| Literature DB >> 32269092 |
Christopher R Mahone1, Erin D Goley2.
Abstract
Bacterial cell division is initiated by the midcell assembly of polymers of the tubulin-like GTPase FtsZ. The FtsZ ring (Z-ring) is a discontinuous structure made of dynamic patches of FtsZ that undergo treadmilling motion. Roughly a dozen additional essential proteins are recruited to the division site by the dynamic Z-ring scaffold and subsequently activate cell wall synthesis to drive cell envelope constriction during division. In this Cell Science at a Glance article and the accompanying poster, we summarize our understanding of the assembly and activation of the bacterial cell division machinery. We introduce polymerization properties of FtsZ and discuss our current knowledge of divisome assembly and activation. We further highlight the intimate relationship between the structure and dynamics of FtsZ and the movement and activity of cell wall synthases at the division site, before concluding with a perspective on the most important open questions on bacterial cell division.Entities:
Keywords: Bacteria; Bacterial cell biology; Cell division; Cytokinesis; FtsZ; Peptidoglycan
Mesh:
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Year: 2020 PMID: 32269092 PMCID: PMC7157936 DOI: 10.1242/jcs.237057
Source DB: PubMed Journal: J Cell Sci ISSN: 0021-9533 Impact factor: 5.285