Controlled expression of lysis gene E by a mutant of the promoter pL of the thermo-inducible lambda cI857-pL system
文献类型： 外文期刊
作者： Fu, L. X. 1 ; Gong, J. S. 3 ; Gao, B. 1 ; Ji, D. J. 1 ; Han, X. G. 2 ; Zeng, L. B. 4 ;
作者机构： 1.Yangzhou Univ, Coll Anim Sci & Technol, Jiangsu Key Lab Zoonosis, Yangzhou, Jiangsu, Peoples R China
2.Chinese Acad Agr Sci, Shanghai Vet Res Inst, Shanghai, Peoples R China
3.Chinese Acad Agr Sci, Poultry Inst, Yangzhou, Jiangsu, Peoples R China
4.Chinese Acad Fishery Sci, Yangtze River Fisheries Res Inst, Minist Agr, Key Lab Freshwater Biodivers Conservat, Wuhan, Hubei, Peoples R China
关键词： bacterial ghosts; cI857 repressor; Escherichia coli; lysis gene E; promoter pL; Salmonella enteritidis
期刊名称：JOURNAL OF APPLIED MICROBIOLOGY （ 影响因子：3.772； 五年影响因子：3.963 ）
ISSN： 1364-5072
年卷期： 2021 年 130 卷 6 期
页码：
收录情况： SCI
摘要： Aims To identify a lambda promoter pL mutant that could extend the thermal stability of the thermo-inducible lambda cI857-pR/pL system and to evaluate the effects of the modified system for the controlled expression of lysis gene E during the production of bacterial ghosts (BGs). Methods and results The promoter pL mutant was identified by random mutagenesis and site-directed mutagenesis. The results showed that a T -> 35C mutation in the pL promoter was responsible for the phenotype alteration. Under the same induction conditions, the lysis rates of the modified lytic system on Escherichia coli and Salmonella enteritidis were significantly lower than that of the control, while the lysis rates of Escherichia coli with the thermo-inducible lytic system were significantly higher than that of S. enteritidis with the corresponding plasmid (P < 0 center dot 05). Conclusions Increasing the heat stability of the thermo-inducible lytic systems decreased lysis efficiency during the production of BGs. There exist differences in the lysis efficiency of thermo-inducible lytic systems between different bacterial strains. Significance and Impact of the Study These findings enrich current knowledge about modifications to thermo-inducible systems and provide a reference for the application of these modified systems for the production of BGs and controlled gene expression in bacteria.
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