Glycosaminoglycan polysaccharide biosynthesis and production: today and tomorrow

被引:125
作者
DeAngelis, Paul L. [1 ]
机构
[1] Univ Oklahoma, Dept Biochem & Mol Biol, Oklahoma Ctr Med Glycobiol, Hlth Sci Ctr, Oklahoma City, OK 73126 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
Polysaccharide; Capsule; Synthase; Glycosyltransferase; Hyaluronan; Heparin; Chondroitin; HYALURONIC-ACID PRODUCTION; ESCHERICHIA-COLI K5; 2; ACTIVE-SITES; PASTEURELLA-MULTOCIDA; MOLECULAR-CLONING; CAPSULAR POLYSACCHARIDE; STREPTOCOCCUS-ZOOEPIDEMICUS; HEPARAN-SULFATE; CHEMOENZYMATIC SYNTHESIS; CHONDROITIN POLYMERASE;
D O I
10.1007/s00253-011-3801-6
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 [微生物学]; 090105 [作物生产系统与生态工程];
摘要
Glycosaminoglycans [GAGs] are essential heteropolysaccharides in vertebrate tissues that are also, in certain cases, employed as virulence factors by microbes. Hyaluronan [HA], heparin, and chondroitin sulfate [CS] are GAGs currently used in various medical applications and together are multi-billion dollar products thus targets for production by animal-free manufacture. By using bacteria as the source of GAGs, the pathogen's sword may be converted into a plowshare to help avoid potential liabilities springing from the use of animal-derived GAGs including adventitious agents (e.g., prions, pathogens), antigenicity, degradation of the environment, and depletion of endangered species. HA from microbes, which have a chemical structure identical to human HA, has already been commercialized and sold at the ton-scale. Substantial progress towards microbial heparin and CS has been made, but these vertebrate polymers are more complicated structurally than the unsulfated bacterial polysaccharide precursors thus require additional processing steps. This review provides an overview of GAG structure, medical applications, microbial biosynthesis, and the state of bacterial GAG production systems. Representatives of all glycosyltransferase enzymes that polymerize the sugar chains of the three main GAGs have been identified and serve as the core technology to harness, but the proteins involved in sugar precursor formation and chain export steps of biosynthesis are also essential to the GAG production process. In addition, this review discusses future directions and potential important issues. Overall, this area is poised to make great headway to produce safer (both increased purity and more secure supply chains) non-animal GAG-based therapeutics.
引用
收藏
页码:295 / 305
页数:11
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