大肠杆菌
基因
重组DNA
生物
基因表达
载体(分子生物学)
表达式向量
大肠杆菌
微生物学
遗传学
标识
DOI:10.1002/0471140864.ps0519s50
摘要
Abstract Despite the development of various nonbacterial expression systems, Escherichia coli ( E. coli ) remains the host of choice for recombinant protein expression. Its culture is simple, fast, inexpensive, and highly efficient (tens of milligrams of pure proteins are typically obtained within 48 hours using as little as 1 liter of culture). Unfortunately, many toxic genes (from various organisms) severely interfere with the physiology of E. coli . As a result, expression yields are dramatically diminished, and sometimes abolished. In fact, some genes are so toxic that E. coli cannot maintain their expression vector during the growth phase (the phase during which recombinant gene expression is presumably repressed). Therefore, modified expression vectors, modified E. coli strains, and appropriate cultivation protocols are needed. This overview discusses several special strategies successfully used to express toxic genes in E. coli . Curr. Protoc. Protein Sci . 50:5.19.1‐5.19.13. © 2007 by John Wiley & Sons, Inc.
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