Search results for " Restriction Fragment Length"

showing 10 items of 133 documents

Fumonisin production by Gibberella fujikuroi strains fromPinus species

2003

Abstract Fumonisins are important mycotoxins basically produced by strains from the Gibberella fujikuroi species complex (with anamorphs in Fusarium genus) which contaminate food and feed products representing a risk to human and animal health. In this work, we report for the first time the fumonisin production of Fusarium moniliforme Sheldon strains associated to edible pine nuts of Pinus pinea. P. pinea is an important and widely distributed Pinus species in the Mediterranean area where their pine nuts are consumed raw or slightly processed in diverse food products. In this work, characterization and further identification of those strains were performed by polymerase chain reaction-restr…

FusariumSpecies complexGibberellaFood ContaminationFumonisinsMicrobiologychemistry.chemical_compoundSpecies SpecificityGenusBotanyFumonisinNutsDNA FungalMycotoxinChromatography High Pressure LiquidPhylogenybiologyPinus radiatafood and beveragesGeneral MedicineFungi imperfectiMycotoxinsPinusbiology.organism_classificationchemistryFood MicrobiologyGibberella fujikuroiPolymorphism Restriction Fragment LengthFood ScienceInternational Journal of Food Microbiology
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Characterization of Fusarium spp. isolates by PCR-RFLP analysis of the intergenic spacer region of the rRNA gene (rDNA)

2004

In the present study, 44 Fusarium spp. isolates (5 Fusarium culmorum, 7 Fusarium graminearum, 1 Fusarium cerealis, 1 Fusarium poae, 26 Fusarium oxysporum, and 4 Gibberella fujikuroi species complex) were characterized morphologically, physiologically and genetically. All except one (Dutch Collection: CBS 620.72) were isolated from different hosts grown in various Spanish localizations. Morphological characterization was made according to macroscopic and microscopic aspects. Physiological characterization was based on their ability to produce zearalenone (ZEA) and type B trichothecenes (deoxynivalenol, nivalenol and 3-acetyldeoxynivalenol). ZEA was determined by liquid chromatography and tri…

FusariumTrichotheceneFood ContaminationBiologyPolymerase Chain ReactionMicrobiologyGas Chromatography-Mass SpectrometryMicrobiologychemistry.chemical_compoundFusariumSpecies SpecificityVomitoxinDNA Ribosomal SpacerFusarium oxysporumFusarium culmorumCluster AnalysisDNA FungalMycological Typing TechniquesZearalenonePhylogenyfood and beveragesRNA FungalDNA Restriction EnzymesGeneral Medicinebiology.organism_classificationDNA FingerprintingchemistryRNA RibosomalZearalenoneGibberella fujikuroiRestriction fragment length polymorphismEdible GrainTrichothecenesPolymorphism Restriction Fragment LengthFood ScienceInternational Journal of Food Microbiology
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MboII endonuclease heat inactivation before agarose gel electrophoresis to prevent artifactual bands in restriction patterns

1999

Gel electrophoresisDNA BacterialElectrophoresis Agar GelProtein DenaturationSettore MED/07 - Microbiologia E Microbiologia ClinicaHot TemperaturebiologyMolecular biologyGeneral Biochemistry Genetics and Molecular BiologyRestriction fragmentHeat inactivationElectrophoresischemistry.chemical_compoundRestriction enzymeBiochemistrychemistryAgarose gel electrophoresisEnzyme Stabilitybiology.proteinEscherichia coliDeoxyribonucleases Type II Site-SpecificMboII endonucleaseDNAPolymorphism Restriction Fragment LengthBiotechnology
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Polymerase chain reaction analysis of the Xba I polymorphism of the human complement C4 genes provides evidence for strong haplotype conservation.

