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糖胺聚糖多糖生物合成和生产:今天和明天。

Glycosaminoglycan polysaccharide biosynthesis and production: today and tomorrow.

机构信息

Department of Biochemistry and Molecular Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73126, USA.

出版信息

Appl Microbiol Biotechnol. 2012 Apr;94(2):295-305. doi: 10.1007/s00253-011-3801-6. Epub 2012 Mar 6.

Abstract

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.

摘要

糖胺聚糖 [GAGs] 是脊椎动物组织中必不可少的杂多糖,在某些情况下,微生物也将其用作毒力因子。透明质酸 [HA]、肝素和硫酸软骨素 [CS] 是目前用于各种医疗应用的 GAGs,它们加起来是价值数十亿美元的产品,因此是无动物制造的目标。通过使用细菌作为 GAGs 的来源,可以将病原体的剑转化为犁,以帮助避免使用动物源性 GAGs 带来的潜在责任,包括偶然剂(例如朊病毒、病原体)、抗原性、环境降解和濒危物种枯竭。微生物来源的 HA 与人类 HA 的化学结构相同,已经商业化并以吨级规模销售。在微生物肝素和 CS 的生产方面已经取得了实质性进展,但这些脊椎动物聚合物在结构上比未硫酸化的细菌多糖前体更为复杂,因此需要额外的加工步骤。这篇综述概述了 GAG 的结构、医学应用、微生物生物合成以及细菌 GAG 生产系统的现状。已经鉴定出聚合三种主要 GAG 糖链的所有糖基转移酶酶的代表,它们是利用的核心技术,但参与生物合成中糖前体形成和链输出步骤的蛋白质对于 GAG 生产过程也是必不可少的。此外,本文还讨论了未来的方向和潜在的重要问题。总体而言,该领域有望在生产更安全(更高纯度和更安全的供应链)的非动物 GAG 基治疗药物方面取得重大进展。

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