A Dynamic Network of Proteins Facilitate Cell Envelope Biogenesis in Gram-Negative Bacteria.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
27 Nov 2021
Historique:
received: 14 10 2021
revised: 02 11 2021
accepted: 03 11 2021
entrez: 10 12 2021
pubmed: 11 12 2021
medline: 27 1 2022
Statut: epublish

Résumé

Bacteria must maintain the ability to modify and repair the peptidoglycan layer without jeopardising its essential functions in cell shape, cellular integrity and intermolecular interactions. A range of new experimental techniques is bringing an advanced understanding of how bacteria regulate and achieve peptidoglycan synthesis, particularly in respect of the central role played by complexes of Sporulation, Elongation or Division (SEDs) and class B penicillin-binding proteins required for cell division, growth and shape. In this review we highlight relationships implicated by a bioinformatic approach between the outer membrane, cytoskeletal components, periplasmic control proteins, and cell elongation/division proteins to provide further perspective on the interactions of these cell division, growth and shape complexes. We detail the network of protein interactions that assist in the formation of peptidoglycan and highlight the increasingly dynamic and connected set of protein machinery and macrostructures that assist in creating the cell envelope layers in Gram-negative bacteria.

Identifiants

pubmed: 34884635
pii: ijms222312831
doi: 10.3390/ijms222312831
pmc: PMC8657477
pii:
doi:

Substances chimiques

Bacterial Proteins 0
Penicillin-Binding Proteins 0
Peptidoglycan 0
Periplasmic Proteins 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Biotechnology and Biological Sciences Research Council
ID : BB/M01116X/1
Pays : United Kingdom
Organisme : Diamond Light Source
ID : STU0212
Organisme : Medical Research Council
ID : MR/J003964/1
Pays : United Kingdom

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Auteurs

Chris L B Graham (CLB)

School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.

Hector Newman (H)

School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.

Francesca N Gillett (FN)

School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.
School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.

Katie Smart (K)

School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.

Nicholas Briggs (N)

School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.

Manuel Banzhaf (M)

School of Biosciences, University of Birmingham, Birmingham B15 2TT, UK.

David I Roper (DI)

School of Life Sciences, University of Warwick, Coventry CV4 7AL, UK.

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