Literature DB >> 4930422

Influence of chromosome structure on the frequency of tonB trp deletions in Escherichia coli.

M B Coukell, C Yanofsky.   

Abstract

The frequency of tonB trp deletions varies in different strains and substrains of Escherichia coli. Studies with chromosomal hybrids constructed by transducing various segments of the cysB-trp-suIII region from K-12(Ymel) into K-12(W3110) indicate that the characteristic low deletion frequency of K-12(Ymel) is determined largely by the (genetic) structure of the trp-suIII region of the chromosome. Transduction of the trp region from K-12(W3110) or K-12(Ymel) into strain B has little effect on the frequency of tonB trp deletions in that strain. When tonB trp deletions occur at 42 C rather than at 37 C, there is a significant reduction in the frequency of deletions in all strains examined except K-12(Ymel) and hybrids exhibiting a Ymel deletion pattern. The magnitude of this temperature effect in different K-12 strains increases proportionally with the frequency of tonB trp deletions at 37 C. At 42 C the frequency of tonB trp deletions in all K-12 strains approaches the low frequency observed for Ymel at 37 or 42 C. In contrast, spontaneous deletions in another region of the genome which simultaneously result in resistance to phages T7 and lambda and in proline auxotrophy (tfrA pro deletions) occur at a constant frequency regardless of growth temperature or the structure of the chromosome in the trp region. Two mutants of strain KB30 obtained after treatment with nitrosoguanidine show very low tonB trp deletion frequencies. The alterations in both mutants map in the trp region of the chromosome. These studies indicate that the structure of the cysB-trp-suIII region is responsible for many of the characteristic deletion frequencies observed.

Entities:  

Mesh:

Substances:

Year:  1971        PMID: 4930422      PMCID: PMC248511          DOI: 10.1128/jb.105.3.864-872.1971

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


  14 in total

1.  On the production of deletions in the chromosome of Escherichia coli.

Authors:  J A Spudich; V Horn; C Yanofsky
Journal:  J Mol Biol       Date:  1970-10-14       Impact factor: 5.469

2.  Spontaneous deletion formation in several classes of Escherichia coli mutants deficient in recombination ability.

Authors:  C W Anderson
Journal:  Mutat Res       Date:  1970-02       Impact factor: 2.433

3.  Isolation of an E. coli strain with a mutation affecting DNA polymerase.

Authors:  P De Lucia; J Cairns
Journal:  Nature       Date:  1969-12-20       Impact factor: 49.962

4.  Genetic analysis of an E. coli strain with a mutation affecting DNA polymerase.

Authors:  J Gross; M Gross
Journal:  Nature       Date:  1969-12-20       Impact factor: 49.962

5.  Repair deficiency in a bacterial mutant defective in DNA polymerase.

Authors:  L Kanner; P Hanawalt
Journal:  Biochem Biophys Res Commun       Date:  1970-04-08       Impact factor: 3.575

Review 6.  Current linkage map of Escherichia coli.

Authors:  A L Taylor
Journal:  Bacteriol Rev       Date:  1970-06

7.  Excision-repair properties of an Escherichia coli mutant deficient in DNA polymerase.

Authors:  J M Boyle; M C Paterson; R B Setlow
Journal:  Nature       Date:  1970-05-23       Impact factor: 49.962

8.  Formation of deletion mutations in recombination-deficient mutants of Escherichia coli.

Authors:  J Inselburg
Journal:  J Bacteriol       Date:  1967-10       Impact factor: 3.490

9.  Extraordinary recombinational events in Escherichia coli. Their independence of the rec+ function.

Authors:  N C Franklin
Journal:  Genetics       Date:  1967-04       Impact factor: 4.562

10.  Transposition of the lac region of Escherichia coli. I. Inversion of the lac operon and transduction of lac by phi80.

Authors:  J R Beckwith; E R Signer
Journal:  J Mol Biol       Date:  1966-08       Impact factor: 5.469

View more
  14 in total

1.  IS1 is involved in deletion formation in the gal region of E. coli K12.

Authors:  H J Reif; H Saedler
Journal:  Mol Gen Genet       Date:  1975

2.  Characterization of colicin S4 and its receptor, OmpW, a minor protein of the Escherichia coli outer membrane.

Authors:  H Pilsl; D Smajs; V Braun
Journal:  J Bacteriol       Date:  1999-06       Impact factor: 3.490

3.  Outer membrane peptides of Yersinia pestis mediating siderophore-independent assimilation of iron.

Authors:  D J Sikkema; R R Brubaker
Journal:  Biol Met       Date:  1989

4.  Peptide transport in Salmonella typhimurium: molecular cloning and characterization of the oligopeptide permease genes.

Authors:  I D Hiles; L M Powell; C F Higgins
Journal:  Mol Gen Genet       Date:  1987-01

5.  Iron-regulated outer membrane proteins of Escherichia coli K-12 and mechanism of action of catechol-substituted cephalosporins.

Authors:  N A Curtis; R L Eisenstadt; S J East; R J Cornford; L A Walker; A J White
Journal:  Antimicrob Agents Chemother       Date:  1988-12       Impact factor: 5.191

6.  Positive selection of mutants with deletions of the gal-chl region of the Salmonella chromosome as a screening procedure for mutagens that cause deletions.

Authors:  M D Alper; B N Ames
Journal:  J Bacteriol       Date:  1975-01       Impact factor: 3.490

7.  Induction of protein X in Escherichia coli.

Authors:  J W Little; P C Hanawalt
Journal:  Mol Gen Genet       Date:  1977-02-15

8.  Variations among glyV-derived glycine tRNA suppressors of glutamic acid codons.

Authors:  E J Murgola; N E Prather; K H Hadley
Journal:  J Bacteriol       Date:  1978-06       Impact factor: 3.490

9.  Genetic map of the opp (Oligopeptide permease) locus of Salmonella typhimurium.

Authors:  C F Higgins; M M Hardie; D Jamieson; L M Powell
Journal:  J Bacteriol       Date:  1983-02       Impact factor: 3.490

10.  Effects of mutations of RAD50, RAD51, RAD52, and related genes on illegitimate recombination in Saccharomyces cerevisiae.

Authors:  Y Tsukamoto; J Kato; H Ikeda
Journal:  Genetics       Date:  1996-02       Impact factor: 4.562

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.