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1.
Photochem Photobiol Sci ; 13(5): 739-50, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24637630

RESUMO

UV-resistant Acinetobacter sp. Ver3 isolated from High-Altitude Andean Lakes (HAAL) in Argentinean Puna, one of the highest UV exposed ecosystems on Earth, showed efficient DNA photorepairing ability, coupled to highly efficient antioxidant enzyme activities in response to UV-B stress. We herein present the cloning, expression, and functional characterization of a cyclobutane pyrimidine dimer (CPD)-class I photolyase (Ver3Phr) from this extremophile to prove its involvement in the previously noted survival capability. Spectroscopy of the overexpressed and purified protein identified flavin adenine dinucleotide (FAD) and 5,10-methenyltetrahydrofolate (MTHF) as chromophore and antenna molecules, respectively. All functional analyses were performed in parallel with the ortholog E. coli photolyase. Whereas the E. coli enzyme showed the FAD chromophore as a mixture of oxidised and reduced states, the Ver3 chromophore always remained partly (including the semiquinone state) or fully reduced under all experimental conditions tested. Functional complementation of Ver3Phr in Phr(-)-RecA E. coli strains was assessed by traditional UFC counting and measurement of DNA bipyrimidine photoproducts by HPLC coupled with electrospray ionisation-tandem mass spectrometry (ESI-MS/MS) detection. The results identified strong photoreactivation ability in vivo of Ver3Phr while its nonphotoreactivation function, probably related with the stimulation of nucleotide excision repair (NER), was not as manifest as for EcPhr. Whether this is a question of the approach using an exogenous photolyase incorporated in a non-genuine host or a fundamental different behaviour of a novel enzyme from an exotic environment will need further studies.


Assuntos
Acinetobacter/enzimologia , Acinetobacter/efeitos da radiação , Altitude , Desoxirribodipirimidina Fotoliase/metabolismo , Lagos/microbiologia , Dímeros de Pirimidina/metabolismo , Raios Ultravioleta , Acinetobacter/isolamento & purificação , Desoxirribodipirimidina Fotoliase/química , Desoxirribodipirimidina Fotoliase/classificação , Dados de Sequência Molecular , Filogenia
2.
Plant J ; 76(2): 322-31, 2013 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-23865633

RESUMO

In Arabidopsis thaliana, light signals modulate the defences against bacteria. Here we show that light perceived by the LOV domain-regulated two-component system (Pst-Lov) of Pseudomonas syringae pv. tomato DC3000 (Pst DC3000) modulates virulence against A. thaliana. Bioinformatic analysis and the existence of an episomal circular intermediate indicate that the locus encoding Pst-Lov is present in an active genomic island acquired by horizontal transfer. Strains mutated at Pst-Lov showed enhanced growth on minimal medium and in leaves of A. thaliana exposed to light, but not in leaves incubated in darkness or buried in the soil. Pst-Lov repressed the expression of principal and alternative sigma factor genes and their downstream targets linked to bacterial growth, virulence and quorum sensing, in a strictly light-dependent manner. We propose that the function of Pst-Lov is to distinguish between soil (dark) and leaf (light) environments, attenuating the damage caused to host tissues while releasing growth out of the host. Therefore, in addition to its direct actions via photosynthesis and plant sensory receptors, light may affect plants indirectly via the sensory receptors of bacterial pathogens.


Assuntos
Ilhas Genômicas , Luz , Fotorreceptores Microbianos/genética , Folhas de Planta/microbiologia , Pseudomonas syringae/patogenicidade , Virulência , Arabidopsis/microbiologia , Arabidopsis/efeitos da radiação , Regulação Bacteriana da Expressão Gênica , Transferência Genética Horizontal , Fases de Leitura Aberta , Óperon , Fotorreceptores Microbianos/efeitos da radiação , Doenças das Plantas/microbiologia , Folhas de Planta/efeitos da radiação , Pseudomonas syringae/genética , Percepção de Quorum , Fator sigma/metabolismo
3.
Orig Life Evol Biosph ; 42(2-3): 201-21, 2012 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-22644565

RESUMO

High-Altitude Andean Lakes (HAAL) of the South American Andes are almost unexplored ecosystems of shallow lakes. The HAAL are recognized by a remarkably high UV exposure, strong changes in temperature and salinity, and a high content of toxic elements, especially arsenic. Being exposed to remarkably extreme conditions, they have been classified as model systems for the study of life on other planets. Particularly, Acinetobacter strains isolated from the HAAL were studied for their survival competence under strong UV-B irradiation. Clinical isolates, Acinetobacter baumannii and Acinetobacter johnsonii, served as reference material. Whereas the reference strains rapidly lost viability under UV-B irradiation, most HAAL-derived strains readily survived this exposure and showed less change in cell number after the treatment. Controls for DNA repair activity, comparing dark repair (DR) or photo repair (PR), gave evidence for the involvement of photolyases in the DNA repair. Comparative measurements by HPLC-mass spectrometry detected the number of photoproducts: bipyrimidine dimers under both PR and DR treatments were more efficiently repaired in the HAAL strains (up to 85 % PR and 38 % DR) than in the controls (31 % PR and zero DR ability). Analysis of cosmid-cloned total genomic DNA from the most effective DNA-photorepair strain (Ver3) yielded a gene (HQ443199) encoding a protein with clear photolyase signatures belonging to class I CPD-photolyases. Despite the relatively low sequence similarity of 41 % between the enzymes from Ver3 and from E. coli (PDB 1DNPA), a model-building approach revealed a high structural homology to the CPD-photolyase of E. coli.


Assuntos
Acinetobacter/isolamento & purificação , Altitude , Dano ao DNA , Reparo do DNA , Raios Ultravioleta , Microbiologia da Água , Acinetobacter/classificação , Acinetobacter/genética , Acinetobacter/efeitos da radiação , Sequência de Bases , Primers do DNA , Água Doce/microbiologia , Reação em Cadeia da Polimerase
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