Search results for " fingerprint"

showing 10 items of 157 documents

Estimation of atrazine-degrading genetic potential and activity in three French agricultural soils

2004

The impact of organic amendment (sewage sludge or waste water) used to fertilize agricultural soils was estimated on the atrazine-degrading activity, the atrazine-degrading genetic potential and the bacterial community structure of soils continuously cropped with corn. Long-term application of organic amendment did not modify atrazine-mineralizing activity, which was found to essentially depend on the soil type. It also did not modify atrazine-degrading genetic potential estimated by quantitative PCR targeting atzA, B and C genes, which was shown to depend on soil type. The structure of soil bacterial community determined by RISA fingerprinting was significantly affected by organic amendmen…

DNA BacterialEAU USEEAmendment010501 environmental sciencesBiologyPolymerase Chain ReactionZea mayscomplex mixtures01 natural sciencesApplied Microbiology and BiotechnologyMicrobiologychemistry.chemical_compoundBacterial ProteinsAtrazine[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyBiotransformationSoil MicrobiologyComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciences2. Zero hungerBacteriaEcologybusiness.industryCommunity structureBiodiversity04 agricultural and veterinary sciences15. Life on landSoil typeDNA FingerprintingBiotechnology[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyAgronomyMicrobial population biologyWastewaterchemistrySoil water040103 agronomy & agriculture0401 agriculture forestry and fisheriesAtrazineFrancebusinessSludge
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PCR-DGGE fingerprints of microbial succession during a manufacture of traditional water buffalo mozzarella cheese.

2004

D . E R C O L I N I , G . M A U R I E L L O , G . B L A I O T T A , G . M O S C H E T T I A N D S . C O P P O L A . 2003. Aims: To monitor the process and the starter effectiveness recording a series of fingerprints of the microbial diversity occurring at different steps of mozzarella cheese manufacture and to investigate the involvement of the natural starter to the achievement of the final product. Methods and Results: Samples of raw milk, natural whey culture (NWC) used as starter, curd after ripening and final product were collected during a mozzarella cheese manufacture. Total microbial DNA was directly extracted from the dairy samples as well as bulk colonies collected from the plates…

DNA BacterialElectrophoresisfood.ingredientFood HandlingMicroorganismColony Count MicrobialApplied Microbiology and BiotechnologyPolymerase Chain Reactionchemistry.chemical_compoundfoodStarterCheeseAgarFood microbiologyAnimalsFood scienceLactic AcidPCR-DGGEbiologyChemistrymeshophilic bacteriafood and beveragesStreptococcusGeneral MedicineBiodiversityRaw milkbiology.organism_classificationDNA FingerprintingLactic acidCulture Mediamozzarella cheeseMilkmicrobial diversity natural whey culture PCR–DGGE analysis product identity quality controlstarter effectiveness tracing system water buffalo mozzarella cheeseFood MicrobiologyBacteriaBiotechnologyMesophileSettore AGR/16 - Microbiologia AgrariaJournal of applied microbiology
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Diversity of rhizobia nodulating wild shrubs of Sicily and some neighbouring islands

2008

Abstract Legume shrubs have great potential for rehabilitation of semi-arid degraded soils in Mediterranean ecosystems as they establish mutualistic symbiosis with Nfxing rhizobia. Eighty-eight symbiotic rhizobia were isolated from seven wild legume shrubs native of Sicily (Southern Italy) and grouped in operational taxonomic units (OTU) by analysis of the ribosomal internal transcribed spacer (ITS) polymorphism. Partial sequencing of 16S rRNA gene of representative isolates of each OTU revealed that most Genisteae symbionts are related to Bradyrhizobium canariense, B. japonicum and B. elkanii. Teline monspessulana was the only Genistea nodulated by Mesorhizobium strains, and Anagyris foeti…

