Literature DB >> 10825967

Improving the stereoselectivity of bakers' yeast reductions by genetic engineering.

S Rodríguez1, M Kayser, J D Stewart.   

Abstract

[formula: see text] The stereoselectivities of bakers' yeast catalyzed reductions of beta-keto esters can be manipulated by genetic design. Strains in which two major beta-keto ester reductases are either knocked out or overexpressed have been constructed. The former approach results in whole cell biocatalysts with reversed stereoselectivity from unmodified bakers' yeast while the latter shows useful improvements in stereoselectivity. These results indicate that the "designer yeast" approach can provide useful biocatalysts for these transformations.

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Year:  1999        PMID: 10825967     DOI: 10.1021/ol9901523

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


  2 in total

1.  Towards the discovery of alcohol dehydrogenases: NAD(P)H fluorescence-based screening and characterization of the newly isolated Rhodococcus erythropolis WZ010 in the preparation of chiral aryl secondary alcohols.

Authors:  Chi Yang; Xiangxian Ying; Meilan Yu; Yinjun Zhang; Bin Xiong; Qingqing Song; Zhao Wang
Journal:  J Ind Microbiol Biotechnol       Date:  2012-06-29       Impact factor: 3.346

2.  Yeast cell factories for fine chemical and API production.

Authors:  Beate Pscheidt; Anton Glieder
Journal:  Microb Cell Fact       Date:  2008-08-07       Impact factor: 5.328

  2 in total

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