Efficient synthesis of enantiopure (S)-4-(trimethylsilyl)-3-butyn-2-ol via asymmetric reduction of 4-(trimethylsilyl)-3-butyn-2-one with immobilized Candida parapsilosis CCTCC M203011 cells
Author:
Publisher
Elsevier BV
Subject
Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis
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1. Asymmetric reduction of 4-trimethylsilyl-3-butyn-2-one to (R)-4-trimethylsilyl-3-butyn-2-ol catalyzed by a novel strain lyophilized Acetobacter sp. CCTCC M209061 in an aqueous/ionic liquid biphasic system;Reaction Kinetics, Mechanisms and Catalysis;2022-04-24
2. Enzymatic characterization of a recombinant carbonyl reductase from Acetobacter sp. CCTCC M209061;Bioresources and Bioprocessing;2017-08-28
3. Candida parapsilosis: A versatile biocatalyst for organic oxidation-reduction reactions;Bioorganic Chemistry;2016-10
4. The evaluation of kefir pure culture starter: Liquid-core capsule entrapping microorganisms isolated from kefir grains;Food Science and Technology International;2016-07-09
5. Engineering of a novel carbonyl reductase with coenzyme regeneration in E. coli for efficient biosynthesis of enantiopure chiral alcohols;Journal of Biotechnology;2016-07
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