Reduced peptidoglycan synthesis capacity impairs growth of

bacterial cell envelope penicillin-binding proteins peptidoglycan peptidoglycan hydrolases salt stress

Journal

mBio
ISSN: 2150-7511
Titre abrégé: mBio
Pays: United States
ID NLM: 101519231

Informations de publication

Date de publication:
01 Mar 2024
Historique:
medline: 1 3 2024
pubmed: 1 3 2024
entrez: 1 3 2024
Statut: aheadofprint

Résumé

Gram-negative bacteria have a thin peptidoglycan layer between the cytoplasmic and outer membranes protecting the cell from osmotic challenges. Hydrolases of this structure are needed to cleave bonds to allow the newly synthesized peptidoglycan strands to be inserted by synthases. These enzymes need to be tightly regulated and their activities coordinated to prevent cell lysis. To better understand this process in

Identifiants

pubmed: 38426748
doi: 10.1128/mbio.00325-24
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0032524

Auteurs

Dema Alodaini (D)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.

Victor Hernandez-Rocamora (V)

Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.

Gabriela Boelter (G)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.

Xuyu Ma (X)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.

Micheal B Alao (MB)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.

Hannah M Doherty (HM)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.

Jack A Bryant (JA)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.
School of Life Sciences, University of Nottingham, Nottingham, United Kingdom.

Patrick Moynihan (P)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.

Danesh Moradigaravand (D)

KAUST Computational Bioscience Research Center, King Abdullah University of Science and Technology, Thuwal, Makkah, Saudi Arabia.
Laboratory for Infectious Disease Epidemiology, KAUST Smart-Health Initiative and Biological and Environmental Science and Engineering Division, King Abdullah University of Science and Technology, Thuwal, Makkah, Saudi Arabia.

Monika Glinkowska (M)

Department of Bacterial Molecular Genetics, Faculty of Biology, University of Gdańsk, Gdańsk, Poland.

Waldemar Vollmer (W)

Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.
Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia.

Manuel Banzhaf (M)

Institute of Microbiology and Infection, School of Biosciences, University of Birmingham, Birmingham, United Kingdom.
Biosciences Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom.

Classifications MeSH