Literature DB >> 3532103

Restoration of flagellar clockwise rotation in bacterial envelopes by insertion of the chemotaxis protein CheY.

S Ravid, P Matsumura, M Eisenbach.   

Abstract

When cells of the bacterium Salmonella typhimurium are incubated with penicillin and lysed in a dilute buffer, flagellated cytoplasm-free envelopes are formed. When the envelopes are tethered to glass by their flagella and then energized, some of them spin. The direction of rotation of wild-type envelopes is exclusively counterclockwise (CCW). We perturbed this system by including in the lysis medium (and hence in the envelopes) the chemotaxis protein CheY. As a result, some of the envelopes rotated exclusively clockwise (CW). The fraction of envelopes that did so increased with the concentration of CheY; at a concentration of 48 microM (pH 8), all functional envelopes spun CW. The fraction also increased with the pH of the lysis medium in the range of 6.6-8.4. The results were the same in the presence or absence of intracellular Ca2+. Reconstituted envelopes failed to respond to chemotactic stimuli. None of them changed the direction of their rotation. However, when the intracellular pH was lowered to 6.6 or below, envelopes that spun CW stopped rotating, while envelopes that spun CCW continued to rotate. This phenomenon was reversible. We conclude that CheY per se, without any additional free cytoplasmic mediators, interacts with a switch at the base of the flagellum to cause CW rotation.

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Year:  1986        PMID: 3532103      PMCID: PMC386674          DOI: 10.1073/pnas.83.19.7157

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


  30 in total

1.  Flagellar rotation and the mechanism of bacterial motility.

Authors:  M Silverman; M Simon
Journal:  Nature       Date:  1974-05-03       Impact factor: 49.962

2.  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

3.  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

4.  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

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Authors:  J Adler
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1965

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

Authors:  D R Repaske; J Adler
Journal:  J Bacteriol       Date:  1981-03       Impact factor: 3.490

7.  Molecular cloning of chemotaxis genes and overproduction of gene products in the bacterial sensing system.

Authors:  A L DeFranco; D E Koshland
Journal:  J Bacteriol       Date:  1981-08       Impact factor: 3.490

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

Authors:  M Kihara; R M Macnab
Journal:  J Bacteriol       Date:  1981-03       Impact factor: 3.490

Review 9.  Bacterial chemotaxis: biochemistry of behavior in a single cell.

Authors:  G W Ordal
Journal:  Crit Rev Microbiol       Date:  1985       Impact factor: 7.624

10.  Role of methionine in bacterial chemotaxis.

Authors:  D Aswad; D E Koshland
Journal:  J Bacteriol       Date:  1974-05       Impact factor: 3.490

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  48 in total

1.  The LovK-LovR two-component system is a regulator of the general stress pathway in Caulobacter crescentus.

Authors:  Robert Foreman; Aretha Fiebig; Sean Crosson
Journal:  J Bacteriol       Date:  2012-03-09       Impact factor: 3.490

2.  A chemotactic signaling surface on CheY defined by suppressors of flagellar switch mutations.

Authors:  S J Roman; M Meyers; K Volz; P Matsumura
Journal:  J Bacteriol       Date:  1992-10       Impact factor: 3.490

3.  New structural features of the flagellar base in Salmonella typhimurium revealed by rapid-freeze electron microscopy.

Authors:  S Khan; I H Khan; T S Reese
Journal:  J Bacteriol       Date:  1991-05       Impact factor: 3.490

4.  Involvement of the histidine protein (HPr) of the phosphotransferase system in chemotactic signaling of Escherichia coli K-12.

Authors:  G Grübl; A P Vogler; J W Lengeler
Journal:  J Bacteriol       Date:  1990-10       Impact factor: 3.490

5.  Mutational analysis of the transmembrane helix 2-HAMP domain connection in the Escherichia coli aspartate chemoreceptor tar.

Authors:  Gus A Wright; Rachel L Crowder; Roger R Draheim; Michael D Manson
Journal:  J Bacteriol       Date:  2010-09-24       Impact factor: 3.490

6.  Multiple kinetic states for the flagellar motor switch.

Authors:  S C Kuo; D E Koshland
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

7.  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

8.  Transmembrane signal transduction in bacterial chemotaxis involves ligand-dependent activation of phosphate group transfer.

Authors:  K A Borkovich; N Kaplan; J F Hess; M I Simon
Journal:  Proc Natl Acad Sci U S A       Date:  1989-02       Impact factor: 11.205

9.  A molecular understanding of complementary chromatic adaptation.

Authors:  Arthur R Grossman
Journal:  Photosynth Res       Date:  2003       Impact factor: 3.573

10.  Influence of attractants and repellents on methyl group turnover on methyl-accepting chemotaxis proteins of Bacillus subtilis and role of CheW.

Authors:  D W Hanlon; P B Carpenter; G W Ordal
Journal:  J Bacteriol       Date:  1992-07       Impact factor: 3.490

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