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在携带克隆的phbCAB操纵子的大肠杆菌转化体中,对用于聚羟基丁酸酯(PHB)奇特生物合成的与烟酰胺腺嘌呤二核苷酸磷酸(NADPH)相关的基因zwf和gnd进行扩增。

Amplification of the NADPH-related genes zwf and gnd for the oddball biosynthesis of PHB in an E. coli transformant harboring a cloned phbCAB operon.

作者信息

Lim Sang-Jun, Jung Young-Mi, Shin Hyun-Dong, Lee Yong-Hyun

机构信息

Department of Genetic Engineering, College of Natural Sciences, Kyungpook National University, Daegu 702-701, Korea.

出版信息

J Biosci Bioeng. 2002;93(6):543-9. doi: 10.1016/s1389-1723(02)80235-3.

Abstract

NADPH, a major reducing power in microorganisms, is mostly generated from the pentose phosphate (PP) pathway by glucose-6-phosphate dehydrogenase (G6PDH) and 6-phosphogluconate dehydrogenase (6PGDH) expressed by the zwf and gnd genes, respectively. The characteristics of these two genes in Escherichia coli were compared after their re-introduction into the parent strain for over-expression. zwf encoding G6PDH increased the level of NADPH 3 folds compared to gnd encoding 6PGDH. An excess of NADPH depressed cell growth mainly due to the inhibition of citrate synthase in the TCA cycle. Recombinant plasmids containing zwf or gnd co-integrated with the phbCAB operon from Ralstonia eutropha were constructed, and introduced into E. coli for the oddball biosynthesis of PHB. The amount of PHB increased after enforcing the genes; especially the zwf gene an increase of around 41%, due to the rise in NADPH and the depressed TCA cycle, leading to the metabolic flux of intermediates to the pathway for the biosynthesis of PHB.

摘要

NADPH是微生物中的一种主要还原力,主要由戊糖磷酸(PP)途径产生,该途径分别由zwf和gnd基因表达的葡萄糖-6-磷酸脱氢酶(G6PDH)和6-磷酸葡萄糖酸脱氢酶(6PGDH)催化。将这两个基因重新导入亲本菌株进行过表达后,比较了它们在大肠杆菌中的特性。与编码6PGDH的gnd相比,编码G6PDH的zwf使NADPH水平提高了3倍。过量的NADPH主要通过抑制三羧酸循环中的柠檬酸合酶来抑制细胞生长。构建了含有zwf或gnd与来自真养产碱菌的phbCAB操纵子共整合的重组质粒,并将其导入大肠杆菌用于聚羟基丁酸酯(PHB)的非常规生物合成。增强这些基因后,PHB的量增加;特别是zwf基因使PHB增加了约41%,这是由于NADPH的增加和三羧酸循环受到抑制,导致中间体的代谢通量流向PHB生物合成途径。

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