This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Armitage, J. P.
Right arrow Articles by Ford, R. M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Armitage, J. P.
Right arrow Articles by Ford, R. M.

 Previous Article  |  Next Article 

Journal of Bacteriology, August 1999, p. 4825-4833, Vol. 181, No. 16
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.

Transformations in Flagellar Structure of Rhodobacter sphaeroides and Possible Relationship to Changes in Swimming Speed

Judith P. Armitage,1,* Thomas P. Pitta,2 Margot A.-S. Vigeant,3 Helen L. Packer,1 and Roseanne M. Ford3

Microbiology Unit, Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom1; Rowland Institute of Science, Cambridge, Massachusetts 021422; and Department of Chemical Engineering, University of Virginia, Charlottesville, Virginia 22903-24423

Received 1 March 1999/Accepted 3 June 1999

Rhodobacter sphaeroides is a photosynthetic bacterium which swims by rotating a single flagellum in one direction, periodically stopping, and reorienting during these stops. Free-swimming R. sphaeroides was examined by both differential interference contrast (DIC) microscopy, which allows the flagella of swimming cells to be seen in vivo, and tracking microscopy, which tracks swimming patterns in three dimensions. DIC microscopy showed that when rotation stopped, the helical flagellum relaxed into a high-amplitude, short-wavelength coiled form, confirming previous observations. However, DIC microscopy also revealed that the coiled filament could rotate slowly, reorienting the cell before a transition back to the functional helix. The time taken to reform a functional helix depended on the rate of rotation of the helix and the length of the filament. In addition to these coiled and helical forms, a third conformation was observed: a rapidly rotating, apparently straight form. This form took shape from the cell body out and was seen to form directly from flagella that were initially in either the coiled or the helical conformation. This form was always significantly longer than the coiled or helical form from which it was derived. The resolution of DIC microscopy made it impossible to identify whether this form was genuinely in a straight conformation or was a low-amplitude, long-wavelength helix. Examination of the three-dimensional swimming pattern showed that R. sphaeroides changed speed while swimming, sometimes doubling the swimming speed between stops. The rate of acceleration out of stops was also variable. The transformations in waveform are assumed to be torsionally driven and may be related to the changes in speed measured in free-swimming cells. The roles of and mechanisms that may be involved in the transformations of filament conformations and changes in swimming speed are discussed.


* Corresponding author. Mailing address: Microbiology Unit, Department of Biochemistry, University of Oxford, Oxford OX1 3QU, United Kingdom. Phone: 44 1865 275299. Fax: 44 1865 275297. E-mail: armitage{at}bioch.ox.ac.uk.


Journal of Bacteriology, August 1999, p. 4825-4833, Vol. 181, No. 16
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Pilizota, T., Brown, M. T., Leake, M. C., Branch, R. W., Berry, R. M., Armitage, J. P. (2009). A molecular brake, not a clutch, stops the Rhodobacter sphaeroides flagellar motor. Proc. Natl. Acad. Sci. USA 106: 11582-11587 [Abstract] [Full Text]  
  • Brehm-Stecher, B. F., Johnson, E. A. (2004). Single-Cell Microbiology: Tools, Technologies, and Applications. Microbiol. Mol. Biol. Rev. 68: 538-559 [Abstract] [Full Text]  
  • Ferre, A., de la Mora, J., Ballado, T., Camarena, L., Dreyfus, G. (2004). Biochemical Study of Multiple CheY Response Regulators of the Chemotactic Pathway of Rhodobacter sphaeroides. J. Bacteriol. 186: 5172-5177 [Abstract] [Full Text]  
  • Scharf, B. (2002). Real-Time Imaging of Fluorescent Flagellar Filaments of Rhizobium lupini H13-3: Flagellar Rotation and pH-Induced Polymorphic Transitions. J. Bacteriol. 184: 5979-5986 [Abstract] [Full Text]  
  • Poggio, S., Osorio, A., Corkidi, G., Dreyfus, G., Camarena, L. (2001). The N Terminus of FliM Is Essential To Promote Flagellar Rotation in Rhodobacter sphaeroides. J. Bacteriol. 183: 3142-3148 [Abstract] [Full Text]  
  • Ballado, T., Camarena, L., González-Pedrajo, B., Silva-Herzog, E., Dreyfus, G. (2001). The Hook Gene (flgE) Is Expressed from the flgBCDEF Operon in Rhodobacter sphaeroides: Study of an flgE Mutant. J. Bacteriol. 183: 1680-1687 [Abstract] [Full Text]  
  • Packer, H. L., Armitage, J. P. (2000). Behavioral Responses of Rhodobacter sphaeroides to Linear Gradients of the Nutrients Succinate and Acetate. Appl. Environ. Microbiol. 66: 5186-5191 [Abstract] [Full Text]  
  • Shah, D. S. H., Perehinec, T., Stevens, S. M., Aizawa, S.-I., Sockett, R. E. (2000). The Flagellar Filament of Rhodobacter sphaeroides: pH-Induced Polymorphic Transitions and Analysis of the fliC Gene. J. Bacteriol. 182: 5218-5224 [Abstract] [Full Text]