Detecting Envelope Stress by Monitoring β-Barrel Assembly
Author(s) -
SeungHyun Cho,
Joanna Szewczyk,
Christina Pesavento,
Matylda Zietek,
Manuel Banzhaf,
Paula Roszczenko,
Abir T. Asmar,
Géraldine Laloux,
Ann-Kristin Hov,
Pauline Leverrier,
Charles Van der Henst,
Didier Vertommen,
Athanasios Typas,
JeanFrançois Collet
Publication year - 2014
Publication title -
cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 26.304
H-Index - 776
eISSN - 1097-4172
pISSN - 0092-8674
DOI - 10.1016/j.cell.2014.11.045
Subject(s) - periplasmic space , biology , microbiology and biotechnology , bama , cell envelope , bacterial outer membrane , peptidoglycan , inner membrane , signal transduction , genetics , bacteria , gene , escherichia coli , mitochondrion
The cell envelope protects bacteria from their surroundings. Defects in its integrity or assembly are sensed by signal transduction systems, allowing cells to rapidly adjust. The Rcs phosphorelay responds to outer membrane (OM)- and peptidoglycan-related stress in enterobacteria. We elucidated how the OM lipoprotein RcsF, the upstream Rcs component, senses envelope stress and activates the signaling cascade. RcsF interacts with BamA, the major component of the β-barrel assembly machinery. In growing cells, BamA continuously funnels RcsF through the β-barrel OmpA, displaying RcsF on the cell surface. This process spatially separates RcsF from the downstream Rcs component, which we show is the inner membrane protein IgaA. The Rcs system is activated when BamA fails to bind RcsF and funnel it to OmpA. Newly synthesized RcsF then remains periplasmic, interacting with IgaA to activate the cascade. Thus RcsF senses envelope damage by monitoring the activity of the Bam machinery.
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