» Articles » PMID: 8298044

Torque Generated by the Flagellar Motor of Escherichia Coli

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 1993 Nov 1
PMID 8298044
Citations 82
Authors
Affiliations
Soon will be listed here.
Abstract

Cells of the bacterium Escherichia coli were tethered and spun in a high-frequency rotating electric field at a series of discrete field strengths. This was done first at low field strengths, then at field strengths generating speeds high enough to disrupt motor function, and finally at low field strengths. Comparison of the initial and final speed versus applied-torque plots yielded relative motor torque. For backward rotation, motor torque rose steeply at speeds close to zero, peaking, on average, at about 2.2 times the stall torque. For forward rotation, motor torque remained approximately constant up to speeds of about 60% of the zero-torque speed. Then the torque dropped linearly with speed, crossed zero, and reached a minimum, on average, at about -1.7 times the stall torque. The zero-torque speed increased with temperature (about 90 Hz at 11 degrees C, 140 Hz at 16 degrees C, and 290 Hz at 23 degrees C), while other parameters remained approximately constant. Sometimes the motor slipped at either extreme (delivered constant torque over a range of speeds), but eventually it broke. Similar results were obtained whether motors broke catastrophically (suddenly and completely) or progressively or were de-energized by brief treatment with an uncoupler. These results are consistent with a tightly coupled ratchet mechanism, provided that elastic deformation of force-generating elements is limited by a stop and that mechanical components yield at high applied torques.

Citing Articles

Physical mechanism reveals bacterial slowdown above a critical number of flagella.

Tatulea-Codrean M, Lauga E J R Soc Interface. 2024; 21(220):20240283.

PMID: 39503268 PMC: 11539103. DOI: 10.1098/rsif.2024.0283.


Torque-speed relationship of the flagellar motor with dual-stator systems in .

Wu H, Wu Z, Tian M, Zhang R, Yuan J mBio. 2024; 15(12):e0074524.

PMID: 39475228 PMC: 11633141. DOI: 10.1128/mbio.00745-24.


Flagellar motor remodeling during swarming requires FliL.

Partridge J, Dufour Y, Hwang Y, Harshey R Mol Microbiol. 2023; 120(5):670-683.

PMID: 37675594 PMC: 10942728. DOI: 10.1111/mmi.15148.


Flagellar motor remodeling during swarming requires FliL.

Partridge J, Dufour Y, Hwang Y, Harshey R bioRxiv. 2023; .

PMID: 37503052 PMC: 10370021. DOI: 10.1101/2023.07.14.549092.


A multi-state dynamic process confers mechano-adaptation to a biological nanomachine.

Wadhwa N, Sassi A, Berg H, Tu Y Nat Commun. 2022; 13(1):5327.

PMID: 36088344 PMC: 9464220. DOI: 10.1038/s41467-022-33075-5.


References
1.
Ishihara A, Segall J, Block S, Berg H . Coordination of flagella on filamentous cells of Escherichia coli. J Bacteriol. 1983; 155(1):228-37. PMC: 217673. DOI: 10.1128/jb.155.1.228-237.1983. View

2.
Khan S, DAPICE M, Humayun I . Energy transduction in the bacterial flagellar motor. Effects of load and pH. Biophys J. 1990; 57(4):779-96. PMC: 1280779. DOI: 10.1016/S0006-3495(90)82598-4. View

3.
Blair D . The bacterial flagellar motor. Semin Cell Biol. 1990; 1(2):75-85. View

4.
Berg H, Block S . A miniature flow cell designed for rapid exchange of media under high-power microscope objectives. J Gen Microbiol. 1984; 130(11):2915-20. DOI: 10.1099/00221287-130-11-2915. View

5.
Maurer L, Orndorff P . Identification and characterization of genes determining receptor binding and pilus length of Escherichia coli type 1 pili. J Bacteriol. 1987; 169(2):640-5. PMC: 211826. DOI: 10.1128/jb.169.2.640-645.1987. View