首页> 外文期刊>Molecular Microbiology >Topological regulation of cell division in Escherichia coli involves rapid pole to pole oscillation of the division inhibitor MinC under the control of MinD and MinE.
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Topological regulation of cell division in Escherichia coli involves rapid pole to pole oscillation of the division inhibitor MinC under the control of MinD and MinE.

机译:大肠杆菌中细胞分裂的拓扑调节涉及在MinD和MinE的控制下分裂抑制剂MinC的快速极到极振荡。

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摘要

Placement of the Z ring at midcell in Escherichia coli is assured by the action of the min system, which blocks usage of potential division sites that exist at the cell poles. This activity of min is achieved through the action of an inhibitor of division, MinC, that is activated by MinD and topologically regulated by MinE. In this study, we have used a functional GFP-MinC fusion to monitor the location of MinC. We find that GFP-MinC is a cytoplasmic protein in the absence of the other Min proteins. The addition of MinD, a peripheral membrane protein that interacts with MinC, results in GFP-MinC appearing on the membrane. In the presence of both MinD and MinE, GFP-MinC oscillates rapidly between the halves of the cell. Thus, MinC is positioned by the other Min products, but in a dynamic manner so that it is in position to inhibit Z ring assembly away from midcell.
机译:min系统的作用确保了Z环在大肠杆菌中细胞的位置,这阻止了细胞两极存在的潜在分裂位点的使用。 min的这种活性是通过分裂抑制剂MinC的作用来实现的,该分裂抑制剂受MinD激活并受MinE拓扑调控。在这项研究中,我们使用了功能性GFP-MinC融合体来监测MinC的位置。我们发现GFP-MinC是在没有其他Min蛋白的情况下的细胞质蛋白。 MinD(一种与MinC相互作用的外周膜蛋白)的添加导致GFP-MinC出现在膜上。在MinD和MinE均存在的情况下,GFP-MinC在细胞的两半之间快速振荡。因此,MinC由其他Min产品定位,但以动态方式定位,以使其能够阻止Z环组件离开中孔。

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