大肠杆菌
重组DNA
寄主(生物学)
生产过剩
蛋白质表达
生物
计算生物学
生物技术
生物化学
遗传学
基因
作者
Zixu Zhang,Fang‐Tong Nong,Yu‐Zhou Wang,Chun-Xiao Yan,Yang Gu,Ping Song,Xiao‐Man Sun
标识
DOI:10.1186/s12934-022-01917-y
摘要
Abstract Escherichia coli , one of the most efficient expression hosts for recombinant proteins (RPs), is widely used in chemical, medical, food and other industries. However, conventional expression strains are unable to effectively express proteins with complex structures or toxicity. The key to solving this problem is to alleviate the host burden associated with protein overproduction and to enhance the ability to accurately fold and modify RPs at high expression levels. Here, we summarize the recently developed optimization strategies for the high-level production of RPs from the two aspects of host burden and protein activity. The aim is to maximize the ability of researchers to quickly select an appropriate optimization strategy for improving the production of RPs.
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