Literature DB >> 3042756

Pausing of flagellar rotation is a component of bacterial motility and chemotaxis.

I R Lapidus1, M Welch, M Eisenbach.   

Abstract

When bacterial cells are tethered to glass by their flagella, many of them spin. On the basis of experiments with tethered cells it has generally been thought that the motor which drives the flagellum is a two-state device, existing in either a counterclockwise or a clockwise state. Here we show that a third state of the motor is that of pausing, the duration and frequency of which are affected by chemotactic stimuli. We have recorded on video tape the rotation of tethered Escherichia coli and Salmonella typhimurium cells and analyzed the recordings frame by frame and in slow motion. Most wild-type cells paused intermittently. The addition of repellents caused an increase in the frequency and duration of the pauses. The addition of attractants sharply reduced the number of pauses. A chemotaxis mutant which lacks a large part of the chemotaxis machinery owing to a deletion of the genes from cheA to cheZ did not pause at all and did not respond to repellents by pausing. A tumbly mutant of S. typhimurium responded to repellents by smooth swimming and to attractants by tumbling. When tethered, these cells exhibited a normal rotational response but an inverse pausing response to chemotactic stimuli: the frequency of pauses decreased in response to repellents and increased in response to attractants. It is suggested that (i) pausing is an integral part of bacterial motility and chemotaxis, (ii) pausing is independent of the direction of flagellar rotation, and (iii) pausing may be one of the causes of tumbling.

Entities:  

Mesh:

Year:  1988        PMID: 3042756      PMCID: PMC211337          DOI: 10.1128/jb.170.8.3627-3632.1988

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


  28 in total

Review 1.  Protein methylation in behavioural control mechanisms and in signal transduction.

Authors:  M S Springer; M F Goy; J Adler
Journal:  Nature       Date:  1979-07-26       Impact factor: 49.962

Review 2.  Bacterial motility and the bacterial flagellar motor.

Authors:  R M Macnab; S Aizawa
Journal:  Annu Rev Biophys Bioeng       Date:  1984

3.  Asynchronous switching of flagellar motors on a single bacterial cell.

Authors:  R M Macnab; D P Han
Journal:  Cell       Date:  1983-01       Impact factor: 41.582

Review 4.  Dynamics and energetics of flagellar rotation in bacteria.

Authors:  H C Berg; M D Manson; M P Conley
Journal:  Symp Soc Exp Biol       Date:  1982

5.  Morphology, function and isolation of halobacterial flagella.

Authors:  M Alam; D Oesterhelt
Journal:  J Mol Biol       Date:  1984-07-15       Impact factor: 5.469

6.  Changes in membrane potential of Escherichia coli in response to temporal gradients of chemicals.

Authors:  M Eisenbach
Journal:  Biochemistry       Date:  1982-12-21       Impact factor: 3.162

7.  A miniature flow cell designed for rapid exchange of media under high-power microscope objectives.

Authors:  H C Berg; S M Block
Journal:  J Gen Microbiol       Date:  1984-11

8.  Direction of flagellar rotation in bacterial cell envelopes.

Authors:  S Ravid; M Eisenbach
Journal:  J Bacteriol       Date:  1984-04       Impact factor: 3.490

9.  Correlation between bacteriophage chi adsorption and mode of flagellar rotation of Escherichia coli chemotaxis mutants.

Authors:  S Ravid; M Eisenbach
Journal:  J Bacteriol       Date:  1983-05       Impact factor: 3.490

10.  Bacterial cell envelopes with functional flagella.

Authors:  M Eisenbach; J Adler
Journal:  J Biol Chem       Date:  1981-08-25       Impact factor: 5.157

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  21 in total

1.  An electrostatic mechanism closely reproducing observed behavior in the bacterial flagellar motor.

Authors:  D Walz; S R Caplan
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

2.  Rusty, jammed, and well-oiled hinges: Mutations affecting the interdomain region of FliG, a rotor element of the Escherichia coli flagellar motor.

Authors:  Susan M Van Way; Stephanos G Millas; Aaron H Lee; Michael D Manson
Journal:  J Bacteriol       Date:  2004-05       Impact factor: 3.490

3.  A molecular mechanism of direction switching in the flagellar motor of Escherichia coli.

Authors:  Koushik Paul; Duncan Brunstetter; Sienna Titen; David F Blair
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-03       Impact factor: 11.205

4.  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

5.  Multiple kinetic states for the flagellar motor switch.

Authors:  S C Kuo; D E Koshland
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

6.  Signals, regulatory networks, and materials that build and break bacterial biofilms.

Authors:  Ece Karatan; Paula Watnick
Journal:  Microbiol Mol Biol Rev       Date:  2009-06       Impact factor: 11.056

7.  Rapid Immunocapture of Pseudomonas putida Cells from Lake Water by Using Bacterial Flagella.

Authors:  J A Morgan; C Winstanley; R W Pickup; J R Saunders
Journal:  Appl Environ Microbiol       Date:  1991-02       Impact factor: 4.792

Review 8.  Protein phosphorylation and regulation of adaptive responses in bacteria.

Authors:  J B Stock; A J Ninfa; A M Stock
Journal:  Microbiol Rev       Date:  1989-12

9.  Mechanisms of microbial movement in subsurface materials.

Authors:  P J Reynolds; P Sharma; G E Jenneman; M J McInerney
Journal:  Appl Environ Microbiol       Date:  1989-09       Impact factor: 4.792

10.  Rhodobacter sphaeroides WS8 expresses a polypeptide that is similar to MotB of Escherichia coli.

Authors:  D S Shah; J P Armitage; R E Sockett
Journal:  J Bacteriol       Date:  1995-05       Impact factor: 3.490

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