An Engineered Old Yellow Enzyme that Enables Efficient Synthesis of (4R,6R)-Actinol in a One-Pot Reduction System-Reference-Cited by-同舟云学术

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An Engineered Old Yellow Enzyme that Enables Efficient Synthesis of (4R,6R)-Actinol in a One-Pot Reduction System

Published:2015-01-14 Issue:3 Volume:16 Page:440-445
ISSN:1439-4227
Container-title:ChemBioChem
language:en
Short-container-title:ChemBioChem

Author:

Horita Shoichiro,Kataoka Michihiko,Kitamura Nahoko,Nakagawa Takuya,Miyakawa Takuya,Ohtsuka Jun,Nagata Koji,Shimizu Sakayu,Tanokura Masaru

Publisher

Wiley

Subject

Organic Chemistry,Molecular Biology,Molecular Medicine,Biochemistry

Reference27 articles.

1. Iterative saturation mutagenesis (ISM) for rapid directed evolution of functional enzymes

2. Asymmetric Bioreduction of CC Bonds using Enoate Reductases OPR1, OPR3 and YqjM: Enzyme-Based Stereocontrol

3. Site-Saturation Mutagenesis of Tryptophan 116 of Saccharomyces pastorianus Old Yellow Enzyme Uncovers Stereocomplementary Variants

4. Production of a Doubly Chiral Compound, (4 R ,6 R )-4-Hydroxy-2,2,6-Trimethylcyclohexanone, by Two-Step Enzymatic Asymmetric Reduction

5. Old Yellow Enzyme fromCandida macedoniensisCatalyzes the Stereospecific Reduction of the C=C Bond of Ketoisophorone

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1. Modulation of the catalytic performance of OYE3 by engineering key residues at the entrance of the catalytic pocket;Biotechnology and Applied Biochemistry;2023-04-25

2. Learning Lessons from Protein Engineering;Enzyme Engineering;2023-01-06

3. Engineering a Medium‐chain Alcohol Dehydrogenase for Efficient Synthesis of ( S )‐N−Boc‐3−pyrrolidinol by Adjusting the Conformational Dynamics of Loops;ChemCatChem;2023-01-05

4. Old yellow enzyme of a novel fungi‐specific class;The FEBS Journal;2022-05-19

5. Introduction of Chiral Centers to α- and/or β-Positions of Carbonyl Groups by Biocatalytic Asymmetric Reduction of α,β-Unsaturated Carbonyl Compounds;Natural Product Communications;2022-05

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