Bacterial Cell Biology and Physiology, Swammerdam Institute for Life Science, University of Amsterdam, 1098 XH Amsterdam, The Netherlands.
Int J Mol Sci. 2022 Mar 24;23(7):3537. doi: 10.3390/ijms23073537.
The synthesis of a peptidoglycan septum is a fundamental part of bacterial fission and is driven by a multiprotein dynamic complex called the divisome. FtsW and FtsI are essential proteins that synthesize the peptidoglycan septum and are controlled by the regulatory FtsBLQ subcomplex and the activator FtsN. However, their mode of regulation has not yet been uncovered in detail. Understanding this process in detail may enable the development of new compounds to combat the rise in antibiotic resistance. In this review, recent data on the regulation of septal peptidoglycan synthesis is summarized and discussed. Based on structural models and the collected data, multiple putative interactions within FtsWI and with regulators are uncovered. This elaborates on and supports an earlier proposed model that describes active and inactive conformations of the septal peptidoglycan synthesis complex that are stabilized by these interactions. Furthermore, a new model on the spatial organization of the newly synthesized peptidoglycan and the synthesis complex is presented. Overall, the updated model proposes a balance between several allosteric interactions that determine the state of septal peptidoglycan synthesis.
肽聚糖隔膜的合成是细菌分裂的基本部分,由一个称为分裂体的多蛋白动态复合物驱动。FtsW 和 FtsI 是合成肽聚糖隔膜的必需蛋白,受调节 FtsBLQ 亚基和激活因子 FtsN 控制。然而,它们的调节方式尚未详细揭示。详细了解这一过程可能会促使开发新的化合物来对抗抗生素耐药性的上升。在这篇综述中,总结和讨论了最近关于隔膜肽聚糖合成调节的研究数据。基于结构模型和收集的数据,揭示了 FtsWI 内和与调节剂之间的多个假定相互作用。这阐述并支持了一个早期提出的模型,该模型描述了由这些相互作用稳定的隔膜肽聚糖合成复合物的活性和非活性构象。此外,还提出了一个关于新合成的肽聚糖和合成复合物的空间组织的新模型。总的来说,更新的模型提出了几个变构相互作用之间的平衡,这些相互作用决定了隔膜肽聚糖合成的状态。