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科恩氏菌属质粒pCHAP4的免疫与裂解基因。

The immunity and lysis genes of ColN plasmid pCHAP4.

作者信息

Pugsley A P

机构信息

Unité de Génétique Moléculaire, Institut Pasteur, Paris, France.

出版信息

Mol Gen Genet. 1988 Feb;211(2):335-41. doi: 10.1007/BF00330613.

Abstract

Nucleotide sequencing of part of the plasmid pCHAP4, which encodes the ca. 42,000 Da putative poreforming colicin N, confirmed previous results indicating that the colicin N immunity gene (cni) and the colicin release or lysis gene (cnl) are located immediately downstream from the colicin N structural gene (cna) in the order cna-cni-cnl. The cni gene is transcribed in the opposite direction to cna and probably encodes an Mr 15239 Da protein. The putative immunity protein was detected among the [35S]methionine-labelled proteins produced by minicells carrying cni cloned under lac promoter control, and when the gene was subcloned into expression vectors under the control of a bacteriophage T7 promoter. Deletion of the region immediately upstream from cni completely abolished colicin N immunity, presumably because the natural promoter had been deleted. cnl is in the same operon as cna, and encodes a typical Col plasmid pro-lysis protein comprising a signal peptide and a 34 residue mature polypeptide with high homology to all but one of the other known Col lysis proteins, including the fatty acylated amino-terminal cysteine residue which was specifically labelled with 3H-palmitate. Cell fractionation studies indicated that the cnl gene product was located predominantly in the outer membrane.

摘要

对编码约42,000 Da推定成孔大肠杆菌素N的质粒pCHAP4的部分进行核苷酸测序,证实了先前的结果,表明大肠杆菌素N免疫基因(cni)和大肠杆菌素释放或裂解基因(cnl)按cna - cni - cnl的顺序紧邻大肠杆菌素N结构基因(cna)下游。cni基因的转录方向与cna相反,可能编码一种分子量为15239 Da的蛋白质。在携带在乳糖启动子控制下克隆的cni的小细胞产生的[35S]甲硫氨酸标记的蛋白质中,以及当该基因亚克隆到噬菌体T7启动子控制下的表达载体中时,检测到了推定的免疫蛋白。cni上游紧邻区域的缺失完全消除了大肠杆菌素N的免疫性,推测是因为天然启动子已被删除。cnl与cna在同一个操纵子中,编码一种典型的Col质粒原裂解蛋白,该蛋白包含一个信号肽和一个34个残基的成熟多肽,与所有已知的Col裂解蛋白(除了一个)具有高度同源性,包括用3H - 棕榈酸特异性标记的脂肪酰化氨基末端半胱氨酸残基。细胞分级分离研究表明,cnl基因产物主要位于外膜中。

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