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Peptidoglycan synthesis drives a single population of septal cell wall synthases during division in Bacillus subtilis

Abstract:
Bacterial cell division requires septal peptidoglycan (sPG) synthesis by the divisome complex. Treadmilling of the essential tubulin homologue FtsZ has been implicated in septal constriction, though its precise role remains unclear. Here we used live-cell single-molecule imaging of the divisome transpeptidase PBP2B to investigate sPG synthesis dynamics in Bacillus subtilis. In contrast to previous models, we observed a single population of processively moving PBP2B molecules whose motion is driven by peptidoglycan synthesis and is not associated with FtsZ treadmilling. However, despite the asynchronous motions of PBP2B and FtsZ, a partial dependence of PBP2B processivity on FtsZ treadmilling was observed. Additionally, through single-molecule counting experiments we provide evidence that the divisome synthesis complex is multimeric. Our results support a model for B. subtilis division where a multimeric synthesis complex follows a single track dependent on sPG synthesis whose activity and dynamics are asynchronous with FtsZ treadmilling
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41564-024-01650-9

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Role:
Author
ORCID:
0000-0001-9719-6916
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Role:
Author
ORCID:
0000-0002-1276-9912
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Role:
Author
ORCID:
0000-0003-4674-3291
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Role:
Author
ORCID:
0000-0002-1099-4964
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Institution:
University of Oxford
Role:
Author
ORCID:
0000-0001-8800-7669


Publisher:
Nature Research
Journal:
Nature Microbiology More from this journal
Volume:
9
Issue:
4
Pages:
1064-1074
Publication date:
2024-03-13
DOI:
EISSN:
2058-5276
ISSN:
2058-5276


Language:
English
Keywords:
Pubs id:
1857374
Local pid:
pubs:1857374
Source identifiers:
W4392741267
Deposit date:
2025-12-05
ARK identifier:
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