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

机译:使用大肠杆菌的重组蛋白细胞外产生的基因工程改性和发酵优化

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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.
机译:作为常见的表达宿主,由于最近开发的分泌表达系统,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,这提供了降低的下游生物处理和提高产品质量等优点。这些优点与高密度发酵技术相结合,使其成为工业和农业中使用的许多蛋白质大规模生产的优选系统,降低了工艺成本。为了改善靶蛋白的分泌效率,已经开发出各种策略,包括信号肽优化,周质泄漏和伴侣源共同表达。此外,还考虑了在高密度发酵中的细胞外产生,以降低生产成本,还考虑了优化的发酵条件如温度,诱导剂和培养基,以降低生产成本。在这里,这些策略从基因工程到发酵优化都是总结了使用大肠杆菌的重组蛋白的细胞外产生的指导。

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