Patent Application
20070292923
The present invention relates to, in an oxidation reaction by dehydrogenase using nicotinamide adenine dinucleotide (hereinafter to be abbreviated as NAD+) as a coenzyme, a method of regenerating coenzyme NAD+ using a Streptococcus-derived water-forming NADH oxidase, and a method of producing an optically active compound from an enantiomer mixture utilizing the regeneration method of NAD+.
The whole disclosure of Japanese patent application No. 2004-230139 filed on Aug. 6, 2004 including the specification, claims, drawings and abstract are incorporated hereinto by reference.
The oxidoreductases (e.g., dehydrogenase) classified into E.C.1.1 and E.C.1.4 include those that catalyze a reaction to oxidize alcohol and amino acid to ketone and keto acid in the presence of a coenzyme such as NAD+ and the like. In most cases, since the oxidation reaction by such dehydrogenase is stereoselective, when an enantiomer mixture of alcohols or amino acids is reacted with such enzyme, only one enantiomer is oxidized and the remaining enantiomer is enriched. This reaction is an effective method for the production of an optically active compound.
In the above-mentioned oxidation reaction, however, oxidized coenzyme NAD+ is converted to NADH. Thus, the reaction requires a stoichiometric amount of NAD+. As shown in the following reaction scheme 1, however, it is possible to avoid the use of a stoichiometric amount of NAD+ and reduce the amount thereof to be used, by the coupling of a reaction to convert NADH produced by an oxidation reaction by dehydrogenase to NAD+ (NAD+ regeneration system) (in reaction scheme 1, * shows an asymmetric carbon, and its absolute configuration may be (R) or (S)).
Synthesis methods of optically active compounds utilizing a Lactobacillus brevis-derived water-forming NADH oxidase in a coenzyme regeneration system have been reported heretofore (patent reference 1, non-patent references 1, 2). Oxidase is an enzyme that catalyzes the reaction to oxidize NADH with oxygen to produce NAD+ and water, and the reaction essentially requires the presence of oxygen. The reaction to produce NAD+ from NADH by a water-forming NADH oxidase is irreversible. In addition, as the reaction product other than NAD+, only water is produced and the use of the enzyme for the NAD+ regeneration system is preferable.
However, since a Lactobacillus brevis-derived water-forming NADH oxidase shows high sensitivity to oxidation, the stabilization thereof requires addition of DTT (dithiothreitol) and the like (non-patent reference 1). Accordingly, addition of a stabilizer such as DTT and the like to the reaction system is necessary even when the water-forming NADH oxidase derived from a microorganism is used for the NAD+ regeneration system.
While a synthesis method of an optically active compound utilizing, other than a Lactobacillus brevis, Lactobacillus sanfranciscensis-derived water-forming NADH oxidase as the NAD+ regeneration enzyme has been reported, DTT is also added to the reaction system (non-patent reference 3).
When conventional Lactobacillus brevis and Lactobacillus sanfranciscensis-derived water-forming NADH oxidases are used as NAD+ regeneration enzymes are used, addition of DTT to the reaction system is generally necessary. When addition of DDT is necessary, problems occur such as (1) extra cost for DDT addition, (2) possibility of reaction with added DTT to reduce the yield, depending on the substrate to be used for the reaction and the resultant product, (3) decreased DTT concentration and decreased protection effect for NADH oxidase as a result of the reaction with DDT and the like. These problems need to be particularly considered, for example, for application thereof to industrial production methods.
The present invention aims at provision of an efficient production method of a useful substance such as optically active alcohol, amino acid and the like, which comprises use of a water-forming NADH oxidase, which is superior in the activity, stability and the like and does not require an enzyme protector such as DTT and the like particularly during the reaction, in the NAD+ regeneration system for the stereoselective oxidation reaction by dehydrogenase.
The present inventors have found, with regard to the above-mentioned problems, a microorganism belonging to the genus Streptococcus, more particularly, Streptococcus mutans-derived NADH oxidase, does not require addition of a protector such as DTT and the like for stabilization and is highly advantageous as an NAD+ regeneration enzyme, which resulted in the completion of the present invention.
The present invention further provides the following.
