Carbonyl reductase, gene thereof and method of using the same
View Patent ↗The present invention provides a novel polypeptide efficiently forming (R)-N-benzyl-3-pyrrolidinol, a polynucleotide coding for said polypeptide, and use of the same. The present invention relates to a polypeptide having the physical and chemical properties (1) to (4): (1) activity acting on N-benzyl-3-pyrrolidinone with NADH or NADPH as a coenzyme, to form (R)-N-benzyl-3-pyrrolidinol; (2) optimum pH of 5.5 to 6.0 for activity ; (3) optimum temperature of 50° C. to 55° C. for activity ; (4) molecular weight of about 55,000 as determined by gel filtration analysis, and about 28,000 as determined by SDS polyacrylamide gel electrophoresis analysis. The present invention also relates to a polypeptide comprising the amino acid sequence of SEQ ID NO:1, a polynucleotide coding for said polypeptide, and a transformant producing said polypeptide at high levels.
1. An isolated polynucleotide which is the following (a), (b) or (c):
(a) a polynucleotide comprising the nucleotide sequence of SEQ ID NO:2,
(b) a polynucleotide capable of hybridizing with a polynucleotide comprising the nucleotide sequence fully complementary to the nucleotide sequence of SEQ ID NO:2 under stringent conditions, wherein said stringent conditions comprise washing a filter with 0.1 to 2×SSC solution at 65° C., and coding for a polypeptide having activity in stereoselectively reducing N-benzyl-3-pyrrolidinone represented by the formula (1):
to form (R)-N-benzyl-3-pyrrolidinol represented by the formula (2):
(c) a polynucleotide having at least 90% homology to the nucleotide sequence of SEQ ID NO:2, wherein said polynucleotide encodes a polypeptide with carbonyl reductase activity.
2. An expression vector which contains the polynucleotide according to claim 1 .
3. The expression vector according to claim 2 which is a plasmid pNTDR.
4. The expression vector according to claim 2 which further contains a polynucleotide coding for a polypeptide having glucose dehydrogenase activity.
5. The expression vector according to claim 4 , wherein the polypeptide having glucose dehydrogenase activity is a glucose dehydrogenase derived from Bacillus megaterium .
6. The expression vector according to claim 5 which is a plasmid pNTDRG1.
7. A transformant which is obtainable by transforming an isolated host cell using the expression vector according to claim 2 .
8. The transformant according to claim 7 , wherein the host cell is Escherichia coli.
9. The transformant according to claim 8 which is E. coli HB101(PNTDR) (FERM BP-08457).
10. The transformant according to claim 8 which is E. coli HB101(PNTDRG1) (FERM BP-08458).
11. A method for producing an optically active alcohol which comprises reacting the culture of the transformant according to claim 7 with a carbonyl group-containing compound, wherein the carbonyl group-containing compound is N-benzyl-3-pyrrolidinone represented by the formula (1):
and the above optically active alcohol is (R)-N-benzyl-3-pyrrolidinol represented by the formula (2):
12. A method for producing an optically active alcohol which comprises reacting the culture of the transformant according to claim 7 with a carbonyl group-containing compound, wherein the carbonyl group-containing compound is a 2-tetralone derivative represented by the formula (3):
in the formula, R.sup.1 and R.sup.2 may be the same or different and each represents a hydrogen atom, a hydroxyl group or alkoxy group, and n represents 1 or 2, and
the above optically active alcohol is a 2-tetralol derivative represented by the formula (4):
in the formula, R.sup.1, R.sup.2 and n are the same as defined above.
13. The method according to claim 12 , wherein the above 2-tetralone derivative is 7-methoxy-2-tetralone, and the above 2-tetralol derivative is (R)-7-methoxy-2-tetralol.
14. The method according to claim 12 , wherein the above 2-tetralone derivative is 3 -methoxy-6,7,8,9-tetrahydro-5H-benzocycloheptene-6-One, and the above 2-tetralol derivative is (R)-3-methoxy-6,7,8,9-tetrahydro-5- H-benzocycloheptene-6-ol.
15. A method for producing an optically active alcohol which comprises reacting the culture of the transformant according to claim 7 with a carbonyl group-containing compound, wherein the above carbonyl group-containing compound is a 1-phenylethanone derivative represented by the general formula (5):
in the formula, R.sup.3 and R.sup.4 may be the same or different and each represents a hydrogen or halogen atom or an alkoxy or nitro group, R.sup.5 represents a hydrogen or halogen atom, a hydroxyl group or an alkyl group, which may optionally be substituted, and
the above optically active alcohol is a 1-phenylethanol derivative represented by the general formula (6):
in the formula, R.sup.3, R.sup.4 and R.sup.5 are the same as defined above.
16. The method according to claim 15 , wherein the above 1-phenylethanone derivative is 2-chloro-1-(4′-fluorophenyl)ethanone, and the above 1-phenylethanol derivative is (S)-2-chloro-1-(4′-fluorophenyl)ethanol.
17. The method according to claim 15 , wherein the above 1-phenylethanone derivative is 2-chloro-1-(3′-chlorophenyl)ethanone, and the above 1-phenylethanol derivative is (S)-2-chloro-1-(3′-chlorophenyl)ethanol.