Literature DB >> 23701367

Production of S-acetoin from diacetyl by Escherichia coli transformant cells that express the diacetyl reductase gene of Paenibacillus polymyxa ZJ-9.

J Gao1, Y Y Xu, F W Li, G Ding.   

Abstract

UNLABELLED: S-acetoin (S-AC) is an important four-carbon chiral compound that has unique industrial applications in the asymmetric synthesis of valuable chiral specialty chemicals. However, previous studies showed that the usually low yield and optical purity of S-AC as well as the very high substrate cost have hindered the application of this compound. In the current work, a gene encoding diacetyl reductase (DAR) from a Paenibacillus polymyxa strain ZJ-9 was cloned and expressed in Escherichia coli. Whole cells of the recombinant E. coli were used to produce S-AC from diacetyl (DA). Under optimal conditions, S-AC with high optical purity (purity >99·9%) was obtained with a yield of 13·5 ± 0·24 and 39·4 ± 0·38 g l(-1) under batch and fed-batch culture conditions, respectively. This process featured the biotransformation of DA into S-AC using whole cells of engineered E. coli. The result is a considerable increase in the yield and optical purity of S-AC, which in turn facilitated the practical application of the compound. SIGNIFICANCE AND IMPACT OF THE STUDY: This study demonstrated a highly efficient new method to produce S-acetoin with higher than 99·9% optical purity from diacetyl using whole cells of engineered Escherichia coli. It will therefore decrease the production cost of S-acetoin and highlight its application in asymmetric synthesis of highly valuable chiral compounds.
© 2013 The Society for Applied Microbiology.

Entities:  

Keywords:  S-acetoin; biotransformation; diacetyl; diacetyl reductase; transformant cells

Mesh:

Substances:

Year:  2013        PMID: 23701367     DOI: 10.1111/lam.12107

Source DB:  PubMed          Journal:  Lett Appl Microbiol        ISSN: 0266-8254            Impact factor:   2.858


  6 in total

1.  Enhanced production of optical (S)-acetoin by a recombinant Escherichia coli whole-cell biocatalyst with NADH regeneration.

Authors:  Jian-Xiu Li; Yan-Yan Huang; Xian-Rui Chen; Qi-Shi Du; Jian-Zong Meng; Neng-Zhong Xie; Ri-Bo Huang
Journal:  RSC Adv       Date:  2018-08-29       Impact factor: 4.036

2.  Two-stage pH control strategy based on the pH preference of acetoin reductase regulates acetoin and 2,3-butanediol distribution in Bacillus subtilis.

Authors:  Xian Zhang; Teng Bao; Zhiming Rao; Taowei Yang; Zhenghong Xu; Shangtian Yang; Huazhong Li
Journal:  PLoS One       Date:  2014-03-07       Impact factor: 3.240

3.  Efficient bioconversion of 2,3-butanediol into acetoin using Gluconobacter oxydans DSM 2003.

Authors:  Xiuqing Wang; Min Lv; Lijie Zhang; Kun Li; Chao Gao; Cuiqing Ma; Ping Xu
Journal:  Biotechnol Biofuels       Date:  2013-10-31       Impact factor: 6.040

4.  Electrode-assisted acetoin production in a metabolically engineered Escherichia coli strain.

Authors:  Andreas H Förster; Sebastian Beblawy; Frederik Golitsch; Johannes Gescher
Journal:  Biotechnol Biofuels       Date:  2017-03-14       Impact factor: 6.040

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

Authors:  Yuanzhi He; Feixue Chen; Meijing Sun; Huifang Gao; Zewang Guo; Hui Lin; Jiebo Chen; Wensong Jin; Yunlong Yang; Liaoyuan Zhang; Jun Yuan
Journal:  Molecules       Date:  2018-03-19       Impact factor: 4.411

6.  Efficient whole-cell biocatalyst for acetoin production with NAD+ regeneration system through homologous co-expression of 2,3-butanediol dehydrogenase and NADH oxidase in engineered Bacillus subtilis.

Authors:  Teng Bao; Xian Zhang; Zhiming Rao; Xiaojing Zhao; Rongzhen Zhang; Taowei Yang; Zhenghong Xu; Shangtian Yang
Journal:  PLoS One       Date:  2014-07-18       Impact factor: 3.240

  6 in total

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