Using a water-forming NADH oxidase derived from a microorganism belonging to the genus Streptococcus for a NAD+ regeneration system, regenerative reaction of NAD+ proceeds efficiently even without adding an enzyme stabilizer such as a reducing agent and the like. Accordingly, when the NAD+ regeneration system is coupled with a stereoselective oxidation reaction by dehydrogenase, an enantiomer-enriched compound can be obtained efficiently from an enantiomer mixture.
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1. Water-Forming NADH Oxidase
As the “water-forming NADH oxidase” to be used for the NAD regeneration system of the present invention, one that is stable under oxidative conditions, namely, one free of deactivation, or one wherein remarkable deactivation is suppressed, is used.
In the present specification, being “stable under oxidative conditions” is a concept including catalyzing a reaction to convert NADH to NAD+ without remarkable deactivation in the presence of oxygen, for example, under oxygen supply conditions such as in a buffer without particular deaeration, shaking a test tube containing an enzyme solution and the like. In addition, the concept of being “stable under oxidative conditions” includes a condition stable in the presence of oxygen even without utilizing an enzyme protector as if an enzyme protector was used.
The “water-forming NADH oxidase stable under oxidative conditions” to be used in the present invention maintains not less than about 70%, preferably not less than about 80%, more preferably not less than about 90%, of the activity in the absence of an enzyme protector such as DTT and the like, in the presence of oxygen at about 20° C. for about 3 hr.
The origin of the “water-forming NADH oxidase” of the present invention is, for example, a microorganism belonging to the genus Streptococcus, preferably Streptococcus mutans, more preferably Streptococcus mutans NCIB11723. The amino acid sequence of Streptococcus mutans NCIB11723-derived water-forming NADH oxidase, and the base sequence of DNA encoding the same have already been reported (patent reference: JP-A-8-196281)
SEQ ID NOs: 1, 2 show the amino acid sequence of Streptococcus mutans NCIB11723-derived water-forming NADH oxidase, and the base sequence of DNA encoding the same. The Streptococcus may be a wild strain or a mutant strain. The mutant strain can be obtained by UV irradiation or a treatment with a mutating agent such as N-methyl-N′nitro-N-nitrosoguanidine (NTG), methylethanesulfonate (EMS) and the like by a conventional method. Any mutant strain can be used as a source of NADH oxidase to be used in the present invention, as long as it can produce the NADH oxidase of the present invention.
Unlike the conventional Lactobacillus-derived enzymes, the water-forming NADH oxidase derived from a microorganism belonging to the genus Streptococcus does not require addition of a reducing agent such as DTT and the like for stabilization, and is preferably used for the NAD+ regeneration system, which is the object of the present invention. The water-forming NADH oxidase can be obtained by preparing an enzyme from a culture medium of Streptococcus bacterium. In addition, it can be obtained easily in a large amount by incorporating a DNA encoding the enzyme into a vector, introducing the vector into a host and expressing the enzyme gene in the obtained transformant.
In the present invention, as the “water-forming NADH oxidase”, an enzyme protein substantially the same as the enzyme protein having the amino acid sequence shown in SEQ ID NO: 1 can be used. As for the “substantially the same” enzyme protein, the enzyme protein can be said to be substantially the same when 1, 2, 3, 4, 5, 6, 7, 8, 9, 10 or more substitutions, deletions and/or insertions are introduced into the amino acid sequence of the enzyme protein and the enzyme protein shows an equivalent function. In addition, the enzyme protein to be used in the present invention can be said to be substantially the same when the enzyme protein shows a homology in the amino acid sequence of not less than 60%, preferably not less than 80%, more preferably not less than 90%, and most preferably not less than 99%, with the amino acid sequence shown in SEQ ID NO: 1, and has an equivalent function with the enzyme protein having the amino acid sequence shown in SEQ ID NO: 1.
The above-mentioned “homology” of the amino acid sequence can be determined by comparison with the optimally aligned comparison object sequence. The comparison object sequence may contain addition or deletion after optimal alignment. The homology of amino acid sequences can be calculated, for example, by the Identity value when two amino acid sequences are compared using a sequence similarity searching program FASTA (W. R. Pearson & D. J. Lipman P.N.A.S. (1988) 85:2444-2448) or BLAST (Altschul et. al., J. Mol. Biol. (1990) 215:403-410). The software for the BLAST analysis is publicly available from National Center for Biotechnology Information (http://www.ncbi.nih.gov/).
