Literature DB >> 264676

Bacterial flagella rotating in bundles: a study in helical geometry.

R M Macnab.   

Abstract

Bacterial flagella are semi-rigid helices that undergo true rotation. In peritrichously flagellated bacteria (e.g., Escherichia and Salmonella) there are many flagella on each cell; during translational cell movement these operate as a coordinated bundle that actively disperses upon reversal of the rotation sense. The dynamic behavior of a set of helices originating on separate rotational axes is explored by a working model, geometrical analysis, and hydrodynamic calculations. A critical relationship exists between the interaxial separation and phase difference of parallel helices with overlapping domains; in the subcritical case the filaments are not intertwisted, whereas in the supercritical case they are intertwisted in the same sense (left-handed) as the helices, with one twist per helical turn. During counter-clockwise rotation (the sense operative in forward swimming) any preexisting twists of this kind are automatically cancelled and the helices brought progressively into phase. Hydrodynamic calculations suggest that some wrapping then occurs in a right-handed sense, opposite to that of the helices; this necessitates a distortion from true helical geometry which is minimized by maintaining a coaxial in-phase relationship. A highly coordinated helical bundle results that is capable of operating smoothly for an indefinite period, in agreement with the observed behavior of swimming bacteria. During reverse rotation, the supercritical case develops to cause jamming of the bundle, as has been observed with bacteria in high-viscosity medium. The explosive dispersal of the bundle during reversal in low-viscosity medium is a consequence of a complicating phenomenon, namely, a drastic change in flagellar quaternary structure. The overall conclusion is that bundle formation and function are perfectly compatible with a rotational mechanism for the individual flagella.

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Year:  1977        PMID: 264676      PMCID: PMC393230          DOI: 10.1073/pnas.74.1.221

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  16 in total

1.  The structure of DNA.

Authors:  J D WATSON; F H CRICK
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1953

2.  Flagellar rotation and the mechanism of bacterial motility.

Authors:  M Silverman; M Simon
Journal:  Nature       Date:  1974-05-03       Impact factor: 49.962

3.  Dynamic properties of bacterial flagellar motors.

Authors:  H C Berg
Journal:  Nature       Date:  1974-05-03       Impact factor: 49.962

4.  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

5.  Bacteria swim by rotating their flagellar filaments.

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

6.  Common mechanism for repellents and attractants in bacterial chemotaxis.

Authors:  N Tsang; R Macnab; D E Koshland
Journal:  Science       Date:  1973-07-06       Impact factor: 47.728

7.  Bacterial motility and chemotaxis: light-induced tumbling response and visualization of individual flagella.

Authors:  R Macnab; D E Koshland
Journal:  J Mol Biol       Date:  1974-04-15       Impact factor: 5.469

8.  A note on the helical movement of micro-organisms.

Authors:  A T Chwang; T Y Wu
Journal:  Proc R Soc Lond B Biol Sci       Date:  1971-08-03

9.  Examination of bacterial flagellation by dark-field microscopy.

Authors:  R M Macnab
Journal:  J Clin Microbiol       Date:  1976-09       Impact factor: 5.948

10.  Effect of viscosity on bacterial motility.

Authors:  W R Schneider; R N Doetsch
Journal:  J Bacteriol       Date:  1974-02       Impact factor: 3.490

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  51 in total

1.  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

2.  Microscopic analysis of bacterial motility at high pressure.

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

3.  Rotation and switching of the flagellar motor assembly in Halobacterium halobium.

Authors:  W Marwan; M Alam; D Oesterhelt
Journal:  J Bacteriol       Date:  1991-03       Impact factor: 3.490

4.  From the Cover: Bacterial flagellum as a propeller and as a rudder for efficient chemotaxis.

Authors:  Li Xie; Tuba Altindal; Suddhashil Chattopadhyay; Xiao-Lun Wu
Journal:  Proc Natl Acad Sci U S A       Date:  2011-01-04       Impact factor: 11.205

5.  Hotspots of boundary accumulation: dynamics and statistics of micro-swimmers in flowing films.

Authors:  Arnold J T M Mathijssen; Amin Doostmohammadi; Julia M Yeomans; Tyler N Shendruk
Journal:  J R Soc Interface       Date:  2016-02       Impact factor: 4.118

6.  Release of flagellar filament-hook-rod complex by a Salmonella typhimurium mutant defective in the M ring of the basal body.

Authors:  H Okino; M Isomura; S Yamaguchi; Y Magariyama; S Kudo; S I Aizawa
Journal:  J Bacteriol       Date:  1989-04       Impact factor: 3.490

7.  Synchronization of rotating helices by hydrodynamic interactions.

Authors:  M Reichert; H Stark
Journal:  Eur Phys J E Soft Matter       Date:  2005-08-11       Impact factor: 1.890

8.  On torque and tumbling in swimming Escherichia coli.

Authors:  Nicholas C Darnton; Linda Turner; Svetlana Rojevsky; Howard C Berg
Journal:  J Bacteriol       Date:  2006-12-22       Impact factor: 3.490

9.  Swimming in circles: motion of bacteria near solid boundaries.

Authors:  Eric Lauga; Willow R DiLuzio; George M Whitesides; Howard A Stone
Journal:  Biophys J       Date:  2005-10-20       Impact factor: 4.033

Review 10.  The FliK protein and flagellar hook-length control.

Authors:  Richard C Waters; Paul W O'Toole; Kieran A Ryan
Journal:  Protein Sci       Date:  2007-05       Impact factor: 6.725

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