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枯草芽孢杆菌中青霉素结合蛋白的几种不同定位模式。

Several distinct localization patterns for penicillin-binding proteins in Bacillus subtilis.

作者信息

Scheffers Dirk-Jan, Jones Laura J F, Errington Jeffery

机构信息

Sir William Dunn School of Pathology, University of Oxford, South Parks Road, Oxford OX1 3RE, UK.

出版信息

Mol Microbiol. 2004 Feb;51(3):749-64. doi: 10.1046/j.1365-2958.2003.03854.x.

Abstract

Bacterial cell shape is determined by a rigid external cell wall. In most non-coccoid bacteria, this shape is also determined by an internal cytoskeleton formed by the actin homologues MreB and/or Mbl. To gain further insights into the topological control of cell wall synthesis in bacteria, we have constructed green fluorescent protein (GFP) fusions to all 11 penicillin-binding proteins (PBPs) expressed during vegetative growth of Bacillus subtilis. The localization of these fusions was studied in a wild-type background as well as in strains deficient in FtsZ, MreB or Mbl. PBP3 and PBP4a localized specifically to the lateral wall, in distinct foci, whereas PBP1 and PBP2b localized specifically to the septum. All other PBPs localized to both the septum and the lateral cell wall, sometimes with irregular distribution along the lateral wall or a preference for the septum. This suggests that cell wall synthesis is not dispersed but occurs at specific places along the lateral cell wall. The results implicate PBP3, PBP5 and PBP4a, and possibly PBP4, in lateral wall growth. Localization of PBPs to the septum was found to be dependent on FtsZ, but the GFP-PBP fluorescence patterns were not detectably altered in the absence of MreB or Mbl.

摘要

细菌的细胞形状由坚硬的外部细胞壁决定。在大多数非球菌类细菌中,这种形状还由肌动蛋白同源物MreB和/或Mbl形成的内部细胞骨架决定。为了进一步深入了解细菌细胞壁合成的拓扑控制,我们构建了与枯草芽孢杆菌营养生长期间表达的所有11种青霉素结合蛋白(PBP)的绿色荧光蛋白(GFP)融合体。在野生型背景以及FtsZ、MreB或Mbl缺陷的菌株中研究了这些融合体的定位。PBP3和PBP4a特异性定位于侧壁的不同位点,而PBP1和PBP2b特异性定位于隔膜。所有其他PBP都定位于隔膜和侧壁,有时沿侧壁分布不规则或更倾向于定位于隔膜。这表明细胞壁合成并非分散进行,而是发生在沿侧壁的特定位置。结果表明PBP3、PBP5和PBP4a,可能还有PBP4参与侧壁生长。发现PBP定位于隔膜依赖于FtsZ,但在没有MreB或Mbl的情况下,GFP - PBP荧光模式没有明显改变。

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