The enzyme protein having an equivalent function can be encoded by a DNA containing a nucleotide sequence that hybridizes, under stringent conditions, to a nucleotide chain having a sequence complementary to the nucleotide sequence encoding the enzyme protein.
Examples of the hybridization conditions under stringent conditions preferably include: hybridization in about 7% sodium dodecyl sulfate (SDS), about 0.5 M sodium phosphate, 1 mM EDTA at about 50° C., and washing with about 2×SSC, about 0.1% SDS at 50° C.; more desirably hybridization in about 7% sodium dodecyl sulfate (SDS), about 0.5 M sodium phosphate, about 1 mM EDTA at 50° C., and washing with about 1×SSC, about 0.1% SDS at about 50° C.; more desirably hybridization in about 7% sodium dodecyl sulfate (SDS), about 0.5 M sodium phosphate, about 1 mM EDTA at about 50° C., and washing with about 0.5×SSC, about 0.1% SDS at about 50° C.; more preferably hybridization in about 7% sodium dodecyl sulfate (SDS), about 0.5 M sodium phosphate, about 1 mM EDTA at about 50° C., and washing with about 0.1×SSC, about 0.1% SDS at about 50° C.; and more preferably about 7% sodium dodecyl sulfate (SDS), about 0.5 M sodium phosphate, about 1 mM EDTA at about 50° C., and washing with about 0.0×SSC, about 0.1% SDS at about s 65° C. However, the conditions may vary depending on the length of the nucleotide chain, the sequence, and different environmental parameters. A longer sequence specifically hybridizes at a higher temperature.
A detailed guide of hybridization of nucleic acid can be found, for example, in Tijssen (1993) Laboratory Techniques in Biochemistry and Molecular Biology-Hybridization with Nucleic Acid Probes part I chapter 2, “Overview of principles of hybridization and the strategy of nucleic acid probe assay”, Elsvier, N.Y.
2. Vector
The vector to be used for obtaining the above-mentioned transformant, any can be used as long as it can express the enzyme gene of the present invention in an appropriate host. As such vector, for example, plasmid vector, phage vector, cosmid vector and the like can be mentioned. Moreover, a shuttle vector capable of gene exchange with other hosts can also be used. Such vector contains regulatory elements such as operably linked promoters (e.g., lacUV5 promoter, trp promoter, trc promoter, tac promoter, lpp promoter, tufB promoter, recA promoter, pL promoter) and the like, and can be preferably used as an expression vector containing an expression unit operably linked to the DNA of the present invention. For example, pUCNT (WO94/03613) and the like can be preferably used.
The term “regulatory element” used in the present specification refers to a functional promoter and a base sequence having any related transcription elements (e.g., enhancer, CCAAT box, TATA box, SPI site and the like). The term “operably linked” used in the present specification means that DNA and various control elements such as a promoter, an enhancer and the like that control the expression thereof are so operably linked in the host cell as to express the gene. It is a well-known matter to those of ordinary skill in the art that the type and kind of the regulatory element may vary depending on the host.
3. Transformant
As the host into which a recombinant vector containing the DNA having the gene of the present invention is introduced, bacterium, yeast, fungi, plant cell, animal cell and the like can be mentioned, and Escherichia coli is particularly preferable. The DNA of the present invention can be introduced into a host cell by a conventional method. When Escherichia coli is used as a host cell, for example, the DNA of the present invention can be introduced by a calcium chloride method.
The transformant (or recombinant) in the present specification means a host organism into which a heterologous nucleic acid molecule is introduced. In general, a nucleic acid molecule is stably incorporated into the host genome or present with an extrachromosomal molecule. Such extrachromosomal molecule can replicate autonomously. A transformed cell, tissue or organism is contained not only in the final product of the transformation process but also in its transgenic progeny.
