Nieweg Annette, Bremer Erhard
Department of Biology, University of Konstanz, PO Box 5560, D-78434 Konstanz, Germany.
Philipps University Marburg, Laboratory for Microbiology, Karl-von-Frisch Str., D-35032 Marburg, Germany.
Microbiology (Reading). 1997 Feb;143 ( Pt 2):603-615. doi: 10.1099/00221287-143-2-603.
The Escherichia coli tsx gene encodes an integral outer-membrane protein (Tsx) that functions as a substrate-specific channel for deoxynucleosides and the antibiotic albicidin, and also serves as a receptor for bacteriophages and colicins. We cloned the structural genes of the Tsx proteins from Salmonella typhimurium, Klebsiella pneumoniae and Enterobacter aerogenes and expressed them in an E.coli tsx mutant. The heterologous Tsx proteins fully substituted the E.coli Tsx protein with respect to its function in deoxynucleoside and albicidin uptake, and as receptor for colicin K. The Tsx proteins from K. pneumoniae and Ent. aerogenes were also proficient as receptors for several Tsx-specific bacteriophages, whereas the corresponding protein from S. typhimurium did not confer sensitivity against these phages. The nucleotide sequence of the tsx genes from S. typhimurium, K. pneumoniae and Ent. aerogenes was established. Each of the Tsx proteins is initially synthesized with typical bacterial signal sequence peptides and the predicted mature forms of the Tsx proteins have a calculated M(r) of 30,567 (265 residues), 31,412 (272 residues) and 31,477 (272 residues), respectively. Multiple sequence alignments between the Tsx proteins showed a high degree of sequence identity and revealed the presence of four hypervariable regions, which are thought to constitute segments of the polypeptide chain exposed at the cell surface. Most notable was a deletion of 8 amino acids in one of these hypervariable domains in the S. typhimurium Tsx protein. When this deletion was introduced by site-directed mutagenesis into the corresponding region of the E.coli tsx gene, the mutant Tsx-515 protein lost its phage receptor function but still served as a colicin K receptor and as a substrate-specific channel, indicating that the region between residues 198 and 207 might be part of the bacteriophage receptor area. Multiple sequence alignments, structural predictions and the properties of previously characterized Tsx missense mutants were taken into account to develop a two-dimensional model for the topological organization of the Tsx protein within the outer membrane.
大肠杆菌tsx基因编码一种完整的外膜蛋白(Tsx),它作为脱氧核苷和抗生素杀稻瘟菌素的底物特异性通道,同时也是噬菌体和大肠杆菌素的受体。我们从鼠伤寒沙门氏菌、肺炎克雷伯菌和产气肠杆菌中克隆了Tsx蛋白的结构基因,并在大肠杆菌tsx突变体中进行表达。这些异源Tsx蛋白在脱氧核苷和杀稻瘟菌素摄取功能以及作为大肠杆菌素K受体方面完全替代了大肠杆菌Tsx蛋白。肺炎克雷伯菌和产气肠杆菌的Tsx蛋白也是几种Tsx特异性噬菌体的有效受体,而鼠伤寒沙门氏菌的相应蛋白则不能赋予对这些噬菌体的敏感性。确定了鼠伤寒沙门氏菌、肺炎克雷伯菌和产气肠杆菌tsx基因的核苷酸序列。每个Tsx蛋白最初都与典型的细菌信号序列肽一起合成,预测的Tsx蛋白成熟形式的计算分子量分别为30,567(265个残基)、31,412(272个残基)和31,477(272个残基)。Tsx蛋白之间的多序列比对显示出高度的序列同一性,并揭示了四个高变区存在,这些区域被认为构成了暴露于细胞表面的多肽链片段。最值得注意的是,鼠伤寒沙门氏菌Tsx蛋白的这些高变域之一中缺失了8个氨基酸。当通过定点诱变将此缺失引入大肠杆菌tsx基因的相应区域时,突变的Tsx-515蛋白失去了其噬菌体受体功能,但仍作为大肠杆菌素K受体和底物特异性通道,这表明198至207位残基之间的区域可能是噬菌体受体区域的一部分。考虑到多序列比对、结构预测以及先前表征的Tsx错义突变体的特性,构建了Tsx蛋白在外膜内拓扑组织的二维模型。