterium, or the modified bacterium is unable to synthesize the protein. The phrase "bacterium has been modified to attenuate expression of the gene" also may mean that the bacterium has been modified in such a way that the modified gene encodes a mutant protein with decreased activity.
The presence or absence of the gene in the chromosome of a bacterium can be detected by well-known methods, including PCR, Southern blotting, and the like.
The phrase "inactivation of the gene" means that the modified gene encodes a completely inactive protein. It is also possible that the modified DNA region is unable to naturally express the gene due to deletion of a part of or the entire gene, the shifting of the reading frame of the gene, the introduction of missense/nonsense mutation(s), or the modification of an adjacent region of the gene, including sequences controlling gene expression, such as promoter(s), enhancer(s), attenuator(s), ribosome-binding site(s), etc..
Expression of the gene can be attenuated by introducing a mutation into the gene on the chromosome so that intracellular activity of the protein encoded by the gene is decreased as compared with an unmodified strain. Such a mutation on the gene can be replacement of one base or more to cause an amino acid substitution in the protein encoded by the gene (missense mutation), introduction of a stop codon (nonsense mutation), deletion of one or two bases to cause a frame shift, insertion of a drug-resistance gene, or deletion of a part of the gene or the entire gene (Qiu, Z. and Goodman, M.F., J. Biol. Chem., 272, 8611-8617 (1997);

Kwon, D. H. et al, J. Antimicrob. Chemother 46,193-196 (2000)). Expression of the gene can also be attenuated by modifying an expression regulating sequence such as the promoter, the Shine-Dalgamo (SD) sequence, etc, (W095/34672, Carrier, T.A. and Keasling, J.D., Biotechnoi Prog 15,58-64 (1999)).
For example, the following medthods may be employed to introduce a mutation by gene recombination. A mutant gane encoding a mutant protein having a decreased activity is prepared, and a bacterium is transformed with a DNA fragment containing the mutant gene. Then, the native gene on the chromosome is replaced with the mutant gene by homologous recombination, and the resulting strain is selected. Such gene replacement using homologous recombination can be conducted by the method employing a linear DNA, which is known as "Red-driven integration" (Datsenko, K.A. and Wanner, B.L., Proc. Natl. Acad, Sci. USA, 97, 12, p 6640-6645 (2000)), or by methods employing a plasmid containing a temperature-sensitive replication (U.S. Patent 6,303,383 or JP 05-007491 A). Furthermore, the incorporation of a site-specific mutation by gene substitution using homologous recombination such as set forth above can also be conducted with a plasmid which is unable to replicate in the host.
Expression of the gene can also be attenuated by insertion of a transposon or an IS factor into the coding region of the gene (U.S. Patent No. 5,175,107), or by conventional methods, such as mutagenesis treatment by UV irradiation or nitrosoguanidine (N-methyl-N'-nitro-N-nitrosoguanidine).
Inactivation of the gene can also be performed by conventional methods, such as a mutagenesis treatment using UV irradiation or nitrosoguanidine (N-methyl-N'-nitro-N-nitrosoguanidine), site-directed mutagenesis, gene disruption using homologous recombination, or/and insertion-deletion mutagenesis (Yu, D. et al., Proc. Natl. Acad. Sci. USA, 2000,97:12: 5978-83 and Datsenko, K.A. and Wanner, B.L., Proc. Natl. Acad. Sci. USA, 2000,97:12: 6640-45), also called "Red-driven integration".
Methods for preparation of plasmid DNA, digestion and ligation of DNA, transformation, selection of an oligonucleotide as a primer, and the like may be ordinary methods well known to one skilled in the art. These methods are described, for instance, in Sambrook, J., Fritsch, E.F., and Maniatis, T., "Molecular Cloning A Laboratory Manual, Second Edition", Cold Spring Harbor Laboratory Press (1989).
2. Method of the present invention
The method of the present invention is a method for producing a product of a reacti(

catalyzed by a protein having 2-oxoglurarate-dependent enzyme activity by cultivating the bacterium of the present invention in a culture medium containing a substrate of the reaction, and isolating the produced product from the medium.
According to the product and the specificity of the used protein having 2-oxoglutarate-dependent enzyme activity, the substrate is suitably selected. For example, when the product is (2S,3R,4S)-4-hydroxy-L-isoleucine and the protein has L-isoleucine dioxygenase activity, the substrate may be L-Ieucine.
Thus the method of the present mvention may be a method for producing (2S,3R,4S)-4-hydroxy-L-isoleucine by cultivating the bacterium of the present invention in a culture medium containing L-isoleucine, and isolating produced (2S,3R,4S)-4-hydroxy-L-isoleucine from the medium.
The medium used for culture may be either a synthetic or natural medium, so long as the medium includes a carbon source and a nitrogen source and minerals and, if necessary, appropriate amounts of nutrients which the bacterium requires for growth. The carbon source may include various carbohydrates such as glucose and sucrose, and various organic acids. Depending on the mode of assimilation of the used microorganism, alcohol, including ethanol and glycerol, may be used. As the nitrogen source, various ammonium salts such as ammonia and ammonium sulfate, other nitrogen compounds such as amines, a natural nitrogen source such as peptone, soybean-hydrolysate, and digested fermentative microorganism can be used. As minerals, potassium monophosphate, magnesium sulfate, sodium chloride, ferrous sulfate, manganese sulfate, calcium chloride, and the like can be used. As vitamins, thiamine, yeast extract, and the like, can be used The medium of present invention contained L-isoleucine (20-40 g/1).
The cultivation is preferably performed under aerobic conditions, such as a shaking culture, and a stirring culture with aeration, at a temperature of 20 to 40°C, preferably 30 to 38°C. The pH of the culture is usually between 5 and 9, preferably between 6.5 and 7.2. The pH of the culture can be adjusted with ammonia, calcium carbonate, various acids, various bases, and buffers.
Examples of separation and purification methods may include a method in which the (2S,3R,4S)-4HIL is contacted with an ion exchange resin to adsorb basic amino acids followed by elution and crystallization, and a method in which the product obtained by elution is discolored and filtrated with activated charcoal followed by crystallization to obtain (2S,3R,4S)-4HIL.
With respect to the product other than (2S,3R,4S)-4-hydroxy-L-isoleucine, the culature

