Literature DB >> 4583202

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

M Silverman, M Simon.   

Abstract

In previous work, at least 10 discrete cistrons involved in the synthesis of flagella in Escherichia coli were described. Six cistrons were located between his and uvrC on the genetic map. These were referred to as hag, flaA, flaB, flaC, flaD, and flaE. Four cistrons referred to as mot, flaG, flaH, and flaI were located between uvrC and aroD. In order to determine whether these genes are organized into transcriptional units, a series of Mu phage-induced flagellar mutants was studied. The mutant strains behaved as if they were carrying strong polar mutations. Of 228 independent Mu-induced mutants, 114 with mutations in the his-aroD region of the genetic map were tested by preparing partial diploid strains with episomes carrying a variety of previously defined mutations. The pattern of complementation that emerged indicated that cistrons flaB, flaC, and flaE form a transcriptional unit. Cistron flaO, defined in the course of this study, is also a member of this transcriptional unit. The order of transcription is B-C-O-E. flaA was found to be complex, and it included four cistrons, flaA, flaP, flaQ, and flaR, with the transcriptional order A-P-Q-R. Cistrons flaG and flaH are cotranscribed with the transcriptional order G-H. The remaining genes, flaD, flaI, hag, and mot do not belong to multicistronic transcriptional units. Complementation analysis suggested that the cheC locus is the same as cistron flaA.

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Year:  1973        PMID: 4583202      PMCID: PMC246398          DOI: 10.1128/jb.116.1.114-122.1973

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


  17 in total

1.  Location of genes for motility and chemotaxis on the Escherichia coli genetic map.

Authors:  J B Armstrong; J Adler
Journal:  J Bacteriol       Date:  1969-01       Impact factor: 3.490

2.  Complementation of nonchemotactic mutants of Escherichia coli.

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

3.  Mutation in gal U gene of E. coli blocks phage P1 infection.

Authors:  N C Franklin
Journal:  Virology       Date:  1969-05       Impact factor: 3.616

4.  Insertion of phage Mu. 1 within prophage lambda. A new approach for studying the control of the late functions in bacteriophage lambda.

Authors:  A Toussaint
Journal:  Mol Gen Genet       Date:  1969

5.  Genetical studies of non-flagellate mutants of Salmonella.

Authors:  T Iino; M Enomoto
Journal:  J Gen Microbiol       Date:  1966-06

6.  Nonchemotactic mutants of Escherichia coli.

Authors:  J B Armstrong; J Adler; M M Dahl
Journal:  J Bacteriol       Date:  1967-01       Impact factor: 3.490

7.  A model for three-point analysis of random general transduction.

Authors:  T T Wu
Journal:  Genetics       Date:  1966-08       Impact factor: 4.562

8.  Complementation of non-flagellate Salmonella mutants.

Authors:  T M Joys; B A Stocker
Journal:  J Gen Microbiol       Date:  1965-10

9.  O0 and strong-polar mutations in the gal operon are insertions.

Authors:  E Jordan; H Saedler; P Starlinger
Journal:  Mol Gen Genet       Date:  1968

10.  Bacteriophage Mu integration: on the mechanism of Mu-induced mutations.

Authors:  W Boram; J Abelson
Journal:  J Mol Biol       Date:  1971-11-28       Impact factor: 5.469

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  31 in total

1.  Methylation of a membrane protein involved in bacterial chemotaxis.

Authors:  E N Kort; M F Goy; S H Larsen; J Adler
Journal:  Proc Natl Acad Sci U S A       Date:  1975-10       Impact factor: 11.205

2.  Overproduction of the MotA protein of Escherichia coli and estimation of its wild-type level.

Authors:  M L Wilson; R M Macnab
Journal:  J Bacteriol       Date:  1988-02       Impact factor: 3.490

3.  Isolation and characterization of nondefective transducing lambda bacteriophages carrying fla genes of Escherichia coli K-12.

Authors:  H Kondoh
Journal:  J Bacteriol       Date:  1977-05       Impact factor: 3.490

Review 4.  A complex transcription network controls the early stages of biofilm development by Escherichia coli.

Authors:  Birgit M Prüss; Christopher Besemann; Anne Denton; Alan J Wolfe
Journal:  J Bacteriol       Date:  2006-06       Impact factor: 3.490

5.  Behavioral responses to chemical cues by bacteria.

Authors:  D H Bartlett; P Matsumura
Journal:  J Chem Ecol       Date:  1986-05       Impact factor: 2.626

6.  Co-overproduction and localization of the Escherichia coli motility proteins motA and motB.

Authors:  M L Wilson; R M Macnab
Journal:  J Bacteriol       Date:  1990-07       Impact factor: 3.490

7.  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

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.  Positioning flagellar genes in Escherichia coli by deletion analysis.

Authors:  M Silverman; M Simon
Journal:  J Bacteriol       Date:  1974-01       Impact factor: 3.490

10.  Functional homology of chemotaxis genes in Escherichia coli and Salmonella typhimurium.

Authors:  A L DeFranco; J S Parkinson; D E Koshland
Journal:  J Bacteriol       Date:  1979-07       Impact factor: 3.490

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