Literature DB >> 16892228

Enantioselective reduction of acetophenone and its derivatives with a new yeast isolate Candida tropicalis PBR-2 MTCC 5158.

Pankaj Soni1, Uttam Chand Banerjee.   

Abstract

The enantioselective bioreduction of acetophenone and its various analogues has been carried out using a new yeast strain, Candida tropicalis MTCC 5158, to obtain the corresponding (S)-aryl ethanols with good yield and almost absolute enantioselectivity. The catalytic ability of this microbial strain for acetophenone reduction has been examined and also various parameters of the bioreduction reaction have been optimized. Studies on the catalytic performance showed that this microorganism is capable of carrying out the reduction in a broad range of pH (3-10) and temperature (25-40 degrees C), making it a more versatile biocatalyst. The preparative scale bioreduction of acetophenone using resting cells of Candida tropicalis yielded S-(-)-1-phenyl ethanol with 43% yield and >99% enantiomeric excess.

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Year:  2006        PMID: 16892228     DOI: 10.1002/biot.200500020

Source DB:  PubMed          Journal:  Biotechnol J        ISSN: 1860-6768            Impact factor:   4.677


  4 in total

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4.  A strategy to identify a ketoreductase that preferentially synthesizes pharmaceutically relevant (S)-alcohols using whole-cell biotransformation.

Authors:  Saiful F Haq; Anirudh P Shanbhag; Subbulakshmi Karthikeyan; Imran Hassan; Kannan Thanukrishnan; Abhishek Ashok; Sunilkumar Sukumaran; S Ramaswamy; Nagakumar Bharatham; Santanu Datta; Shalaka Samant; Nainesh Katagihallimath
Journal:  Microb Cell Fact       Date:  2018-12-03       Impact factor: 5.328

  4 in total

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