Ketoreductase polypeptides for the production of azetidinone
View Patent ↗The present disclosure provides engineered ketoreductase enzymes having improved properties as compared to a naturally occurring wild-type ketoreductase enzyme. Also provided are polynucleotides encoding the engineered ketoreductase enzymes, host cells capable of expressing the engineered ketoreductase enzymes, and methods of using the engineered ketoreductase enzymes to synthesize a variety of chiral compounds.
1. An engineered ketoreductase polypeptide capable of converting the substrate, methyl-2-benzamidomethyl-3-oxobutyrate, to the product, 2S,3R-methyl-2-benzamidomethyl-3-hydroxybutyrate, with a percent stereomeric excess of at least 60%, which comprises an amino acid sequence that is at least 90% identical to SEQ ID NO: 4 and in which the residue corresponding to X94 is threonine, the residue corresponding to X199 is alanine, histidine, or asparagine; and the residue corresponding to X202 is valine or leucine.
2. The polypeptide of claim 1 in which the ketoreductase amino acid sequence has additionally one or more of the following features:
residue corresponding to X2 is alanine;
residue corresponding to X4 is cysteine;
residue corresponding to X11 is phenylalanine;
residue corresponding to X40 arginine;
residue corresponding to X80 is threonine;
residue corresponding to X86 is isoleucine;
residue corresponding to X96 is valine or phenylalanine;
residue corresponding to X105 is glycine;
residue corresponding to X129 is threonine;
residue corresponding to X147 is methionine or leucine;
residue corresponding to X153 is alanine or serine;
residue corresponding to X190 is histidine or proline;
residue corresponding to X195 is valine;
residue corresponding to X196 is leucine;
residue corresponding to X206 is phenylalanine;
residue corresponding to X226 is valine;
residue corresponding to X248 is lysine, or arginine;
residue corresponding to X249 is tryptophan;
wherein optionally the amino acid sequence has one or more residue differences at other amino acid residue positions as compared to the polypeptide sequence of SEQ ID NO: 4.
3. The polypeptide of claim 2 in which the ketoreductase amino acid sequence has additionally one or more of the following features:
residue corresponding to X40 is arginine; and
residue corresponding to X147 is methionine or leucine.
4. The polypeptide of claim 2 in which the ketoreductase amino acid sequence has the following additional features:
residue corresponding to X40 is arginine;
residue corresponding to X96 is valine or phenylalanine;
residue corresponding to X147 is methionine or leucine; and
wherein optionally the amino acid sequence has one or more residue differences at other amino acid residue positions as compared to the polypeptide sequence of SEQ ID NO: 4.
5. The polypeptide of claim 2 in which the ketoreductase amino acid sequence has the following additional features:
residue corresponding to X96 is valine or phenylalanine;
residue corresponding to X147 is methionine or leucine;
residue corresponding to X195 is valine;
residue corresponding to X196 is leucine; and
wherein optionally the amino acid sequence has one or more residue differences at other amino acid residue positions as compared to the polypeptide sequence of SEQ ID NO: 4.
6. The polypeptide of claim 2 in which the ketoreductase amino acid sequence has the following additional feature: residue corresponding to X40 is arginine.
7. The polypeptide of claim 2 in which the ketoreductase amino acid sequence has the following additional feature: residue corresponding to X147 is methionine or leucine.
8. The polypeptide of claim 2 in which the ketoreductase amino acid sequence has the following additional features: residue corresponding to X40 is arginine; and the residue corresponding to X147 is methionine or leucine.
9. The polypeptide of claim 1 , which comprises an amino acid sequence corresponding to SEQ ID NO: 6, 10, 12, 20, 22, 24, 30, 32, 34, 36, and 38.
10. The polypeptide of claim 1 , which is capable of converting the substrate to the product with a percent stereomeric excess of at least 95%.
11. The polypeptide of claim 10 , which comprises an amino acid sequence corresponding to SEQ ID NO: 6, 10, 12, 20, 22, 24, 30, 32, 34, 36, and 38.
