电穿孔
质粒
大肠杆菌
周质间隙
转化(遗传学)
生物
表达式向量
基因表达
计算生物学
分子生物学
基因
发起人
化学
重组DNA
生物化学
作者
Alain Bernard,Mark A. Payton
标识
DOI:10.1002/0471140864.ps0502s00
摘要
This unit lists the most useful expression strains of E. coli for fermentation processes. Standard procedures are provided for several expression systems, namely, temperature induction via the p(L) promoter and chemical induction via the trp promoter, lac or tac promoters, and the T7 promoter. These protocols require that the gene encoding the protein of interest has been identified and cloned into an appropriate expression vector using standard molecular biology techniques. Transformation of a suitable host strain (e.g., by electroporation) is also described and is a prerequisite. Protocols for the analysis of plasmid stability and subsequent storage are provided. Support protocols describe how to prepare samples for electrophoresis, how to analyze the solubility of the expressed proteins, and how to make samples of periplasmic extracts and extracellular media (using TCA precipitation). Many of the support protocols are small-scale analysis procedures that are used to guide subsequent purification strategies and determine the suitability of the expression system for further development and scale-up.
科研通智能强力驱动
Strongly Powered by AbleSci AI