Search results for " PCR"

showing 10 items of 153 documents

A real-time PCR assay for detection and quantification of 2-branched (1,3)-β-D–glucan producing lactic acid bacteria in cider

2010

28 p.-1 fig.-4 tab.

DNA Bacterialbeta-GlucansFood spoilageMicrobiologyMelting curve analysisMicrobiologyPolysaccharidesLactobacillus(13)(12)--D-glucanLactic acid bacteriaFood sciencePediococcusOenococcusOenococcus oeniDNA PrimersbiologyBacteriaSpoilageReverse Transcriptase Polymerase Chain ReactionAlcoholic BeveragesGeneral MedicineAmpliconbiology.organism_classificationBacterial Typing TechniquesLactobacillusCidersGenes BacterialGlucosyltransferasesFood MicrobiologyPediococcusProteoglycansOenococcusBacteriaFood ScienceReal-time PCR
researchProduct

Population Data of Nine STR Loci From Western Sicily, Italy

2008

DNA PCR STR
researchProduct

Salt drying: a low-cost, simple and efficient method for storing plants in the field and preserving biological repositories for DNA diversity researc…

2013

Although a variety of methods have been optimized for the collection and storage of plant specimens, most of these are not suited for field expeditions for a variety of logistic reasons. Drying specimens with silica gel in polyethylene bags is currently the standard for field-sampling methods that are suitable for subsequent DNA extraction. However, silica-gel repositories are not readily available in remote areas, and its use is not very cost-effective for the long-term storage of collections or in developing countries with limited research budgets. Salting is an ancient and traditional drying process that preserves food samples by dehydrating tissues and inhibiting water-dependent cellula…

DNA PlantFood spoilagePreservation BiologicalSalt (chemistry)Silica GelBacterial growthBiologySodium Chloridechemistry.chemical_compoundGeneticsmedicineDehydrationDesiccationEcology Evolution Behavior and Systematicschemistry.chemical_classificationbusiness.industrySilica gelSaltingPlantsPulp and paper industrymedicine.diseaseDNA extractionBiotechnologychemistrybusinessApplications of PCRBiotechnologyMolecular ecology resources
researchProduct

Characterization of microbial communities in pest colonized books by molecular biology tools

2011

This work presents the identification of bacteria and fungi colonies in insect infesting books, by cultural-independent methodologies based on molecular biology techniques. Microbial genomic DNA extraction,<em> in vitro</em> amplification of specific target sequences by polymerase chain reactions (PCR), sequencing and sequence analysis were performed. These procedures minimized the samples amount, optimized the diagnostic studies on bacteria and fungi colonization and allowed the identification of many species also in complex microbial consortia. The molecular techniques for sure accomplish and integrate the microbiological standard methods (<em>in vitro</em>&nbs…

EcologySequence analysisMicroorganismSettore BIO/11 - Biologia MolecolareStandard methodsBiologybiology.organism_classificationMolecular biologygenomic DNAgenomic DNA paper biodeteriorationPCR termites infestationInsect Sciencelcsh:ZoologyIdentification (biology)PEST analysisgenomic DNA paper biodeterioration PCR termites infestation.lcsh:QL1-991Ecology Evolution Behavior and SystematicsBacteriaJournal of Entomological and Acarological Research
researchProduct

Protective role of glutathione addition against wine-related stress in Oenococcus oeni

2016

FIliació URV: SIInclòs a la memòria: SI Oenococcus oeni is the main species responsible for the malolactic fermentation (MLF) of wine due to its ability to survive in this environment. Some wine-related stress factors, such as ethanol and low pH, may alter the cell redox balance of O. oeni. For the first time, the ability to uptake glutathione (GSH), an almost universal tripeptide with antioxidant properties, has been associated to the improvement of stress response in O. oeni. Despite the inability of O. oeni to synthesize GSH, this bacterium can capture it from the media. The ability of 30 O. oeni strains to uptake GSH was assessed in this study. Although all of the strains tested were ab…

Enologia0301 basic medicineAntioxidantEnologíamedicine.medical_treatment030106 microbiologyExpressionStressLactic-acid bacteriaGeneVi -- Fermentació malolàcticaWine conditions03 medical and health scienceschemistry.chemical_compoundQuantificationMalolactic fermentationmedicineFatty acidsAdaptationSelectionOenococcus oeniWineEthanolEthanolbiologyMalolactic fermentationLactococcus lactis[ SDV.IDA ] Life Sciences [q-bio]/Food engineeringGlutathionebiology.organism_classificationGlutathioneQuantitative pcrOenologyBiochemistrychemistryLactococcus-lactis0963-9969GlutatióAnisotropyOenococcus oeniBacteriaFood ScienceFood Research International
researchProduct

Real-time PCR detection of Ochroconis lascauxensis involved in the formation of black stains in the Lascaux Cave, France