4. Reaction
In one embodiment of the present invention, an enantiomer enrichment reaction by stereoselective oxidation by dehydrogenase characteristically utilizes an NAD+ regeneration system using a Streptococcus bacterium-derived water-forming NADH oxidase. Therefore, in one aspect, the present invention is characterized by the coupling of a stereoselective oxidation reaction and a NAD+ regeneration system using a Streptococcus-derived water-forming NADH oxidase, where the present invention is not at all limited by the kind of the enantiomer-enriched compound to be produced, and further, the kind of the dehydrogenase to be used for the reaction.
5. Substrate
The starting material of the enantiomer-enriched compound to be produced by the present invention includes an enantiomer mixture. As the “enantiomer mixture” of the present invention, a compound having an asymmetric carbon wherein the carbon is bonded to hydroxyl group, amino group, formyl group and the like that can be oxidized by dehydrogenase can be mentioned. Specifically, alcohol derivatives inclusive of diol derivative and the like, hydroxy acid derivative, amino acid derivative and the like can be mentioned.
The “derivative” means a compound produced due to a structural change in a small part of a certain compound. A compound wherein hydrogen atom or a particular atomic group in the compound has been substituted by other atom or atomic group is considered to be a derivative of the compound.
6. Dehydrogenase
For production of the above-mentioned alcohol derivative and hydroxy acid derivative, any enzyme group classified as E.C.1.1.1, which shows enantiomer selective reaction and can utilize NAD+ as a coenzyme, can be used. For production of the above-mentioned amino acid derivative, any enzyme group classified as E.C.1.4.1, which shows enantiomer selective reaction and can utilize NAD+ as a coenzyme, can be used. As an example, dehydrogenase derived from Celluromonas sp. strain we have previously found (Japanese Patent Application No. 2004-182926) is an NAD dependent enzyme having a stereoselective oxidation activity to (R)-forms of 1,2-butanediol and 1,3-butanediol. Moreover, the above-mentioned enzyme has a stereoselective oxidation activity to an (S)-form of 3-chloro-1,2-propanediol.
Accordingly, when the above-mentioned enzyme is used as the dehydrogenase of the present invention, an (S) -form enantiomer enriched 1,2-butanediol or 1,3-butanediol can be obtained from an enantiomer mixture of the above-mentioned diol. Moreover, (when the above-mentioned enzyme is used as the dehydrogenase of the present invention,) an (R)-form enantiomer enriched 3-chloro-1,2-propanediol can be obtained from an enantiomer mixture of the above-mentioned diol.
In addition, a dehydrogenase derived from Candida maris IF010003 strain (WO01/005996) catalyzes a stereoselective oxidation reaction of (R) form of 1-phenylethanol.
Therefore, when the above-mentioned enzyme is used as the dehydrogenase of the present invention, an enantiomer-enriched compound in an (S)-form can be obtained from an enantiomer mixture of 1-phenylethanol. Moreover, when an L-form or D-form-specific amino acid dehydrogenase is used, an enantiomer-enriched amino acid derivative in a D-form or an L-form can be obtained from an enantiomer mixture of the amino acid derivative, respectively.
7. Enantiomer Enrichment
The “enantiomer-enriched compound” in the present invention means a compound containing the object optical enantiomer in a proportion of not less than 50% by mol, preferably not less than about 70%, more preferably not less than about 90%, in a mixture with the other optical enantiomer.
The enantiomer enrichment reaction in the present invention can be performed as in the following. First of all, an enantiomer mixture, a dehydrogenase having an oxidation activity on only one of the enantiomers, a water-forming NADH oxidase and NAD+ are added to a suitable solvent and the mixture is stirred.
The water-forming NADH oxidase of the present invention can be used in combination with a stereoselective dehydrogenase, for which NAD+ is a coenzyme. As used herein, “used in combination” means a case where both enzymes of water-forming NADH oxidase and dehydrogenase are simultaneously added to the reaction mixture, and a case where both enzymes are added at different time points as long as they coexist in the reaction mixture.
