Literature DB >> 7009571

Change in intracellular pH of Escherichia coli mediates the chemotactic response to certain attractants and repellents.

D R Repaske, J Adler.   

Abstract

Changes in the membrane potential, pH gradient, proton motive force, and intracellular pH of Escherichia coli were followed during the chemotactic responses to a variety of potentially membrane-active compounds. Lipophilic weak acids, decreases in extracellular pH, and nigericin each caused a repellent response. Lipophilic weak bases, increases in extracellular pH, and valinomycin in the presence of K+ each caused an attractant response. Changes in membrane potential, pH gradient, and proton motive force did not correlate with the behavioral responses to these treatments, but changes in intracellular pH did correlate. Furthermore, the strength of the response to a weak acid was correlated with the magnitude of the change of the intracellular pH, and many compounds which could alter the intracellular pH were found to be chemotactically active. Apparently these attractants and repellents are not detected by specific chemoreceptors but rather are detected via the ability of cells to sense and respond to changes in intracellular pH. The pathway of sensory transduction which proceeds through methyl-accepting chemotaxis protein I was found to be involved in the response to a change in intracellular pH.

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Year:  1981        PMID: 7009571      PMCID: PMC217120          DOI: 10.1128/jb.145.3.1196-1208.1981

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


  43 in total

1.  Negative chemotaxis in Escherichia coli.

Authors:  W W Tso; J Adler
Journal:  J Bacteriol       Date:  1974-05       Impact factor: 3.490

2.  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

3.  Change in direction of flagellar rotation is the basis of the chemotactic response in Escherichia coli.

Authors:  S H Larsen; R W Reader; E N Kort; W W Tso; J Adler
Journal:  Nature       Date:  1974-05-03       Impact factor: 49.962

4.  The gradient-sensing mechanism in bacterial chemotaxis.

Authors:  R M Macnab; D E Koshland
Journal:  Proc Natl Acad Sci U S A       Date:  1972-09       Impact factor: 11.205

5.  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

6.  Antibiotic-mediated transport of alkali ions across lipid barriers.

Authors:  B C Pressman; E J Harris; W S Jagger; J H Johnson
Journal:  Proc Natl Acad Sci U S A       Date:  1967-11       Impact factor: 11.205

7.  Ion transport induced by light and antibiotics IN CHROMATOPHORES FROM Rhodospirillum rubrum.

Authors:  J B Jackson; A R Crofts; L V von Stedingk
Journal:  Eur J Biochem       Date:  1968-10-17

8.  Development of K+-Na+ discrimination in experimental bimolecular lipid membranes by macrocyclic antibiotics.

Authors:  P Mueller; D O Rudin
Journal:  Biochem Biophys Res Commun       Date:  1967-02-21       Impact factor: 3.575

9.  Escherichia coli mutants defective in chemotaxis toward specific chemicals.

Authors:  G L Hazelbauer; R E Mesibov; J Adler
Journal:  Proc Natl Acad Sci U S A       Date:  1969-12       Impact factor: 11.205

10.  Chemotaxis toward amino acids in Escherichia coli.

Authors:  R Mesibov; J Adler
Journal:  J Bacteriol       Date:  1972-10       Impact factor: 3.490

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  88 in total

Review 1.  More than one way to sense chemicals.

Authors:  G Alexandre; I B Zhulin
Journal:  J Bacteriol       Date:  2001-08       Impact factor: 3.490

Review 2.  Bacterial chemotaxis toward environmental pollutants: role in bioremediation.

Authors:  Gunjan Pandey; Rakesh K Jain
Journal:  Appl Environ Microbiol       Date:  2002-12       Impact factor: 4.792

3.  Nutrient-dependent methylation of a membrane-associated protein of Escherichia coli.

Authors:  C C Young; J D Alvarez; R W Bernlohr
Journal:  J Bacteriol       Date:  1990-09       Impact factor: 3.490

4.  Alkaline induction of a novel gene locus, alx, in Escherichia coli.

Authors:  R J Bingham; K S Hall; J L Slonczewski
Journal:  J Bacteriol       Date:  1990-04       Impact factor: 3.490

5.  Evidence for symmetry in the elementary process of bidirectional torque generation by the bacterial flagellar motor.

Authors:  Shuichi Nakamura; Nobunori Kami-ike; Jun-ichi P Yokota; Tohru Minamino; Keiichi Namba
Journal:  Proc Natl Acad Sci U S A       Date:  2010-09-27       Impact factor: 11.205

6.  Extracellular oxidoreduction potential modifies carbon and electron flow in Escherichia coli.

Authors:  C Riondet; R Cachon; Y Waché; G Alcaraz; C Diviès
Journal:  J Bacteriol       Date:  2000-02       Impact factor: 3.490

7.  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

8.  Murine Models for the Investigation of Colonization Resistance and Innate Immune Responses in Campylobacter Jejuni Infections.

Authors:  Soraya Mousavi; Stefan Bereswill; Markus M Heimesaat
Journal:  Curr Top Microbiol Immunol       Date:  2021       Impact factor: 4.291

9.  Direction of flagellar rotation in bacterial cell envelopes.

Authors:  S Ravid; M Eisenbach
Journal:  J Bacteriol       Date:  1984-04       Impact factor: 3.490

10.  Behavioral responses of Escherichia coli to changes in redox potential.

Authors:  V A Bespalov; I B Zhulin; B L Taylor
Journal:  Proc Natl Acad Sci U S A       Date:  1996-09-17       Impact factor: 11.205

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