DNA BacterialGenotypeRhizobium · Bradyrhizobium · 16SrDNA · Symbiotic genes · Mediterranean wild legumes · Genisteae · Thermopsideae · Soil rehabilitation · Nodule occupancyMolecular Sequence DataGenisteaeSettore BIO/19 - Microbiologia GeneraleSoil rehabilitationSymbiotic geneDNA RibosomalPlant RootsBiochemistryMicrobiologyBradyrhizobiumRhizobiaBacterial ProteinsSymbiosisRhizobiaceaeRNA Ribosomal 16SDNA Ribosomal SpacerBotanyGeneticsCluster AnalysisBradyrhizobiaceaeBiomassBradyrhizobiumInternal transcribed spacerSicilyMolecular BiologyPhylogenyPolymorphism Geneticbiology16SrDNAMesorhizobiumfood and beveragesFabaceaeBiodiversitySequence Analysis DNAGeneral Medicinebiology.organism_classificationGenisteaeDNA FingerprintingNodule occupancyThermopsideaeRhizobiumMediterranean wild legumeAcyltransferasesRhizobium
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Genotypic characterization of Bradyrhizobium strains nodulating small Senegalese legumes by 16S-23S rRNA intergenic gene spacers and amplified fragme…

2000

ABSTRACT We examined the genotypic diversity of 64 Bradyrhizobium strains isolated from nodules from 27 native leguminous plant species in Senegal (West Africa) belonging to the genera Abrus , Alysicarpus , Bryaspis , Chamaecrista , Cassia , Crotalaria , Desmodium , Eriosema , Indigofera , Moghania , Rhynchosia , Sesbania , Tephrosia , and Zornia , which play an ecological role and have agronomic potential in arid regions. The strains were characterized by intergenic spacer (between 16S and 23S rRNA genes) PCR and restriction fragment length polymorphism (IGS PCR-RFLP) and amplified fragment length polymorphism (AFLP) fingerprinting analyses. Fifty-three reference strains of the different B…

DNA BacterialGenotypeTECHNIQUE RFLPBACTERIEBiologyDNA RibosomalPolymerase Chain ReactionApplied Microbiology and BiotechnologyBradyrhizobiumPlant MicrobiologyIntergenic regionRNA Ribosomal 16SGenotypeBotanyCluster AnalysisBradyrhizobiumSYMBIOSERibosomal DNA[SDV.EE]Life Sciences [q-bio]/Ecology environmentGeneticsPlants MedicinalEcologyFIXATION BIOLOGIQUE DE L'AZOTELEGUMINEUSEfood and beveragesFabaceaeRibosomal RNAbiology.organism_classificationDNA FingerprintingAmplified Ribosomal DNA Restriction AnalysisSenegalBacterial Typing TechniquesGENOTYPERNA Ribosomal 23S[SDV.EE] Life Sciences [q-bio]/Ecology environmentNODOSITE VEGETALEPOLYMORPHISME GENETIQUEDNA IntergenicAmplified fragment length polymorphismRestriction fragment length polymorphismANALYSE GENETIQUEPolymorphism Restriction Fragment LengthFood ScienceBiotechnology
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Acidobacteria dominate the active bacterial communities of Arctic tundra with widely divergent winter-time snow accumulation and soil temperatures.

2012

The timing and extent of snow cover is a major controller of soil temperature and hence winter-time microbial activity and plant diversity in Arctic tundra ecosystems. To understand how snow dynamics shape the bacterial communities, we analyzed the bacterial community composition of windswept and snow-accumulating shrub-dominated tundra heaths of northern Finland using DNA- and RNA-based 16S rRNA gene community fingerprinting (terminal restriction fragment polymorphism) and clone library analysis. Members of the Acidobacteria and Proteobacteria dominated the bacterial communities of both windswept and snow-accumulating habitats with the most abundant phylotypes corresponding to subdivision …

DNA BacterialLibraryMolecular Sequence DataApplied Microbiology and BiotechnologyMicrobiologySoilRNA Ribosomal 16SSnowBotanyProteobacteriaEcosystemEcosystemFinlandSoil MicrobiologyEcologybiologyBacteriaBase SequenceEcologyArctic RegionsTemperatureGenes rRNAPlantsbiology.organism_classificationSnowTundraAcidobacteriaRNA BacterialHabitatSeasonsProteobacteriaCommunity Fingerprintinghuman activitiesAcidobacteriaFEMS microbiology ecology
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Effect of natamycin on the enumeration, genetic structure and composition of bacterial community isolated from soils and soybean rhizosphere

