Literature DB >> 2121899

Inducible UV repair potential of Pseudomonas aeruginosa PAO.

C S Simonson1, T A Kokjohn, R V Miller.   

Abstract

Pseudomonas aeruginosa PAO lacks UV-inducible Weigle reactivation and Weigle mutagenesis of UV-damaged bacteriophages. This lack of UV-inducible, error-prone DNA repair appears to be due to the absence of efficiently expressed umuDC-like genes in this species. When the P. aeruginosa recA gene is introduced into a recA(Def) mutant of Escherichia coli K12, the P. aeruginosa recA gene product is capable of mediating UV-induced mutagenesis, indicating that it could participate in a recA-lexA-like regulatory network and function in inducible DNA repair pathways if such existed in P. aeruginosa. The presence of the IncP9, UV-resistance plasmid R2 in RecA+ strains of P. aeruginosa PAO allows UV-inducible, mutagenic DNA repair of UV-irradiated bacteriophages. R2 also greatly stimulates the ability of UV radiation to induce mutagenesis of the bacterial chromosome. When R2 is introduced into P. aeruginosa strains containing either the recA908 or recA102 mutation, plasmid-mediated UV resistance and Weigle reactivation are not observed. These observations suggest that the increased protection afforded to P. aeruginosa by R2 is derived from a RecA-mediated, DNA-damage-inducible, error-prone DNA repair system which complements the lack of a chromosomally encoded umuDC-like operon.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2121899     DOI: 10.1099/00221287-136-7-1241

Source DB:  PubMed          Journal:  J Gen Microbiol        ISSN: 0022-1287


  14 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.  Regulation of the rulAB mutagenic DNA repair operon of Pseudomonas syringae by UV-B (290 to 320 nanometers) radiation and analysis of rulAB-mediated mutability in vitro and in planta.

Authors:  J J Kim; G W Sundin
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

3.  Influence of infected cell growth state on bacteriophage reactivation levels.

Authors:  D R Kadavy; J J Shaffer; S E Lott; T A Wolf; C E Bolton; W H Gallimore; E L Martin; K W Nickerson; T A Kokjohn
Journal:  Appl Environ Microbiol       Date:  2000-12       Impact factor: 4.792

4.  Prevalence of broad-host-range lytic bacteriophages of Sphaerotilus natans, Escherichia coli, and Pseudomonas aeruginosa.

Authors:  E C Jensen; H S Schrader; B Rieland; T L Thompson; K W Lee; K W Nickerson; T A Kokjohn
Journal:  Appl Environ Microbiol       Date:  1998-02       Impact factor: 4.792

5.  General and inducible hypermutation facilitate parallel adaptation in Pseudomonas aeruginosa despite divergent mutation spectra.

Authors:  Michael R Weigand; George W Sundin
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-06       Impact factor: 11.205

6.  Characterization of Pseudomonas aeruginosa bacteriophage UNL-1, a bacterial virus with a novel UV-A-inducible DNA damage reactivation phenotype.

Authors:  J J Shaffer; L M Jacobsen; J O Schrader; K W Lee; E L Martin; T A Kokjohn
Journal:  Appl Environ Microbiol       Date:  1999-06       Impact factor: 4.792

7.  The uvrB gene of Pseudomonas aeruginosa is not DNA damage inducible.

Authors:  E Rivera; L Vila; J Barbé
Journal:  J Bacteriol       Date:  1996-09       Impact factor: 3.490

8.  Chlorella virus PBCV-1 encodes a homolog of the bacteriophage T4 UV damage repair gene denV.

Authors:  M Furuta; J O Schrader; H S Schrader; T A Kokjohn; S Nyaga; A K McCullough; R S Lloyd; D E Burbank; D Landstein; L Lane; J L Van Etten
Journal:  Appl Environ Microbiol       Date:  1997-04       Impact factor: 4.792

9.  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

10.  Increased mutagenesis mediated by cloned plasmid CAM-OCT genes: potential for expanding substrate ranges of Pseudomonas spp.

Authors:  D L McBeth; B Hauer
Journal:  Appl Environ Microbiol       Date:  1996-09       Impact factor: 4.792

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.