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MicrobiologybioRxiv
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A single conserved residue in FlhA couples export gate activation to substrate specificity switching

Miki KinoshitaiD, Tohru MinaminoiD, Motoshi Sakai, Norihiro TakekawaiD, Takayuki UchihashiiD, Akio KitaoiD, Katsumi ImadaiD, Keiichi NambaiD

Abstract

FlhA is a core component of the bacterial flagellar type III secretion system that functions as both an export engine and a switch regulator of substrate specificity. How these two processes are mechanistically coupled remains unclear. Here we identify a single conserved residue in FlhA, Arg-391, as a key molecular node that links export gate activation to substrate specificity switching. The R391A substitution blocks the transition from hook-type to filament-type secretion, resulting in polyhooks lacking filaments. An intermolecular salt-bridge formation of Arg-391 with Glu-351 of an adjacent FlhA subunit stabilizes the filament-type FlhA ring. Suppressor mutations in FlhA and the ruler protein FliK restore this interaction, indicating that FliK promotes the intermolecular salt-bridge formation during export switching. Moreover, Arg-391 is required for efficient ATPase-independent activation of the export gate. Together, these findings reveal an electrostatic mechanism by which FlhA coordinates export gate activation and substrate specificity switching during flagellar assembly.

PDFDOI

02 /Specification & Classification

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