Search results for "Domo"

showing 10 items of 508 documents

Genetic potential, diversity and activity of an atrazine-degrading community enriched from a herbicide factory effluent

2008

Aims:  To characterize an atrazine-degrading bacterial community enriched from the wastewater of a herbicide factory. Methods and Results:  The community mineralized 81·4 ± 1·9% of [14C-ring]atrazine and 31·0 ± 1·8% of [14C-ethyl]atrazine within 6 days of batch cultivation in mineral salts medium containing atrazine as the sole nitrogen source. Degradation activity of the community towards different chloro- and methylthio-substituted s-triazine compounds was also demonstrated. Restriction analysis of amplified 16S rDNA revealed high diversity of bacterial populations forming the community, with Pseudomonas species dominating in the clone library. Atrazine-degrading genetic potential of the …

DNA BacterialCOMMUNAUTE BACTERIENNEBioaugmentationWASTEWATERLibraryATRAZINEIndustrial WasteBACTERIAL COMMUNITYBIODEGRADATIONQUANTITATIVE PCRBiologyPolymerase Chain ReactionApplied Microbiology and Biotechnology03 medical and health scienceschemistry.chemical_compoundBiotransformationPseudomonasRNA Ribosomal 16STRZAtrazineGenetic variabilityFood science030304 developmental biology0303 health sciencesGenetic diversityBacteriaHerbicidesTriazines030306 microbiologybusiness.industryGeneral Medicine16S ribosomal RNAbiology.organism_classification6. Clean waterBiotechnology[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitologyatrazine ; biodegradation ; atz ; trz ; bacterial community ; wastewater ; quantitative PCRchemistryATZbusinessBacteriaPlasmidsBiotechnologyJournal of Applied Microbiology
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Pseudomonas litolaris sp. nov., isolated from mediterranean seawater

2012

Strains 2SM5T and 2SM6, two strictly aerobic chemo-organotrophic gammaproteobacteria, were isolated from Mediterranean seawater off the coast of Vinaroz, Castellón, Spain, in February, 1990. They were extensively characterized by a polyphasic study that placed them in the genus Pseudomonas. Phylogenetic analysis of 16S rRNA gene sequences showed that both strains shared 100 % sequence similarity and were closely related to members of the Pseudomonas pertucinogena clade, with less than 97.3 % similarity to strains of established species; Pseudomonas xiamenensis was the closest relative. Analysis of sequences of three housekeeping genes, rpoB, rpoD and gyrB, further confirmed the phylogenetic…

DNA BacterialGenotypeMolecular Sequence DataBiologyDNA RibosomalMicrobiologyPseudomonas pertucinogenaBacterial ProteinsSpecies SpecificityPseudomonasRNA Ribosomal 16SGammaproteobacteriaBotanySeawaterCladePhylogenyEcology Evolution Behavior and SystematicsBase CompositionPhylogenetic treeMediterranean RegionFatty AcidsPseudomonasQuinonesGenes rRNASequence Analysis DNAGeneral MedicinerpoB16S ribosomal RNAbiology.organism_classificationLipidsBacterial Typing TechniquesHousekeeping genePhenotypeSpain
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Bronchial microbiome of severe COPD patients colonised by Pseudomonas aeruginosa

2014

The bronchial microbiome in severe COPD during stability and exacerbation in patients chronically colonised by Pseudomonas aeruginosa (PA), has not been defined. Our objective was to determine the characteristics of the bronchial microbiome of severe COPD patients colonised and not colonised by P. aeruginosa and its changes during exacerbation. COPD patients with severe disease and frequent exacerbations were categorised according to chronic colonisation by P. aeruginosa. Sputum samples were obtained in stability and exacerbation, cultured, and analysed by 16S rRNA gene amplification and pyrosequencing. Sixteen patients were included, 5 of them showing chronic colonisation by P. aeruginosa.…

