Yuan Lin, Qin Yan-Li, Zou Zhi-Cheng, Appiah Bright, Huang Hao, Yang Zhong-Hua, Qun Can
School of Chemistry and Chemical Engineering, Wuhan University of Science and Technology, Wuhan 430081, China.
School of Chemistry and Chemical Engineering, Wuhan University of Science and Technology, Wuhan 430081, China; Key Laboratory of Hubei Province for Coal Conversion and New Carbon Materials, Wuhan University of Science and Technology, Wuhan 430081, China.
J Biosci Bioeng. 2022 Dec;134(6):528-533. doi: 10.1016/j.jbiosc.2022.08.010. Epub 2022 Oct 9.
The intracellular NAD(P)H insufficiency is the key factor which limits the reduced product (such as chiral alcohols) synthesis by whole cell biocatalysis or microbial cell factory. In this paper, we reported a novel solution to increase NADPH supply through strengthening the pentose phosphate pathway (PPP) flux with overexpression of extra zwf (gene for glucose 6-phosphatedehydrogenase) and glk (gene for glucokinase) by recombinant Escherichia coli BL21(DE3)/pETDuet-1-glk-zwf and pET28a-bccr containing a carbonyl reductase gene bccr. The amount of intracellular NADPH was significantly increased from 150.3 μmol/L to 681.8 μmol/L after strengthening the PPP flux, which was 4.5-fold to that of the control. It was applied to improve the asymmetric reduction of 4-chloroacetoacetate to ethyl S-4-chloro-3-hydroxybutylate catalyzed by the BcCR, which increased the reaction yield 2.8-fold to the control. This strategy provides a new way to increase NADPH supply in E. coli cell factories.
细胞内NAD(P)H不足是限制全细胞生物催化或微生物细胞工厂合成还原产物(如手性醇)的关键因素。在本文中,我们报道了一种新的解决方案,即通过重组大肠杆菌BL21(DE3)/pETDuet-1-glk-zwf和含有羰基还原酶基因bccr的pET28a-bccr过表达额外的zwf(葡萄糖6-磷酸脱氢酶基因)和glk(葡萄糖激酶基因)来增强磷酸戊糖途径(PPP)通量,从而增加NADPH供应。增强PPP通量后,细胞内NADPH的量从150.3 μmol/L显著增加到681.8 μmol/L,是对照的4.5倍。将其应用于改善由BcCR催化的4-氯乙酰乙酸不对称还原为S-4-氯-3-羟基丁酸乙酯的反应,反应产率比对照提高了2.8倍。该策略为增加大肠杆菌细胞工厂中NADPH供应提供了一种新方法。