Literature DB >> 11882287

How myxobacteria glide.

Charles Wolgemuth1, Egbert Hoiczyk, Dale Kaiser, George Oster.   

Abstract

BACKGROUND: Many microorganisms, including myxobacteria, cyanobacteria, and flexibacteria, move by gliding. Although gliding always describes a slow surface-associated translocation in the direction of the cell's long axis, it can result from two very different propulsion mechanisms: social (S) motility and adventurous (A) motility. The force for S motility is generated by retraction of type 4 pili. A motility may be associated with the extrusion of slime, but evidence has been lacking, and how force might be generated has remained an enigma. Recently, nozzle-like structures were discovered in cyanobacteria from which slime emanated at the same rate at which the bacteria moved. This strongly implicates slime extrusion as a propulsion mechanism for gliding.
RESULTS: Here we show that similar but smaller nozzle-like structures are found in Myxococcus xanthus and that they are clustered at both cell poles, where one might expect propulsive organelles. Furthermore, light and electron microscopical observations show that slime is secreted in ribbons from the ends of cells. To test whether the slime propulsion hypothesis is physically reasonable, we construct a mathematical model of the slime nozzle to see if it can generate a force sufficient to propel M. xanthus at the observed velocities. The model assumes that the hydration of slime, a cationic polyelectrolyte, is the force-generating mechanism.
CONCLUSIONS: The discovery of nozzle-like organelles in various gliding bacteria suggests their role in prokaryotic gliding. Our calculations and our observations of slime trails demonstrate that slime extrusion from such nozzles can account for most of the observed properties of A motile gliding.

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Year:  2002        PMID: 11882287     DOI: 10.1016/s0960-9822(02)00716-9

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  90 in total

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2.  The motility of mollicutes.

Authors:  Charles W Wolgemuth; Oleg Igoshin; George Oster
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3.  Membrane localization of motility, signaling, and polyketide synthetase proteins in Myxococcus xanthus.

Authors:  Vesna Simunovic; Frank C Gherardini; Lawrence J Shimkets
Journal:  J Bacteriol       Date:  2003-09       Impact factor: 3.490

4.  AglZ is a filament-forming coiled-coil protein required for adventurous gliding motility of Myxococcus xanthus.

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Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

5.  Waves and aggregation patterns in myxobacteria.

Authors:  Oleg A Igoshin; Roy Welch; Dale Kaiser; George Oster
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9.  Characterization of myxobacterial A-motility: insights from microcinematographic observations.

Authors:  Matthias K Koch; Egbert Hoiczyk
Journal:  J Basic Microbiol       Date:  2013-01-15       Impact factor: 2.281

10.  Flavobacterium johnsoniae GldH is a lipoprotein that is required for gliding motility and chitin utilization.

Authors:  Mark J McBride; Timothy F Braun; Jessica L Brust
Journal:  J Bacteriol       Date:  2003-11       Impact factor: 3.490

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