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Simulations suggest a constrictive force is required for Gram-negative bacterial cell division

机译:模拟表明革兰氏阴性细菌细胞分裂需要收缩力

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To divide, Gram-negative bacterial cells must remodel cell wall at the division site. It remains debated, however, whether this cell wall remodeling alone can drive membrane constriction, or if a constrictive force from the tubulin homolog FtsZ is required. Previously, we constructed software (REMODELER 1) to simulate cell wall remodeling during growth. Here, we expanded this software to explore cell wall division (REMODELER 2). We found that simply organizing cell wall synthesis complexes at the midcell is not sufficient to cause invagination, even with the implementation of a make-before-break mechanism, in which new hoops of cell wall are made inside the existing hoops before bonds are cleaved. Division can occur, however, when a constrictive force brings the midcell into a compressed state before new hoops of relaxed cell wall are incorporated between existing hoops. Adding a make-before-break mechanism drives division with a smaller constrictive force sufficient to bring the midcell into a relaxed, but not necessarily compressed, state.
机译:为了分裂,革兰氏阴性细菌细胞必须在分裂部位重塑细胞壁。然而,仍然有争议的是,这种细胞壁重塑是否可以单独驱动膜收缩,或者是否需要来自微管蛋白同源物FtsZ的收缩力。以前,我们构建了软件(REMODELER 1)来模拟细胞壁在生长过程中的重塑。在这里,我们扩展了该软件以探索细胞壁分裂(REMODELER 2)。我们发现,即使在先断裂机制的实现下,仅在中部细胞组织细胞壁合成复合物仍不足以引起内陷,在先断裂机制中,在分裂之前先在现有的环内部制造新的细胞壁环。但是,当收缩力使中层细胞进入压缩状态,然后在现有箍之间合并新的松弛细胞壁箍时,会发生分裂。添加“先断后合”机制可以以较小的收缩力驱动分裂,该收缩力足以使中层细胞进入松弛状态(但不一定是压缩状态)。

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