condition, the separation and pufification methods and the line are similarily selected depending on the nature of the used bacterium and the target product
Examples
The present invention will be explained in further detail with reference to examples shown below, however, the invention is not limited thereto.
Example 1. Construction of MG1655 rpELAC-IDOfLvs. 23)] and MG1655rPL-brnQ)[pELAC-IDO(Lvs. 23)1 strains.
1.1.Construction of the pMW119-IDQ(Lys. 23) plasmid.
An 0.8 kb DNA fragment of the chromosome of the Bacillus thuringiemis strain 2-e-2 was amplified using oligonucleotides SVS 170 (SEQ ID No: 15) and SVS 169 (SEQ ID No: 16) as a primers and purified chromosomal DNA as a template. The PCR protocol was as follows: initial cycle for 30 seconds at 94°C; 4 cycles for 40 seconds at 94°C; 30 seconds at 49°C; 40 seconds at 72°C; 35 cycles for 30 seconds at 94°C; 30 seconds at 54''C; 30 seconds at 72°C. The PCR fragment was digested with BamHI and Sad endonucleases and then ligated into the pMW11 9 vector which had been previously treated with the same restrictases.
1.2. Construction of the PELAC-IDO CLVS. 23) plasmid.
A 0.76 kb DNA Augment was excised from the pMWl I9-IDO(Lys, 23) plasmid withXbal, Sad endonucleases, and than cloned into the pELAC-ilvA/A/XaI-SacI vector (see Reference example 1), resulting in the recombinant plasmid pELAC-IDO (Lys, 23) (Fig. 3).
1.3. Construction of the MG1655 (Pf-bmO) strain.
The expression of the He-transporter BrnQ was increased in the MG1655 strain to improve the He influx. A1.9 kbp DNA fragment harboring a Cm marker and the Pt-promoter was PCR-amplified using oligonucleotides SVS 179(SEQ ID No: 17) and SVS 180(SEQ ID No: 18) as primers and chromosomal DNA of the B W25113 cat-Pi-yddG (EP1449918A1, Russian patent RU2222596) strain as a template. Conditions for PCR were as follows: denaturation step for 3 min at 95°C; profile for two first cycles: 1 min at 95°C, 30 sec at 50°C, 40 sec at 72''C; profile for the last 25 cycles: 30 sec at 95°C, 30 sec at 54°C, 40 sec at 72°C; final step: 5 min at 72°C.

A 1.9 kbp PCR product was obtained and purified in agarose gel and was used for electroporation of the E. coli strain MG1655 (ATCC 700926), which contains the plasmid pKD46 which has a temperature-sensitive replication origin The plasmid pKD46 (Datsenko, K.A. and Wanner, B.L., Proc. Natl. Acad. Sci. USA, 2000,97:12:6640-45) includes a 2,154 nucleotide DNA fragment of phage (nucleotide positions 31088 to 33241, GenBank accession no. J02459), and contains genes of the X. Red homologous recombination system (y, P, exo genes) under the control of the arabinose-inducible ParaB promoter. The plasmid pKD46 is necessary for integration of the PCR product into the chromosome of strain MGl 655.
Electrocompetent cells were prepared as follows: E. coli MG1655/pKD46 was grown overnight at 30°C in LB medium containing ampicillin (100 mg/1), and the culture was diluted 100 times with 5 ml of SOB medium (Sambrook et al, "Molecular Cloning: A Laboratory Manual, Second Edition", Cold Spring Harbor Laboratory Press, 1989) containing ampicillin and L-arabinose (1 mM). The cells were grown with aeration at 30°C to an ODgoo of M3.6 and then were made electrocompetent by concentrating 100-fold and washing three times with ice-cold deionized H2O. Electroporation was performed using 70µ\ of cells and w100 ng of the PCR product. Cells after electroporation were incubated with 1 ml of SOC medium (Sambrook et al, "Molecular Cloning: A Laboratory Manual, Second Edition", Cold Spring Harbor Laboratory Press, 1989) at 37°C for 2.5 hours and then were plated onto L-agar containing chloramphenicol (30 g/ml) and grown at 37°C to select CmR recombinants. Then, to eliminate the pKD46 plasmid, two passages on L-agar with Cm at 42C were performed and the obtained colonies were tested for sensitivity to ampicillin.
Thus E. coli MGl655 (PL-bmQ) strain was constructed (Fig.4).
1.4. Construction of MG1655 rpELAC-IDO(Lvs. 23)1 and MG1655fP^-brnQDELACIDO(Lys. 21)] strains.
The cells of the strains MG1655 and MG1655 (PL-brnQ) were each transformed with plasmid pELAC-IDO (Lys, 23). Resulting clones were selected on the X-gal/IPTG agar-plate (blue/white test). Thus, the strains MG1655 [pELAC-IDO(Lys, 23)] and MG1655(PL-brnQ[pELAC-IDO(Lys, 23)], respectively, were obtained.
Example 2. Production of 4HIL bv Ecoli strain MG1655fPL-bronQ)rpELAC-IDOrLvs. 23'>] To test the effect of enhanced expression of a gene coding for L-isoleucine transporter