While the reaction conditions vary depending on the substrate, oxidoreductase and the like to be used, the reaction is generally carried out at a temperature of about 5-80° C., preferably about 10-50° C., at a pH of about 4-10, preferably about 5-9. The enantiomer mixture to be the substrate can be added at a charge concentration of about 0.1-80% (w/v), preferably about 1-60%. NAD+ is added at a concentration of about 0.00001-1 mol%, preferably about 0.00001-0.1% (w/v), relative to the substrate. Since oxygen is necessary for the reaction of NADH oxidase, the reaction mixture is preferably reacted in the air or in the presence of comparatively pure oxygen. To accelerate dissolution of oxygen in the reaction mixture, the reaction is preferably carried out by shaking or under stirring conditions. Furthermore, a reaction under pressurization at not less than the atmospheric pressure may afford more efficient progress of the reaction, since the solubility of oxygen in the reaction mixture is improved.
8. Enzyme
The enzyme to be used in the present invention, such as dehydrogenase and water-forming NADH oxidase may be a uniformly or partially purified enzyme, and a culture of an organism (e.g., microorganism) that produces such enzyme and a treated product of the culture can also be used. As used herein, the “culture of microorganism” means a culture medium containing a bacterium or cultivated bacterium, and the “treated product” means, for example, a crude extract, lyophilized bacterium, acetone dry bacterium, milled cells thereof, a mixture thereof and the like. Furthermore, they can be used as the enzyme itself or bacterium itself after being immobilized by a known means (e.g., crosslinking method, physical adsorption method, entrapment and the like).
When a reaction is to be carried out, moreover, by the use of a culture of a transformant wherein both the dehydrogenase and the water-forming NADH oxidase have been introduced into the same host cell (e.g., transformant microorganism) or a treated product of the culture, an enantiomer-enriched compound can be produced at a lower cost since microorganisms separately expressing the both enzymes do not need to be cultivated.
In addition, for example, using a transformant microorganism expressing the both enzymes in the same cell, the reaction can proceed using the intracellular NAD+ of the microorganism, which in turn obviates separate addition of NAD+ from the outside, or the amount of NAD+ to be added can be drastically reduced. Such transformant can be produced by incorporating a DNA encoding the dehydrogenase to be used and a DNA encoding the water-forming NADH oxidase into the same vector, and introducing the vector into a host. Such transformant can also be produced by respectively incorporating these two kinds of DNAs into two kinds of vectors of different incompatible groups and introducing the vectors into the same host.
In other words, a transformant containing a recombinant vector containing a DNA encoding a dehydrogenase to be used and a DNA encoding a NADH oxidase, and a transformant containing a first recombinant vector containing a DNA encoding a dehydrogenase to be used and a second recombinant vector containing a DNA encoding a NADH oxidase can be used.
The “composition” of the present invention, which comprises a stereoselective dehydrogenase, for which NAD+ is a coenzyme, and a water-forming NADH oxidase is produced by mixing the both enzymes and, where desired, a carrier. Such composition can also contain other active substances and conventional additives, for example, stabilizer, wetting agent, emulsifier, flavor, buffer and the like. The composition of the present invention can be used for the method of the present invention.
The present invention is explained in more detail in the following by referring to Examples, which are not to be construed as limitative.
For expression of Streptococcus mutans-derived water-forming NADH oxidase in Escherichia coli, a recombinant vector used for transformation was prepared. First, a double stranded DNA, wherein a NdeI site was added to the starting point of a NADH oxidase structural gene, and a new stop codon and a PstI site were added to immediately after the stop codon, was obtained by the following method.
PCR was performed using a combination of synthetic primers depicted by 5′-gaggatttgcatatgagtaaaatcgttattg-3′ (primer-1: SEQ ID NO: 3) and 5′-atgaaaacatgtgaattcccattgacatatc-3′ (primer-2: SEQ ID NO: 4) and, as a template, plasmid pSSW61 (Biosci. Biotech. Biochem., 60(l), 39-43, 1996) containing water-forming NADH oxidase gene, whereby a double stranded DNA1 was synthesized. Similarly, PCR was performed using a combination of synthetic primers of 5′-gatatgtcaatgggaattcacatgttttcat-3′ (primer-3: SEQ ID NO: 5) and 5′-tttctgcagttatcatttagcttttaatgct-3′ (primer-4: SEQ ID NO: 6) and, as a template, plasmid pSSW61 (Biosci. Biotech. Biochem., 60(1), 39-43, 1996) containing water-forming NADH oxidase gene, whereby a double stranded DNA2 was synthesized.
