大肠杆菌
巨芽孢杆菌
脱氢酶
生物化学
生物
酶
化学
细菌
基因
遗传学
作者
Xiangwei Wang,Xiang Xing,Qinglin Ma
标识
DOI:10.1080/13102818.2016.1196121
摘要
This study devised an effective method for the direct production of hydroxyfatty acids (HFAs) from free fatty acids (FFAs) using Escherichia coli. By employing fatty acid hydroxylase P450BM3 and glucose dehydrogenase (GDH) to convert FFAs to HFAs, high-specificity production of C12 HFAs was achieved. By further knocking out the endogenous fadD gene of E. coli, an engineered strain capable of producing 702.3 mg/L C12 HFA was finally obtained, accounting for 92.9% of the total HFAs production, representing a higher titre reported in shake flask so far. This study provides an attractive strategy for increasing HFAs production in E. coli by increasing NADPH accumulation.
科研通智能强力驱动
Strongly Powered by AbleSci AI