» Articles » PMID: 33876769

Mechanosensitive Remodeling of the Bacterial Flagellar Motor is Independent of Direction of Rotation

Overview
Specialty Science
Date 2021 Apr 20
PMID 33876769
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Motility is important for the survival and dispersal of many bacteria, and it often plays a role during infections. Regulation of bacterial motility by chemical stimuli is well studied, but recent work has added a new dimension to the problem of motility control. The bidirectional flagellar motor of the bacterium recruits or releases torque-generating units (stator units) in response to changes in load. Here, we show that this mechanosensitive remodeling of the flagellar motor is independent of direction of rotation. Remodeling rate constants in clockwise rotating motors and in counterclockwise rotating motors, measured previously, fall on the same curve if plotted against torque. Increased torque decreases the off rate of stator units from the motor, thereby increasing the number of active stator units at steady state. A simple mathematical model based on observed dynamics provides quantitative insight into the underlying molecular interactions. The torque-dependent remodeling mechanism represents a robust strategy to quickly regulate output (torque) in response to changes in demand (load).

Citing Articles

Ultrasensitivity without conformational spread: A mechanical origin for non-equilibrium cooperativity in the bacterial flagellar motor.

Mattingly H, Tu Y ArXiv. 2025; .

PMID: 39975436 PMC: 11838781.


Measuring Bacterial Flagellar Motor Dynamics via a Bead Assay.

Hoffmann W, Biquet-Bisquert A, Pedaci F, Nord A Methods Mol Biol. 2024; 2881():43-64.

PMID: 39704937 DOI: 10.1007/978-1-0716-4280-1_2.


Interplay between environmental yielding and dynamic forcing modulates bacterial growth.

Hancock A, Datta S Biophys J. 2024; 123(8):957-967.

PMID: 38454600 PMC: 11052696. DOI: 10.1016/j.bpj.2024.03.008.


Engineered Extracellular Vesicles Driven by Erythrocytes Ameliorate Bacterial Sepsis by Iron Recycling, Toxin Clearing and Inflammation Regulation.

Li Y, Qu G, Dou G, Ren L, Dang M, Kuang H Adv Sci (Weinh). 2024; 11(13):e2306884.

PMID: 38247172 PMC: 10987154. DOI: 10.1002/advs.202306884.


Flagellar motors of swimming bacteria contain an incomplete set of stator units to ensure robust motility.

Niu Y, Zhang R, Yuan J Sci Adv. 2023; 9(44):eadi6724.

PMID: 37922360 PMC: 10624342. DOI: 10.1126/sciadv.adi6724.


References
1.
Kojima S, Imada K, Sakuma M, Sudo Y, Kojima C, Minamino T . Stator assembly and activation mechanism of the flagellar motor by the periplasmic region of MotB. Mol Microbiol. 2009; 73(4):710-8. DOI: 10.1111/j.1365-2958.2009.06802.x. View

2.
Chang Y, Zhang K, Carroll B, Zhao X, Charon N, Norris S . Molecular mechanism for rotational switching of the bacterial flagellar motor. Nat Struct Mol Biol. 2020; 27(11):1041-1047. PMC: 8129871. DOI: 10.1038/s41594-020-0497-2. View

3.
Hug I, Deshpande S, Sprecher K, Pfohl T, Jenal U . Second messenger-mediated tactile response by a bacterial rotary motor. Science. 2017; 358(6362):531-534. DOI: 10.1126/science.aan5353. View

4.
Chen X, Berg H . Torque-speed relationship of the flagellar rotary motor of Escherichia coli. Biophys J. 2000; 78(2):1036-41. PMC: 1300707. DOI: 10.1016/S0006-3495(00)76662-8. View

5.
Chevance F, Hughes K . Coordinating assembly of a bacterial macromolecular machine. Nat Rev Microbiol. 2008; 6(6):455-65. PMC: 5963726. DOI: 10.1038/nrmicro1887. View