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利用大肠杆菌通过遗传工程修饰和发酵优化进行重组蛋白的胞外生产。

Genetic engineering modification and fermentation optimization for extracellular production of recombinant proteins using Escherichia coli.

机构信息

Hubei Collaborative Innovation Center for Green Transformation of Bio-Resources, Hubei Key Laboratory of Industrial Biotechnology, The College of Life Science, Hubei University, Wuhan, 430062, People's Republic of China.

出版信息

Appl Microbiol Biotechnol. 2018 Feb;102(4):1545-1556. doi: 10.1007/s00253-017-8700-z. Epub 2017 Dec 21.

Abstract

As a common expression host, Escherichia coli has received more and more attention due to the recently developed secretory expression system, which offers advantages like reduced downstream bioprocesses and improved product quality. These advantages, coupled with high-density fermentation technology, make it a preferred system for large-scale production of many proteins utilized in industry and agriculture at a reduced process cost. To improve the secretion efficiency of target proteins, various strategies, including signal peptide optimization, periplasmic leakage, and chaperones co-expression have been developed. In addition, the optimization of the fermentation conditions such as temperature, inducer, and medium were also taken into account for the extracellular production in the high-density fermentation to reduce the cost of production. Here, these strategies ranging from genetic engineering to fermentation optimization were summarized for the future guidance of extracellular production of recombinant proteins using E. coli.

摘要

作为一种常见的表达宿主,大肠杆菌由于最近开发的分泌表达系统而受到越来越多的关注,该系统具有减少下游生物处理和提高产品质量等优点。这些优点,再加上高密度发酵技术,使其成为工业和农业中许多蛋白质大规模生产的首选系统,可降低工艺成本。为了提高目标蛋白的分泌效率,已经开发了各种策略,包括信号肽优化、周质渗漏和伴侣蛋白共表达。此外,还考虑了发酵条件的优化,如温度、诱导剂和培养基,以便在高密度发酵中进行细胞外生产,从而降低生产成本。在这里,从遗传工程到发酵优化的这些策略进行了总结,为使用大肠杆菌进行重组蛋白的细胞外生产提供未来指导。

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