| Literature DB >> 25682229 |
Yu-Cai He1, Dan-Ping Zhang2, Zhi-Cheng Tao2, Yun Lu2, Yun Ding2, Feng Liu2, Zheng-Zhong Zhu2, Huan Rui2, Gao-Wei Zheng3, Xian Zhang4.
Abstract
To reduce dependence on the expensive cofactor and effectively biotransform ethyl 4-chloro-3-oxobutanoate, L-glutamine and glycine were found to enhance the content of intracellular NADH and the reductase activity. Adding the mixture of 200 mM of L-glutamine and 500 mM of glycine to the reaction media, a 1.67-fold of reductase activity was increased over the control without the addition of the two compounds. Moreover, β-cyclodextrin (0.4 mol β-cyclodextrin/mol ethyl 4-chloro-3-oxobutanoate) was also added into this reaction media, and the biocatalytic activity of the whole-cell biocatalyst of Escherichia coli CCZU-K14 was increased by 1.34-fold than that without β-cyclodextrin. In this β-cyclodextrin-water media containing L-glutamine (200 mM) plus glycine (500 mM), ethyl (S)-4-chloro-3-hydroxybutanoate (>99% ee) could be obtained from 3000 mM ethyl 4-chloro-3-oxobutanoate in the yield of 98.0% after 8h. All the positive features demonstrate the potential applicability of the bioprocess for the large-scale production of ethyl (S)-4-chloro-3-hydroxybutanoate.Entities:
Keywords: Ethyl (S)-4-chloro-3-hydroxybutanoate; Ethyl 4-chloro-3-oxobutanoate; Glycine; l-Glutamine; β-Cyclodextrin
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Year: 2015 PMID: 25682229 DOI: 10.1016/j.biortech.2015.01.111
Source DB: PubMed Journal: Bioresour Technol ISSN: 0960-8524 Impact factor: 9.642