on 4HIL production, cells of the MG1655 [pELAC-IDO(Lys, 23)] and MGl655(Pz:-brnQ[pELAC-IDO(Lys, 23)] strains were grown in LB medium supplemented with ampicillin (200 µg/ml) and IPTG (1 mM) at 37°C for about 4-5 hours. Specific IDO activity was measured in crude protein extracts for each grown recombinant E. coli strain as follows. Cells from 5 ml of culture were harvested by centrifiigation at 4°C, re-suspended in 0.5 ml of buffer A*(50 mM TRIZMA, 5% glycerol, 1 mM EDTA, 1 mM DTT, pH 7 adjusted by HCl) and disrupted by sonication at 4°C. The reaction mixture (50 µl) contained 50 mM HEPES pH 7.0; 5 mM lle; 0.5mM a-ketogjutarate; 5 mM ascorbate; 5 mM FeSO4 and an aliquot of the protein preparation. The reaction was incubated at 34C for 1 hour with shaking. 4HIL was detected using TLC or HPLC analysis as follows. TLC analysis: thin-layer silica gel plate (10x15 cm) spotted with an aliquot (1-2µ1) of the reaction solution was developed with a developing solvent (2-propanol: acetone: ammonia: water =100:100 : 25 : 16) and 4HIL was detected with the ninhydrin reagent. HPLC analysis: High pressure chromatograph (Waters, USA) with spectrofluorometer 1100 series (Agilent, USA) was used. The chosen detection wave range: excitation wavelength at 250 run, range of emission wavelengths were 320-560 nm. The separation by the accq-tag method was performed in a column Nova-Pak ™C18 150 X 3.9 mm, 4µm (Waters, USA) at +40°C. The injection volume of the sample was 5µl. The formation of amino acid derivatives and their separation was performed according to Waters manufacturer's recommendation (Liu, H. et al, J. Chromatogr. A, 828, 383-395 (1998); Waters accq-tag chemistry package. Instruction manual. Millipore Corporation, pp. 1-9 (1993)). To obtain amino acid derivatives with 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate, the kit Accq-Fluor™ (Waters, USA) was used- The analysis by accq-tag method was performed using concentrated Accq-tag Eluent A (Waters, USA). All solutions were prepared using Milli-Q water, standard solutions were stored at + 4°C. Results of measuring of IDO activity in crude extract of IDO-producing strains are shown in Table 1.
Cells of the MG1655 [pELAC-IIX)(Lys, 23)] and MG1655(PL-67-BRNQ[PELAC-IDO(Lys, 23)] strains were harvested by centrifiigation and re-suspended up to a final volume of 2 ml (to an OD540 ==0.03-0.04) in the medium MI30ch (50 mM KH2PO4 (pH7, adjusted by NaOH); 20 mM NH4CI, 2 mM MgSO4, chalk - 1.25 g/100ml, 30 g/1 He, 2 mM FeSO4,2 mM ascorbate, ampicillin 200 mg/1) supplemented with L-isoleucine and ketoglutarate, glucose or glycerol in various combinations (see Table 2, Table 3). Cells were cultivated for about 15 hours at 32C with vigorous agitation. Then, accumulation of 4HIL was investigated by HPLC-analysis as described above. The results of measuring of the 4HIL produced by the

MG1655 [pELAC-IDCKLys, 23)] and MG1655{Pl-brnQ)[pELAC-IDO(Lys, 23)] strains depending on the a-ketoglutarate, glucose, and glycerol are shown in Table 2(at least 3 test tubes). The results of measuring of the 4HIL produced by the MG1655 [pELAC-IDO(Lys, 23)] and MG1655(PL-brnQ[pELAC-IDO(Lys, 23)] strains depending on the different concentrations of glycerol are shown in Table 3 (at least 3 test tubes). As follows from Table 2 and Table 3, MG1655(PL-brnQ)[pELAC-IDO(Lys, 23)] produced a higher amount of 4HIL, as compared with MG1655 [pELAC-IDO(Lys, 23)].



Example 3. Construction of MG1655 (AsucAB. AaceAK. Pi-brnO) rpELAC-IDOCLvs. 22)} strain.
3.1. Construction of MG1655 (AsucAB) strain.
To delete the si4cAB genes, the following manipulations were carried out. A 1.8 kb DNA fragment containing a Cm*^ -marker and the P,ac promoter was amplified by PCR with oligonucleotides SVS-192(SEQ ID No:19) and SVS-193((SEQ ID No:20) as primers and chromosomal DNAof MG1655(attR-Cm-attL-PMc) strain (Katashkina J.I. et al., Molekulamaya biologiya(RU), v.39, No.5,1-10 (2005)) as a template. Conditions for PCR were as follows: denaturation step for 3 min at 95''C; profile for two first cycles: 1 min at 95'»C, 30 sec at 50°C, 40 sec at 72°C; profile for the last 25 cycles: 30 sec at 95°C, 30 sec at 54*C, 40 sec at 72''C; final step: 5 min at 72°C.
A1.8 kbp PCR prodxict was obtained and purified in agarose gel and was used for electroporation of the £. coli strain MG1655 , which contains the plasmid pKD46 having a temperature-sensitive replication.
Electroporation was performed as described above. Cells after electroporation were incubated with 1 ml of SOC medium at 37^ for 2.5 hours and then were plated onto L-agar containing chloramphenicol (30 ^g/ml) and grown at 37''C to select CmR recombinants. Then, to eliminate the pKD46 plasmid, two passages on L-agar with Cm at 42''C were performed and the obtained colonies were tested for sensitivity to ampicillin.
Thus E. coli MG1655 (AsucAB) strain was constructed.

