Literature DB >> 19346306

Elevated mutation frequency in surviving populations of carbon-starved rpoS-deficient Pseudomonas putida is caused by reduced expression of superoxide dismutase and catalase.

Kairi Tarassova1, Radi Tegova, Andres Tover, Riho Teras, Mariliis Tark, Signe Saumaa, Maia Kivisaar.   

Abstract

RpoS is a bacterial sigma factor of RNA polymerase which is involved in the expression of a large number of genes to facilitate survival under starvation conditions and other stresses. The results of our study demonstrate that the frequency of emergence of base substitution mutants is significantly increased in long-term-starved populations of rpoS-deficient Pseudomonas putida cells. The increasing effect of the lack of RpoS on the mutation frequency became apparent in both a plasmid-based test system measuring Phe(+) reversion and a chromosomal rpoB system detecting rifampin-resistant mutants. The elevated mutation frequency coincided with the death of about 95% of the cells in a population of rpoS-deficient P. putida. Artificial overexpression of superoxide dismutase or catalase in the rpoS-deficient strain restored the survival of cells and resulted in a decline in the mutation frequency. This indicated that, compared to wild-type bacteria, rpoS-deficient cells are less protected against damage caused by reactive oxygen species. 7,8-Dihydro-8-oxoguanine (GO) is known to be one of the most stable and frequent base modifications caused by oxygen radical attack on DNA. However, the spectrum of base substitution mutations characterized in rpoS-deficient P. putida was different from that in bacteria lacking the GO repair system: it was broader and more similar to that identified in the wild-type strain. Interestingly, the formation of large deletions was also accompanied by a lack of RpoS. Thus, the accumulation of DNA damage other than GO elevates the frequency of mutation in these bacteria. It is known that oxidative damage of proteins and membrane components, but not that of DNA, is a major reason for the death of cells. Since the increased mutation frequency was associated with a decline in the viability of bacteria, we suppose that the elevation of the mutation frequency in the surviving population of carbon-starved rpoS-deficient P. putida may be caused both by oxidative damage of DNA and enzymes involved in DNA replication and repair fidelity.

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Year:  2009        PMID: 19346306      PMCID: PMC2681911          DOI: 10.1128/JB.01803-08

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


  76 in total

Review 1.  Mutagenicity, toxicity and repair of DNA base damage induced by oxidation.

Authors:  Svein Bjelland; Erling Seeberg
Journal:  Mutat Res       Date:  2003-10-29       Impact factor: 2.433

2.  Escherichia coli cells bearing a ribosomal ambiguity mutation in rpsD have a mutator phenotype that correlates with increased mistranslation.

Authors:  Sergey Balashov; M Zafri Humayun
Journal:  J Bacteriol       Date:  2003-08       Impact factor: 3.490

3.  General stress response regulator RpoS in adaptive mutation and amplification in Escherichia coli.

Authors:  Mary-Jane Lombardo; Ildiko Aponyi; Susan M Rosenberg
Journal:  Genetics       Date:  2004-02       Impact factor: 4.562

4.  Error-prone DNA polymerase IV is controlled by the stress-response sigma factor, RpoS, in Escherichia coli.

Authors:  Jill C Layton; Patricia L Foster
Journal:  Mol Microbiol       Date:  2003-10       Impact factor: 3.501

5.  Stress-induced mutagenesis in bacteria.

Authors:  Ivana Bjedov; Olivier Tenaillon; Bénédicte Gérard; Valeria Souza; Erick Denamur; Miroslav Radman; François Taddei; Ivan Matic
Journal:  Science       Date:  2003-05-30       Impact factor: 47.728

6.  Different spectra of stationary-phase mutations in early-arising versus late-arising mutants of Pseudomonas putida: involvement of the DNA repair enzyme MutY and the stationary-phase sigma factor RpoS.

Authors:  Signe Saumaa; Andres Tover; Lagle Kasak; Maia Kivisaar
Journal:  J Bacteriol       Date:  2002-12       Impact factor: 3.490

7.  Involvement of error-prone DNA polymerase IV in stationary-phase mutagenesis in Pseudomonas putida.

Authors:  Radi Tegova; Andres Tover; Kairi Tarassova; Mariliis Tark; Maia Kivisaar
Journal:  J Bacteriol       Date:  2004-05       Impact factor: 3.490

Review 8.  Diversity of structures and properties among catalases.

Authors:  P Chelikani; I Fita; P C Loewen
Journal:  Cell Mol Life Sci       Date:  2004-01       Impact factor: 9.261

Review 9.  Mutagenic potentials of damaged nucleic acids produced by reactive oxygen/nitrogen species: approaches using synthetic oligonucleotides and nucleotides: survey and summary.

Authors:  Hiroyuki Kamiya
Journal:  Nucleic Acids Res       Date:  2003-01-15       Impact factor: 16.971

10.  Proteome reference map of Pseudomonas putida strain KT2440 for genome expression profiling: distinct responses of KT2440 and Pseudomonas aeruginosa strain PAO1 to iron deprivation and a new form of superoxide dismutase.

Authors:  S Heim; M Ferrer; H Heuer; D Regenhardt; M Nimtz; K N Timmis
Journal:  Environ Microbiol       Date:  2003-12       Impact factor: 5.491

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  5 in total

1.  Molecular analysis of two bacterioferritin genes, bfralpha and bfrbeta, in the model rhizobacterium Pseudomonas putida KT2440.

Authors:  Shicheng Chen; William F Bleam; William J Hickey
Journal:  Appl Environ Microbiol       Date:  2010-06-18       Impact factor: 4.792

2.  The Metabolic Redox Regime of Pseudomonas putida Tunes Its Evolvability toward Novel Xenobiotic Substrates.

Authors:  Özlem Akkaya; Danilo R Pérez-Pantoja; Belén Calles; Pablo I Nikel; Víctor de Lorenzo
Journal:  MBio       Date:  2018-08-28       Impact factor: 7.867

3.  Pseudomonas putida mt-2 tolerates reactive oxygen species generated during matric stress by inducing a major oxidative defense response.

Authors:  Nanna B Svenningsen; Danilo Pérez-Pantoja; Pablo I Nikel; Mette H Nicolaisen; Víctor de Lorenzo; Ole Nybroe
Journal:  BMC Microbiol       Date:  2015-10-06       Impact factor: 3.605

4.  Normal mutation rate variants arise in a Mutator (Mut S) Escherichia coli population.

Authors:  María-Carmen Turrientes; Fernando Baquero; Bruce R Levin; José-Luis Martínez; Aida Ripoll; José-María González-Alba; Raquel Tobes; Marina Manrique; Maria-Rosario Baquero; Mario-José Rodríguez-Domínguez; Rafael Cantón; Juan-Carlos Galán
Journal:  PLoS One       Date:  2013-09-12       Impact factor: 3.240

5.  Colonization efficiency of Pseudomonas putida is influenced by Fis-controlled transcription of nuoA-N operon.

Authors:  Annika Teppo; Andrio Lahesaare; Hanna Ainelo; Kadri Samuel; Maia Kivisaar; Riho Teras
Journal:  PLoS One       Date:  2018-08-02       Impact factor: 3.240

  5 in total

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