1995

The genes coding for the two isotypes of the fourth component of human complement, C4A and C4B, are located between the HLA-B and -DR loci of the MHC. We studied the linkage relationship of the previously described XbaI RFLP to obtain further insight into the evolution of the tandemly arranged C4 genes. Using exon-specific PCR amplification followed by restriction analysis and direct DNA sequencing, the polymorphic site could be located in exon 40 of the C4 gene (cDNA position 5095). The polymorphism does not change an amino acid residue. Using nested PCR amplification with isotype-specific primers to amplify either C4A or C4B alleles the haplotype arrangement of the XbaI sites in both isot…

Genetic LinkageImmunologyMolecular Sequence DataBiologyPolymerase Chain Reactionlaw.inventionExonlawComplementary DNAImmunology and AllergyHumansDeoxyribonucleases Type II Site-SpecificGenePolymerase chain reactionGeneticsPolymorphism GeneticBase SequenceHaplotypeIntronChromosome MappingComplement C4General MedicineMolecular biologyRestriction siteHaplotypesRestriction fragment length polymorphismPolymorphism Restriction Fragment LengthHuman immunology
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pcaH, a molecular marker for estimating the diversity of the protocatechuate-degrading bacterial community in the soil environment

2007

Microorganisms degrading phenolic compounds play an important role in soil carbon cycling as well as in pesticide degradation. The pcaH gene encoding a key ring-cleaving enzyme of the -ketoadipate pathway was selected as a functional marker. Using a degenerate primer pair, pcaH fragments were cloned from two agricultural soils. Restriction fragment length polymorphism (RFLP) screening of 150 pcaH clones yielded 68 RFLP families. Comparison of 86 deduced amino acid sequences displayed 70% identity to known PcaH sequences. Phylogenetic analysis results in two major groups mainly related to PcaH sequences from Actinobacteria and Proteobacteria phyla. This confirms that the developed primer pai…

Genetic Markers[SDV]Life Sciences [q-bio]Molecular Sequence DataBACTERIAL COMMUNITYSequence alignmentProtocatechuate-34-DioxygenaseActinobacteriaSOIL DNAchemistry.chemical_compoundBacterial ProteinsSequence Analysis ProteinMolecular markerProteobacteriaAmino Acid SequencePesticidesPhylogenySoil MicrobiologyPROTOCATECHUATE 34-DIOXYGENASEDNA PrimersGeneticsbiologyPhylogenetic treeRESTRICTION FRAGMENT LENGTH POLYMORPHISMPOLYMORPHISME DE RESTRICTIONBiodiversityGeneral Medicinebiology.organism_classificationCarbonActinobacteriaBiodegradation EnvironmentalchemistryGenetic markerInsect Science[SDE]Environmental SciencesRFLPProteobacteriaRestriction fragment length polymorphismSequence AlignmentAgronomy and Crop ScienceSoil microbiologyPolymorphism Restriction Fragment LengthPest Management Science
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Amplified fragment length polymorphism (AFLP) and biochemical typing of Photobacterium damselae subsp. damselae.

2002

Aims: The aim of the present study was to characterize subspecifically Photobacterium damselae subsp. damselae strains isolated from cultured Sparus aurata and Dicentrarchus labrax by means of phenotypic and molecular typing techniques (amplified fragment length polymorphism, AFLP). Methods and Results: Seventy-one strains of P. damselae subsp. damselae were isolated from 38 cultured fishes at different fish farms located on the Mediterranean coast near Valencia, Spain. Most fish studied were asymptomatic and some were recovered during infectious outbreaks. Phenotypic characterization revealed a considerable degree of variability within the subspecies, including some characters, such as pro…

GeneticsDNA BacterialPhotobacteriumDendrogramUPGMAGeneral MedicinePhenotypic traitAquacultureBiologySubspeciesPhotobacteriumbiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyBacterial Typing TechniquesPerciformesFish DiseasesPhotobacterium damselaePhenotypeAnimalsAmplified fragment length polymorphismTypingGram-Negative Bacterial InfectionsPolymorphism Restriction Fragment LengthBiotechnologyJournal of applied microbiology
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DNA polymorphism of the human complement C8 beta gene: formal genetics and intragenic localization.

