Chaperone‐mediated coupling of subunit availability to activation of flagellar Type III secretion

• DOI: 10.1111/mmi.14731
• Publication Date: 2021-04-24T00:26:44Z
• Authors: Owain J. Bryant; Betty Y.‐W. Chung; Gillian M. Fraser
• Keywords: Adenosine Triphosphatases; Salmonella typhimurium; 0301 basic medicine; 0303 health sciences; Cell Membrane; proton motive force; Membrane Proteins; Proton-Motive Force; protein export; RESEARCH ARTICLES; Enzyme Activation; RESEARCH ARTICLE; Protein Transport; Type III secretion system; 03 medical and health sciences; Bacterial Proteins; Flagella; Type III Secretion Systems; bacterial flagella biogenesis; Molecular Chaperones

AbstractBacterial flagellar subunits are exported across the cell membrane by the flagellar Type III Secretion System (fT3SS), powered by the proton motive force (pmf) and a specialized ATPase that enables the flagellar export gate to utilize the pmf electric potential (ΔΨ). Export gate activation is mediated by the ATPase stalk, FliJ, but how this process is regulated to prevent wasteful dissipation of pmf in the absence of subunit cargo is not known. Here, we show that FliJ activation of the export gate is regulated by flagellar export chaperones. FliJ binds unladen chaperones and, by using novel chaperone variants specifically defective for FliJ binding, we show that disruption of this interaction attenuates motility and cognate subunit export. We demonstrate in vitro that chaperones and the FlhA export gate component compete for binding to FliJ, and show in vivo that unladen chaperones, which would be present in the cell when subunit levels are low, sequester FliJ to prevent activation of the export gate and attenuate subunit export. Our data indicate a mechanism whereby chaperones couple availability of subunit cargo to pmf‐driven export by the fT3SS.