DNA BacterialMaleMicrobiology (medical)ExacerbationMolecular Sequence DataBronchiBiologymedicine.disease_causeDNA RibosomalArticleMicrobiologyCohort StudiesPulmonary Disease Chronic ObstructiveRNA Ribosomal 16SHaemophilusmedicineCluster AnalysisHumansMicrobiomeMoraxellaPhylogenyAgedAged 80 and overStreptococcusPseudomonas aeruginosaMicrobiotaSputumGeneral MedicineSequence Analysis DNAMiddle Agedbiology.organism_classificationrespiratory tract diseasesColonisationInfectious DiseasesSputumFemalemedicine.symptomEuropean Journal of Clinical Microbiology & Infectious Diseases
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A novel VIM‐type metallo‐beta‐lactamase (VIM‐14) in a Pseudomonas aeruginosa clinical isolate from a neonatal intensive care unit

2011

AbstractA Pseudomonas aeruginosa highly resistant to carbapenems was isolated in a neonatal intensive care unit in Palermo, Italy. The strain was found to carry a novel VIM‐type enzyme, classified as VIM‐14. The novel enzyme differs from VIM‐4 in a G31S mutation. VIM‐14 was harboured in a class 1 integron with a new organization. The integron carried the genes aac7, blaVIM‐14, blaOXA‐20 and aac4 in that order.

DNA BacterialMicrobiology (medical)Settore MED/07 - Microbiologia E Microbiologia ClinicaNeonatal intensive care unitSettore MED/17 - Malattie Infettivemetallo-b-lactamaseAntibiotic resistancemetallo-β-lactamasemedicine.medical_treatmentMolecular Sequence DataMicrobial Sensitivity TestsBiologySettore MED/42 - Igiene Generale E Applicatamedicine.disease_causeIntegronbeta-LactamasesIntegronscarbapenemlaw.inventionMicrobiologyAntibiotic resistancelawDrug Resistance Multiple BacterialIntensive Care Units Neonatalpolycyclic compoundsmedicineHumansVIM-14Antibacterial agentBase SequencePseudomonas aeruginosaInfant Newbornmetallo‐β‐lactamaseAntibiotic resistance; carbapenems; metallo-b-lactamase; Pseudomonas aeruginosa; VIM-14Sequence Analysis DNAGeneral Medicinebiochemical phenomena metabolism and nutritionbacterial infections and mycosesbiology.organism_classificationIntensive care unitInfectious DiseasesPseudomonas aeruginosaBeta-lactamasebiology.proteinbacteriacarbapenemsVIM‐14PseudomonadaceaeClinical Microbiology and Infection
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Distribution and diversity of type III secretion system-like genes in saprophytic and phytopathogenic fluorescent pseudomonads

2004

Type three secretion systems (TTSSs) are protein translocation mechanisms associated with bacterial pathogenicity in host plants, and hypersensitive reactions in non-host plants. Distribution and diversity of TTSS-like genes within a collection of saprophytic and phytopathogenic fluorescent pseudomonads were characterized. This collection included 16 strains belonging to 13 pathogenic species, and 87 strains belonging to five saprophytic species isolated from plant rhizosphere and soil. Presence of conserved hypersensitive reaction/pathogenicity (hrp) genes (hrc RST) was assessed both by PCR using primers designed to amplify the corresponding sequence and by dot-blot hybridization using a P…

DNA BacterialMolecular Sequence DataBiologyPlant RootsPolymerase Chain ReactionApplied Microbiology and BiotechnologyMicrobiologyFluorescenceMicrobiologyType three secretion systemlaw.inventionPSEUDOMOMAS FLUORESCENS03 medical and health sciencesBacterial ProteinslawPseudomonasRNA Ribosomal 16SGenotypeGene[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologySoil MicrobiologyPolymerase chain reactionComputingMilieux_MISCELLANEOUSPlant Diseases030304 developmental biology2. Zero hungerGenetics0303 health sciencesEcology030306 microbiologyGenetic transferGenetic VariationSequence Analysis DNAPlants16S ribosomal RNAbiology.organism_classification[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyPOUVOIR PATHOGENERestriction fragment length polymorphismPolymorphism Restriction Fragment LengthBacteria
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Diversity of chlorophenol-degrading bacteria isolated from contaminated boreal groundwater