1989

The eighth component of human complement consists of three subunits of different molecular mass, which are coded for by three separate genetic loci. Polymorphisms have been described at the protein level for the alpha and beta subunits by means of sodium dodecyl sulfate gel electrophoresis and isoelectric focusing. Using a full-length human C8 beta cDNA probe, we have studied more than 100 individuals by Southern blot analysis to detect DNA polymorphisms. We have found two restriction fragment length polymorphisms (RFLPs) with the enzymes Taq I and Bam HI. The Taq I polymorphism is defined by two alleles, i.e., a single 4.9 kb fragment or two 2.8/2.1 kb fragments. The allele frequencies are…

GeneticsGel electrophoresisDeoxyribonuclease BamHIImmunologyBiologyMolecular biologyComplement C8Restriction fragmentBlotting SouthernGene mappingComplementary DNAGeneticsbiology.proteinHumansRestriction fragment length polymorphismDeoxyribonucleases Type II Site-SpecificGeneAllele frequencyAllelesPolymorphism Restriction Fragment LengthSouthern blotImmunogenetics
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Amplified fragment length polymorphisms and sequence data in the phylogenetic analysis of polyploids: multiple origins of Veronica cymbalaria (Planta…

2007

Summary • The origin of polyploid Veronica cymbalaria (Plantaginaceae) was investigated using DNA sequence data and amplified fragment length polymorphism (AFLP) fingerprints to reveal the parentage of this taxon. The use of AFLP fingerprints in phylogenetic analysis is problematic and various methods have therefore been compared. • DNA sequence data (for the internal transcribed spacer (ITS) region and the plastid trnL-F region (trnL intron, 3’exon, and trnL-F spacer)) and polymerase chain reaction–restriction fragment length polymorphism (PCR-RFLP) analysis of the ITS region suggested a reliable hypothesis for the evolution of the V. cymbalaria complex. This hypothesis allowed evaluation …

GeneticsGenetic MarkersJaccard indexPolymorphism GeneticPhylogenetic treebiologyPhysiologyfood and beveragesPlant ScienceSequence Analysis DNAbiology.organism_classificationPolymerase Chain ReactionDNA sequencingPolyploidyTaxonPolyploidPlantaginaceaeAmplified fragment length polymorphismInternal transcribed spacerAmplified Fragment Length Polymorphism AnalysisPlantagoPhylogenyPolymorphism Restriction Fragment LengthThe New phytologistReferences
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Forensics of birds of prey by DNA fingerprinting with 32P-labeled oligonucleotide probes.

1991

Paternity tests on confiscated families of eight species of birds of prey were carried out successfully by DNA fingerprinting with 32P-labeled oligonucleotide probes. Variations in the number of hybridized fragments, depending on the species of birds, are observed using the same probe, as well as differences of polymorphism by hybridizing the DNA samples with several oligonucleotide probes.

GeneticsMaleBase CompositionBase SequenceOligonucleotideClinical BiochemistryPhosphorus IsotopesBiologyBiochemistryDNA FingerprintingAnalytical ChemistryPredationBirdschemistry.chemical_compoundchemistryDNA profilingPolymorphism (computer science)Paternity testsAnimalsBase sequenceMolecular probeOligonucleotide ProbesDNAPolymorphism Restriction Fragment LengthRepetitive Sequences Nucleic AcidElectrophoresis
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Rapid characterization of wild and collection strains of the genus Zygosaccharomyces according to mitochondrial DNA patterns

1997

Several wild and collection strains of the genus Zygosaccharomyces were characterized using a rapid and simple method of restriction analysis of mitochondrial DNA. Patterns obtained with three endonucleases (HaeIII, HinfI and RsaI) made it possible to differentiate each species and to identify the wild strains, isolated from the same spoiled concentrated must, as belonging to the species Z. rouxii. The HinfI restriction enzyme produced a strain-specific pattern which allowed us to recognize that the seven wild isolates belonged to only three strains.

GeneticsMitochondrial DNAGenus ZygosaccharomycesZygosaccharomycesBiologybiology.organism_classificationDNA MitochondrialMicrobiologyHaeIIIRestriction enzymeEndonucleasechemistry.chemical_compoundSpecies SpecificitychemistrySaccharomycetalesFood MicrobiologyGeneticsmedicinebiology.proteinMolecular BiologyPolymorphism Restriction Fragment LengthDNAmedicine.drugFEMS Microbiology Letters
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