Literature DB >> 4957395

Chemotaxis in bacteria.

J Adler.   

Abstract

Motile Escherichia coli placed at one end of a capillary tube containing an energy source and oxygen migrate out into the tube in one or two bands, which are clearly visible to the naked eye and can also be demonstrated by photography, microscopy, and densitometry and by assaying for bacteria throughout the tube. The formation of two bands is not due to heterogeneity among the bacteria, since the bacteria in each band, when reused, will form two more bands. If an anaerobically utilizable energy source such as galactose is present in excess over the oxygen, the first band consumes all the oxygen and a part of the sugar and the second band uses the residual sugar anaerobically. On the other hand, if oxygen is present in excess over the sugar, the first band oxidizes all the sugar and leaves behind unused oxygen, and the second band uses up the residual oxygen to oxidize an endogenous energy source. The essence of the matter is that the bacteria create a gradient of oxygen or of an energy source, and then they move preferentially in the direction of the higher concentration of the chemical. As a consequence, bands of bacteria (or rings of bacteria in the case of agar plates) form and move out. These results show that E. coli is chemotactic toward oxygen and energy sources such as galactose, glucose, aspartic acid, threonine, or serine. The full repertoire of chemotactic responses by E. coli is no doubt greater than this, and a more complete list remains to be compiled. The studies reported here demonstrate that chemotaxis allows bacteria to find that environment which provides them with the greatest supply of energy. It is clearly an advantage for bacteria to be able to carry out chemotaxis, since by this means they can avoid unfavorable conditions and seek optimum surroundings. Finally, it is necessary to acknowledge the pioneering work of Englemann, Pfeffer, and the other late-19thcentury biologists who discovered chemotaxis in bacteria, and to point out that the studies reported here fully confirm the earlier reports of Beijerinck (4) and Sherris and his collaborators (5,6) on a band of bacteria chemotactic toward oxygen. By using a chemically defined medium instead of a complex broth, it has been possible to study this band more closely and to demonstrate in addition the occurrence of a second band of bacteria chemotactic toward an energy source. Beijerinck (4) did, in fact, sometimes observe a second band, but he did not offer an explanation for it.

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Year:  1966        PMID: 4957395     DOI: 10.1126/science.153.3737.708

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  318 in total

Review 1.  Biological factors underlying regularity and chaos in aquatic ecosystems: simple models of complex dynamics.

Authors:  A B Medvinsky; S V Petrovskii; D A Tikhonov; I A Tikhonova; G R Ivanitsky; H Malchow
Journal:  J Biosci       Date:  2001-03       Impact factor: 1.826

2.  A nonlinear stimulus-response relation in bacterial chemotaxis.

Authors:  A M Stock
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

3.  Role of the receptor for bacteriophage lambda in the functioning of the maltose chemoreceptor of Escherichia coli.

Authors:  G L Hazelbauer
Journal:  J Bacteriol       Date:  1975-10       Impact factor: 3.490

4.  Attractant regulation of the aspartate receptor-kinase complex: limited cooperative interactions between receptors and effects of the receptor modification state.

Authors:  J A Bornhorst; J J Falke
Journal:  Biochemistry       Date:  2000-08-08       Impact factor: 3.162

5.  Nonstationary dynamics of bacterial population waves.

Authors:  M A Tsyganov; G V Aslanidi; V Shakhbazian; V N Biktashev; G R Ivanitsky
Journal:  Dokl Biochem Biophys       Date:  2001 Sep-Oct       Impact factor: 0.788

6.  A sensitive, versatile microfluidic assay for bacterial chemotaxis.

Authors:  Hanbin Mao; Paul S Cremer; Michael D Manson
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-18       Impact factor: 11.205

7.  New motion analysis system for characterization of the chemosensory response kinetics of Rhodobacter sphaeroides under different growth conditions.

Authors:  Mila Kojadinovic; Antoine Sirinelli; George H Wadhams; Judith P Armitage
Journal:  Appl Environ Microbiol       Date:  2011-04-22       Impact factor: 4.792

8.  Isolation and characterization of Escherichia coli mutants blocked in production of membrane-derived oligosaccharides.

Authors:  A C Weissborn; M K Rumley; E P Kennedy
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

9.  Mechanisms of microbial movement in subsurface materials.

Authors:  P J Reynolds; P Sharma; G E Jenneman; M J McInerney
Journal:  Appl Environ Microbiol       Date:  1989-09       Impact factor: 4.792

10.  Motility and chemotaxis in Agrobacterium tumefaciens surface attachment and biofilm formation.

Authors:  Peter M Merritt; Thomas Danhorn; Clay Fuqua
Journal:  J Bacteriol       Date:  2007-08-31       Impact factor: 3.490

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