Furthermore, PCR was performed using the aforementioned two kinds of synthetic primers (primer-1, primer-4) and, as a template, a mixture of double stranded DNA1 and DNA2 obtained above, whereby a double stranded DNA was obtained. The obtained DNA fragment was digested with NdeI and PstI, and inserted into the NdeI, PstI sites at the downstream of lac promoter of plasmid pUCNT (WO94/03613), whereby a recombinant plasmid pNTNX was obtained.
The recombinant Escherichia coli HB101(pNTNX) obtained in Example 1 was cultured in 2×YT medium (Bacto Tryptone 1.6% (w/v), Bacto yeast extract 1.0% (w/v), NaCl 0.5% (w/v), 100 μg/ml ampicillin, pH 7.0) supplemented with 100 μg/ml of ampicillin and glycerol 0.8% (w/v), and the cells were harvested, suspended in 100 mM Tris-HCl buffer (pH 7), and disrupted by an ultrasonication disruption method to give a cell-free extract. The specific activity of the NADH oxidase in the cell-free extract was 30 U/mg protein. [NADH oxidase activity measurement conditions] An enzyme solution (0.05 ml) was added to a reaction mixture (0.95 ml) containing 100 mM phosphate buffer (pH 7.0), NADH 0.17 mM, EDTA 0.2 mM and FAD 0.02 mM, and the activity was assayed by the measurement of a decrease in the absorbance at 30° C. and wavelength 340 nm. The enzyme activity necessary for oxidation of 1 μmol of NADH to NAD+ in 1 min under such reaction conditions was defined to be 1 unit.
The recombinant Escherichia coli HB101(pNTNX) expressing NADH oxidase obtained in Example 1 was inoculated to 80 ml of the medium described in Example 2, which was sterilized in a 500 ml-Sakaguchi-flask, and subjected to shaking culture at 30° C. for 32 hr. After cell harvest, the cells were suspended in 10 ml of 100 mM phosphate buffer (pH 7.0), disrupted by an ultrasonication disruption method, and centrifuged to give a cell-free extract containing NADH oxidase.
Then, E. coli HB101(pNTFP) (deposit number FERM BP-7116) expressing Candida maris-derived dehydrogenase and E. coli HB101(pTSCS) (FERM BP-10024) expressing Celluromonas sp.-derived dehydrogenase were each inoculated to 60 ml of a semi-synthetic medium (glycerol 1.5% (w/v), yeast extract 0.3% (w/v), Na2HPO4 0.6% (w/v), KH2HPO4 0.3% (w/v), NaCl 0.2% (w/v), MGSO4.7H20 0.5% (w/v), 100 μg/ml ampicillin, pH 6.0), which was sterilized in a 500 ml-Sakaguchi-flask, and subjected to culture at 37° C. for 37 hr. After cell harvest, the cells were suspended in 10 ml of 100 mM phosphate buffer (pH 7.0), disrupted by an ultrasonication disruption method, and centrifuged to give a cell-free extract containing two kinds of NAD dependent dehydrogenases. The cell-free extract prepared from HB101(pTSCS) and HB101(pNTFP) showed an oxidation activity of 10 U/mg for 1,2-butanediol and an oxidation activity of 5 U/mg for 1-phenylethanol.
An enzyme solution (0.05 ml) was added to a reaction mixture (0.95 ml) containing 100 mM phosphate buffer (pH 7.0), 1,2-butanediol or 1-phenylethanol 20 mM, and NAD+ 0.17 mM, and-the activity was assayed by the measurement of an increase in the absorbance at 30° C. and wavelength 340 nm. The enzyme activity necessary for oxidation of 1 μmol of NADH to NAD+ in 1 min under such reaction conditions was defined to be 1 unit.
E. coli HB101(pNTFP)(FERM-7116) was deposited on Apr. 11, 2000, and E. coli HB101(pTSCS)(FERM BP-10024) was deposited on May 12, 2004 under each deposit number mentioned above in the International Patent Organism Depositary, National Institute of Advanced Industrial Science and Technology (IPOD: 305-8566 Tsukuba Central 6, 1-1-1 Higashi, Tsukuba, Ibaraki Japan).