3.2. Construction of MG1655 (AaceAK) strain.
To delete the aceAK genes, the following manipulations were carried out. A 1.8 kb DNA fragment containing the Km'^ -marker and ?UK promoter was amplified by PCR with oUgonucleotidesSVS-199(SEQIDNo:21)and SVS-200 (SEQ ID No:22) as primers and pMWl 1 Z-{XattL-Km^-XattR) (see RefCTKice example 2) plasmid DNA as a template.
Conditions for PCR were as follows: denaturation step for 3 min at 95°C; profile for two first cycles: 1 min at 95°C, 30 sec at 50°C, 40 sec at 72°C; profile for the last 25 cycles: 30 sec at 95°C, 30 sec at 54°C, 40 sec at 72''C; final step: 5 min at 72°C.
A 1.8 kbp PCR product was obtained and purified in agarose gel and was used for electroporation of the E. coli strain MG1655 , wiiich contains the plasmid pKD46 which has a temperature-sensitive replication origin.
Electroporation was performed as described above. Cells after electroporation were incubated with 1 ml of SOC medium at 37*'C for 2.5 hours and then were plated onto L-agar containing kanamycine (20 ^ig/ml) and grown at 37°C to select Km recombinants. Then, to eliminate the pKD46 plasmid, two passives on L-agar with Km at 42°C were performed and the obtained colonies were tested for sensitivity to ampicillin.
Thus E. coli MG1655 (A aceAK) strain was constructed.
3.3. Construction of MG1655 (Aw/cAB. AaceAK. Vi-brnO) strain.
To eliminate the chloramphenicol resistance marker fi^om the strain MG1655 (P^,-6rwQ), cells were transformed with the plasmid pMW 118-int-xis (Ap*^) (WO2605/010175). Ap*^ clones were grown on LB agar plates containing 150 mg/1 ampicillin at 30°C. Several tens of Ap"^ clones were picked up and tested for chloramphenicol sensitivity. The plasmid pMWl 18-int-xis was eliminated fi-om the Cm^ cells by incubation on LB agar plates at 42°C. The obtained strain was used for fiirtiier construction.
DNA fi-agments ftova the chromosome of the E. coli MG\655{iSsucAE) strain were transferred to the strain obtaii^ after elimination of the chloramphenicol resistance marker fi-om the strain MG1655 (Pi-6r/iQ) by PI transduction (Miller, J.H. Experiments in Molecular Genetics, Cold Spring Harbor Lab. Press, 1972, Plainview, NY). Thus, MG1655 (A^wcAB, P^. 6r/rQ) strain was constructed. DNA fiagments fiom the chromosome of the E. coli MG1655(AflceAK) strain were transferred to the strain MG1655 (A^MCAB, Pi,.6rnQ). Thus, MG1655 (AsucAB, AaceAK, P£.femQ) strain was constructed.
The cells of the strain MG1655 (AsucAB, AaceAK, P/..6rwQ) were transformed with

plasmid pELAC-IDO (Lys, 23). Resulting dones were selected on the X-gal/IPTG agar-plate (blue/white test). Thus, the strafais MG1655 (AsucAB, A^eAK, ?iJ)rnQ) [pELAC-IDCXLys, 23)] was obtained.
3.4. Investigation of growth of strains MG1655. MG1655 (Ay^cAB. AaceAK. P^-brnOX MG1655 rpELAC-IDCXLvs. 23)1 and MG1655 (AsucAB. AaceAK. Pf-hrrK)) rpELAC-IDOfLvs. 23)1.
Strains MG1655 and MG1655 (AsucAB, AaceAK, Pc-brnQ) were grown in the following cultivation media:
A - M9 salts + glucose (0.4%);
B - M9 salts + glucose (0.4%) + DAP, Met, Lys (40 mg/1 of each);
C - M9 salts + glycerol (0.4%);
D - M9 salts + glycerol (0.4%) + DAP, Met, Lys (40 mg/1 of each).
Strains were cultivated in test tube at 37°C and optical density of cells culture (A555) was measured every hour. As it can be seen from Figure 5, strain MG1655 (AsucAB, AaceAK, Pi-bmQ) lacks succinyl-CoA and cannot grow in the media A or C. Only addition of lysine, methionine and diaminopimelate (DAP) restored growth of the strain.
Futher, strains MG1655[pELAC-IDO(Lys, 23)] and MG1655 (A^wcAB, AaceAK, ?L-brnQ) [pELAC-IDO(Lys, 23)] strains were grown in following media:
G - M9 salts + glucose (137 mM)
GI - M9 salts + glucose (137mM) + L-isoleucine (137 mM)
Y - M9 salts + glycerol (136 mM)
YI - M9 salts + glycerol (136 mM) + L-isoleucine (137 mM)
Each medium contained ampicillin (100 mg/1). Strains were cultivated in test tube at 3TC and optical density of cells culture (A555) was measured every hoxir.
Expression of IDG gene restores growth of strain MG1655 (AsucAB, AaceAK, P^-ferwQ) on the M9-salts medium supplemented wiA L-isoleucine (Fig. 6). It proves the idea of the authors of the present invention that isoleucine hydroxylation leads to the growth of the strain.
Example 4. Production of 4HIL bv E. coli strain MG1655 (A^MCAB. AaceAK, P^-ferwO) rpELAC-IDQ(Lvs. 23)1.
To test the effect of attenuated expression of genes coding for oxoglutarate dehydrogenase, isocitrate lyase, and isocitrate dehydrogenase phosphatase, cells of the

