Change of waveform in bacterial flagella : the role of mechanics at the molecular level

Abstract The flagella of Salmonella and other bacteria are constructed from molecules of the protein flagellin in a way which permits relatively easy transition between members of a family of distinct stable left and right-handed helical waveforms. Changes of waveform, particularly between “normal” (left-handed) and “curly” (right-handed) play an important role in the switch from smooth swimming to tumbling in chemotaxis. This paper establishes some mechanical properties of model flagella built from bi-stable subunits, which in turn clarifies the mechanics of the changes of waveform which occur, in a viscous fluid environment, at various points in the swimming cycle. Available data on the joining of different helical waveforms in a single filament, supplemented by information on the way in which helical filaments flatten down in preparation for electron microscopy, are well-fitted by the mechanical behaviour of an assembly of mechanical subunits having some simple distinctive design features. The same arrangement makes possible an explanation for the formation of flagellar-like but straight polymers from Salmonella flagellin in the presence of high concentrations of NaCl.

[1]  C. Calladine Construction of bacterial flagella , 1975, Nature.

[2]  H. Berg,et al.  Chemotaxis in Escherichia coli analysed by Three-dimensional Tracking , 1972, Nature.

[3]  J. Adler,et al.  The sensing of chemicals by bacteria. , 1976, Scientific American.

[4]  M. Simon,et al.  Flagellar rotation and the mechanism of bacterial motility , 1974, Nature.

[5]  C. Calladine Design requirements for the construction of bacterial flagella. , 1976, Journal of theoretical biology.

[6]  D E Koshland,et al.  Bacterial motility and chemotaxis: light-induced tumbling response and visualization of individual flagella. , 1974, Journal of molecular biology.

[7]  T. Kuroiwa,et al.  Polymorphism in a flagellar-shape mutant of Salmonella typhimurium. , 1974, Journal of general microbiology.

[8]  S. Harrison,et al.  Tomato bushy stunt virus at 5.5-Å resolution , 1977, Nature.

[9]  M. A. Jaswon,et al.  Atomic displacements in the austenite–martensite transformation , 1948 .

[10]  K. Wakabayashi,et al.  A Phenomenological Theory of Polymorphism of Salmonella Flagella. I. A Model , 1972 .

[11]  S. Asakura,et al.  Formation of a flagella-like but straight polymer of Salmonella flagellin. , 1974, Journal of molecular biology.

[12]  M. Yanagida,et al.  Structure of straight flagellar filaments from a mutant of Escherichia coli. , 1975, Journal of molecular biology.

[13]  R M Macnab,et al.  Normal-to-curly flagellar transitions and their role in bacterial tumbling. Stabilization of an alternative quaternary structure by mechanical force. , 1977, Journal of molecular biology.

[14]  S. Asakura,et al.  Left-handed to right-handed helix conversion in Salmonella flagella , 1975, Nature.

[15]  J. Adler,et al.  Change in direction of flagellar rotation is the basis of the chemotactic response in Escherichia coli , 1974, Nature.

[16]  A. Pijper Shape of Bacterial Flagella , 1955, Nature.

[17]  S. Asakura,et al.  Polymorphism of Salmonella flagella as investigated by means of in vitro copolymerization of flagellins derived from various strains. , 1972, Journal of molecular biology.

[18]  P. Bennett,et al.  Structure of straight flagella from a mutant Salmonella. , 1972, Journal of molecular biology.

[19]  S. Asakura,et al.  Helical transformations of Salmonella flagella in vitro. , 1976, Journal of molecular biology.

[20]  H. Berg,et al.  Dynamic properties of bacterial flagellar motors , 1974, Nature.

[21]  E. Leifson,et al.  MORPHOLOGICAL CHARACTERISTICS OF FLAGELLA OF PROTEUS AND RELATED BACTERIA , 1955, Journal of bacteriology.

[22]  H. Hotani Light microscope study of mixed helices in reconstituted Salmonella flagella. , 1976, Journal of molecular biology.