Carbonyl reductase, gene thereof and method of using the same
View Patent ↗The present invention provides a novel polypeptide producing (S)-N-benzyl-3-pyrrolidinol, a DNA coding for it and a method of using them. A polypeptide having the following physicochemical properties (1) to (5): (1) Action: It asymmetrically reduces N-benzyl-3-pyrrolidinone to produce (S)-N-benzyl-3-pyrrolidinol with NADPH as a coenzyme; (2) Optimum action pH: 4.5 to 5.5; (3) Optimum action temperature: 40° C. to 45° C.; (4) Molecular weight: About 29,000 as determined by gel filtration analysis, about 35,000 as determined by SDS-polyacrylamide gel electrophoresis analysis; (5) Inhibitor: It is inhibited by the divalent copper ion. Further, a polypeptide having the amino acid sequence shown under SEQ ID NO:1 in the sequence listing; or a polypeptide having an amino acid sequence obtainable from the amino acid sequence shown under SEQ ID NO:1 in the sequence listing by substitution, insertion, deletion and/or addition of one or more amino acids and having enzyme activity in asymmetrically reducing N-benzyl-3-pyrrolidinone to produce (S)-N-benzyl-3-pyrrolidinol.
1. An isolated and purified DNA molecule encoding a polypeptide comprising SEQ ID NO: 1.
2. An isolated and purified DNA molecule encoding a polypeptide wherein the polypeptide comprises the enzyme activity of asymmetrically reducing N-benzyl-3-pyrrolidinone into (S)-N-benzyl-3-pyrrolidinol, and wherein the DNA molecule hybridizes to SEQ ID NO: 2 under stringent conditions at 65° C. in the presence of 0.7 to 1.0 M NaCl.
3. An expression vector comprising the isolated DNA molecule of claim 1 .
4. The expression vector of claim 3 , wherein the vector is a plasmid pTSBH.
5. The expression vector of claim 3 , which further comprises an isolated DNA molecule encoding a polypeptide having glucose dehydrogenase activity.
6. The expression vector of claim 5 , wherein the polypeptide having glucose dehydrogenase activity is a Bacillus megaterium -derived glucose dehydrogenase.
7. The expression vector of claim 6 , wherein the vector is a plasmid pTSBG1.
8. An isolated host cell transformed with the expression vector of claim 3 .
9. An isolated host cell transformed with both the expression vector of claim 3 and an expression vector comprising a DNA molecule encoding a polypeptide having glucose dehydrogenase activity.
10. The transformant of claim 9 , wherein the polypeptide having glucose dehydrogenase activity is a Bacillus megaterium -derived glucose dehydrogenase.
11. The transformant of claim 8 , wherein the host is Escherichia coli.
12. The transformant of claim 11 , wherein the transformant is Escherichia coli HB101 (pTSBH) obtained by transforming Escherichia coli using the recombinant plasmid pTSBH.
13. An isolated transformed host cell, wherein the transformant is Escherichia coli HB101 (pTSBG1) obtained by transforming Escherichia coli HB101 using the recombinant plasmid pTSBG 1.
14. The transformant of claim 9 , wherein the transformant is Escherichia coli HB101 (pTSBH, pSTVG) obtained by transforming Escherichia coli HB101 using both the recombinant plasmid pTSBH and the recombinant plasmid pSTVG.
15. A method of producing (S)-N-benzyl-3-pyrrolidinol comprising:
a) culturing the transformant of claim 8 in presence of N-benzyl-3-pyrrolidinone, and
b) harvesting the (S)-N-benzyl-3-pyrrolidinol produced in a).
16. The method of claim 15 , wherein step (a) is carried out in the presence of a coenzyme regenerating system.
17. An expression vector comprising the isolated DNA-molecule of claim 2 .
18. An isolated and purified polypeptide encoded by the DNA molecule of claim 1 .
19. An isolated and purified polypeptide encoded by the DNA molecule of claim 2 , wherein said polypeptide comprises the enzyme activity of asymmetrically reducing N-benzyl-3-pyrrolidinone into (S)-N-benzyl-3-pyrrolidinol.