Cell cycle dependent coordination of surface layer biogenesis in Caulobacter crescentus.


Journal

Nature communications
ISSN: 2041-1723
Titre abrégé: Nat Commun
Pays: England
ID NLM: 101528555

Informations de publication

Date de publication:
18 Apr 2024
Historique:
received: 23 06 2023
accepted: 04 04 2024
medline: 19 4 2024
pubmed: 19 4 2024
entrez: 18 4 2024
Statut: epublish

Résumé

Surface layers (S-layers) are proteinaceous, two-dimensional paracrystalline arrays that constitute a major component of the cell envelope in many prokaryotic species. In this study, we investigated S-layer biogenesis in the bacterial model organism Caulobacter crescentus. Fluorescence microscopy revealed localised incorporation of new S-layer at the poles and mid-cell, consistent with regions of cell growth in the cell cycle. Light microscopy and electron cryotomography investigations of drug-treated bacteria revealed that localised S-layer insertion is retained when cell division is inhibited, but is disrupted upon dysregulation of MreB or lipopolysaccharide. We further uncovered that S-layer biogenesis follows new peptidoglycan synthesis and localises to regions of high cell wall turnover. Finally, correlated cryo-light microscopy and electron cryotomographic analysis of regions of S-layer insertion showed the presence of discontinuities in the hexagonal S-layer lattice, contrasting with other S-layers completed by defined symmetric defects. Our findings present insights into how C. crescentus cells form an ordered S-layer on their surface in coordination with the biogenesis of other cell envelope components.

Identifiants

pubmed: 38637514
doi: 10.1038/s41467-024-47529-5
pii: 10.1038/s41467-024-47529-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

3355

Subventions

Organisme : Human Frontier Science Program (HFSP)
ID : RGY0074/2021
Organisme : Wellcome Trust (Wellcome)
ID : 225317/Z/22/Z
Organisme : Leverhulme Trust
ID : Philip Leverhulme Prize

Informations de copyright

© 2024. The Author(s).

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Auteurs

Matthew Herdman (M)

Sir William Dunn School of Pathology, University of Oxford, Oxford, OX1 3RE, UK.

Buse Isbilir (B)

Structural Studies Division, MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.

Andriko von Kügelgen (A)

Sir William Dunn School of Pathology, University of Oxford, Oxford, OX1 3RE, UK.
Structural Studies Division, MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.

Ulrike Schulze (U)

Cell Biology Division, MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK.

Alan Wainman (A)

Sir William Dunn School of Pathology, University of Oxford, Oxford, OX1 3RE, UK.

Tanmay A M Bharat (TAM)

Structural Studies Division, MRC Laboratory of Molecular Biology, Cambridge, CB2 0QH, UK. tbharat@mrc-lmb.cam.ac.uk.

Classifications MeSH