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 language | English |
|---|---|
| Pages (from-to) | 114-118 |
| Number of pages | 5 |
| Journal | Journal of Molecular Catalysis - B Enzymatic |
| Volume | 70 |
| Issue number | 3-4 |
| DOIs | |
| State | Published - 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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