代谢工程
1,3-丙二醇
甘油
发酵
化学
辅因子
生物化学
代谢途径
丙二醇
大肠杆菌
食品科学
新陈代谢
酶
有机化学
基因
作者
Yufei Zhang,Junhua Yun,Hossain M. Zabed,Yuan Dou,Guoyan Zhang,Mei Zhao,Mohammad J. Taherzadeh,Arthur J. Ragauskas,Xianghui Qi
标识
DOI:10.1016/j.biortech.2022.128438
摘要
3-Hydroxypropionic acid (3-HP) and 1,3-propanediol (1,3-PDO) are value-added chemicals with versatile applications in the chemical, pharmaceutical, and food industries. Nevertheless, sustainable production of 3-HP and 1,3-PDO is often limited by the lack of efficient strains and suitable fermentation configurations. Herein, attempts have been made to improve the co-production of both metabolites through metabolic engineering of Escherichia coli and process optimization. First, the 3-HP and 1,3-PDO co-biosynthetic pathways were recruited and optimized in E. coli, followed by coupling the pathways to the transhydrogenase-mediated cofactor regeneration systems that increased cofactor availability and product synthesis. Next, pathway rebalancing and block of by-product formation significantly improved 3-HP and 1,3-PDO net titer. Subsequently, glycerol flux toward 3-HP and 1,3-PDO synthesis was maximized by removing metabolic repression and fine-tuning the glycerol oxidation pathway. Lastly, the combined fermentation process optimization and two-stage pH-controlled fed-batch fermentation co-produced 140.50 g/L 3-HP and 1,3-PDO, with 0.85 mol/mol net yield.
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