Literature DB >> 6305913

Interactions between chemotaxis genes and flagellar genes in Escherichia coli.

J S Parkinson, S R Parker, P B Talbert, S E Houts.   

Abstract

Escherichia coli mutants defective in cheY and cheZ function are motile but generally nonchemotactic; cheY mutants have an extreme counterclockwise bias in flagellar rotation, whereas cheZ mutants have a clockwise rotational bias. Chemotactic pseudorevertants of cheY and cheZ mutants were isolated on semisolid agar and examined for second-site suppressors in other chemotaxis-related loci. Approximately 15% of the cheZ revertants and over 95% of the cheY revertants contained compensatory mutations in the flaA or flaB locus. When transferred to an otherwise wild-type background, most of these suppressor mutations resulted in a generally nonchemotactic phenotype: suppressors of cheY caused a clockwise rotational bias; suppressors of cheZ produced a counterclockwise rotational bias. Chemotactic double mutants containing a che and a fla mutation invariably exhibited flagellar rotation patterns in between the opposing extremes characteristic of the component mutations. This additive effect on flagellar rotation resulted in essentially wild-type swimming behavior and is probably the major basis of suppressor action. However, suppression effects were also allele specific, suggesting that the cheY and cheZ gene products interact directly with the flaA and flaB products. These interactions may be instrumental in establishing the unstimulated swimming pattern of E. coli.

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Year:  1983        PMID: 6305913      PMCID: PMC217677          DOI: 10.1128/jb.155.1.265-274.1983

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


  28 in total

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

Authors:  J S Parkinson
Journal:  J Bacteriol       Date:  1976-05       Impact factor: 3.490

2.  Flagellar rotation and the mechanism of bacterial motility.

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

3.  Dynamic properties of bacterial flagellar motors.

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

4.  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

5.  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

6.  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

7.  Complementation of nonchemotactic mutants of Escherichia coli.

Authors:  J B Armstrong; J Adler
Journal:  Genetics       Date:  1969-01       Impact factor: 4.562

8.  Transient response to chemotactic stimuli in Escherichia coli.

Authors:  H C Berg; P M Tedesco
Journal:  Proc Natl Acad Sci U S A       Date:  1975-08       Impact factor: 11.205

9.  Salmonella typhimurium mutants generally defective in chemotaxis.

Authors:  A L Collins; B A Stocker
Journal:  J Bacteriol       Date:  1976-12       Impact factor: 3.490

10.  Genetic analysis of flagellar mutants in Escherichia coli.

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

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  80 in total

1.  Characterization of photodamage to Escherichia coli in optical traps.

Authors:  K C Neuman; E H Chadd; G F Liou; K Bergman; S M Block
Journal:  Biophys J       Date:  1999-11       Impact factor: 4.033

2.  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

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.  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

5.  Diffusion of Bacterial Cells in Porous Media.

Authors:  Nicholas A Licata; Bitan Mohari; Clay Fuqua; Sima Setayeshgar
Journal:  Biophys J       Date:  2016-01-05       Impact factor: 4.033

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.  Flagellar switch of Salmonella typhimurium: gene sequences and deduced protein sequences.

Authors:  M Kihara; M Homma; K Kutsukake; R M Macnab
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

10.  DNA sequence analysis, gene product identification, and localization of flagellar motor components of Escherichia coli.

Authors:  J Malakooti; Y Komeda; P Matsumura
Journal:  J Bacteriol       Date:  1989-05       Impact factor: 3.490

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