Literature DB >> 4895049

Spontaneous lethal sectoring, a further feature of Escherichia coli strains deficient in the function of rec and uvr genes.

K Haefner.   

Abstract

Eight recombination-deficient (Rec(-)) mutants of Escherichia coli were studied. Progeny lines were obtained on solid media, by means of micromanipulation, and the colony-forming ability of individual cells was analyzed. Cells of all eight strains gave rise to colony-forming as well as non-colony-forming descendants ("lethal sectoring"). Lethal sectors, i.e., groups of non-colony-forming cells which originate from a common ancestor, appeared with frequencies per generation ranging between 4 and 20% in Rec(-) strains, whereas lethal sectors were rare in Rec(+) strains (less than 1%). A strain carrying a mutation (uvrA6) in one of the genes involved in pyrimidine dimer excision from deoxyribonucleic acid (DNA) showed twice as many lethal sectors per generation as a strain with the genotype uvrA(+). Similarly, a double mutant (AB2480, uvrA6, recA13) showed twice as much spontaneous lethal sectoring as the corresponding Rec(-) strain (uvrA(+), recA13). The kinetics of growth curves obtained in nutrient broth and the frequency of non-colony-forming units in stationary-phase broth cultures indicate clearly that lethal sectors occur in liquid cultures too. The causes for spontaneous lethal sectoring are unknown at present. It seems reasonable to assume that gene uvrA and the rec genes are somehow involved in the repair of spontaneously occurring DNA lesions, since a deficiency in this type of repair may cause lethal sectors. The extent to which spontaneous lethal sectoring (observed in all Rec(-) strains of E. coli studied) may contribute indirectly to the failure to form recombinants is discussed.

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Year:  1968        PMID: 4895049      PMCID: PMC252355          DOI: 10.1128/jb.96.3.652-659.1968

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


  18 in total

1.  THE DISAPPEARANCE OF THYMINE DIMERS FROM DNA: AN ERROR-CORRECTING MECHANISM.

Authors:  R B SETLOW; W L CARRIER
Journal:  Proc Natl Acad Sci U S A       Date:  1964-02       Impact factor: 11.205

2.  ISOLATION AND CHARACTERIZATION OF RECOMBINATION-DEFICIENT MUTANTS OF ESCHERICHIA COLI K12.

Authors:  A J CLARK; A D MARGULIES
Journal:  Proc Natl Acad Sci U S A       Date:  1965-02       Impact factor: 11.205

3.  Recombination and segregation in Escherichia coli.

Authors:  T F ANDERSON
Journal:  Cold Spring Harb Symp Quant Biol       Date:  1958

4.  GENETIC STRUCTURE OF RECOMBINANT CHROMOSOMES FORMED AFTER MATING IN ESCHERICHIA COLI K12.

Authors:  J Tomizawa
Journal:  Proc Natl Acad Sci U S A       Date:  1960-01       Impact factor: 11.205

5.  The beginning of a genetic analysis of recombination proficiency.

Authors:  A J Clark
Journal:  J Cell Physiol       Date:  1967-10       Impact factor: 6.384

6.  The enzymatic repair of DNA. I. Formation of circular lambda-DNA.

Authors:  M L Gefter; A Becker; J Hurwitz
Journal:  Proc Natl Acad Sci U S A       Date:  1967-07       Impact factor: 11.205

7.  The genetic constitution of the radiation-sensitive mutant Escherichia coli Bs-1.

Authors:  I E Mattern; H Zwenk; A Rörsch
Journal:  Mutat Res       Date:  1966-10       Impact factor: 2.433

8.  DNA repair and genetic recombination: studies on mutants of Escherichia coli defective in these processes.

Authors:  P Howard-Flanders; R P Boyce
Journal:  Radiat Res       Date:  1966       Impact factor: 2.841

9.  Genetic recombination in Escherichia coli: clone heterogeneity and the kinetics of segregation.

Authors:  T H Wood
Journal:  Science       Date:  1967-07-21       Impact factor: 47.728

10.  Properties of four mutants of Escherichia coli defective in genetic recombination.

Authors:  P van de Putte; H Zwenk; A Rörsch
Journal:  Mutat Res       Date:  1966-10       Impact factor: 2.433

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  33 in total

1.  DNA degradation in minicells of Escherichia coli K-12. II. Effect of recA1 and recB21 mutations on DNA degradation in minicells and detection of exonuclease V activity.

Authors:  G G Khachatourians; M C Paterson; R J Sheehy; B V Dorp; T E Worthy
Journal:  Mol Gen Genet       Date:  1975-06-19

2.  Isolation and characterization of mutants of Haemophilus influenzae deficient in an adenosine 5'-triphosphate-dependent deoxyribonuclease activity.

Authors:  K W Wilcox; H O Smith
Journal:  J Bacteriol       Date:  1975-05       Impact factor: 3.490

3.  A Roadblock-and-Kill Mechanism of Action Model for the DNA-Targeting Antibiotic Ciprofloxacin.

Authors:  Nikola Ojkic; Elin Lilja; Susana Direito; Angela Dawson; Rosalind J Allen; Bartlomiej Waclaw
Journal:  Antimicrob Agents Chemother       Date:  2020-08-20       Impact factor: 5.191

4.  Specific effects of a recB mutation on the HfrH strain of Escherichia coli.

Authors:  D Dermić; Z Trgovcević
Journal:  J Bacteriol       Date:  1999-02       Impact factor: 3.490

5.  Metabolic characterization of the viable, residually dividing and nondividing cell classes of recombination-deficient strains of Escherichia coli.

Authors:  J E Miller; S D Barbour
Journal:  J Bacteriol       Date:  1977-04       Impact factor: 3.490

6.  Cell division and DNA synthesis in uvrA recA double mutants of E. coli K12.

Authors:  K Suzuki
Journal:  Mol Gen Genet       Date:  1974-03-27

7.  Analysis of the growth of recombination-deficient strains of Escherichia coli K-12.

Authors:  F N Capaldo; G Ramsey; S D Barbour
Journal:  J Bacteriol       Date:  1974-04       Impact factor: 3.490

Review 8.  Mutator genes in different species.

Authors:  G Mohn; F E Würgler
Journal:  Humangenetik       Date:  1972

9.  Degradation of bacteriophage lambda deoxyribonucleic acid after restriction by Escherichia coli K-12.

Authors:  V F Simmon; S Lederberg
Journal:  J Bacteriol       Date:  1972-10       Impact factor: 3.490

10.  Non-essentiality of the recA- mutation in the phenomenon of bacteriophage M13-induced elimination of F' factors.

Authors:  S R Palchoudhury; V N Iyer
Journal:  J Bacteriol       Date:  1971-06       Impact factor: 3.490

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