Literature DB >> 20071211

Practical chiral alcohol manufacture using ketoreductases.

Gjalt W Huisman1, Jack Liang, Anke Krebber.   

Abstract

Over the past two years the application of ketoreductases in the commercial synthesis of chiral alcohols has undergone a revolution. Biocatalysts are now often the preferred catalyst for the synthesis of chiral alcohols via ketone reduction and are displacing reagents and chemocatalysts that only recently were considered break-through process solutions themselves. Tailor-made enzymes can now be generated from advanced, non-natural variants using HTP screening and modern molecular biology techniques. At the same time, global economic and environmental pressures direct industrial process development toward versatile platforms that can be applied to the different stages of product development. We will discuss the technologies that have emerged over the past years that have guided biocatalysis from the bottom of the toolbox, to the power tool of choice. Copyright 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 20071211     DOI: 10.1016/j.cbpa.2009.12.003

Source DB:  PubMed          Journal:  Curr Opin Chem Biol        ISSN: 1367-5931            Impact factor:   8.822


  31 in total

1.  In vivo enzyme immobilization by inclusion body display.

Authors:  Björn Steinmann; Andreas Christmann; Tim Heiseler; Janine Fritz; Harald Kolmar
Journal:  Appl Environ Microbiol       Date:  2010-06-25       Impact factor: 4.792

2.  Efficient PCR-based amplification of diverse alcohol dehydrogenase genes from metagenomes for improving biocatalysis: screening of gene-specific amplicons from metagenomes.

Authors:  Nobuya Itoh; Satomi Kariya; Junji Kurokawa
Journal:  Appl Environ Microbiol       Date:  2014-08-01       Impact factor: 4.792

3.  Accessing non-natural reactivity by irradiating nicotinamide-dependent enzymes with light.

Authors:  Megan A Emmanuel; Norman R Greenberg; Daniel G Oblinsky; Todd K Hyster
Journal:  Nature       Date:  2016-12-14       Impact factor: 49.962

4.  Novel Aldo-Keto Reductases for the Biocatalytic Conversion of 3-Hydroxybutanal to 1,3-Butanediol: Structural and Biochemical Studies.

Authors:  Taeho Kim; Robert Flick; Joseph Brunzelle; Alex Singer; Elena Evdokimova; Greg Brown; Jeong Chan Joo; George A Minasov; Wayne F Anderson; Radhakrishnan Mahadevan; Alexei Savchenko; Alexander F Yakunin
Journal:  Appl Environ Microbiol       Date:  2017-03-17       Impact factor: 4.792

5.  Isolation and characterization of a novel Rhodococcus strain with switchable carbonyl reductase and para-acetylphenol hydroxylase activities.

Authors:  Rui Zhang; Jie Ren; Yu Wang; Qiaqing Wu; Min Wang; Dunming Zhu
Journal:  J Ind Microbiol Biotechnol       Date:  2012-09-27       Impact factor: 3.346

6.  Thermostable alcohol dehydrogenase from Thermococcus kodakarensis KOD1 for enantioselective bioconversion of aromatic secondary alcohols.

Authors:  Xi Wu; Chong Zhang; Izumi Orita; Tadayuki Imanaka; Toshiaki Fukui; Xin-Hui Xing
Journal:  Appl Environ Microbiol       Date:  2013-01-25       Impact factor: 4.792

7.  Origins of stereoselectivity in evolved ketoreductases.

Authors:  Elizabeth L Noey; Nidhi Tibrewal; Gonzalo Jiménez-Osés; Sílvia Osuna; Jiyong Park; Carly M Bond; Duilio Cascio; Jack Liang; Xiyun Zhang; Gjalt W Huisman; Yi Tang; Kendall N Houk
Journal:  Proc Natl Acad Sci U S A       Date:  2015-12-07       Impact factor: 11.205

8.  A Biocatalytic Route to Highly Enantioenriched β-Hydroxydioxinones.

Authors:  Rick C Betori; Eric R Miller; Karl A Scheidt
Journal:  Adv Synth Catal       Date:  2017-03-02       Impact factor: 5.837

9.  Activity prediction of substrates in NADH-dependent carbonyl reductase by docking requires catalytic constraints and charge parameterization of catalytic zinc environment.

Authors:  Gaurao V Dhoke; Christoph Loderer; Mehdi D Davari; Marion Ansorge-Schumacher; Ulrich Schwaneberg; Marco Bocola
Journal:  J Comput Aided Mol Des       Date:  2015-11-03       Impact factor: 3.686

10.  Asymmetric reduction of 4-hydroxy-2-butanone to (R)-1,3-butanediol with absolute stereochemical selectivity by a newly isolated strain of Pichia jadinii.

Authors:  Taowei Yang; Zaiwei Man; Zhiming Rao; Meijuan Xu; Xian Zhang; Zhenghong Xu
Journal:  J Ind Microbiol Biotechnol       Date:  2014-10-12       Impact factor: 3.346

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