MG1655(Pi-6rw0[pELAC-IDO(Lys, 23)] and MGl655(AsucAB, AaceAK ,Pi-6r«0[pELAC-IDO(Lys, 23)] strains wsre each gro^wi in medium A [(NH4)2S04 -1.5 g/100 ml; KH2PO4- 0-15 g/100 ml; MgS04 - O.I g /lOO ml (MgS04-7H20 - 0.205 g/100 ml); He -220 mM; FeCh - 2 mM, 1 mM IPTG, chalk - 2 g/100 ml] supplemented with glucose (300 mM) or glycerol (500 mM) at 32*<^ for 72 hours with vigorous agitation. Then, accumulation of 4HIL was investigated by HPLC-analysis as described above. The results of measuring of the 4HIL produced by the MG1655(PL-6rn0[pELAC-IDO(Lys, 23)] and MG1655(A sucAB, AaceAK ,P£,-6rn0[pELAC-IIX)(Lys, 23)] strains are shown in Table 4(at least 3 test tubes). As follows from Table 4, MG1655(AywcAB, AaceAK ,Pz.-6rn0[pELAC-IIX)(Lys, 23)] produced a higher amount of 4HIL, as con^ared with MG1655(Pi-6r«<2)[pELAC-IDO(Lys, 23)].
Table 4

Example 5. Production of 4HIL bv £. coli strain MG1655 (AsucAB. AaceAK, Pf-hrnQ)* rpEL-IDO(Lvs. 23^1.
5.1. Construction of the PEL-IDO(LVS. 23) plasmid.
Due to the presence of/oc/gene ia the pELAC-IDO(Lys, 23) plasmid, addition of IPTG is necessary to induce IDO expression during the biotransformation process of 4-HIL production. To avoid such IPTG-dependence, large part of the /ac/gene was deleted from pELAC-IDO(Lys, 23) plasmid (Fig. 1) by excision of the Sphl-EcoRV DNA fragment using corresp)onding restrictases followed by ligation of the remaining part of the plasmid. Thus, pEL-IDO(Lys, 23) plasmid has been constructed.

5.2. Production of 4HIL
MG1655 (AyucAB, AaceAK, ?L-brrrQj* strain was obtained by sequential excisions of Cm and Kn markers from MG1655 (Asi^AB, AoceAK, ?L-bmQ) strain using plasmid pMWl Ig-int-xis-CAp*^) (WO2005/010175) as described above. Plasmids pELAC-IDO(Lys, 23) and pEL-IDO(Lys, 23) wo^e introduced into resulted strain. Thus, MG1655 (AJMCAB, AaceAK, ?L-brnQ)* [pELAC-IDO(Lys, 23)] and MG1655 {AsucAB, AaceAK, ?/.-6rnQ)*[pEL-ID0(Lys, 23)] strains were obtained.
A piece of biomass of MG1655 (AsucAB, AaceAK, Pi-brnQ)* [pELAC-IDO(Lys, 23)] or MG1655 (A5«cAB, AaceAK, Pi-6r«Q)*[pEL-nX)(Lys, 23)] strain from fresh-made LB-agar plate was separately inoculated in 50 ml of LB broth supplemented with Ap (100 mg/1) and cultivated at 37°C for about 4 hours in 750 ml-flask. Obtained cell cultures were used as inoculums in the biotransformation carried out in "Marubischi" fermenters. The following cultivation parameters were used: starting culture volume - 500 ml; agitation - 1200 rev/min; air - 1:1; cultivation temperature - 34°C; pH 7.0 was stabilized using 2.5 M NH4OH.
Inoculum of MG1655 (AsucAB, AaceAK, Pi-6rnQ)* [pELAC-IDO] strain was added to 450 ml of medium containing (NH4)2S04 - 5 g/1; KH2PO4 - 1.5 g/1; MgS04 7H2O - 1 g/1; FeS04 7H2O - 0,01 g/1; isoleucine - 22-23 g/1 (=170 mM); glucose - 50 g/1; ImM IPTG (pH 7 adjusted by KOH, final volume = 500 ml) and cultivated for about 20 hours.
Inoculvun of MG1655 (AsucAB, AaceAK^ ?L-brnQ)* [pEL-IDO] strain was added to 450 ml of the above medium without IPTG and cultivated for about 20 hours. Concentrations of 4HIL and L-isoleucine were determined using HPLC analysis as above. As it is seen from the Table 5, use of pEL-IDO plasmid allows to avoid IPTG -dependence.


