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首页> 外文期刊>eLife journal >An essential Staphylococcus aureus cell division protein directly regulates FtsZ dynamics
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An essential Staphylococcus aureus cell division protein directly regulates FtsZ dynamics

机译:必需的金黄色葡萄球菌细胞分裂蛋白直接调节FtsZ动态

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Binary fission has been well studied in rod-shaped bacteria, but the mechanisms underlying cell division in spherical bacteria are poorly understood. Rod-shaped bacteria harbor regulatory proteins that place and remodel the division machinery during cytokinesis. In the spherical human pathogen Staphylococcus aureus , we found that the essential protein GpsB localizes to mid-cell during cell division and co-constricts with the division machinery. Depletion of GpsB arrested cell division and led to cell lysis, whereas overproduction of GpsB inhibited cell division and led to the formation of enlarged cells. We report that S. aureus GpsB, unlike other Firmicutes GpsB orthologs, directly interacts with the core divisome component FtsZ. GpsB bundles and organizes FtsZ filaments and also stimulates the GTPase activity of FtsZ. We propose that GpsB orchestrates the initial stabilization of the Z-ring at the onset of cell division and participates in the subsequent remodeling of the divisome during cytokinesis.
机译:在杆状细菌中对二元裂变已经进行了很好的研究,但对球形细菌中细胞分裂的潜在机制了解甚少。杆状细菌带有调节蛋白,可在胞质分裂过程中放置​​并重塑分裂机制。在球形人类病原体金黄色葡萄球菌中,我们发现必需蛋白GpsB在细胞分裂过程中定位于中层细胞,并与分裂机制共同收缩。 GpsB的耗尽会阻止细胞分裂并导致细胞裂解,而GpsB的过量生产会抑制细胞分裂并导致形成扩大的细胞。我们报告金黄色葡萄球菌GpsB,不同于其他Firmicutes GpsB直系同源物,直接与核心divisome组件FtsZ相互作用。 GpsB捆扎并组织FtsZ细丝,还刺激FtsZ的GTPase活性。我们建议,GpsB协调在细胞分裂开始时Z环的初始稳定,并在胞质分裂过程中参与对divisome的后续重塑。

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