Production of intracellular heparosan and derived oligosaccharides by lyase expression in metabolically engineered E. coli K-12

被引:33
|
作者
Barreteau, Helene [1 ]
Richard, Emeline [1 ]
Drouillard, Sophie [1 ]
Samain, Eric [1 ]
Priem, Bernard [1 ]
机构
[1] CNRS, Ctr Rech Macromol Vegetales, Grp Chim & Biotechnol Oligosaccharides, F-38041 Grenoble 09, France
关键词
Glycosaminoglycans; E; coli; K5; polysaccharide; Heparosan; Lyase; Metabolic engineering; ESCHERICHIA-COLI; CAPSULAR POLYSACCHARIDE; K5; POLYSACCHARIDE; GENE-CLUSTER; CLONING; HEPARIN; VECTORS;
D O I
10.1016/j.carres.2012.07.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The cluster of genes of capsular K5 heparosan is composed of three regions, involved in the synthesis and the exportation of the polysaccharide. The region 2 possesses all the necessary genes involved in the synthesis of heparosan, namely kfiA, encoding alpha-4-N-acetylglucosaminyltransferase, kfiD, encoding beta-3-glucuronyl transferase, kfiC, encoding UDP-glucose dehydrogenase (UDP-glucuronic acid synthesis), and kfiB encoding a protein of unknown function. The cloning and expression of kfiADCB into Escherichia coli K-12 were found to be sufficient for the production of heparosan, which accumulates in the cells due to a lack of the exporting system. The concentration of recombinant heparosan reached one gram per liter under fed-batch cultivation. The cytoplasmic localization of heparosan inside the bacteria allowed subsequent enzymatic modifications such as a partial degradation with K5 lyase when expressed intracellularly. Under these conditions, the production of DP 2-10 oligosaccharides occurred intracellularly, at a concentration similar to that of recombinant intracellular heparosan. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:19 / 24
页数:6
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