Controlling enantioselectivity of esterase in asymmetric hydrolysis of aryl prochiral diesters by introducing aromatic interactions-Reference-Cited by-同舟云学术

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Controlling enantioselectivity of esterase in asymmetric hydrolysis of aryl prochiral diesters by introducing aromatic interactions

Published:2014-04-25 Issue:9 Volume:111 Page:1729-1739
ISSN:0006-3592
Container-title:Biotechnology and Bioengineering
language:en
Short-container-title:Biotechnol. Bioeng.

Author:

Guo Fei¹,Franzen Stefan²,Ye Lidan¹,Gu Jiali¹,Yu Hongwei¹

Affiliation:

1. Institute of Bioengineering; Department of Chemical and Biological Engineering; Zhejiang University; Hangzhou PR China

2. Department of Chemistry; Zhejiang University; Hangzhou PR China

Funder

Natural Science Foundation of China

Open Funding Project of the State Key Laboratory of Bioreactor Engineering

Outstanding Young Scholar of Zhejiang Province

Program for Zhejiang Leading Team of S&T Innovation

Publisher

Wiley

Subject

Applied Microbiology and Biotechnology,Bioengineering,Biotechnology

Reference42 articles.

1. Complete inversion of enantioselectivity towards acetylated tertiary alcohols by a double mutant of a Bacillus subtilis esterase;Bartsch;Angew Chem Int Ed,2008

2. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding;Bradford;Anal Biochem,1976

3. Asymmetric hydrolysis of dimethyl 3-phenylglutarate catalyzed by Lecitase Ultra®;Cabrera;Enzyme Microb Technol,2008

4. Enantioselective desymmetrization of prochiral diesters catalyzed by immobilized Rhizopus oryzae lipase;Cabrera;Tetrahedron Asymmetry,2011

5. Directed evolution and axial chirality: Optimization of the enantioselectivity of Pseudomonas aeruginosa lipase towards the kinetic resolution of a racemic allene;Carballeira;Chem Commun,2007

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