Literature DB >> 3129410

Expression of the recA gene of Pseudomonas aeruginosa PAO is inducible by DNA-damaging agents.

R V Miller1, T A Kokjohn.   

Abstract

Western (immunoblot) analysis using Escherichia coli anti-RecA antiserum revealed that expression of the RecA protein of Pseudomonas aeruginosa PAO is induced upon exposure of the bacterium to UV irradiation or norfloxacin, a quinolone related to nalidixic acid.

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Year:  1988        PMID: 3129410      PMCID: PMC211135          DOI: 10.1128/jb.170.5.2385-2387.1988

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


  9 in total

1.  The sequence and function of the recA gene and its protein in Pseudomonas aeruginosa PAO.

Authors:  Y Sano; M Kageyama
Journal:  Mol Gen Genet       Date:  1987-07

2.  Isolation of protease-proficient, recombinase-deficient recA mutants of Escherichia coli K-12.

Authors:  E S Tessman; P K Peterson
Journal:  J Bacteriol       Date:  1985-08       Impact factor: 3.490

3.  Measurement of in vivo expression of the recA gene of Escherichia coli by using lacZ gene fusions.

Authors:  J M Weisemann; C Funk; G M Weinstock
Journal:  J Bacteriol       Date:  1984-10       Impact factor: 3.490

Review 4.  Protein blotting: principles and applications.

Authors:  J M Gershoni; G E Palade
Journal:  Anal Biochem       Date:  1983-05       Impact factor: 3.365

Review 5.  Mutagenesis and inducible responses to deoxyribonucleic acid damage in Escherichia coli.

Authors:  G C Walker
Journal:  Microbiol Rev       Date:  1984-03

6.  Cloned truncated recA genes in E. coli II. Effects of truncated gene products on in vivo recA+ protein activity.

Authors:  G T Yarranton; S G Sedgwick
Journal:  Mol Gen Genet       Date:  1982

7.  Characterization of the Pseudomonas aeruginosa recA analog and its protein product: rec-102 is a mutant allele of the P. aeruginosa PAO recA gene.

Authors:  T A Kokjohn; R V Miller
Journal:  J Bacteriol       Date:  1987-04       Impact factor: 3.490

8.  Effects of norfloxacin on DNA metabolism in Pseudomonas aeruginosa.

Authors:  D M Benbrook; R V Miller
Journal:  Antimicrob Agents Chemother       Date:  1986-01       Impact factor: 5.191

9.  Molecular cloning and characterization of the recA gene of Pseudomonas aeruginosa PAO.

Authors:  T A Kokjohn; R V Miller
Journal:  J Bacteriol       Date:  1985-08       Impact factor: 3.490

  9 in total
  7 in total

1.  Study of the response of a biofilm bacterial community to UV radiation.

Authors:  M O Elasri; R V Miller
Journal:  Appl Environ Microbiol       Date:  1999-05       Impact factor: 4.792

2.  The CAM-OCT plasmid enhances UV responses of Pseudomonas aeruginosa recA mutants.

Authors:  D L McBeth
Journal:  J Bacteriol       Date:  1990-03       Impact factor: 3.490

3.  Effect of degradative plasmid CAM-OCT on responses of Pseudomonas bacteria to UV light.

Authors:  D L McBeth
Journal:  J Bacteriol       Date:  1989-02       Impact factor: 3.490

4.  Regulation of pyocin genes in Pseudomonas aeruginosa by positive (prtN) and negative (prtR) regulatory genes.

Authors:  H Matsui; Y Sano; H Ishihara; T Shinomiya
Journal:  J Bacteriol       Date:  1993-03       Impact factor: 3.490

5.  Characterization of the Burkholderia thailandensis SOS response by using whole-transcriptome shotgun sequencing.

Authors:  Ricky L Ulrich; David Deshazer; Tara A Kenny; Melanie P Ulrich; Anna Moravusova; Timothy Opperman; Sina Bavari; Terry L Bowlin; Donald T Moir; Rekha G Panchal
Journal:  Appl Environ Microbiol       Date:  2013-07-19       Impact factor: 4.792

6.  Characterization of stress-responsive behavior in Pseudomonas aeruginosa PAO: isolation of Tn3-lacZYA fusions with novel damage-inducible (din) promoters.

Authors:  A L Warner-Bartnicki; R V Miller
Journal:  J Bacteriol       Date:  1992-03       Impact factor: 3.490

7.  Molecular cloning of the recA analog from the marine fish pathogen Vibrio anguillarum 775.

Authors:  J T Singer
Journal:  J Bacteriol       Date:  1989-11       Impact factor: 3.490

  7 in total

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