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Production of intracellular heparosan and derived oligosaccharides by lyase expression in metabolically engineered E. coli K-12
被引:34
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.
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页码:19 / 24
页数:6
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