Ketoreductase polypeptides for the synthesis of chiral compounds

US12410410B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-12410410-B2
Application numberUS-202117553455-A
CountryUS
Kind codeB2
Filing dateDec 16, 2021
Priority dateFeb 10, 2015
Publication dateSep 9, 2025
Grant dateSep 9, 2025

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

Official abstract text for this publication.

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.

First claim

Opening claim text (preview).

What is claimed is: 1. An engineered polypeptide comprising an amino acid sequence with at least 95% sequence identity to SEQ ID NO: 240, wherein the residue corresponding to X150 is a tryptophan, the residue corresponding to X173 is a non-polar or aliphatic residue, the residue corresponding to X211 is an aromatic, acidic, or polar residue, and wherein the residue corresponding to X249 is glycine and wherein said polypeptide has ketoreductase activity with at least 2-fold greater selectivity to the chiral compound 2a relative to chiral compound 2c as compared to SEQ ID NO:2. 2. The engineered polypeptide of claim 1 , wherein said amino acid sequence further comprises at least one of the following: the residue corresponding to X68 is a non-polar, or aliphatic residue; the residue corresponding to X94 is a polar, or non-polar residue; the residue corresponding to X102 is an acidic residue; the residue corresponding to X110 is an acidic, or aromatic residue; the residue corresponding to X114 is a non-polar residue; the residue corresponding to X135 is a basic residue; the residue corresponding to X144 is a non-polar, or aromatic residue; the residue corresponding to X145 is an aromatic residue; the residue corresponding to X147 is a non-polar, or aliphatic residue; the residue corresponding to X149 is a polar residue; the residue corresponding to X153 is a polar, or aromatic residue; the residue corresponding to X158 is a non-polar, or aliphatic residue; the residue corresponding to X175 is a polar residue; the residue corresponding to X190 is an aromatic, aliphatic, non-polar, or polar residue; the residue corresponding to X196 is an aromatic, polar, basic, non-polar, or aliphatic residue; the residue corresponding to X197 is an aromatic residue; the residue corresponding to X198 is a non-polar, polar residue; the residue corresponding to X199 is an acidic residue; the residue corresponding to X201 is a polar residue; the residue corresponding to X202 is an aromatic, or basic residue; the residue corresponding to X203 is an aromatic, non-polar, or aliphatic residue; the residue corresponding to X205 is a polar residue; the residue corresponding to X206 is an aromatic residue; the residue corresponding to X207 is an aromatic, acidic, non-polar, or aliphatic residue; the residue corresponding to X209 is an aromatic, acidic, non-polar, polar, or aliphatic residue; the residue corresponding to X210 is a non-polar, or aliphatic residue; the residue corresponding to X212 is an aromatic, basic, non-polar, aliphatic, or acidic residue; the residue corresponding to X213 is an aromatic, basic, acidic, polar, non-polar, or aliphatic residue; the residue corresponding to X217 is a polar, or aromatic residue; the residue corresponding to X233 is a polar residue; the residue corresponding to X250 is a non-polar residue; and the residue corresponding to X252 is an aromatic residue. 3. The engineered polypeptide of claim 1 , comprising at least one substitution selected from X68V, X94G/M/Q, X102D, X110E/W, X114G, X135K, X144G/W, X145W, X147L, X149S, X153H/P/T/V/C, X158V, X173L, X175T, X196H/I/K/N/Q, X196I, X196K/N/Q, X197Y, X198G/S, X199E, X201N, X202F/H/R/Y, X203G/L/W, X205T, X206H/W/Y, X207D/G/V/Y, X209E/F/G/I/M/T/V/W, X210L/P, X211E/H/P/S, X212A/E/G/H/N/P/R/V, X213D/E/G/H/K/M/N/R, X217H/N, X233Q/T, X250G, and X252W. 4. The engineered polypeptide of claim 1 , comprising a substitution at position X190 as compared to SEQ ID NO: 2. 5. The engineered polypeptide of claim 4 , wherein the substitution at position X190 is selected from P, A, T, or Q. 6. An engineered polypeptide of claim 1 having ketoreductase activity, wherein the polypeptide comprises SEQ ID NO: 240.

Assignees

Inventors

Classifications

  • containing a carboxyl group {including Peroxycarboxylic acids} · CPC title

  • containing a six-membered hetero ring · CPC title

  • containing a hydroxy group · CPC title

  • by oxidation/reduction reactions · CPC title

  • Carbonyl reductase (NADPH) (1.1.1.184) · CPC title

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What does patent US12410410B2 cover?
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…
Who is the assignee on this patent?
Codexis Inc
What technology area does this patent fall under?
Primary CPC classification C12N9/0006. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Sep 09 2025 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).