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首页> 外文期刊>Journal of bacteriology >Genetic and Mass Spectrometry Analyses of the Unusual Type IV-Like Pili of the Archaeon Methanococcus maripaludis
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Genetic and Mass Spectrometry Analyses of the Unusual Type IV-Like Pili of the Archaeon Methanococcus maripaludis

机译:遗传和质谱分析古罗马产甲烷球菌的异常IV型菌毛

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摘要

The structure of pili from the archaeon Methanococcus maripaludis is unlike that of any bacterial pili. However, genetic analysis of the genes involved in the formation of these pili has been lacking until this study. Pili were isolated from a nonflagellated (ΔflaK) mutant and shown by sodium dodecyl sulfate-polyacrylamide gel electrophoresis to consist primarily of subunits with an apparent molecular mass of 17 kDa. In-frame deletions were created in three genes, MMP0233, MMP0236, and MMP0237, which encode proteins with bacterial type IV pilin-like signal peptides previously identified by in silico methodology as likely candidates for pilus structural proteins. Deletion of MMP0236 or MMP0237 resulted in mutant cells completely devoid of pili on the cell surface, while deletion of the third pilin-like gene, MMP0233, resulted in cells greatly reduced in the number of pili on the surface. Complementation with the deleted gene in each case returned the cells to a piliated state. Surprisingly, mass spectrometry analysis of purified pili identified the major structural pilin as another type IV pilin-like protein, MMP1685, whose gene is located outside the first pilus locus. This protein was found to be glycosylated with an N-linked branched pentasaccharide glycan. Deletion and complementation analysis confirmed that MMP1685 is required for piliation.
机译:产自古细菌的甲烷单球菌的菌毛的结构不同于任何细菌菌毛的结构。但是,直到进行这项研究之前,都缺乏对这些菌毛形成相关基因的遗传分析。菌毛是从无鞭毛的(Δ flaK )突变体中分离得到的,十二烷基硫酸钠-聚丙烯酰胺凝胶电泳显示主要由表观分子量为17 kDa的亚基组成。在三个基因中创建了框内缺失,分别是 MMP0233 MMP0236 MMP0237 ,它们编码具有细菌IV型菌毛蛋白样信号肽的蛋白先前被 in silico 方法确定为菌毛结构蛋白的候选对象。删除 MMP0236 MMP0237 导致突变细胞完全没有菌毛在细胞表面,而删除了第三个菌毛蛋白样基因 MMP0233 ,导致细胞表面菌毛数量大大减少。在每种情况下,与缺失基因的互补使细胞返回到毛细血管状态。出乎意料的是,对纯化菌毛的质谱分析发现,主要结构菌毛蛋白是另一种IV型菌毛蛋白样蛋白MMP1685,其基因位于第一个菌毛基因座之外。发现该蛋白质被N-连接的支链五糖聚糖糖基化。缺失和互补分析证实,MMP1685是必需的。

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