Literature DB >> 8816755

Behavioral responses of Escherichia coli to changes in redox potential.

V A Bespalov1, I B Zhulin, B L Taylor.   

Abstract

Escherichia coli bacteria sensed the redox state in their surroundings and they swam to a niche that had a preferred reduction potential. In a spatial redox gradient of benzoquinone/benzoquinol, E. coli cells migrated to form a sharply defined band. Bacteria swimming out of either face of the band tumbled and returned to the preferred conditions at the site of the band. This behavioral response was named redox taxis. Redox molecules, such as substituted quinones, that elicited redox taxis, interact with the bacterial electron transport system, thereby altering electron transport and the proton motive force. The magnitude of the behavioral response was dependent on the reduction potential of the chemoeffector. The Tsr, Tar, Trg, Tap, and CheR proteins, which have a role in chemotaxis, were not essential for redox taxis. A cheB mutant had inverted responses in redox taxis, as previously demonstrated in aerotaxis. A model is proposed in which a redox effector molecule perturbs the electron transport system, and an unknown sensor in the membrane detects changes in the proton motive force or the redox status of the electron transport system, and transduces this information into a signal that regulates phosphorylation of the CheA protein. A similar mechanism has been proposed for aerotaxis. Redox taxis may play an important role in the distribution of bacterial species in natural environments.

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Year:  1996        PMID: 8816755      PMCID: PMC38340          DOI: 10.1073/pnas.93.19.10084

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  43 in total

1.  Mg2+, Ca2+-dependent adenosine triphosphatase as receptor for divalent cations in bacterial sensing.

Authors:  R S Zukin; D E Koshland
Journal:  Science       Date:  1976-07-30       Impact factor: 47.728

Review 2.  Mechanism of oxidative phosphorylation.

Authors:  E C Slater
Journal:  Annu Rev Biochem       Date:  1977       Impact factor: 23.643

3.  Inversion of aerotactic response in Escherichia coli deficient in cheB protein methylesterase.

Authors:  C V Dang; M Niwano; J Ryu; B L Taylor
Journal:  J Bacteriol       Date:  1986-04       Impact factor: 3.490

4.  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

5.  Intrinsic and extrinsic light responses of Salmonella typhimurium and Escherichia coli.

Authors:  B L Taylor; D E Koshland
Journal:  J Bacteriol       Date:  1975-08       Impact factor: 3.490

6.  Change in membrane potential during bacterial chemotaxis.

Authors:  S Szmelcman; J Adler
Journal:  Proc Natl Acad Sci U S A       Date:  1976-12       Impact factor: 11.205

7.  Identification of a methyl-accepting chemotaxis protein for the ribose and galactose chemoreceptors of Escherichia coli.

Authors:  H Kondoh; C B Ball; J Adler
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

8.  Phototaxis and membrane potential in the photosynthetic bacterium Rhodospirillum rubrum.

Authors:  S Harayama; T Iino
Journal:  J Bacteriol       Date:  1977-07       Impact factor: 3.490

9.  Chemotaxis in bacteria.

Authors:  J Adler
Journal:  Science       Date:  1966-08-12       Impact factor: 47.728

10.  Sensory electrophysiology of bacteria: relationship of the membrane potential to motility and chemotaxis in Bacillus subtilis.

Authors:  J B Miller; D E Koshland
Journal:  Proc Natl Acad Sci U S A       Date:  1977-11       Impact factor: 11.205

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  25 in total

1.  Loss of cytochrome c oxidase activity and acquisition of resistance to quinone analogs in a laccase-positive variant of Azospirillum lipoferum.

Authors:  G Alexandre; R Bally; B L Taylor; I B Zhulin
Journal:  J Bacteriol       Date:  1999-11       Impact factor: 3.490

Review 2.  More than one way to sense chemicals.

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

Review 3.  PAS domains: internal sensors of oxygen, redox potential, and light.

Authors:  B L Taylor; I B Zhulin
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

4.  Energy taxis is the dominant behavior in Azospirillum brasilense.

Authors:  G Alexandre; S E Greer; I B Zhulin
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

5.  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

6.  Differentiation between electron transport sensing and proton motive force sensing by the Aer and Tsr receptors for aerotaxis.

Authors:  Jessica C Edwards; Mark S Johnson; Barry L Taylor
Journal:  Mol Microbiol       Date:  2006-09-21       Impact factor: 3.501

Review 7.  The two-component signaling pathway of bacterial chemotaxis: a molecular view of signal transduction by receptors, kinases, and adaptation enzymes.

Authors:  J J Falke; R B Bass; S L Butler; S A Chervitz; M A Danielson
Journal:  Annu Rev Cell Dev Biol       Date:  1997       Impact factor: 13.827

8.  Energy sensors for aerotaxis in Escherichia coli: something old, something new.

Authors:  A M Stock
Journal:  Proc Natl Acad Sci U S A       Date:  1997-09-30       Impact factor: 11.205

9.  Magneto-aerotaxis in marine coccoid bacteria.

Authors:  R B Frankel; D A Bazylinski; M S Johnson; B L Taylor
Journal:  Biophys J       Date:  1997-08       Impact factor: 4.033

Review 10.  Bacterial energy taxis: a global strategy?

Authors:  Tobias Schweinitzer; Christine Josenhans
Journal:  Arch Microbiol       Date:  2010-04-22       Impact factor: 2.552

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