首页> 美国卫生研究院文献>Journal of Bacteriology >Anchoring of DNA to the bacterial cytoplasmic membrane through cotranscriptional synthesis of polypeptides encoding membrane proteins or proteins for export: a mechanism of plasmid hypernegative supercoiling in mutants deficient in DNA topoisomerase I.
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Anchoring of DNA to the bacterial cytoplasmic membrane through cotranscriptional synthesis of polypeptides encoding membrane proteins or proteins for export: a mechanism of plasmid hypernegative supercoiling in mutants deficient in DNA topoisomerase I.

机译:通过共转录合成编码膜蛋白或输出蛋白的多肽将DNA锚定到细菌细胞质膜上:DNA拓扑异构酶I缺乏突变体中质粒超负超螺旋的机制。

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摘要

A homologous set of plasmids expressing tet, lacY, and melB, genes encoding integral cytoplasmic membrane proteins, and tolC and ampC, genes encoding proteins for export through the cytoplasmic membrane, was constructed for studying the effects of transcription and translation of such genes on the hypernegative supercoiling of plasmids in Escherichia coli cells deficient in DNA topoisomerase I. The results support the view that intracellular bacterial DNA is anchored to the cytoplasmic membrane at many points through cotranscriptional synthesis of membrane proteins or proteins designated for export across the cytoplasmic membrane; in the latter case, the presence of the signal peptide appears to be unnecessary for cotranscriptional membrane association.
机译:构建了一组同源的表达tet,lacY和melB(编码完整细胞质膜蛋白的基因)和tolC和ampC(编码通过细胞质膜输出的蛋白的基因)的质粒,以研究此类基因在转录和翻译上的影响。 DNA拓扑异构酶I缺乏的大肠杆菌细胞中质粒的超负超螺旋。结果支持以下观点:细胞内细菌DNA通过膜蛋白或指定跨细胞膜输出的蛋白的共转录合成在许多点锚定到细胞质膜上。在后一种情况下,信号肽的存在似乎对于共转录膜缔合是不必要的。

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