1999

Chlorophenol-degrading bacteria from a long-term polluted groundwater aquifer were characterized. All isolates degraded 2,4,6-trichlorophenol and 2,3,4,6-tetrachlorophenol at concentrations detected in the contaminated groundwater (10 mg 1(-1)). Pentachlorophenol was degraded by three isolates when present alone. In two gram-positive isolates, 2,3,4,6-tetrachlorophenol was required as an inducer for the degradation of pentachlorophenol. The gram-positive isolates were sensitive to pentachlorophenol, with an IC50 value of 5 mg/l. Isolates belonging to the Cytophaga/Flexibacter/Bacteroides phylum had IC50 values of 25 and 63 mg/l. Isolates belonging to alpha-, beta- and gamma-Proteobacteria g…

DNA BacterialPentachlorophenolfood.ingredientCaulobacterMolecular Sequence DataFresh WaterAquiferGram-Positive BacteriaBiochemistryMicrobiologyMicrobiology03 medical and health sciencesfoodRalstoniaRNA Ribosomal 16SGram-Negative BacteriaGeneticsMolecular BiologyPhylogeny030304 developmental biologyBase Composition0303 health sciencesgeographygeography.geographical_feature_categoryBacteriabiology030306 microbiologyPseudomonasNocardioidesGenetic VariationGeneral Medicinebiology.organism_classification6. Clean waterBiodegradation EnvironmentalEnvironmental chemistryWater MicrobiologyPolymorphism Restriction Fragment LengthWater Pollutants ChemicalBacteriaGroundwaterFlavobacteriumChlorophenolsArchives of Microbiology
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Absence of endo-1,4-β-glucanase KOR1 alters the Jasmonate-dependent defence response to Pseudomonas syringae in Arabidopsis

2014

During plant-pathogen interactions, the plant cell wall forms part of active defence against invaders. In recent years, cell wall-editing enzymes, associated with growth and development, have been related to plant susceptibility or resistance. Our previous work identified a role for several tomato and Arabidopsis endo-1,4-β-glucanases (EGs) in plant-pathogen interactions. Here we studied the response of the Arabidopsis thaliana T-DNA insertion mutant lacking EG Korrigan1 (KOR1) infected with Pseudomonas syringae. KOR1 is predicted to be an EG which is thought to participate in cellulose biosynthesis. We found that kor1-1 plants were more susceptible to P. syringae, and displayed severe dise…

DNA BacterialPhysiologyLipoxygenaseendo-glucanasesMutantArabidopsisPseudomonas syringaeCyclopentanesPlant ScienceMicrobiologychemistry.chemical_compoundCellulaseCell WallGene Expression Regulation PlantArabidopsisPseudomonas syringaeArabidopsis thalianaOxylipinsJasmonateplant responsePlant DiseasesbiologyArabidopsis ProteinsJasmonic acidfungiCalloseMembrane Proteinsfood and beveragesGlucanasebiology.organism_classificationchemistrycell wallSalicylic AcidAgronomy and Crop ScienceJournal of Plant Physiology
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Fitness drift of an atrazine-degrading population under atrazine selection pressure.

2008

International audience; Pseudomonas sp. ADP harbouring the atrazine catabolic plasmid ADP1 was subcultured in liquid medium containing atrazine as sole source of nitrogen. After approximately 320 generations, a new population evolved which replaced the initial population. This newly evolved population grew faster and degraded atrazine more rapidly than the initial population. Plasmid profiles and Southern blot analyses revealed that the evolved strain, unlike the ancestral strain, presented a tandem duplication of the atzB gene encoding the second enzyme of the atrazine catabolic pathway responsible for the transformation of hydroxyatrazine to N-isopropylammelide. This duplication resulted …

DNA BacterialPopulationBiologyMicrobiologyPSEUDOMONAS SP03 medical and health scienceschemistry.chemical_compoundPlasmidGene DuplicationPseudomonasGene duplicationELEMENTSDirect repeatAtrazineInsertion sequenceSelection GeneticADAPTATIONeducationEcology Evolution Behavior and Systematics030304 developmental biologyGenetics0303 health scienceseducation.field_of_study030306 microbiologySALMONELLA-TYPHIMURIUMSTRAIN ADPCATABOLISM GENESTransformation (genetics)Blotting Southern[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryGenes BacterialBACTERIADNA Transposable ElementsGROWTHAtrazineTandem exon duplicationPLASMIDRESISTANCEPlasmidsEnvironmental microbiology
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Comparison of different primer sets for use in Automated Ribosomal Intergenic Spacer Analysis of complex bacterial communities.

