The cell cycle regulator GpsB functions as cytosolic adaptor for multiple cell wall enzymes
Robert M. Cleverley,
Zoe J. Rutter,
Jeanine Rismondo,
Federico Corona,
Ho-Ching Tiffany Tsui,
Fuad A. Alatawi,
Richard A. Daniel,
Sven Halbedel,
Orietta Massidda,
Malcolm E. Winkler and
Richard J. Lewis ()
Additional contact information
Robert M. Cleverley: University of Newcastle
Zoe J. Rutter: University of Newcastle
Jeanine Rismondo: Robert Koch Institute
Federico Corona: Università di Cagliari
Ho-Ching Tiffany Tsui: Indiana University Bloomington
Fuad A. Alatawi: University of Newcastle
Richard A. Daniel: University of Newcastle
Sven Halbedel: Robert Koch Institute
Orietta Massidda: Università di Cagliari
Malcolm E. Winkler: Indiana University Bloomington
Richard J. Lewis: University of Newcastle
Nature Communications, 2019, vol. 10, issue 1, 1-17
Abstract:
Abstract Bacterial growth and cell division requires precise spatiotemporal regulation of the synthesis and remodelling of the peptidoglycan layer that surrounds the cytoplasmic membrane. GpsB is a cytosolic protein that affects cell wall synthesis by binding cytoplasmic mini-domains of peptidoglycan synthases to ensure their correct subcellular localisation. Here, we describe critical structural features for the interaction of GpsB with peptidoglycan synthases from three bacterial species (Bacillus subtilis, Listeria monocytogenes and Streptococcus pneumoniae) and suggest their importance for cell wall growth and viability in L. monocytogenes and S. pneumoniae. We use these structural motifs to identify novel partners of GpsB in B. subtilis and extend the members of the GpsB interactome in all three bacterial species. Our results support that GpsB functions as an adaptor protein that mediates the interaction between membrane proteins, scaffolding proteins, signalling proteins and enzymes to generate larger protein complexes at specific sites in a bacterial cell cycle-dependent manner.
Date: 2019
References: Add references at CitEc
Citations: View citations in EconPapers (1)
Downloads: (external link)
https://www.nature.com/articles/s41467-018-08056-2 Abstract (text/html)
Related works:
This item may be available elsewhere in EconPapers: Search for items with the same title.
Export reference: BibTeX
RIS (EndNote, ProCite, RefMan)
HTML/Text
Persistent link: https://EconPapers.repec.org/RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-018-08056-2
Ordering information: This journal article can be ordered from
https://www.nature.com/ncomms/
DOI: 10.1038/s41467-018-08056-2
Access Statistics for this article
Nature Communications is currently edited by Nathalie Le Bot, Enda Bergin and Fiona Gillespie
More articles in Nature Communications from Nature
Bibliographic data for series maintained by Sonal Shukla () and Springer Nature Abstracting and Indexing ().