Reference example 1. Constnicticm of the pELAC-ilvA plasmicL
The plasmid pET-ilvA was constructed as follows. A 1.5 kb fragment of the E. coli MG1655 strain chromosomal DNA was amplified using PCR with oligonucleotides ilvA-5 (SEQ ID NO: 23) and iIvA-3 (SEQ ID NO: 24) as primers. A piece of cell culture of £. coli MG1655 strain from LB-agar plate was used as a source of the template DNA for the PCR procedure. As a result, the DNA fr^m^it contained the ilvA gene and was flanked by the Ndel and BamHi restriction sites. It was cloned into the pET22 (b+) vector (Novagen, Germany) between the Ndel-BamHl sites. Tlius, recombinant plasmid pET-ilvA was constructed (Fig. 2).
The pELAC-ilvA plasmid was constructed from pET-ilvA by replacing the BglH-Xbal fragment containing the T7 promoter with the Bglll-Xbal fragment containing the Piac promoter (SEQ ID NO: 25).
Reference example 2. Construction of the pMW118-(Xfl//I-Km'-Xar//?) plasmid.
The pMW 118-(XattL-Km^-Xa/r/?) plasmid was constructed based on the pMWl 18-attL-Tc-attR (WO2005/010175) plasmid by substitution of the tetracycline resistance marker gene with the kanamycin resistance marker gene from the pUC4K plasmid (Vieira, J. and Messing, J., Gene, 19(3): 259-68 (1982)).
For that purpose, the large £coRI - HiruRW. fragment from pMWl 18-attL-Tc-attR plasmid was ligated to two fragments from the pUC4K plasmid: Hindlll - Pstl fragment (676 bp) and £coRI - Hindlll fragment (585 bp).
Basic pMW118-attL-Tc-attR v/as obtained by ligation of the following four DNA fragments:
1) the BglU-EcoRl fragment (114 bp) carrying attL (SEQ ID NO: 26) which was obtained by PCR amplification of tiie corresponding region of the E. coli W3350 (contained X proph^e) chromosome usii^ oligonucleotides P3 and P4 (SEQ ID NOS: 27 and 28) as primers (these primers contained the subsidiary recognition sites for Bglll and EcoRl endonucleases);
2) the Pstl-Hindm fragment (182 bp) carrying attR (SEQ ID NO: 29) which was obtained by PCR amplification of the corresponding region of the E. coli W3350 (contained "K prophage) chromosome using the oligonucleotides P5 and P6 (SEQ ID NOS: 30 and 31) as primers (these primers contained the subsidiary recognition sites
. for Pstl and Hindlll endonucleases);

3) the large Bglil-Hindm firagmeni (3916 bp) of pMW118-ter_/T«5. The plasmid
pMWl 1 %-X&cjrnB was obtained b\^ ligation of the following three DNA fragments:
a) the large DNA fragment (2359 bp) carrjing the AatU-EcoRl fragment of pMWl 18 that was obtained by the following way: pMWl 18 was digested with EcoRl restriction endonuclease, treated with Kleiww fragment of DNA polymerase I, and then digested with AatU restriction end
Medium A (300 ml): D-glucose (20 g/L), MgS04-7H20 (1 g/L);
Medium B (700 ml): ammonium sul&te (5 g/L), KH2PO4 (1.5 g/L), sodium ascorbate (0.01 g/L), FeS04 7H2O(0.1 g/L), adjusted pH to 7.0 with KOH.
The media A and B were s^arately autoclaved at IIQ^C for 20 min, and mixed after cooling.
The D-glucose concentration (g/L) and the 4-hydroxy-proline concentration (mM) are shown in Table 6. D-glucose was analyzed widi a glucose analyzer (S AKURA SI, Japan). 4-Hydroxy-proline was analyzed by HPLC with Simiichiral OA-5000 (Sumika Analysis Center, Japan) (Mobile phase: 2 mM cupper sulfate aqueous solution, column temperature: 30°C, flow rate: 1 ml/min, detection: UV 254 nm).

As a result, it was confirmed that MG1655 (AsucAB, bjoceAK, PL-bmQ)*/ ptrp4_PD0 could utilize D-glucose more efficiently for production reaction of hydroxyproline compared with MG1655/ ptrp4_PD0.

Example 7-1. Construction of E. coli strain MG1655 (∆sucA, AaceAK) and E. coli strain MG1655 (∆sucB. ∆aceAK).
To confirm whether the Pl-brnQ mutation is mandatory for the efficient utilization of D-giucose or not, the following experiments were carried out.
To construct a strain deficient in 2-oxoglutarate dehydrogenase (sucA and sucB), isocitrate lyase (aceA) and isocitrate dehydrogenase kinase/phosphatase (aceK) without any mutation in PL-brnQ, AaceAK was introduced into E. coli strain MG1655 AsucA strain (JW0715) and E. coli strain MG1655 AsucB strain (JW0716) of E. coli Keio Knockout Collection (http://ecoli.naisLjp) to obtain E. coli strain MG1655 (AsucA, AaceAK) and E. coli strain MG1655 (AsucB, AaceAK). The deficiency of one of sucA and sucB results in the deficiency of 2-oxoglutarate dehydrogenase activity.
To delete the aceAK genes, the following manipulations were carried out. A 1.6 kb DNA Segment containing the CmR-marker was amplified by PCR with oligonucleotides SVS-199 (SEQ ID N0:21) and SVS-200 (SEQ ID NO:22) as primers and pMW118-(λattL-Cmr-λattR) (WO2005/010175) plasmid DNA as a template.
Conditions for PCR were as follows: denaturation step for 3 min at 94''C; profile for 30 cycles: 30 sec at 94C, 30 sec at 50C, 2 min at 72°C.
A 1.6 kbp PCR product was obtained and purified in agarose gel and was used for electroporation of the E. coli strain MG1655 (AsucA), E. coli strain MG1655 (AsucB), which contains the plasmid pKD46 (WO2005/010175) which has a temperature-sensitive replication origin.

