Literature DB >> 17189361

On torque and tumbling in swimming Escherichia coli.

Nicholas C Darnton1, Linda Turner, Svetlana Rojevsky, Howard C Berg.   

Abstract

Bacteria swim by rotating long thin helical filaments, each driven at its base by a reversible rotary motor. When the motors of peritrichous cells turn counterclockwise (CCW), their filaments form bundles that drive the cells forward. We imaged fluorescently labeled cells of Escherichia coli with a high-speed charge-coupled-device camera (500 frames/s) and measured swimming speeds, rotation rates of cell bodies, and rotation rates of flagellar bundles. Using cells stuck to glass, we studied individual filaments, stopping their rotation by exposing the cells to high-intensity light. From these measurements we calculated approximate values for bundle torque and thrust and body torque and drag, and we estimated the filament stiffness. For both immobilized and swimming cells, the motor torque, as estimated using resistive force theory, was significantly lower than the motor torque reported previously. Also, a bundle of several flagella produced little more torque than a single flagellum produced. Motors driving individual filaments frequently changed directions of rotation. Usually, but not always, this led to a change in the handedness of the filament, which went through a sequence of polymorphic transformations, from normal to semicoiled to curly 1 and then, when the motor again spun CCW, back to normal. Motor reversals were necessary, although not always sufficient, to cause changes in filament chirality. Polymorphic transformations among helices having the same handedness occurred without changes in the sign of the applied torque.

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Year:  2006        PMID: 17189361      PMCID: PMC1855780          DOI: 10.1128/JB.01501-06

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  28 in total

1.  Torque-speed relationship of the flagellar rotary motor of Escherichia coli.

Authors:  X Chen; H C Berg
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

2.  Real-time imaging of fluorescent flagellar filaments.

Authors:  L Turner; W S Ryu; H C Berg
Journal:  J Bacteriol       Date:  2000-05       Impact factor: 3.490

Review 3.  Flagellar movement driven by proton translocation.

Authors:  David F Blair
Journal:  FEBS Lett       Date:  2003-06-12       Impact factor: 4.124

Review 4.  The rotary motor of bacterial flagella.

Authors:  Howard C Berg
Journal:  Annu Rev Biochem       Date:  2002-12-11       Impact factor: 23.643

5.  Biomechanics: bacterial flagellar switching under load.

Authors:  Karen A Fahrner; William S Ryu; Howard C Berg
Journal:  Nature       Date:  2003-06-26       Impact factor: 49.962

6.  Reversal of flagellar rotation in monotrichous and peritrichous bacteria: generation of changes in direction.

Authors:  B L Taylor; D E Koshland
Journal:  J Bacteriol       Date:  1974-08       Impact factor: 3.490

7.  Change in direction of flagellar rotation is the basis of the chemotactic response in Escherichia coli.

Authors:  S H Larsen; R W Reader; E N Kort; W W Tso; J Adler
Journal:  Nature       Date:  1974-05-03       Impact factor: 49.962

8.  Bacteria swim by rotating their flagellar filaments.

Authors:  H C Berg; R A Anderson
Journal:  Nature       Date:  1973-10-19       Impact factor: 49.962

9.  Chemotaxis in Escherichia coli analysed by three-dimensional tracking.

Authors:  H C Berg; D A Brown
Journal:  Nature       Date:  1972-10-27       Impact factor: 49.962

10.  Nonchemotactic mutants of Escherichia coli.

Authors:  J B Armstrong; J Adler; M M Dahl
Journal:  J Bacteriol       Date:  1967-01       Impact factor: 3.490

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  99 in total

1.  Motor-driven bacterial flagella and buckling instabilities.

Authors:  R Vogel; H Stark
Journal:  Eur Phys J E Soft Matter       Date:  2012-02-29       Impact factor: 1.890

2.  Stochastic coordination of multiple actuators reduces latency and improves chemotactic response in bacteria.

Authors:  Michael W Sneddon; William Pontius; Thierry Emonet
Journal:  Proc Natl Acad Sci U S A       Date:  2011-12-27       Impact factor: 11.205

3.  Microscopic analysis of bacterial motility at high pressure.

Authors:  Masayoshi Nishiyama; Yoshiyuki Sowa
Journal:  Biophys J       Date:  2012-04-18       Impact factor: 4.033

4.  Dynamics of bacterial swarming.

Authors:  Nicholas C Darnton; Linda Turner; Svetlana Rojevsky; Howard C Berg
Journal:  Biophys J       Date:  2010-05-19       Impact factor: 4.033

5.  Visualization of Flagella during bacterial Swarming.

Authors:  Linda Turner; Rongjing Zhang; Nicholas C Darnton; Howard C Berg
Journal:  J Bacteriol       Date:  2010-04-02       Impact factor: 3.490

6.  Force-extension curves of bacterial flagella.

Authors:  R Vogel; H Stark
Journal:  Eur Phys J E Soft Matter       Date:  2010-11-04       Impact factor: 1.890

7.  Counterclockwise circular motion of bacteria swimming at the air-liquid interface.

Authors:  Laurence Lemelle; Jean-François Palierne; Elodie Chatre; Christophe Place
Journal:  J Bacteriol       Date:  2010-10-01       Impact factor: 3.490

8.  Bacterial Motility Reveals Unknown Molecular Organization.

Authors:  Ismaël Duchesne; Simon Rainville; Tigran Galstian
Journal:  Biophys J       Date:  2015-11-17       Impact factor: 4.033

9.  Direct observation of rotation and steps of the archaellum in the swimming halophilic archaeon Halobacterium salinarum.

Authors:  Yoshiaki Kinosita; Nariya Uchida; Daisuke Nakane; Takayuki Nishizaka
Journal:  Nat Microbiol       Date:  2016-08-26       Impact factor: 17.745

10.  Single-cell E. coli response to an instantaneously applied chemotactic signal.

Authors:  Takashi Sagawa; Yu Kikuchi; Yuichi Inoue; Hiroto Takahashi; Takahiro Muraoka; Kazushi Kinbara; Akihiko Ishijima; Hajime Fukuoka
Journal:  Biophys J       Date:  2014-08-05       Impact factor: 4.033

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