大肠杆菌
重组DNA
辣木
伴侣(临床)
生物技术
计算生物学
生物
基因表达
生物化学
食品科学
基因
医学
病理
作者
Nallaiah Hemamalini,Selvaram Ezhilmathi,A. Angela Mercy
摘要
Escherichia coli is the most extensively used organism in recombinant protein production. It has several advantages including a very short life cycle, ease of genetic manipulation and the well-known cell biology etc. which makes E. coli as the perfect host for recombinant protein expression. Despite many advantages, E. coli also have few disadvantages such as coupled transcription and translation and lack of eukaryotic post-translational modifications. These challenges can be overcome by adopting several strategies such as, using different E. coli expression vectors, changing the gene sequence without altering the functional domain, modified E. coli strain usage, changing the culture parameters and co-expression with a molecular chaperone. In this review, we present the level of strategies used to enhance the recombinant protein expression and its stability in E. coli.
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