Publication:
Oxidative responses and defense mechanism of hyperpigmented p. Aeruginosa as characterized by proteomics and metabolomics

dc.contributor.authorChadinee Thippakornen_US
dc.contributor.authorChartchalerm Isarankura-Na-ayudhyaen_US
dc.contributor.authorSupitcha Pannengpetchen_US
dc.contributor.authorPatcharee Isarankura-Na-Ayudhyaen_US
dc.contributor.authorNalini Schaduangraten_US
dc.contributor.authorChanin Nantasenamaten_US
dc.contributor.authorVirapong Prachayasittikulen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherThammasat Universityen_US
dc.date.accessioned2019-08-23T10:16:30Z
dc.date.available2019-08-23T10:16:30Z
dc.date.issued2018-06-13en_US
dc.description.abstract© 2018, Leibniz Research Centre for Working Environment and Human Factors. All rights reserved. Pseudomonas aeruginosa is known to produce multiple types of pigment which are involved in its pathogenicity and survival in certain environments. Herein, we reported the identification of P. aeruginosa dark-brown hyperpigmented (HP) strains which have been isolated from clinical samples. In order to study the role of these darkbrown containing secretions, alterations of metabolic processes and cellular responses under microenvironment of this bacterial pathogen, two-dimensional gel electrophoresis (2-DE) in conjunction with peptide mass fingerprinting (PMF) were performed. Protein spots showing the most significant differences and high spot optical density values were selected for further characterization. Fold difference of protein expression levels among those spots were calculated. Three major groups of proteins including anti-oxidant enzyme such as catalase, alkyl hydroperoxide reductase and also iron-superoxide dismutase (Fe-SOD), transmembrane proteins as well as proteins involved in energy metabolism such as ATP synthase and pyruvate/2-oxoglutarate dehydrogenase were significantly decreased in P. aeruginosa HP. Whereas, malate syntase and isocitrate lyase, the key enzyme in glyoxylate cycle as well as alcohol dehydrogenase were significantly increased in P. aeruginosa HP, as compared to the reference strain ATCC 27853. Moreover, the HP exerted SOD-like activity with its IC50 equal to 0.26 mg/ml as measured by NBT assay. Corresponding to secretomic metabolome identification, elevated amounts of anti-oxidant compounds are detected in P. aeruginosa HP than those observed in ATCC 27853. Our findings indicated successful use of proteomics and metabolomics for understanding cell responses and defense mechanisms of P. aeruginosa dark-brown hyperpigmented strains upon surviving in its microenvironment.en_US
dc.identifier.citationEXCLI Journal. Vol.17, (2018), 544-562en_US
dc.identifier.doi10.17179/excli2018-1238en_US
dc.identifier.issn16112156en_US
dc.identifier.other2-s2.0-85051457604en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/44734
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85051457604&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleOxidative responses and defense mechanism of hyperpigmented p. Aeruginosa as characterized by proteomics and metabolomicsen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85051457604&origin=inwarden_US
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