2004

ABSTRACT ITSF and ITSReub, constituting a new primer set designed for the amplification of the 16S-23S rRNA intergenic transcribed spacers, have been compared with primer sets consisting of 1406F and 23Sr (M. M. Fisher and E. W. Triplett, Appl. Environ. Microbiol. 65:4630-4636, 1999) and S-D-Bact-1522-b-S-20 and L-D-Bact-132-a-A-18 (L. Ranjard et al., Appl. Environ. Microbiol. 67:4479-4487, 2001), previously proposed for automated ribosomal intergenic spacer analysis (ARISA) of complex bacterial communities. An agricultural soil and a polluted soil, maize silage, goat milk, a small marble sample from the façade of the Certosa of Pavia (Pavia, Italy), and brine from a deep hypersaline anoxi…

DNA BacterialRibosomal Intergenic Spacer analysisDIVERSITYRNA GENESSettore BIO/19 - Microbiologia GeneralePolymerase Chain ReactionSensitivity and SpecificityApplied Microbiology and BiotechnologyMicrobial Ecologychemistry.chemical_compoundIntergenic regionDNA Ribosomal SpacerEnvironmental MicrobiologyMICROORGANISMSGEO/02 - GEOLOGIA STRATIGRAFICA E SEDIMENTOLOGICAMICROBIAL COMMUNITIESRibosomal DNAEcosystemSoil MicrobiologyDNA PrimersGeneticsBacteriological TechniquesBacteriaBase SequenceEcologybiologyDNASpacer DNARibosomal RNABIO/19 - MICROBIOLOGIA GENERALEbiology.organism_classificationPseudomonas stutzeriLENGTH HETEROGENEITYSOILPCRITSFchemistryACIDFood MicrobiologyITSReubANALYSIS FINGERPRINTSDNABacteriaFood ScienceBiotechnology
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Shifts in diversity and microscale distribution of the adapted bacterial phenotypes due to Hg(II) spiking in soil.

2003

In a previous experiment [Ranjard et al. (2000) FEMS Microbiol Ecol 31:107–115], the spatial heterogeneity of a mercury impact on soil bacterial community was revealed by an increase of mercury-resistant (HgR) bacterial numbers in the outer fraction and the sand fractions when compared to those in the silt fractions. The objectives of the present study were (i) to investigate whether mercury exposure affects the diversity and the distribution within the various fractions of the HgR populations and (ii) to evaluate the contribution of the HgR populations to the overall community adaptation. A total of 236 strains isolated before (104 isolates) and 30 days (132 isolates) after spiking were ch…

DNA BacterialRibosomal Intergenic Spacer analysisMolecular Sequence DataAdaptation BiologicalSoil ScienceStreptomycesPolymerase Chain Reaction03 medical and health sciencesXanthomonasPseudomonasRNA Ribosomal 16SGenotypeEcology Evolution Behavior and SystematicsComputingMilieux_MISCELLANEOUSEcosystemSoil Microbiology2. Zero hungerGenetics[SDV.EE]Life Sciences [q-bio]/Ecology environment0303 health sciencesEcologyPhylogenetic treebiologyBase Sequence030306 microbiology04 agricultural and veterinary sciencesMercuryBIOLOGIE MOLECULAIREbiology.organism_classification16S ribosomal RNAAmplified Ribosomal DNA Restriction AnalysisSpatial heterogeneity[SDV.EE] Life Sciences [q-bio]/Ecology environment040103 agronomy & agriculture0401 agriculture forestry and fisheriesDNA IntergenicMicrobial ecology
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