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首页> 外文期刊>FEMS Microbiology Letters >Heat-inactivation of plasmid-encoded CI857 repressor induces gene expression from Ind- lambda prophage in recombinant Escherichia coli.
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Heat-inactivation of plasmid-encoded CI857 repressor induces gene expression from Ind- lambda prophage in recombinant Escherichia coli.

机译:质粒编码的CI857阻遏物的热失活诱导了重组大肠杆菌中Ind-λ噬菌体的基因表达。

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摘要

We have observed significant cell lysis upon temperature up-shift of recombinant Escherichia coli cultures harboring CI857-repressed lambda-based expression vectors. This event, that becomes evident about 30-40 min after the heat shock, takes place when using the lambda promoter system in Ind- lysogenic strains, but not in others commonly employed for recombinant gene expression. These results strongly suggest that the thermosensitive CI857 repressor, encoded by the expression vector, competes with CI Ind- molecules for binding to the prophage operator region, allowing for expression of lytic genes from the integrated Ind- viral genome upon temperature up-shift. Transcription of viral lytic genes does not include unspecific expression of a reporter sulA::lacZ gene fusion carried in the prophage genome. These results prompt, however, to carefully evaluate the limitations of expression systems based on pL/pR-CI857 in bacterial strains modified through lambda Ind- gene transfer vehicles.
机译:我们已经观察到,带有CI857抑制的基于λ的表达载体的重组大肠杆菌培养物温度升高时,细胞裂解作用显着。当在Indlysogenic菌株中使用lambda启动子系统时,在热休克后约30-40分钟会发生此事件,而在通常用于重组基因表达的其他菌株中则没有此事件。这些结果强烈表明,由表达载体编码的热敏CI857阻遏物与CI Ind分子竞争结合到噬菌体操纵子区域,从而允许在温度升高时从整合的Ind-病毒基因组表达裂解基因。病毒裂解基因的转录不包括原噬菌体基因组中携带的报告基因sulA :: lacZ基因融合体的非特异性表达。但是,这些结果促使人们仔细评估基于pL / pR-CI857的表达系统在通过λInd基因转移载体修饰的细菌菌株中的局限性。

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