Literature DB >> 7009572

Cytoplasmic pH mediates pH taxis and weak-acid repellent taxis of bacteria.

M Kihara, R M Macnab.   

Abstract

Bacteria migrate away from an acid pH and from a number of chemicals, including organic acids such as acetate; the basis for detection of these environmental cues has not been demonstrated. Membrane-permeant weak acids caused prolonged tumbling when added to Salmonella sp. or Escherichia coli cells at pH 5.5. Tethered Salmonella cells went from a prestimulus behavior of 14% clockwise rotation to 80% clockwise rotation when 40 mM acetate was added and remained this way for more than 30 min. A low external pH in the absence of weak acid did not markedly affect steady-state tumbling frequency. Among the weak acids tested, the rank for acidity (salicylate greater than benzoate greater than acetate greater than 5,5-dimethyl-2,4-oxazolidinedione) was the same as the rank for the ability to collapse the transmembrane pH gradient and to cause tumbling. At pH 7.0, the tumbling responses caused by the weak acids were much briefer. Indole, a non-weak-acid repellent, did not cause prolonged tumbling at low pH. Two chemotaxis mutants (a Salmonella mutant defective in the chemotaxis methylesterase and an E. coli mutant defective in the methyl-accepting protein in MCP I) showed inverse responses of enhanced counterclockwise rotation in the first 1 min after acetate addition. The latter mutant had been found previously to be defective in the sensing of gradients of extracellular pH and (at neutral pH) of acetate. We conclude (i) that taxes away from acid pH and membrane-permeant weak acids are both mediated by a pH-sensitive component located either in the cytoplasm or on the cytoplasmic side of the membrane, rather than by an external receptor (as in the case of the attractants), and (ii) that both of these taxes involve components of the chemotaxis methylation system, at least in the early phase of the response.

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Year:  1981        PMID: 7009572      PMCID: PMC217121          DOI: 10.1128/jb.145.3.1209-1221.1981

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


  49 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.  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

3.  Chemotaxis in Escherichia coli analysed by three-dimensional tracking.

Authors:  H C Berg; D A Brown
Journal:  Nature       Date:  1972-10-27       Impact factor: 49.962

4.  An S-adenosylmethionine requirement for chemotaxis in Escherichia coli.

Authors:  J B Armstrong
Journal:  Can J Microbiol       Date:  1972-11       Impact factor: 2.419

5.  Nonsense motility mutants in Salmonella typhimurium.

Authors:  P S Vary; B A Stocker
Journal:  Genetics       Date:  1973-02       Impact factor: 4.562

6.  Effect of pH on the kinetics of frog muscle phosphofructokinase.

Authors:  B Trivedi; W H Danforth
Journal:  J Biol Chem       Date:  1966-09-10       Impact factor: 5.157

Review 7.  Chemoreceptors in bacteria.

Authors:  J Adler
Journal:  Science       Date:  1969-12-26       Impact factor: 47.728

8.  Chemotactic responses by motile bacteria.

Authors:  F W Seymour; R N Doetsch
Journal:  J Gen Microbiol       Date:  1973-10

9.  Oxidative phosphorylation in Escherichia coli K12. Mutations affecting magnesium ion- or calcium ion-stimulated adenosine triphosphatase.

Authors:  J D Butlin; G B Cox; F Gibson
Journal:  Biochem J       Date:  1971-08       Impact factor: 3.857

10.  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

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  96 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

2.  The fast tumble signal in bacterial chemotaxis.

Authors:  Shahid Khan; Sanjay Jain; Gordon P Reid; David R Trentham
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

3.  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

4.  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

5.  pH regulates genes for flagellar motility, catabolism, and oxidative stress in Escherichia coli K-12.

Authors:  Lisa M Maurer; Elizabeth Yohannes; Sandra S Bondurant; Michael Radmacher; Joan L Slonczewski
Journal:  J Bacteriol       Date:  2005-01       Impact factor: 3.490

Review 6.  The acetate switch.

Authors:  Alan J Wolfe
Journal:  Microbiol Mol Biol Rev       Date:  2005-03       Impact factor: 11.056

7.  Motility response of Rhodobacter sphaeroides to chemotactic stimulation.

Authors:  P S Poole; J P Armitage
Journal:  J Bacteriol       Date:  1988-12       Impact factor: 3.490

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.  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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