Manipulation of the precursor supply for high-level production of longifolene by metabolically engineered Escherichia coli

被引:27
|
作者
Cao, Yujin [1 ]
Zhang, Rubing [1 ]
Liu, Wei [1 ]
Zhao, Guang [1 ]
Niu, Wei [2 ]
Guo, Jiantao [2 ]
Xian, Mo [1 ]
Liu, Huizhou [1 ]
机构
[1] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, CAS Key Lab Biobased Mat, Qingdao, Peoples R China
[2] Univ Nebraska, Dept Chem, Lincoln, NE 68588 USA
基金
中国国家自然科学基金;
关键词
MEVALONATE PATHWAY; BIOSYNTHESIS; DIPHOSPHATE; SYNTHASES; EXPRESSION; EVOLUTION; TOXICITY; ACID;
D O I
10.1038/s41598-018-36495-w
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Longifolene is a naturally occurring tricyclic sesquiterpene widely used in many different fields. Up to now, this valuable terpene was mainly manufactured from the high-boiling fraction of certain pine resins. Microbial production can be a promising alternative to the extraction from natural plant sources. Here, we present the metabolic engineering strategy to assemble biosynthetic pathway for longifolene production in Escherichia coli. E. coli was rendered to produce longifolene by heterologously expressing a codon optimized longifolene synthase from Picea abies. Augmentation of the metabolic flux to farnesyl pyrophosphate (FPP) by different FPP synthases conferred a 1.8-fold increase in longifolene production. An additional enhancement of longifolene production (up to 2.64 mg/L) was achieved by introducing an exogenous mevalonate pathway. Underfed-batch conditions, the best-performing strain was able to produce 382 mg/L of longifolene in a 5 L bioreactor. These results demonstrated the feasibility of producing longifolene by microbial fermentation and could serve as the basis for the construction of more robust strains in the future.
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页数:10
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