Literature DB >> 8962029

Symmetries in bacterial motility.

H C Berg1.   

Abstract

Descriptions are given of three kinds of symmetries encountered in studies of bacterial locomotion, and of the ways in which they are circumvented or broken. A bacterium swims at very low Reynolds number: it cannot propel itself using reciprocal motion (by moving through a sequence of shapes, first forward and then in reverse); cyclic motion is required. A common solution is rotation of a helical filament, either right- or left-handed. The flagellar rotary motor that drives each filament generates the same torque whether spinning clockwise or counterclockwise. This symmetry is broken by coupling to the filament. Finally, bacterial populations, grown in a nutrient medium from an inoculum placed at a single point, usually move outward in symmetric circular rings. Under certain conditions, the cells excrete a chemoattractant, and the rings break up into discrete aggregates that can display remarkable geometric order.

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Year:  1996        PMID: 8962029      PMCID: PMC34465          DOI: 10.1073/pnas.93.25.14225

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


  16 in total

1.  Complex patterns formed by motile cells of Escherichia coli.

Authors:  E O Budrene; H C Berg
Journal:  Nature       Date:  1991-02-14       Impact factor: 49.962

2.  Dynamics of formation of symmetrical patterns by chemotactic bacteria.

Authors:  E O Budrene; H C Berg
Journal:  Nature       Date:  1995-07-06       Impact factor: 49.962

Review 3.  A physicist looks at bacterial chemotaxis.

Authors:  H C Berg
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1988

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

Authors:  R M Macnab
Journal:  Proc Natl Acad Sci U S A       Date:  1977-01       Impact factor: 11.205

5.  Normal-to-curly flagellar transitions and their role in bacterial tumbling. Stabilization of an alternative quaternary structure by mechanical force.

Authors:  R M Macnab; M K Ornston
Journal:  J Mol Biol       Date:  1977-05-05       Impact factor: 5.469

6.  Flagellar rotation and the mechanism of bacterial motility.

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

7.  Chemomechanical coupling without ATP: the source of energy for motility and chemotaxis in bacteria.

Authors:  S H Larsen; J Adler; J J Gargus; R W Hogg
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

8.  Growth and movement of rings of chemotactic bacteria.

Authors:  R Nossal
Journal:  Exp Cell Res       Date:  1972-11       Impact factor: 3.905

9.  Adaptation kinetics in bacterial chemotaxis.

Authors:  S M Block; J E Segall; H C Berg
Journal:  J Bacteriol       Date:  1983-04       Impact factor: 3.490

10.  Chemotaxis in bacteria.

Authors:  J Adler
Journal:  Science       Date:  1966-08-12       Impact factor: 47.728

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  4 in total

1.  Single particle tracking of correlated bacterial dynamics.

Authors:  G V Soni; B M Jaffar Ali; Y Hatwalne; G V Shivashankar
Journal:  Biophys J       Date:  2003-04       Impact factor: 4.033

2.  An ABC transporter plays a developmental aggregation role in Myxococcus xanthus.

Authors:  M J Ward; K C Mok; D P Astling; H Lew; D R Zusman
Journal:  J Bacteriol       Date:  1998-11       Impact factor: 3.490

3.  Radial and spiral stream formation in Proteus mirabilis colonies.

Authors:  Chuan Xue; Elena O Budrene; Hans G Othmer
Journal:  PLoS Comput Biol       Date:  2011-12-29       Impact factor: 4.475

4.  Rapid, high-throughput tracking of bacterial motility in 3D via phase-contrast holographic video microscopy.

Authors:  Fook Chiong Cheong; Chui Ching Wong; YunFeng Gao; Mui Hoon Nai; Yidan Cui; Sungsu Park; Linda J Kenney; Chwee Teck Lim
Journal:  Biophys J       Date:  2015-03-10       Impact factor: 4.033

  4 in total

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