详细信息

Optimization and Scale-up of a Bioreduction Process for Preparation of Ethyl (S)-4-Chloro-3-hydroxybutanoate  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Optimization and Scale-up of a Bioreduction Process for Preparation of Ethyl (S)-4-Chloro-3-hydroxybutanoate

作者:Pan, Jiang[1];Zheng, Gao-Wei[1];Ye, Qin[1];Xu, Jian-He[1]

机构:[1]E China Univ Sci & Technol, State Key Lab Bioreactor Engn, Lab Biocatalysis & Synthet Biotechnol, Shanghai 200237, Peoples R China

年份:2014

卷号:18

期号:6

起止页码:739

外文期刊名:ORGANIC PROCESS RESEARCH & DEVELOPMENT

收录:;EI(收录号:20142717882946);WOS:【SCI-EXPANDED(收录号:WOS:000337870900009)】;

基金:This work was financially supported by the National Natural Science Foundation of China (nos. 21276082 & 31200050), Ministry of Science and Technology, P. R. China (nos. 2011CB710800 & 2011AA02A210), and the Innovation Program of Shanghai Municipal Education Commission (no. 11431921600).

语种:英文

外文关键词:Coenzymes

摘要:Ethyl 4-chloro-3-oxobutanoate (CUBE) was asymmetrically reduced with Escherichia coli cells expressing a reductase (ScCR) from Streptomyces coelicolor to afford enantiopure ethyl (S)-4-chloro-3-hydroxybutanoate [(S)-CHBE], which is an important precursor for preparing the drug atorvastatin. The substrate load was fixed at 100 g/L, and the concentration of coenzyme NAD(+) was limited to 0.1 mM based on cost considerations. Under these conditions, the other reaction parameters were optimized as 25 degrees C and pH 6.5, with a biocatalyst dose of 10 kU/L in the presence of isopropanol (1.5 equiv of CUBE), which acted as a cosubstrate for regenerating NADH. The reaction was performed in a toluene aqueous biphasic system (1:1, v/ v), with agitation at the maximal linear rate of 0.88 m/s. Finally, the bioreaction was performed on a pilot scale using a SO L thermostated stirred-tank-reactor, affording (S)-CHBE in 85.4% yield and 99.9% ee, and a total turnover number (TTN) of 6060 for the cofactor NAD(+). The specific production was calculated to be 36.8 g(product)/g(dcw), which is the highest value reported to date among the whole-cell-mediated processes for producing (S)-CHBE.

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