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Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis

(3S)-Acetoin and (2S,3S)-2,3-butanediol are important platform chemicals widely applied in the asymmetric synthesis of valuable chiral chemicals. However, their production by fermentative methods is difficult to perform. This study aimed to develop a whole-cell biocatalysis strategy for the producti...

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Autores principales: He, Yuanzhi, Chen, Feixue, Sun, Meijing, Gao, Huifang, Guo, Zewang, Lin, Hui, Chen, Jiebo, Jin, Wensong, Yang, Yunlong, Zhang, Liaoyuan, Yuan, Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017632/
https://www.ncbi.nlm.nih.gov/pubmed/29562693
http://dx.doi.org/10.3390/molecules23030691
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author He, Yuanzhi
Chen, Feixue
Sun, Meijing
Gao, Huifang
Guo, Zewang
Lin, Hui
Chen, Jiebo
Jin, Wensong
Yang, Yunlong
Zhang, Liaoyuan
Yuan, Jun
author_facet He, Yuanzhi
Chen, Feixue
Sun, Meijing
Gao, Huifang
Guo, Zewang
Lin, Hui
Chen, Jiebo
Jin, Wensong
Yang, Yunlong
Zhang, Liaoyuan
Yuan, Jun
author_sort He, Yuanzhi
collection PubMed
description (3S)-Acetoin and (2S,3S)-2,3-butanediol are important platform chemicals widely applied in the asymmetric synthesis of valuable chiral chemicals. However, their production by fermentative methods is difficult to perform. This study aimed to develop a whole-cell biocatalysis strategy for the production of (3S)-acetoin and (2S,3S)-2,3-butanediol from meso-2,3-butanediol. First, E. coli co-expressing (2R,3R)-2,3-butanediol dehydrogenase, NADH oxidase and Vitreoscilla hemoglobin was developed for (3S)-acetoin production from meso-2,3-butanediol. Maximum (3S)-acetoin concentration of 72.38 g/L with the stereoisomeric purity of 94.65% was achieved at 24 h under optimal conditions. Subsequently, we developed another biocatalyst co-expressing (2S,3S)-2,3-butanediol dehydrogenase and formate dehydrogenase for (2S,3S)-2,3-butanediol production from (3S)-acetoin. Synchronous catalysis together with two biocatalysts afforded 38.41 g/L of (2S,3S)-butanediol with stereoisomeric purity of 98.03% from 40 g/L meso-2,3-butanediol. These results exhibited the potential for (3S)-acetoin and (2S,3S)-butanediol production from meso-2,3-butanediol as a substrate via whole-cell biocatalysis.
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spelling pubmed-60176322018-11-13 Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis He, Yuanzhi Chen, Feixue Sun, Meijing Gao, Huifang Guo, Zewang Lin, Hui Chen, Jiebo Jin, Wensong Yang, Yunlong Zhang, Liaoyuan Yuan, Jun Molecules Article (3S)-Acetoin and (2S,3S)-2,3-butanediol are important platform chemicals widely applied in the asymmetric synthesis of valuable chiral chemicals. However, their production by fermentative methods is difficult to perform. This study aimed to develop a whole-cell biocatalysis strategy for the production of (3S)-acetoin and (2S,3S)-2,3-butanediol from meso-2,3-butanediol. First, E. coli co-expressing (2R,3R)-2,3-butanediol dehydrogenase, NADH oxidase and Vitreoscilla hemoglobin was developed for (3S)-acetoin production from meso-2,3-butanediol. Maximum (3S)-acetoin concentration of 72.38 g/L with the stereoisomeric purity of 94.65% was achieved at 24 h under optimal conditions. Subsequently, we developed another biocatalyst co-expressing (2S,3S)-2,3-butanediol dehydrogenase and formate dehydrogenase for (2S,3S)-2,3-butanediol production from (3S)-acetoin. Synchronous catalysis together with two biocatalysts afforded 38.41 g/L of (2S,3S)-butanediol with stereoisomeric purity of 98.03% from 40 g/L meso-2,3-butanediol. These results exhibited the potential for (3S)-acetoin and (2S,3S)-butanediol production from meso-2,3-butanediol as a substrate via whole-cell biocatalysis. MDPI 2018-03-19 /pmc/articles/PMC6017632/ /pubmed/29562693 http://dx.doi.org/10.3390/molecules23030691 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
He, Yuanzhi
Chen, Feixue
Sun, Meijing
Gao, Huifang
Guo, Zewang
Lin, Hui
Chen, Jiebo
Jin, Wensong
Yang, Yunlong
Zhang, Liaoyuan
Yuan, Jun
Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis
title Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis
title_full Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis
title_fullStr Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis
title_full_unstemmed Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis
title_short Efficient (3S)-Acetoin and (2S,3S)-2,3-Butanediol Production from meso-2,3-Butanediol Using Whole-Cell Biocatalysis
title_sort efficient (3s)-acetoin and (2s,3s)-2,3-butanediol production from meso-2,3-butanediol using whole-cell biocatalysis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017632/
https://www.ncbi.nlm.nih.gov/pubmed/29562693
http://dx.doi.org/10.3390/molecules23030691
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