Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated Reduction
(<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol is an important pharmaceutical intermediate of a chemokine CCR5 antagonist. In the present study, a bioprocess for the asymmetric reduction of 4-(trifluoromethyl)acetophenone to (<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanol wa...
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doaj-49535d7d0a224ab09ee600ce66feca4c2020-11-25T02:01:07ZengMDPI AGCatalysts2073-43442019-04-019439110.3390/catal9040391catal9040391Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated ReductionYing Chen0Nana Xia1Yuewang Liu2Pu Wang3College of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, ChinaCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, ChinaCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, ChinaCollege of Pharmaceutical Science, Zhejiang University of Technology, Hangzhou 310014, China(<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol is an important pharmaceutical intermediate of a chemokine CCR5 antagonist. In the present study, a bioprocess for the asymmetric reduction of 4-(trifluoromethyl)acetophenone to (<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanol was developed by recombinant <i>Escherichia coli</i> cells with excellent enantioselectivity. In order to overcome the conversion limitation performed in the conventional buffer medium resulting from poor solubility of non-natural substrate, we subsequently established a polar organic solvent-aqueous medium to improve the efficacy. Isopropanol was selected as the most suitable cosolvent candidate, based on the investigation on a substrate solubility test and cell membrane permeability assay in different organic solvent-buffer media. Under the optimum conditions, the preparative-scale asymmetric reduction generated a 99.1% yield with >99.9% product enantiomeric excess (ee) in a 15% (<i>v</i>/<i>v</i>) isopropanol proportion, at 100 mM of 4-(trifluoromethyl)acetophenone within 3 h. Compared to bioconversion in the buffer medium, the developed isopropanol-aqueous system enhanced the substrate concentration by 2-fold with a remarkably improved yield (from 62.5% to 99.1%), and shortened the reaction time by 21 h. Our study gave the first example for a highly enantioselective production of (<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanol by a biological method, and the bioreduction of 4-(trifluoromethyl)acetophenone in a polar organic solvent-aqueous system was more efficient than that in the buffer solution only. This process is also scalable and has potential in application.https://www.mdpi.com/2073-4344/9/4/391(<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanolasymmetric bioreductionrecombinant whole-cell catalysispolar organic solvent-aqueous system |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ying Chen Nana Xia Yuewang Liu Pu Wang |
spellingShingle |
Ying Chen Nana Xia Yuewang Liu Pu Wang Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated Reduction Catalysts (<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanol asymmetric bioreduction recombinant whole-cell catalysis polar organic solvent-aqueous system |
author_facet |
Ying Chen Nana Xia Yuewang Liu Pu Wang |
author_sort |
Ying Chen |
title |
Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated Reduction |
title_short |
Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated Reduction |
title_full |
Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated Reduction |
title_fullStr |
Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated Reduction |
title_full_unstemmed |
Efficient Biocatalytic Preparation of Optically Pure (<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol by Recombinant Whole-Cell-Mediated Reduction |
title_sort |
efficient biocatalytic preparation of optically pure (<i>r</i>)-1-[4-(trifluoromethyl)phenyl]ethanol by recombinant whole-cell-mediated reduction |
publisher |
MDPI AG |
series |
Catalysts |
issn |
2073-4344 |
publishDate |
2019-04-01 |
description |
(<i>R</i>)-1-[4-(Trifluoromethyl)phenyl]ethanol is an important pharmaceutical intermediate of a chemokine CCR5 antagonist. In the present study, a bioprocess for the asymmetric reduction of 4-(trifluoromethyl)acetophenone to (<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanol was developed by recombinant <i>Escherichia coli</i> cells with excellent enantioselectivity. In order to overcome the conversion limitation performed in the conventional buffer medium resulting from poor solubility of non-natural substrate, we subsequently established a polar organic solvent-aqueous medium to improve the efficacy. Isopropanol was selected as the most suitable cosolvent candidate, based on the investigation on a substrate solubility test and cell membrane permeability assay in different organic solvent-buffer media. Under the optimum conditions, the preparative-scale asymmetric reduction generated a 99.1% yield with >99.9% product enantiomeric excess (ee) in a 15% (<i>v</i>/<i>v</i>) isopropanol proportion, at 100 mM of 4-(trifluoromethyl)acetophenone within 3 h. Compared to bioconversion in the buffer medium, the developed isopropanol-aqueous system enhanced the substrate concentration by 2-fold with a remarkably improved yield (from 62.5% to 99.1%), and shortened the reaction time by 21 h. Our study gave the first example for a highly enantioselective production of (<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanol by a biological method, and the bioreduction of 4-(trifluoromethyl)acetophenone in a polar organic solvent-aqueous system was more efficient than that in the buffer solution only. This process is also scalable and has potential in application. |
topic |
(<i>R</i>)-1-[4-(trifluoromethyl)phenyl]ethanol asymmetric bioreduction recombinant whole-cell catalysis polar organic solvent-aqueous system |
url |
https://www.mdpi.com/2073-4344/9/4/391 |
work_keys_str_mv |
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