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Production of chiral compound using recombinant Escherichia coli cells co-expressing reductase and glucose dehydrogenase in an ionic liquid/water two phase system

  • Hye Jeong Choi
  • , Ki Nam Uhm
  • , Hyung Kwoun Kim
  • The Catholic University of Korea
  • Cronbio Ltd.

Research output: Contribution to journalArticlepeer-review

32 Scopus citations

Abstract

(S)-3-Chloro-1-phenyl-1-propanol ((S)-CPPO) is a useful chiral building block for the synthesis of anti-depressant drugs. The yeast reductase, YOL151W, evidences enantioselective reduction activity, converting 3-chloro-1-phenyl-1- propanone (3-CPP) into (S)-CPPO. Escherichia coli whole cells co-expressing YOL151W and Bacillus subtilis glucose dehydrogenase were employed for the synthesis of CPPO following permeabilization treatment. A reaction system employing these recombinant E. coli whole cells could convert 30 mM 3-CPP enantioselectively into (S)-CPPO. In an effort to enhance substrate solubility and to prevent substrate/product inhibition during the enzyme reaction process, a variety of ionic liquids were tested and [Bmim][NTf2] was ultimately selected for the ionic liquid/water two phase system. Tween 40 was added to accomplish the efficient mixing of the two phases. Using these recombinant E. coli whole cells and the [Bmim][NTf2]/water two phase system, 100 mM (S)-CPPO was generated with an enantiomeric excess of >99%.

Original languageEnglish
Pages (from-to)114-118
Number of pages5
JournalJournal of Molecular Catalysis - B Enzymatic
Volume70
Issue number3-4
DOIs
StatePublished - Jul 2011

Bibliographical note

Funding Information:
This work was supported by the 21C Frontier Microbial Genomics and Applications Center Program , Ministry of Education, Science & Technology, Republic of Korea , and Gyeonggi Regional Research Center (GRRC) at the Catholic University of Korea.

Keywords

  • Chiral intermediate
  • Enantioselectivity
  • Ionic liquid
  • Reductase
  • Whole cell bioconversion

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