2012

A real-time Polymerase Chain Reaction (PCR) assay was developed to detect and quantify Ochroconis lascauxensis in the Lascaux Cave in France. This fungus is the principal causal agent of the black stains threatening the Paleolithic paintings of this UNESCO World Heritage Site. The black stains outbreak could not be stopped in spite of using intensive biocide treatments. A sensitive and time-saving protocol is needed for determining the extent of the colonization. Sets of primers that target the ITS and RPB2 regions were designed and evaluated for specificity against O. lascauxensis. Genomic DNA extracted from five species of Ochroconis and 13 other fungal species frequently isolated from ca…

Environmental Engineering[SDV]Life Sciences [q-bio]Pcr assayFungal outbreaksFungusUnesco world heritageReal-Time Polymerase Chain Reactionlaw.inventionMicrobiology03 medical and health sciencesAscomycotaCavelaw[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular Biology[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyEnvironmental Chemistry[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyColoring AgentsDNA FungalWaste Management and Disposal[SDV.MP.MYC]Life Sciences [q-bio]/Microbiology and Parasitology/MycologyPolymerase chain reactionDNA Primers030304 developmental biology0303 health sciencesgeographygeography.geographical_feature_categoryBase Sequencebiology030306 microbiologyEcologyLascaux CaveOchroconis lascauxensisbiology.organism_classification[SDV.MP.MYC] Life Sciences [q-bio]/Microbiology and Parasitology/MycologyPollution3. Good healthgenomic DNAReal-time polymerase chain reactionOchroconis lascauxensis[SDE]Environmental SciencesFranceReal-time PCRScience of The Total Environment
researchProduct

Use of functional genes to quantify denitrifiers in the environment.

2006

During the last decade, application of molecular methods using cultivation-independent approaches has provided new insights into the composition and structure of denitrifying communities in various environments. However, little is known about their abundance, and quantification is still performed using cultivation-based approaches, which are not only biased by the inability to cultivate of many micro-organisms but also fastidious and time-consuming. Two types of cultivation-independent approaches have recently been developed to quantify denitrifiers. The first type, which is based on the hybridization technique, comprises the use of Southern hybridization and DNA arrays. The second type, ba…

Fastidious organismNitratesEcologyNucleic Acid HybridizationFunctional genesComputational biologyBiologyEnvironmentBiochemistryPolymerase Chain ReactionCompetitive pcrlaw.inventionlawMost probable numberGenes BacterialPolymerase chain reactionNitritesSoil MicrobiologySouthern blotOligonucleotide Array Sequence AnalysisBiochemical Society transactions
researchProduct

Indigenous yeast communities in the environment of ‘‘Rovello bianco’’ grape variety and their use in commercial white wine fermentation

2009

The indigenous yeast communities associated with several vineyard habitats were analysed. Wild yeasts were isolated, differentiated at strain level and identified. A phylogenetic tree based on partial 26S rRNA genes was constructed. The strains were characterized and the indigenous Saccharomyces cerevisiae GR1 was then used to carry out a vinification process and compared with a commercial yeast. Wines obtained were subjected to chemical and sensory analysis. The comparison between the two products highlighted differences due to the fer- menting strains employed. The vineyard environment was found to strongly influence the composition of yeast communities, thus, confirming the theory of ‘te…

Fermentation in winemakingWinebiologyAscomycotaPhylogenetic treeBirds Grape variety ‘‘Rovello bianco’’ or ‘‘Greco muscio’’ PCR-DGGE Saccharomyces cerevisiae Vineyard environment Wild yeasts Wine fermentationPhysiologySaccharomyces cerevisiaefood and beveragesGeneral Medicinebiology.organism_classificationApplied Microbiology and BiotechnologyVineyardYeastBirds Grape variety ‘‘Rovello bianco’’ or ‘‘Greco muscio’’ PCR-DGGEBotanyFermentationBiotechnologySettore AGR/16 - Microbiologia Agraria
researchProduct

IL PROCESSO INFIAMMATORIO E LA FIBRILLAZIONE ATRIALE: RELAZIONE FRA I LIVELLI EMATICI DI PCR, FIBRINOGENO C E MMP-9 E DIFFERENTI PATTERN CLINICI DELL…

2011

Fibrillazzione atrialeMMP-9 Fibrinogeno PCR
researchProduct

GIV noroviruses and other enteric viruses in bivalves: a preliminary study.

2012

We evaluated the presence of the enteric viruses: norovirus, adenovirus, enterovirus, astrovirus, hepatitis A virus, and hepatitis E virus in bivalves using nested PCR methods and cell culture assays. Noroviruses GII.4 and GIV.1, adenoviruses types 1 and 2, hepatitis A, and echovirus type 7 were detected in the shellfish tested, which were often co-infected. This is the first study to detect such a high level of viral contamination in Italian mussels (up to four different viral groups in a single sample), and the first to document the presence of GIV NoV in shellfish.

GIV noroviruMicrobiology (medical)PCR assayEnteric viruseEnteric viruses; GIV norovirus; PCR assays; Shellfish; Microbiology (medical)Shellfish
researchProduct