12. The polypeptide of claim 1 , which is capable of converting the substrate to the product with a percent stereomeric excess of at least 99%.
13. The polypeptide of claim 12 , which comprises an amino acid sequence corresponding to SEQ ID NO: 6, 10, 12, 20, 22, 24, 30, 32, and 34.
14. The polypeptide of claim 1 , which is capable of converting the substrate to the product at a rate that is at least 15 times greater than the reference polypeptide of SEQ ID NO: 4.
15. The polypeptide of claim 14 , which comprises an amino acid sequence corresponding to SEQ ID NO: 6, 10, 12, 20, 22, 24, 30, 32, and 34.
16. A composition comprising a ketoreductase of claim 1 and compound methyl-2-benzamidomethyl-3-oxobutyrate or compound 2S,3R-methyl-2-benzamidomethyl-3-hydroxybutyrate.
17. The composition of claim 16 , further comprising a cofactor regenerating system.
18. The composition of claim 17 in which the cofactor regenerating system comprises glucose dehydrogenase and glucose; formate dehydrogenase and formate; or isopropanol and a secondary alcohol dehydrogenase.
19. A method for reducing the substrate methyl-2-benzamidomethyl-3-oxobutyrate, to the product 2S,3R-methyl-2-benzamidomethyl-3-hydroxybutyrate, which comprises contacting or incubating the substrate with a ketoreductase polypeptide of claim 1 under reaction conditions suitable for reducing the substrate to the product.
20. The method of claim 19 in which the product is present at a stereomeric excess greater than 99%.
21. The method of claim 19 which is carried out with whole cells that express the ketoreductase enzyme, or an extract or lysate of such cells.
22. The method of claim 19 in which the ketoreductase is isolated and/or purified and the reduction reaction is carried out in the presence of a cofactor for the ketoreductase and optionally a cofactor regenerating system.
23. The method of claim 22 in which the cofactor regenerating system comprises glucose dehydrogenase and glucose; formate dehydrogenase and formate; or isopropanol and a secondary alcohol dehydrogenase.
24. The method of claim 23 in which the secondary alcohol dehydrogenase is the ketoreductase.
25. In a method for the synthesis of the intermediate of formula (IVa),
wherein R 1 is H or a hydroxyl protecting group, and R 10 is a halogen, or —OAc, where Ac is acetate,
a step in the method comprises contacting or reacting the substrate methyl-2-benzamidomethyl-3-oxobutyrate with the ketoreductases of claim 1 under reaction conditions suitable for reducing or converting the substrate to the product 2S,3R-methyl-2-benzamidomethyl-3-hydroxybutyrate.
26. In a method for the synthesis of the intermediate of structural formula (IX),
wherein R 2 is H or a C1-C4 alkyl (e.g., —CH 3 ); R 3 is H, or a hydroxyl protecting group; R 4 is H, carboxy protecting group, ammonia group, alkali metal, or alkaline earth metal; and X is OH or a leaving group,
a step in the method comprises contacting or reacting the substrate methyl-2-benzamidomethyl-3-oxobutyrate with the ketoreductase of claim 1 under reaction conditions suitable for reducing or converting the substrate to the product 2S,3R-methyl-2-benzamidomethyl-3-hydroxybutyrate.
27. In a method for the synthesis of a carbapenem of structural formula (V):
or solvates, hydrates, salts, and prodrugs thereof, wherein R 2 is H or —CH 3 ; R 5 is selected from substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted heterocycloalkyl, and substituted or unsubstituted heteroarylalkyl; and R 6 is H or a progroup,
a step in the method comprises contacting or reacting the substrate methyl-2-benzamidomethyl-3-oxobutyrate with the ketoreductase of claim 1 under reaction conditions suitable for reducing or converting the substrate to the product 2S,3R-methyl-2-benzamidomethyl-3-hydroxybutyrate.