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重建实验和基因缺失揭示了棒状杆菌属中两种主要细胞壁通道的存在。

Reconstitution experiments and gene deletions reveal the existence of two-component major cell wall channels in the genus Corynebacterium.

机构信息

Rudolf Virchow Center, University of Würzburg, D-97078 Würzburg, Germany.

出版信息

J Bacteriol. 2010 Feb;192(3):786-800. doi: 10.1128/JB.01142-09. Epub 2009 Dec 4.

Abstract

Two small polypeptides, PorA and PorH, are known to form cell wall channels in Corynebacterium glutamicum and in Corynebacterium efficiens. The genes coding for both polypeptides are localized in close proximity to one another between the genes coding for GroEl2 and a polyphosphate kinase (PKK2). In this study, we investigated the relationship of PorA and PorH to one another. The results suggested that the major cell wall channels of Corynebacterium glutamicum, Corynebacterium efficiens, and Corynebacterium diphtheriae need the obligatory presence of two distinct polypeptides, one of class PorA and one of class PorH, to form an active cell wall channel. Identification of genes coding for homologous proteins in the chromosome of Corynebacterium callunae suggested a similar result for this strain. Contrary to our previous reports on channel-forming proteins in these strains, a heterooligomeric structure composed of PorA and PorH is needed in all of them to form the major cell wall channel. This was concluded from complementation experiments using a porH- and porA-deficient C. glutamicum strain. The stringent necessity of proteins of either class to recover the wild-type channels was demonstrated by black lipid bilayer experiments using detergent or organic solvent extracts of the complemented porH- and porA-deficient C. glutamicum strain. The channel-forming capability of recombinant expressed, affinity-purified PorA and PorH proteins of C. glutamicum revealed that the channels consisted solely of these two components. This agreed with results obtained from a transcript coding for both channel-forming components identified in C. glutamicum by Northern blot analysis and reverse transcription-PCR analysis. The transcription start point of the genes was determined by the rapid amplification of cDNA ends approach, allowing the prediction of the -35 and -10 regions of the promoter. The results demonstrate that the cell wall channels within the genus Corynebacterium may be formed by two-component oligomers.

摘要

两种小的多肽 PorA 和 PorH 被认为在谷氨酸棒杆菌和有效棒杆菌中形成细胞壁通道。编码这两种多肽的基因位于 GroEl2 基因和多聚磷酸激酶 (PKK2) 编码基因之间的紧密接近位置。在这项研究中,我们研究了 PorA 和 PorH 之间的关系。结果表明,谷氨酸棒杆菌、有效棒杆菌和白喉棒杆菌的主要细胞壁通道需要两种不同的多肽,一种是 PorA 类,另一种是 PorH 类,才能形成活性细胞壁通道。在棒杆菌属 cal l uneae 的染色体中鉴定出编码同源蛋白的基因,这表明该菌株也存在类似的结果。与我们之前在这些菌株中关于通道形成蛋白的报告相反,所有这些菌株都需要由 PorA 和 PorH 组成的异源寡聚体结构才能形成主要的细胞壁通道。这是通过使用 porH 和 porA 缺陷型 C. glutamicum 菌株进行的互补实验得出的结论。使用去污剂或互补的 porH 和 porA 缺陷型 C. glutamicum 菌株的有机溶剂提取物进行黑质双层实验,证明了这两种蛋白质中的任何一种恢复野生型通道的严格必要性。使用谷氨酸棒杆菌的重组表达、亲和纯化的 PorA 和 PorH 蛋白进行的通道形成能力实验表明,这些通道仅由这两种成分组成。这与通过 Northern blot 分析和逆转录-PCR 分析在谷氨酸棒杆菌中鉴定出的两种通道形成成分的转录物编码结果一致。通过快速扩增 cDNA 末端方法确定了基因的转录起始点,允许预测启动子的 -35 和 -10 区域。结果表明,棒杆菌属内的细胞壁通道可能由两种成分的寡聚物形成。

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