Literature DB >> 18205368

Inverting the enantioselectivity of a carbonyl reductase via substrate-enzyme docking-guided point mutation.

Dunming Zhu1, Yan Yang, Stephanie Majkowicz, Thoris Hsin-Yuan Pan, Katherine Kantardjieff, Ling Hua.   

Abstract

Substrate-enzyme docking-guided point mutation of a carbonyl reductase from Sporobolomyces salmonicolor led to mutant enzymes, which reversed the enantiopreference and enhanced the enantioselectivity toward the reduction of para-substituted acetophenones. Such a dramatic change in the enantioselectivity indicates that the 245 residue in the catalytic site plays a critical role in determining the enantioselectivity of these ketone reductions, providing valuable insight into our understanding of how residues involved in substrate binding affect the orientation of bound substrate and thus control the reduction stereoselectivity.

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Year:  2008        PMID: 18205368     DOI: 10.1021/ol702638j

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Enantioselective, ketoreductase-based entry into pharmaceutical building blocks: ethanol as tunable nicotinamide reductant.

Authors:  Sylvain Broussy; Ross W Cheloha; David B Berkowitz
Journal:  Org Lett       Date:  2009-01-15       Impact factor: 6.005

2.  Utilization of one novel deep-sea microbial protease sin3406-1 in the preparation of ethyl (S)-3-hydroxybutyrate through kinetic resolution.

Authors:  Jinlong Huang; Yongkai Xu; Yun Zhang; Aijun Sun; Yunfeng Hu
Journal:  World J Microbiol Biotechnol       Date:  2018-08-06       Impact factor: 3.312

Review 3.  Computational tools for rational protein engineering of aldolases.

Authors:  Michael Widmann; Jürgen Pleiss; Anne K Samland
Journal:  Comput Struct Biotechnol J       Date:  2012-11-13       Impact factor: 7.271

  3 in total

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