Electroporation was perfonned as ckscribed above. Cells after electroporation were incubated with 1 ml of SOC medium at 37° C for 1 hours and then were plated onto L-agar containing Cm (25µ g/ml) and grown at 37°C to select CmR recombinants. Then, to eliminate the pKD46 plasmid, two passages on L-agar with Cm at 42°C were performed and the obtained colonies were tested for sensitivity to ampicillin.
After that, CmR-marker was ranoved using plasmid pMW118-int-xis-ts (ApR) (WO2005/010175) as described above.
Thus E. coli strain MG1655 (∆sucA,∆ aceAK) and E. coli strain MG1655( ∆sucB, ∆aceAK) strain were constructed.
Example 7-2. Production of 4HIL bv E. coli strain MG1655[pEL-IDCXLvs. 23)]1. E. coli strain
«
MG1655 ∆(sucA. a∆cgy^n∆roEL-IDCXLvs. 23')1. and E. coli strain MO 1655 (AxucB. ∆aceAK) rpEL-lDO(Lvs. 23)1.
pEL-IDO(Lys, 23) plasmid was introduced into each of E. coli strain MG1655 as well as E. coli strain MG1655 (AsucA, ∆aceAK) and E. coli strain MG1655 (AsucB, AaceAK) obtained by the above method to obtain transformants E. coli strain MG1655[pEL-IDO(Lys, 23)], E . coli strain MG1655 (∆sucA, ∆aceAK[pEL-IDO(Lys, 23)], and £. coli stram MG1655 (AsucB, AaceAK) [pEL-IDO(Lys, 23)].
These strains were cultivated in LB medium containing 100 mg/1 ampicillin at 30°C for 24 hours, and 300µL of the culture was inoculated to 3 ml of LB medium containing 100 mg/1 ampicillin and cultivated at 37° C for 6 hours. To a test tube containing L-Ile and calcium carbonate so that their final concentrations were 10 g/1 and 20 g/1, respectively, the obtained culture (0.3 ml) and the following cultivation media (2.7 ml) were added:

Medium A (300 ml): D-glucose (20 g/L), MgSO4-7H2O (1 g/L);
Medium B (700 ml): ammonium sulfate (5 g/L), KH2PO4 (1.5 g/L), sodium ascorbate (0.01 g/L), FeS04 7H2O (0.1 g/L), adjusted pH to 7.0 with KOH.
The media A and B were separately autoclaved at 102° C for 20 min, and mixed after cooling.
The remaining D-glucose and the produced 4-hydroxy-isoleucine in the medium are shown in Table 7. D-glucose was analyzed with a glucose analyzer (SAKURA SI, Japan). 4-Hydroxy-isoleucine was analyzed by HPLC with MCI GEL CRS10W (Mitsubishi Kagaku,

Japan) (Mobile phase: 1 mM CuSO, 5% MeOH, column temperature: 30°C, flow rate: 1 ml/min, detection: UV 254 nm).
As a result, it was confirmed that in the reaction using E. coli strain MGl 655 (AsucA, Aflcea/k[pEL-IDO(Lys, 23)], and E coli strain MG1655 (AsucB, ∆aceAK) [pEL-IDO(Lys, 23)] without the PL-brnQ mutation, D-glucose could be more efficiently utilized for the conversion reaction by He dioxygenase compared with MG1655[pEL-IDO(Lys, 23)].
From these results, it is confirmed that strains deficient in the genes of ∆sucAB, AsucA, AsucB, and AaceAK, such as E. coli MGl655 (AsucAB, AaceAK), E. coli strain MGl655 (AsucA, AaceAK), and E. coli strain MGl655 {AsucB, AaceAK) can be widely used for the 2-oxoglutrate-dependent enzymes.

Explanation of sequences 1: L-isoleucine dioxygenase gene fiom Bacillus thuringiensis strain 2-e-2 2: L-isoleucine dioxygenase fiom Bacillus thuringiensis strain 2-e-2 3: brnQ gene fit>m E. coli 4: BrnQ fiom E. coli 5: sucA gene fit)m E. coli 6: SucA fix)m E. coli 7: sucB gene from E. coli 8: SucB fiom E. coli 9: aceA gene from E. coli 10: AceA from E. coli 11: aceK gene from E. coli 12: AceK from E. coli

13: ilvE gene from E. coli
14: IlvE from E. coli
15: primer SVS 170
16: primer SVS 169
17: primer SVS 179
18: primer SVS 180
19: primer SVS 192
20: primer SVS 193
21: primer SVS 199
22: primer SVS 200
23: primer IlvA-5
24: primer ilvA-3
25: Bgtll-Xbal fragment containing the Plac promoter
26: fragment attL
27: primer P3
28: primer P4
29: fragment attR
30: primer P5
31: primer P6
32: primer P7
33: primer P8
34: primer P9
35: primer P10
36: fragment of pML-Tc-ter_thrL
37: primer P11
38: primer P12
39: L-proline 4-hydroxylase gene from Dactylosporangium sp.
40: L-proline 4-hydroxylase from Dactylosporangium sp.
While the invention has been described in detail with reference to preferred embodiments thereof, it will be apparent to one skilled in the art that various changes can be made, and equivalents employed, without departing from the scope of the invention. All the cited references herein are incorporated as a part of this application by reference.

