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与生长速率相关的中间FtsZ环形成调控

Growth rate-dependent regulation of medial FtsZ ring formation.

作者信息

Weart Richard B, Levin Petra Anne

机构信息

Department of Biology, Washington University, St. Louis, Missouri 63130, USA.

出版信息

J Bacteriol. 2003 May;185(9):2826-34. doi: 10.1128/JB.185.9.2826-2834.2003.

Abstract

FtsZ is an essential cell division protein conserved throughout the bacteria and archaea. In response to an unknown cell cycle signal, FtsZ polymerizes into a ring that establishes the future division site. We conducted a series of experiments examining the link between growth rate, medial FtsZ ring formation, and the intracellular concentration of FtsZ in the gram-positive bacterium Bacillus subtilis. We found that, although the frequency of cells with FtsZ rings varies as much as threefold in a growth rate-dependent manner, the average intracellular concentration of FtsZ remains constant irrespective of doubling time. Additionally, expressing ftsZ solely from a constitutive promoter, thereby eliminating normal transcriptional control, did not alter the growth rate regulation of medial FtsZ ring formation. Finally, our data indicate that overexpressing FtsZ does not dramatically increase the frequency of cells with medial FtsZ rings, suggesting that the mechanisms governing ring formation are refractile to increases in FtsZ concentration. These results support a model in which the timing of FtsZ assembly is governed primarily through cell cycle-dependent changes in FtsZ polymerization kinetics and not simply via oscillations in the intracellular concentration of FtsZ. Importantly, this model can be extended to the gram-negative bacterium Escherichia coli. Our data show that, like those in B. subtilis, average FtsZ levels in E. coli are constant irrespective of doubling time.

摘要

FtsZ是一种在细菌和古菌中都保守的必需细胞分裂蛋白。响应未知的细胞周期信号,FtsZ聚合形成一个环,确定未来的分裂位点。我们进行了一系列实验,研究革兰氏阳性细菌枯草芽孢杆菌的生长速率、中间FtsZ环形成与FtsZ细胞内浓度之间的联系。我们发现,尽管带有FtsZ环的细胞频率以生长速率依赖的方式变化多达三倍,但FtsZ的平均细胞内浓度与倍增时间无关,保持恒定。此外,仅从组成型启动子表达ftsZ,从而消除正常的转录控制,并没有改变中间FtsZ环形成的生长速率调节。最后,我们的数据表明,过表达FtsZ不会显著增加带有中间FtsZ环的细胞频率,这表明控制环形成的机制对FtsZ浓度的增加具有抗性。这些结果支持了一个模型,其中FtsZ组装的时间主要通过FtsZ聚合动力学中依赖细胞周期的变化来控制,而不仅仅是通过FtsZ细胞内浓度的振荡。重要的是,这个模型可以扩展到革兰氏阴性细菌大肠杆菌。我们的数据表明,与枯草芽孢杆菌中的情况一样,大肠杆菌中的平均FtsZ水平与倍增时间无关,保持恒定。

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