2004

Natamycin is commonly used to control fungal growth on agar media used for bacterial enumeration or strain isolation. However, there is no conclusive report on the possible effect of this antibiotic on bacterial growth or on the diversity of the recovered soil bacteria. Therefore, the possible effects of natamycin on the numbers of bacteria isolated at 12 degrees C from three different soils and soybean rhizosphere soil were investigated using natamycin concentrations ranging from 0 to 200 mg l(-1). Our results demonstrate that natamycin concentrations, which inhibit the growth of fungi on the media, have a small but significant inhibitory effect on the number of bacterial colony forming un…

DNA BacterialMicrobiology (medical)Antifungal Agentsfood.ingredientNatamycinRibosomal Intergenic Spacer analysisColony Count MicrobialBacterial growthBiologyPlant RootsMicrobiologyMicrobiologyBacterial genetics03 medical and health sciencesNatamycinfoodRNA Ribosomal 16SDNA Ribosomal SpacermedicineAgar[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyMolecular BiologySoil MicrobiologyComputingMilieux_MISCELLANEOUS030304 developmental biologyPrincipal Component Analysis0303 health sciencesRhizosphereBacteria030306 microbiologyGenetic VariationDNA Restriction Enzymesbiology.organism_classificationDNA Fingerprinting[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologySoybeansSoil microbiologyBacteriamedicine.drugJournal of Microbiological Methods
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DNA Amplification Fingerprinting for Subtyping Neisseria gonorrhoeae Strains

1995

Background and Objectives DNA amplification fingerprinting is used in most epidemiologic studies as a substitute for conventional typing methods. DNA amplification fingerprinting and conventional typing methods were compared in this epidemiologic study of Neisseria gonorrhoeae. Goal of This Study To differentiate 70 Neisseria gonorrhoeae isolates from untreated patients with urogenital gonococcal infection. Study Design Gonococcal strains were characterized by auxo-typing, serotyping, plasmid profile, antibiotic sensitivity, and DNA amplification fingerprinting. The method of unweighted pair-group average linkage was used for cluster analysis. Discriminatory power was calculated applying Si…

DNA BacterialMicrobiology (medical)SerotypeSexually transmitted diseasePenicillin ResistanceMolecular Sequence DataMicrobial Sensitivity TestsDermatologyBiologymedicine.disease_causechemistry.chemical_compoundPlasmidmedicineHumansSerotypingElectrophoresis Agar GelGeneticsBase SequencePublic Health Environmental and Occupational HealthNucleic acid amplification techniquebiology.organism_classificationDNA FingerprintingVirologyNeisseria gonorrhoeaeSubtypingBacterial Typing TechniquesInfectious DiseaseschemistryNeisseria gonorrhoeaeNeisseriaceaeNucleic Acid Amplification TechniquesDNASexually Transmitted Diseases
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Identification of bacterial groups preferentially associated with mycorrhizal roots of Medicago truncatula

2007

ABSTRACT The genetic structures of bacterial communities associated with Medicago truncatula Gaertn. cv. Jemalong line J5 (Myc + Nod + ) and its symbiosis-defective mutants TRV48 (Myc + Nod − ) and TRV25 (Myc − Nod − ) were compared. Plants were cultivated in a fertile soil (Châteaurenard, France) and in soil from the Mediterranean basin showing a low fertility (Mas d'Imbert, France). Plant growth, root architecture, and the efficiency of root symbiosis of the three plant genotypes were characterized in the two soils. Structures of the bacterial communities were assessed by automated-ribosomal intergenic spacer analysis (A-RISA) fingerprinting from DNA extracted from the rhizosphere soil an…

