谷氨酸棒杆菌
葡萄糖激酶
磷酸烯醇丙酮酸羧激酶
PEP群易位
生物化学
琥珀酸
化学
突变体
葡萄糖转运蛋白
生物
酶
基因
内分泌学
胰岛素
作者
Zhonggao Zhou,Chen Wang,Hongtao Xu,Zhongjun Chen,Heng Cai
出处
期刊:Journal of Industrial Microbiology & Biotechnology
[Oxford University Press]
日期:2015-05-07
卷期号:42 (7): 1073-1082
被引量:29
标识
DOI:10.1007/s10295-015-1630-9
摘要
Abstract Succinic acid synthesized from glucose shows potential as a bio-based platform chemical. However, the need for a high glucose concentration, and the accompanying low yields, limit its industrial applications. Despite efficient glucose uptake by the phosphotransferase system (PTS), 1 mol of phosphoenolpyruvate is required for each mole of internalized glucose. Therefore, a PTS-defective Corynebacterium glutamicum mutant was constructed to increase phosphoenolpyruvate availability for succinic acid synthesis, resulting in a lower glucose utilization rate and slower growth. The transcriptional regulator iolR was also deleted to enable the PTS-defective mutant to utilize glucose via iolT-mediated glucose transport. Deletion of iolR and overexpression of iolT1 and ppgk (polyphosphate glucokinase) in the PTS-deficient C. glutamicum strain completely restored glucose utilization, increasing production by 11.6 % and yield by 32.4 % compared with the control. This study revealed for the first time that iolR represses the expression of the two glucokinase genes (glk and ppgk).
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