Nanoscale-length control of the flagellar driveshaft requires hitting the tethered outer membrane
Author(s) -
Eli J. Cohen,
Josie L. Ferreira,
Mark S. Ladinsky,
Morgan Beeby,
Kelly T. Hughes
Publication year - 2017
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aam6512
Subject(s) - flagellum , periplasmic space , nanoscopic scale , bacterial outer membrane , mechanism (biology) , enhanced data rates for gsm evolution , biophysics , nanotechnology , biology , physics , bacteria , materials science , computer science , artificial intelligence , genetics , escherichia coli , gene , quantum mechanics
The bacterial flagellum exemplifies a system where even small deviations from the highly regulated flagellar assembly process can abolish motility and cause negative physiological outcomes. Consequently, bacteria have evolved elegant and robust regulatory mechanisms to ensure that flagellar morphogenesis follows a defined path, with each component self-assembling to predetermined dimensions. The flagellar rod acts as a driveshaft to transmit torque from the cytoplasmic rotor to the external filament. The rod self-assembles to a defined length of ~25 nanometers. Here, we provide evidence that rod length is limited by the width of the periplasmic space between the inner and outer membranes. The length of Braun's lipoprotein determines periplasmic width by tethering the outer membrane to the peptidoglycan layer.
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