Industrial Applicability
According to the present invention, production of (2S,3R,4S)-4-hydroxy-L-isoleucine can be enhanced. This compound is useful as a component of pharmaceutical compositions with insulinotropic activity. Production of (2S,3R,4S)-4-hydroxy-L-isoleucine is enhanced by using a bacterium transformed with a DNA fragment containing a gene coding for a protein having L-isoleucine dioxygenase activity.

CLAIMS

1. A bacterium transformed with a DNA fragment containing a gene coding for a protein having 2-oxoglutarate-dependent enzyme activity, wherein said bacterium has been modified to attenuate the expression of a gene coding for oxoglutarate dehydrogenase, and wherein said bacterium has the ability to produce a product of a reaction catalyzed by the protein.

2. The bacterium according to claim 1, wherein said expression is attenuated by inactivating said genes coding for oxoglutarate dehydrogenase.

3. The bacterium according to claim 1, wherein said bacterium has been modified to attenuate the expression of genes coding for oxoglutarate dehydrogenase and isocitrate lyase.

4. The bacterium according to claim 3, wherein said expression is attenuated by inactivating said genes coding for oxoglutarate dehydrogenase and isocitrate lyase.

5. The bacterium according to claim 1, wherein said bacterium has been modified to attenuate the expression of genes coding for oxoglutarate dehydrogenase, isocitrate lyase, and isocitrate dehydrogenase phosphatase.

6. The bacterium according to claim 5, wherein said expression is attenuated by inactivating said genes coding for oxoglutarate dehydrogenase, isocitrate lyase, and isocitrate dehydrogenase phosphatase.

7. The bacterium according to any of claims 1-6, wherein the bacterium belongs to a genus selected from the group consisting of Escherichia, Pseudomonas, Corynebacterium, Arthrobacter, Aspergillus, and Bacillus.

8. The bacterium according to claim 7, wherein the bacterium is selected from the group consisting of Escherichia coli, Arthrobacter simplex, Corynebacterium glutamicum, Arthrobacter globiformis, Arthrobacter sulfureus, Arthrobacter viscosus, and Bacillus subtilis.

9. A method for manufacturing a product of a reaction catalyzed by a protein having 2-oxoglutarate-dependent enzyme activity, comprising:
cultivating a bacterium according to any one of claims I to 8 in a culture medium containing a substrate of the reaction; and isolating the product.

10. The bacterium according to claim 1, wherein said protein has L-isoleucine dioxygenase activity, and the product is (2S,3R,4S)-4-hydroxy-L-isoleucine.

11. The bacterium according to claim 6. wherein said bacterium has been modified to overexpress a gene coding for an L-isoleucine transporter.

12. The bacterium according to claim 10, wherein the gene coding for the protein having L-isoleucine dioxygenase activity is selected from the group consisting of:

(a) a DNA comprising the nucleotide sequonce of SEQ ED No: 1;

(b) a DNA that hybridizes under stringent conditions with a DNA comprising a nucleotide sequence complementary to the nucleotide sequence of SEQ ID No: 1 and wherein said DNA encodes a protein having L-isoleucine dioxygenase activity;

(c) a DNA comprising a nucleotide sequence that encodes a protein comprising the amino acid sequence of SEQ ID No: 2;

(d) a DNA comprising a nucleotide sequence that encodes a protein comprising an amino acid sequence of SEQ ID NO. 2, except that said amino acid sequence contains a substitution, deletion, insertion, addition, or inversion of one or several amino acid residues, and wherein said protein has L-isoleucine dioxygenase activity; and

(e) a DNA comprising a nucleotide sequence that encodes a protein comprising an amino acid sequence that is at least 98% homologous to the amino acid sequence of SEQ ID NO: 2, and wherein said protein has L-isoleucine dioxygenase activity.

13. The bacterium according to claim 10, wherein the bacterium has been modified to enhance the activity of L-isoleucine dioxygenase.

14. The bacterium according to claim 13, wherein the activity of L-isoleucine dioxygenase is enhanced by increasing the expression of the gene encoding L-isoleucine dioxygenase.

15. The bacterium according to claim 14, wherein the expression of L-isoleucine dioxygenase is increased by modifying an expression control sequence of the gene encoding L-isoleucine dioxygenase or by increasing the copy number of the gene encoding L-isoleucine dioxygenase.

16. The bacterium according to claim 11, wherein the gene coding for the L-isoleucine transporter is the brnQ gene from Escherichia coli.

17. The bacterium according to claim 10, which is additionally modified to attenuate expression of a gene coding for a branched-chain amino-acid aminotransferase.

18. The bacterium according to claim 17,wherein said expression is attenuated by inactivating said gene.

19. A method for manufacturing (2S,3R,4S)-4-hydroxy-L-isoleucine or a salt thereof, comprising:

cultivating a bacterium according to any of claims 10 to 18 in a culture medium
containing L-isoleucine; and isolating (2S,3R,4S)-4-hydroxy-L-isoileucine .

20. The method according to claim 19, wherein the culture medium contains a carbon source selected from the group consisting of a carbohydrate, and an alcohol.
21. The method according to claim 20, wherein said carbohydrate is glucose, and said alcohol is glycerol.

22. The bacterium according to claim 1, wherein said protein has L-proline hydroxylase activity, and the product is 4-hydroxy-L-proline.

23. A method for manufacturing 4-hydroxy-L-proline or a salt thereof, comprising:
cultivating a bacterium according to claim 22 in a culture medium containing L-proline; and isolating 4-hydroxy-L-proline.