Literature DB >> 3881399

Chemotactic signaling in filamentous cells of Escherichia coli.

J E Segall, A Ishihara, H C Berg.   

Abstract

Video techniques were used to record chemotactic responses of filamentous cells of Escherichia coli stimulated iontophoretically with aspartate. Long, nonseptate cells were produced from polyhook strains either by introducing a cell division mutation or by growth in the presence of cephalexin. Markers indicating rotation of flagellar motors were attached with anti-hook antibodies. Aspartate was applied by iontophoretic ejection from a micropipette, and the effects on the direction of rotation of the markers were measured. Motors near the pipette responded, whereas those sufficiently far away did not, even when the pipette was near the cell surface. The response of a given motor decreased as the pipette was moved away, but it did so less steeply when the pipette remained near the cell surface than when it was moved out into the external medium. This shows that there is an internal signal, but its range is short, only a few micrometers. These experiments rule out signaling by changes in membrane potential, by simple release or binding of a small molecule, or by diffusion of the receptor-attractant complex. A likely candidate for the signal is a protein or ligand that is activated by the receptor and inactivated as it diffuses through the cytoplasm. The range of the signal was found to be substantially longer in a cheZ mutant, suggesting that the product of the cheZ gene contributes to this inactivation.

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Year:  1985        PMID: 3881399      PMCID: PMC214834          DOI: 10.1128/jb.161.1.51-59.1985

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  59 in total

1.  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

2.  Common mechanism for repellents and attractants in bacterial chemotaxis.

Authors:  N Tsang; R Macnab; D E Koshland
Journal:  Science       Date:  1973-07-06       Impact factor: 47.728

3.  A method for measuring chemotaxis and use of the method to determine optimum conditions for chemotaxis by Escherichia coli.

Authors:  J Adler
Journal:  J Gen Microbiol       Date:  1973-01

Review 4.  Bacterial chemotaxis.

Authors:  A Boyd; M Simon
Journal:  Annu Rev Physiol       Date:  1982       Impact factor: 19.318

5.  Separation of signal transduction and adaptation functions of the aspartate receptor in bacterial sensing.

Authors:  A F Russo; D E Koshland
Journal:  Science       Date:  1983-06-03       Impact factor: 47.728

6.  Impulse responses in bacterial chemotaxis.

Authors:  S M Block; J E Segall; H C Berg
Journal:  Cell       Date:  1982-11       Impact factor: 41.582

7.  Methyl-accepting chemotaxis proteins are distributed in the membrane independently from basal ends of bacterial flagella.

Authors:  P Engström; G L Hazelbauer
Journal:  Biochim Biophys Acta       Date:  1982-03-23

8.  Isolation and behavior of Escherichia coli deletion mutants lacking chemotaxis functions.

Authors:  J S Parkinson; S E Houts
Journal:  J Bacteriol       Date:  1982-07       Impact factor: 3.490

9.  A voltage clamp inhibits chemotaxis of Spirochaeta aurantia.

Authors:  E A Goulbourne; E P Greenberg
Journal:  J Bacteriol       Date:  1983-02       Impact factor: 3.490

10.  Coordination of flagella on filamentous cells of Escherichia coli.

Authors:  A Ishihara; J E Segall; S M Block; H C Berg
Journal:  J Bacteriol       Date:  1983-07       Impact factor: 3.490

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  49 in total

Review 1.  How signals are heard during bacterial chemotaxis: protein-protein interactions in sensory signal propagation.

Authors:  A Bren; M Eisenbach
Journal:  J Bacteriol       Date:  2000-12       Impact factor: 3.490

2.  Evolutionary conservation of methyl-accepting chemotaxis protein location in Bacteria and Archaea.

Authors:  J E Gestwicki; A C Lamanna; R M Harshey; L L McCarter; L L Kiessling; J Adler
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

3.  Cooperativity between bacterial chemotaxis receptors.

Authors:  Joseph J Falke
Journal:  Proc Natl Acad Sci U S A       Date:  2002-05-14       Impact factor: 11.205

4.  Bacteria are not too small for spatial sensing of chemical gradients: an experimental evidence.

Authors:  Roland Thar; Michael Kuhl
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-28       Impact factor: 11.205

Review 5.  Bacterial chemotaxis: a new player in response regulator dephosphorylation.

Authors:  John S Parkinson
Journal:  J Bacteriol       Date:  2003-03       Impact factor: 3.490

6.  Binding of the Escherichia coli response regulator CheY to its target measured in vivo by fluorescence resonance energy transfer.

Authors:  Victor Sourjik; Howard C Berg
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-13       Impact factor: 11.205

7.  Mutational analysis of N381, a key trimer contact residue in Tsr, the Escherichia coli serine chemoreceptor.

Authors:  Khoosheh K Gosink; Yimin Zhao; John S Parkinson
Journal:  J Bacteriol       Date:  2011-09-30       Impact factor: 3.490

Review 8.  Reaction-diffusion systems in intracellular molecular transport and control.

Authors:  Siowling Soh; Marta Byrska; Kristiana Kandere-Grzybowska; Bartosz A Grzybowski
Journal:  Angew Chem Int Ed Engl       Date:  2010-06-07       Impact factor: 15.336

9.  Control of transducer methylation levels in Escherichia coli: investigation of components essential for modulation of methylation and demethylation reactions.

Authors:  C B Russell; R C Stewart; F W Dahlquist
Journal:  J Bacteriol       Date:  1989-07       Impact factor: 3.490

10.  Role of CheW protein in coupling membrane receptors to the intracellular signaling system of bacterial chemotaxis.

Authors:  J D Liu; J S Parkinson
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

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