代谢工程
大肠杆菌
生物化学
合成生物学
吲哚试验
代谢途径
化学
新陈代谢
檀香
生物
酶
计算生物学
历史
基因
考古
作者
Yan Wang,Shenting Zhou,Qian Liu,Seong-Hee Jeong,Liyan Zhu,Xiang Yu,Xiaojian Zheng,Gongyuan Wei,Seon-Won Kim,Chonglong Wang
标识
DOI:10.1021/acs.jafc.1c05486
摘要
α-Santalene belongs to a class of natural compounds with many physiological functions and medical applications. Advances in metabolic engineering enable non-native hosts (e.g., Escherichia coli) to produce α-santalene, the precursor of sandalwood oil. However, imbalances in enzymatic activity often result in a metabolic burden on hosts and repress the synthetic capacity of the desired product. In this work, we manipulated ribosome binding sites (RBSs) to optimize an α-santalene synthetic operon in E. coli, and the best engineered E. coli NA-IS3D strain could produce α-santalene at a titer of 412 mg·L-1. Concerning the observation of the inverse correlation between indole synthesis and α-santalene production, this study speculated that indole-associated amino acid metabolism would be competitive to the synthesis of α-santalene rather than indole toxicity itself. The deletion of tnaA could lead to a 1.5-fold increase in α-santalene production to a titer of 599 mg·L-1 in E. colitnaA- NA-IS3D. Our results suggested that the optimization of RBS sets of the synthetic module and attenuation of the competitive pathway are promising approaches for improving the production of terpenoids including α-santalene.
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