Literature DB >> 770453

cheA, cheB, and cheC genes of Escherichia coli and their role in chemotaxis.

J S Parkinson.   

Abstract

Motile but generally nonchemotatic (che) mutants of Escherichia coli were isolated by a simple screening method. A total of 172 independent mutants were examined, and four genes were defined on the basis of mapping and complemenvestigated by determining their null phenotypes with nonsense or bacteriophage Mu-induced mutations. The cheA and cheB products were essential in producing changes of swimming direction and flagellar rotation. The checC product appeared to be an essential component of the flagellum; however, specific mutational alterations of this component allowed flagellar assembly but prevented directional changes in swimming. Since some cheB mutants changed directions incessantly, this gene product may also serve to control the direction of flagellar rotation in response to chemoreceptor signals. Thus most or all of the common elements in the signalling process were involved in the generation and regulation of changes in the direction of flagellar rotation.

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Year:  1976        PMID: 770453      PMCID: PMC233211          DOI: 10.1128/jb.126.2.758-770.1976

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


  33 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.  Dynamic properties of bacterial flagellar motors.

Authors:  H C Berg
Journal:  Nature       Date:  1974-05-03       Impact factor: 49.962

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.  Bacteria swim by rotating their flagellar filaments.

Authors:  H C Berg; R A Anderson
Journal:  Nature       Date:  1973-10-19       Impact factor: 49.962

5.  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

6.  Nonsense motility mutants in Salmonella typhimurium.

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

7.  Genetic analysis of bacteriophage Mu-induced flagellar mutants in Escherichia coli.

Authors:  M Silverman; M Simon
Journal:  J Bacteriol       Date:  1973-10       Impact factor: 3.490

8.  Rapid mapping of conditional and auxotrophic mutations in Escherichia coli K-12.

Authors:  B Low
Journal:  J Bacteriol       Date:  1973-02       Impact factor: 3.490

9.  Genetic analysis of flagellar mutants in Escherichia coli.

Authors:  M Silverman; M Simon
Journal:  J Bacteriol       Date:  1973-01       Impact factor: 3.490

10.  Temporal stimulation of chemotaxis in Escherichia coli.

Authors:  D A Brown; H C Berg
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

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  115 in total

1.  Clustering of the chemoreceptor complex in Escherichia coli is independent of the methyltransferase CheR and the methylesterase CheB.

Authors:  S R Lybarger; J R Maddock
Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

2.  Crosslinking snapshots of bacterial chemoreceptor squads.

Authors:  Claudia A Studdert; John S Parkinson
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-09       Impact factor: 11.205

3.  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

4.  Chemotactic signaling by an Escherichia coli CheA mutant that lacks the binding domain for phosphoacceptor partners.

Authors:  Knut Jahreis; Tom B Morrison; Andrés Garzón; John S Parkinson
Journal:  J Bacteriol       Date:  2004-05       Impact factor: 3.490

5.  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

6.  Mutant MotB proteins in Escherichia coli.

Authors:  D F Blair; D Y Kim; H C Berg
Journal:  J Bacteriol       Date:  1991-07       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.  Three types of taxis used in the response of Acidovorax sp. strain JS42 to 2-nitrotoluene.

Authors:  Christine A Rabinovitch-Deere; Rebecca E Parales
Journal:  Appl Environ Microbiol       Date:  2012-01-27       Impact factor: 4.792

9.  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

10.  Predataxis behavior in Myxococcus xanthus.

Authors:  James E Berleman; Jodie Scott; Tatiana Chumley; John R Kirby
Journal:  Proc Natl Acad Sci U S A       Date:  2008-10-24       Impact factor: 11.205

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