DNA BacterialMolecular Sequence DataApplied Microbiology and BiotechnologyPlant RootsMicrobial Ecology03 medical and health scienceschemistry.chemical_compoundSymbiosisMolecular markerMycorrhizaeBotanyDNA Ribosomal SpacerMedicago truncatulaMycorrhizaRELATION PLANTE-MICROORGANISMESymbiosisSoil Microbiology030304 developmental biologyOxalobacteraceae2. Zero hunger[SDV.EE]Life Sciences [q-bio]/Ecology environment0303 health sciencesRhizosphereEcologybiology030306 microbiologyBetaproteobacteriaSequence Analysis DNA15. Life on landbiology.organism_classificationDNA FingerprintingMedicago truncatulachemistrySoil fertilitySoil microbiologyFood ScienceBiotechnology
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Lactobacillus oeni sp. nov., from wine.

2009

Ten Lactobacillus strains, previously isolated from different Bobal grape wines from the Utiel-Requena Origin Denomination of Spain, were characterized phylogenetically, genotypically and phenotypically. The 16S rRNA genes were sequenced and phylogenetic analysis showed that they form a tight phylogenetic clade that is closely related to reference strains Lactobacillus satsumensis NRIC 0604T, ‘Lactobacillus uvarum’ 8 and Lactobacillus mali DSM 20444T. DNA–DNA hybridization results confirmed the separation of the strains from other Lactobacillus species. Genotypically, the strains could be differentiated from their closest neighbours by 16S amplified rDNA restriction analysis and random ampl…

DNA BacterialMolecular Sequence DataWineMicrobiologyDNA RibosomalMicrobiologyAesculinchemistry.chemical_compoundPhylogeneticsLactobacillusRNA Ribosomal 16SGenotypeCluster AnalysisAnaerobiosisEcology Evolution Behavior and SystematicsPhylogenyWinebiologyPhylogenetic treefood and beveragesNucleic Acid HybridizationGeneral MedicineSequence Analysis DNAbiology.organism_classification16S ribosomal RNACatalaseDNA FingerprintingBacterial Typing TechniquesRandom Amplified Polymorphic DNA TechniqueLactobacilluschemistrySpainBacteriaPolymorphism Restriction Fragment LengthInternational journal of systematic and evolutionary microbiology
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Characterization of Bacterial and Fungal Soil Communities by Automated Ribosomal Intergenic Spacer Analysis Fingerprints: Biological and Methodologic…

2001

ABSTRACT Automated rRNA intergenic spacer analysis (ARISA) was used to characterise bacterial (B-ARISA) and fungal (F-ARISA) communities from different soil types. The 16S-23S intergenic spacer region from the bacterial rRNA operon was amplified from total soil community DNA for B-ARISA. Similarly, the two internal transcribed spacers and the 5.8S rRNA gene (ITS1-5.8S-ITS2) from the fungal rRNA operon were amplified from total soil community DNA for F-ARISA. Universal fluorescence-labeled primers were used for the PCRs, and fragments of between 200 and 1,200 bp were resolved on denaturing polyacrylamide gels by use of an automated sequencer with laser detection. Methodological (DNA extracti…

DNA BacterialRibosomal Intergenic Spacer analysisBiologyPolymerase Chain ReactionApplied Microbiology and Biotechnology03 medical and health sciencesIntergenic regionRNA Ribosomal 16SDNA Ribosomal SpacerMethodsDNA FungalComputingMilieux_MISCELLANEOUSEcosystemSoil Microbiology030304 developmental biology[SDV.EE]Life Sciences [q-bio]/Ecology environmentGenetics[ SDE.BE ] Environmental Sciences/Biodiversity and Ecology0303 health sciencesBacteriaEcology030306 microbiologyFungiReproducibility of ResultsGenes rRNASpacer DNABIOLOGIE MOLECULAIRERibosomal RNADNA FingerprintingDNA extraction[SDV.EE] Life Sciences [q-bio]/Ecology environmentRNA Ribosomal 23SDNA profilingRRNA Operon[SDE.BE]Environmental Sciences/Biodiversity and EcologySoil microbiologyFood ScienceBiotechnologyApplied and Environmental Microbiology
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