大肠杆菌
突变体
质粒
转化(遗传学)
基因
同源重组
pUC19型
生物
化学
拉伤
微生物学
分子生物学
遗传学
解剖
作者
Xiaona Chen,Ning Zhu,Guangrui Yang,Xiao-Peng Guo,Shangchen Sun,Feifan Leng,Yonggang Wang
标识
DOI:10.1002/jobm.202400113
摘要
ABSTRACT One of the fundamental techniques in genetic engineering is the creation of Escherichia coli competent cells using the CaCl 2 method. However, little is known about the mechanism of E. coli competence formation. We have previously found that the cspA gene may play an indispensable role in the preparation of E. coli DH5α competent cells through multiomics analysis. In the present study, the cellular localization, physicochemical properties, and function of the protein expressed by the cspA gene were analyzed. To investigate the role of the cspA gene in E. coli transformation, cspA‐ deficient mutant was constructed by red homologous recombination. The growth, transformation efficiency, and cell morphology of the cspA‐ deficient strain and E. coli were compared. It was found that there were no noticeable differences in growth and morphology between E. coli and the cspA‐ deficient strain cultured at 37°C, but the mutant exhibited increased transformation efficiencies compared to E. coli DH5α for plasmids pUC19, pET‐32a, and p1304, with enhancements of 2.23, 2.24, and 3.46 times, respectively. It was proved that cspA gene is an important negative regulatory gene in the CaCl 2 preparation of competent cells.
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