Engineering Escherichia coli for high-yield production of ectoine

被引:15
作者
Wang, Daoan [1 ,3 ]
Chen, Jiamin [1 ,3 ]
Wang, Yang [1 ,2 ]
Du, Guocheng [1 ,2 ]
Kang, Zhen [1 ,2 ]
机构
[1] Jiangnan Univ, Sci Ctr Future Foods, Wuxi 214122, Peoples R China
[2] Jiangnan Univ, Key Lab Carbohydrate Chem & Biotechnol, Minist Educ, Wuxi 214122, Peoples R China
[3] Jiangnan Univ, Sch Biotechnol, Key Lab Ind Biotechnol, Minist Educ, Wuxi 214122, Peoples R China
基金
中国国家自然科学基金;
关键词
Ectoine; Escherichia coli; Metabolic engineering; RBS design; COMPATIBLE SOLUTE ECTOINE; L-ASPARTATE; BIOSYNTHESIS; EXPRESSION; GENES; HYDROXYECTOINE; CONSTRUCTION; OPTIMIZATION; EXTREMOLYTES; PLASMIDS;
D O I
10.1016/j.gce.2021.09.002
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Ectoine is a natural macromolecule protector and synthesized by some extremophiles. It provides protections against radiation-mediated oxidative damages and is widely used as a bioactive ingredient in pharmaceutics and cosmetics. To meet its growing commercial demands, we engineered Escherichia coli strains for the high-yield production of ectoine. The ectABC gene cluster from the native ectoine producer Halomonas elongata was introduced into different Escherichia coli (E. Coil) strains via plasmids and 0.8 g L-1 of ectoine was produced in flask cultures by engineered E. coli BL21 (DE3). Subsequently, we designed the ribosome-binding sites of the gene cluster to fine-tune the expressions of genes ectA, ectB, and ectC, which increased the ectoine yield to 1.6 g L-1. After further combinatorial overexpression of Corynebacterium glutamicum aspartate kinase mutant (G1A, C932T) and the H. elongate aspartate-semialdehyde dehydrogenase to increase the supply of the precursor, the titer of ectoine reached to 5.5 g L-1 in flask cultures. Finally, the engineered strain produced 60.7 g L-1 ectoine in fedbatch cultures with a conversion rate of 0.25 g/g glucose.
引用
收藏
页码:217 / 223
页数:7
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