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  1. Article: Timing of TolA and TolQ Recruitment at the Septum Depends on the Functionality of the Tol-Pal System

    Baccelli, Pauline / Rachedi, Raphaël / Serrano, Bastien / Petiti, Mélissa / Bernard, Christophe S / Houot, Laetitia / Duche, Denis

    Journal of molecular biology. 2022 Apr. 15, v. 434, no. 7

    2022  

    Abstract: Efficient cell division of Gram-negative bacteria requires the presence of the Tol-Pal system to coordinate outer membrane (OM) invagination with inner membrane invagination (IM) and peptidoglycan (PG) remodeling. The Tol-Pal system is a trans-envelope ... ...

    Abstract Efficient cell division of Gram-negative bacteria requires the presence of the Tol-Pal system to coordinate outer membrane (OM) invagination with inner membrane invagination (IM) and peptidoglycan (PG) remodeling. The Tol-Pal system is a trans-envelope complex that connects the three layers of the cell envelope through an energy-dependent process. It is composed of the three IM proteins, TolA, TolQ and TolR, the periplasmic protein TolB and the OM lipoprotein Pal. The proteins of the Tol-Pal system are dynamically recruited to the cell septum during cell division. TolA, the central hub of the Tol-Pal system, has three domains: a transmembrane helix (TolA₁), a long second helical periplasmic domain (TolA₂) and a C-terminal globular domain (TolA₃). The TolQR complex uses the PMF to energize TolA, allowing its cyclic interaction via TolA₃ with the OM TolB-Pal complex. Here, we confirm that TolA₂ is sufficient to address TolA to the site of constriction, whereas TolA₁ is recruited by TolQ. Analysis of the protein localization as function of the bacterial cell age revealed that TolA and TolQ localize earlier at midcell in the absence of the other Tol-Pal proteins. These data suggest that TolA and TolQ are delayed from their septal recruitment by the multiple interactions of TolA with TolB-Pal in the cell envelope providing a new example of temporal regulation of proteins recruitment at the septum.
    Keywords cell division ; lipoproteins ; molecular biology ; peptidoglycans
    Language English
    Dates of publication 2022-0415
    Publishing place Elsevier Ltd
    Document type Article
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2022.167519
    Database NAL-Catalogue (AGRICOLA)

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  2. Article ; Online: Timing of TolA and TolQ Recruitment at the Septum Depends on the Functionality of the Tol-Pal System.

    Baccelli, Pauline / Rachedi, Raphaël / Serrano, Bastien / Petiti, Mélissa / Bernard, Christophe S / Houot, Laetitia / Duche, Denis

    Journal of molecular biology

    2022  Volume 434, Issue 7, Page(s) 167519

    Abstract: Efficient cell division of Gram-negative bacteria requires the presence of the Tol-Pal system to coordinate outer membrane (OM) invagination with inner membrane invagination (IM) and peptidoglycan (PG) remodeling. The Tol-Pal system is a trans-envelope ... ...

    Abstract Efficient cell division of Gram-negative bacteria requires the presence of the Tol-Pal system to coordinate outer membrane (OM) invagination with inner membrane invagination (IM) and peptidoglycan (PG) remodeling. The Tol-Pal system is a trans-envelope complex that connects the three layers of the cell envelope through an energy-dependent process. It is composed of the three IM proteins, TolA, TolQ and TolR, the periplasmic protein TolB and the OM lipoprotein Pal. The proteins of the Tol-Pal system are dynamically recruited to the cell septum during cell division. TolA, the central hub of the Tol-Pal system, has three domains: a transmembrane helix (TolA
    MeSH term(s) Bacterial Outer Membrane Proteins/metabolism ; Cell Division ; Escherichia coli/cytology ; Escherichia coli/metabolism ; Escherichia coli Proteins/metabolism ; Lipoproteins/metabolism ; Peptidoglycan/metabolism
    Chemical Substances Bacterial Outer Membrane Proteins ; Escherichia coli Proteins ; ExcC protein, E coli ; Lipoproteins ; Peptidoglycan ; tolA protein, E coli ; tolQ protein, E coli (110736-92-0)
    Language English
    Publishing date 2022-02-28
    Publishing country Netherlands
    Document type Journal Article
    ZDB-ID 80229-3
    ISSN 1089-8638 ; 0022-2836
    ISSN (online) 1089-8638
    ISSN 0022-2836
    DOI 10.1016/j.jmb.2022.167519
    Database MEDical Literature Analysis and Retrieval System OnLINE

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