Transcriptional Engineering of Escherichia coli K4 for Fructosylated Chondroitin Production

被引:39
作者
Wu, Qiulin [1 ,2 ,3 ]
Yang, Aihua [1 ]
Zou, Wei [1 ]
Duan, Zuoying [1 ]
Liu, Jie [4 ]
Chen, Jian [2 ]
Liu, Liming [1 ,2 ,3 ]
机构
[1] Jiangnan Univ, State Key Lab Food Sci & Technol, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Key Lab Ind Biotechnol, Minist Educ, Wuxi 214122, Jiangsu, Peoples R China
[3] Jiangnan Univ, Lab Food Microbial Mfg Engn, Wuxi 214122, Jiangsu, Peoples R China
[4] Jiangsu Jiangshan Pharmaceut Co Ltd, Jingjiang 214500, Jiangsu, Peoples R China
关键词
capsule polysaccharide; chondroitin sulfate; E; coli K4; slyA; transcriptional regulation; CAPSULE GENE-CLUSTER; HYALURONIC-ACID PRODUCTION; SALMONELLA-TYPHIMURIUM; H-NS; SLYA; POLYSACCHARIDES; BIOSYNTHESIS; EXPRESSION; OVEREXPRESSION; REGULATOR;
D O I
10.1002/btpr.1777
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The capsule polysaccharide (CPS) of Escherichia coli K4 (K4CPS) is identical to fructosylated chondroitin, which can be modified to chondroitin sulfate, a commercially valuable biopolymer commonly used in pharmaceutical applications. In this study, we homologously overexpressed the transcriptional regulator SlyA to enhance the expression of K4 capsule gene cluster and production of CPS. The iTRAQ quantificaton of proteomics revealed 77 up-regulated proteins and 143 down-regulated proteins in E. coli THslyA. Most enzymes of glycolysis and citrate cycle pathway were weakened, while proteins associated with K4CPS synthesis were up-regulated, showing a shift of carbon flux from cell growth to K4CPS production. Further, the production of K4CPS by the recombinant strain was 1 and 2.6 g/L in a shake flask and 7-L batch bioreactor, which was 1.85- and 1.53-fold higher than that of the wild-type strain, respectively. Thus, this study provides a viable strategy for improving the production of K4CPS through a transcriptional-level manipulation. (c) 2013 American Institute of Chemical Engineers Biotechnol. Prog., 29:1140-1149, 2013
引用
收藏
页码:1140 / 1149
页数:10
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