A reaction mixture (1 ml) containing the HB101(pTSCS) cell-free extract (dehydrogenase) 70 μl and HB101(pNTNX) cell-free extract (NADH oxidase) 28 μl, both prepare in Example 3, 10 mg of racemate of 1,2-butanediol, and 300 mM potassium phosphate buffer (pH 7.0) was shaken in a test tube at 20° C. for 23 hr to carry out the reaction. The reaction mixture (200 μl) was saturated with ammonium sulfate, and 1,2-butanediol was extracted with ethyl acetate (400 μl). The solvent was removed from 100 μl of the extract under reduced pressure, trifluoroacetic anhydride (200 μl) was added to the residue and the mixture was stood at room temperature for 10 min to allow trifluoroacetylation, and unreacted trifluoroacetic anhydride was removed under reduced pressure. Ethyl acetate (500 μl) was further added to dissolve trifluorinated 1,2-butanediol, and the optical purity was analyzed by capillary gas chromatography. The above-mentioned enzyme reaction mixture (100 μl) was saturated with ammonium sulfate, 1,2-butanediol was extracted with ethyl acetate (1000 μl), and the 1,2-butanediol content of the extract was analyzed by gas chromatography. As a result, a 1,2-butanediol (S)-form having an optical purity of 97% was produced in a yield of 49%.
[Optical Purity Analysis Conditions]
A reaction mixture (1 ml) containing the HB101(pNTFP) cell-free extract (dehydrogenase) 19 μl and HB101(pNTNX) cell-free extract (NADH oxidase enzyme) 28 μl, both prepared in Example 3, 10 mg of racemate of 1-phenylethanol, and 300 mM potassium phosphate buffer was shaken at 20° C. for 23 hr to carry out the reaction. The reaction mixture (100 μl) was saturated with ammonium sulfate, and 1-phenylethanol was extracted with ethyl acetate (700 μl). The optical purity and content of 1-phenylethanol in the extract were analyzed by HPCL (column: manufactured by Daicel Chemical Industries, LTD., Chiralcell OD-H (0.46×25 cm), column temperature: 25° C., eluent: n-hexane/2-propanol=9/1, flow rate: 0.5 ml/min, elution time: (R) form-12.2 min, (S) form-13.3 min). As a result, a 1-phenylethanol (S)-form having an optical purity of 100% was produced in a yield of 48%.
Optical Purity, Content Analysis Conditions]
A reaction mixture (1 ml) containing the HB101(pNTFP) cell-free extract (dehydrogenase) 10 μl and HB101(pNTNX) cell-free extract (NADH oxidase) 5 μl, both prepared in Example 3, 10 mg of racemate of 1-phenylethanol, and 300 mM potassium phosphate buffer, and a reaction mixture (1 ml) containing this reaction mixture and 5 mM DTT were shaken at 20° C. for 6 hr to carry out the reaction. Thereafter, the content and optical purity of 1-phenylethanol in the reaction mixtures were measured in the same manner as in Example 5. As a result, 1-phenylethanol having an optical purity of 95% was produced in a yield of 50% and 1-phenylethanol having an optical purity of 94% was produced in a yield of 51%, in the reaction mixtures without or with addition of DTT, respectively. As shown above, the same level of reaction proceeded even without addition of DTT to the reaction mixture, as with the addition of DTT, and the addition of DTT was not substantially necessary.
An HB101(pNTNX) cell-free extract (0.1 ml) containing water-forming NADH oxidase, which was prepared in Example 3, was added to 100 mM phosphate buffer (0.9 ml) or 100 mM phosphate buffer (0.9 ml) containing 5 mM DTT, the mixture was stood still or maintained under shaking condition at 300 rpm (oxygen supply condition) in a small test tube at 20° C. for 3 hr, and the residual NADH oxidase activity was assayed. The results are shown in Table 1. Under any conditions, the activity of not less than 90% was maintained.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2004-230139 | Aug 2004 | JP | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/JP05/14007 | 8/1/2005 | WO | 2/6/2007 |
