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Journal of Bacteriology, September 2000, p. 5218-5224, Vol. 182, No. 18
Microbiology Unit, Biochemistry Department,
University of Oxford, Oxford OX1 3QU,1
School of Biological Sciences, Sutton Bonnington Campus,
University of Nottingham, Sutton Bonnington, Leicestershire LE12
5RD,3 and Immunology
Division4 and Institute of
Genetics,5 University of Nottingham, Queens
Medical Centre, Nottingham NG7 2UH, United Kingdom, and
Department of Bioscience, Teikyo University, 1-1 Toyosatodai, Utsunomiya 320, Japan2
Received 22 December 1999/Accepted 20 June 2000
Flagellar motility in Rhodobacter sphaeroides is
notably different from that in other bacteria. R. sphaeroides moves in a series of runs and stops produced by the
intermittent rotation of the flagellar motor. R. sphaeroides has a single, plain filament whose conformation
changes according to flagellar motor activity. Conformations adopted
during swimming include coiled, helical, and apparently straight forms.
This range of morphological transitions is larger than that in other
bacteria, where filaments alternate between left- and right-handed
helical forms. The polymorphic ability of isolated R. sphaeroides filaments was tested in vitro by varying pH and ionic
strength. The isolated filaments could form open-coiled, straight,
normal, or curly conformations. The range of transitions made by the
R. sphaeroides filament differs from that reported for
Salmonella enterica serovar Typhimurium. The sequence of
the R. sphaeroides fliC gene, which encodes the flagellin
protein, was determined. The gene appears to be controlled by a
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Copyright © 2000, American Society for Microbiology. All rights reserved.
The Flagellar Filament of Rhodobacter
sphaeroides: pH-Induced Polymorphic Transitions and Analysis of
the fliC Gene
28-dependent promoter. It encodes a predicted peptide of
493 amino acids. Serovar Typhimurium mutants with altered polymorphic
ability usually have amino acid changes at the terminal portions of
flagellin or a deletion in the central region. There are no obvious
major differences in the central regions to explain the difference in polymorphic ability. In serovar Typhimurium filaments, the termini of
flagellin monomers have a coiled-coil conformation. The termini of
R. sphaeroides flagellin are predicted to have a lower
probability of coiled coils than are those of serovar Typhimurium
flagellin. This may be one reason for the differences in polymorphic
ability between the two filaments.
*
Corresponding author. Mailing address: Institute of
Genetics, University of Nottingham, Queens Medical Centre, Nottingham NG7 2UH, United Kingdom. Phone: 44-115-9194496. Fax: 44-115-9709906. E-mail: liz.sockett{at}nottingham.ac.uk.
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