Search results for "Gel electrophoresi"

showing 10 items of 321 documents

Comparison of pulsed-field gel electrophoresis and whole-genome-sequencing-based typing confirms the accuracy of pulsed-field gel electrophoresis for…

2020

Summary Aim To determine whether pulsed-field gel electrophoresis (PFGE) accurately recognizes isolates belonging to clusters defined by techniques based on whole-genome sequencing (WGS) using Pseudomonas aeruginosa as a model. Methods We selected 65 isolates of ST395 P. aeruginosa isolated in seven European hospitals between 1998 and 2012. Isolates were typed by PFGE and sequenced by WGS. A core genome multi-locus sequence typing (cgMLST) analysis based on 3831 genes was performed with a homemade pipeline. Findings PFGE identified eight pulsotypes and cgMLST differentiated nine clusters and nine singletons. Five cgMLST clusters and pulsotypes (31/65 isolates) coincided perfectly. Isolates …

Bacterial typingMicrobiology (medical)030501 epidemiologymedicine.disease_causeGenomeDisease Outbreaks03 medical and health sciencesPulsed-field gel electrophoresisHumansMedicinePseudomonas InfectionsTypingPulsed-field gel electrophoresisReference standardsGel electrophoresisWhole genome sequencingGeneticsWhole-genome sequencing0303 health sciencesWhole Genome Sequencing030306 microbiologybusiness.industryPseudomonas aeruginosaOutbreaksReproducibility of ResultsOutbreakGeneral MedicineBacterial Typing TechniquesElectrophoresis Gel Pulsed-FieldEurope[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyInfectious DiseasesPseudomonas aeruginosacgMLST0305 other medical sciencebusinessGenome BacterialMultilocus Sequence TypingJournal of Hospital Infection
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Shifts in size, genetic structure and activity of the soil denitrifier community by nematode grazing

2010

International audience; Bacterial-feeding nematodes represent an important driver of the soil microbial activity and diversity. This study aimed at characterizing the impact of nematode grazing on a model functional bacterial guild involved in N-cycling, the denitrifiers. Bacterial-feeding nematodes (Cephalobus pseudoparvus) were inoculated into soil microcosms whose indigenous nematofauna had previously been removed. The size, genetic structure and activity of the soil denitrifier community were characterized 15 and 45 days after nematodes inoculation using quantitative PCR of the nirK, nirS and nosZ denitrification genes, fingerprinting of the nirK and nirS genes and denitrification enzym…

BacterivoreDenitrification[SDV]Life Sciences [q-bio]Soil biologyDENITRIFIERSSoil ScienceSOIL BACTERIAL FEEDING NEMATODESBiologyMicrobiologyGrazing pressure03 medical and health sciencesCEPHALOBUS PSEUDOPARVUSGrazingBotanyDGGERelative species abundance030304 developmental biology2. Zero hunger0303 health sciences04 agricultural and veterinary sciences15. Life on landQPCRInsect Science[SDE]Environmental Sciences040103 agronomy & agriculture0401 agriculture forestry and fisheriesMicrocosmTemperature gradient gel electrophoresisEuropean Journal of Soil Biology
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Glomerular basement membrane: evidence for collagenous domain of the alpha 3 and alpha 4 chains of collagen IV.

1990

Abstract A collagenous component(s) of Mr = 60K was extracted from glomerular basement membrane with urea and was purified. Upon digestion, it yielded a collagenase-resistant fragment(s) of Mr = 23.5K. Both component and fragment showed immunochemical identity with the noncollagenous domains of the new α3 & α4 chains of collagen IV. The component is characterized by a collagenous domain of about 280 residues and a noncollagenous domain of about 250 residues. These findings further establish these new chains as distinct entities of collagen IV.

Basement membraneGel electrophoresischemistry.chemical_classificationChemistryRenal glomerulusMacromolecular SubstancesProtein ConformationProtein subunitGlomerular basement membraneKidney GlomerulusBiophysicsBiological membraneCell BiologyBiochemistryBasement Membranemedicine.anatomical_structureBiochemistryDomain (ring theory)medicineAnimalsCattleCollagenAmino AcidsGlycoproteinMolecular BiologyBiochemical and biophysical research communications
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Synthesis of a New Disulfide Affinity Adsorbent for Purification of Human Uterine Progesterone Receptor

2005

For purification of the human uterine progesterone receptor, an affinity adsorbent was synthesized in which the specific ligand (16 alpha-ethyl-3-oxo-19nor-androst-4-ene 17 beta-carboxylic acid) was bound to derivatized celulose using a disulfide-group-containing spacer. The purified receptor protein, isolated by reductive cleavage of the disulfide bond, bound the synthetic gestagen R5020 with high affinity (Kd 12.2 nmol/l). The affinity gel was highly efficient. A 24000-fold purification of progesterone receptor with a recovery of 40% could be achieved in a single step within 6 h. By means of dodecyl sulphate/polyacrylamide gel electrophoresis two main polypeptides with molecular weights o…

Binding CompetitiveBiochemistryChromatography Affinitychemistry.chemical_compoundCytosolAdsorptionPregnenedionesProgesterone receptorCentrifugation Density GradientHumansCelluloseReceptorPolyacrylamide gel electrophoresisChromatographyProgesterone CongenersMolecular massUterusDisulfide bondLigand (biochemistry)Resins SyntheticchemistryBiochemistryElectrophoresis Polyacrylamide GelFemaleAdsorptionReceptors ProgesteroneEuropean Journal of Biochemistry
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Use of Biocides for the Control of Fungal Outbreaks in Subterranean Environments: The Case of the Lascaux Cave in France

2012

The Lascaux Cave in France suffered an outbreak of the fungus Fusarium solani in 2001. Biocides were applied for three years to control this outbreak. Four months after the initial biocide application, a new outbreak appeared in the form of black stains that progressively invaded the cave. The black stains on the ceiling and passage banks were so evident by 2007 that they became one of the caves major problems. Therefore, biocides were used again in 2008. The present study investigated the fungal communities associated with the black stains and the effectiveness of the biocides applied, by using cloning, denaturing gradient gel electrophoresis, and culture-dependent methods. A novel species…

Biocide[SDV]Life Sciences [q-bio]Molecular Sequence DataHerpotrichiellaceaeZoologyFungusDisease Outbreaks03 medical and health sciencesFusariumCaveDNA Ribosomal SpacerEnvironmental ChemistryPhylogeny[SDV.MP.MYC]Life Sciences [q-bio]/Microbiology and Parasitology/Mycology030304 developmental biology0303 health sciencesgeographygeography.geographical_feature_categorybiologyDenaturing Gradient Gel Electrophoresis030306 microbiologyEcologyOutbreakGeneral ChemistryOchroconis lascauxensisbiology.organism_classification[SDV.MP.MYC] Life Sciences [q-bio]/Microbiology and Parasitology/Mycology3. Good healthCavesMycosesRNA Ribosomal[SDE]Environmental SciencesFranceFusarium solaniTemperature gradient gel electrophoresisDisinfectants
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Differential Proteomics Based on 2D-Difference In-Gel Electrophoresis and Tandem Mass Spectrometry for the Elucidation of Biological Processes in Ant…

2017

Proteomics based on 2D-Difference In Gel Electrophoresis (2D-DIGE) coupled with mass spectrometry (MS) procedures can be considered a “gold standard” to determine quantitatively and comparatively protein abundances in cell extracts from different biological sources/conditions according to a gel-based approach. In particular, 2D-DIGE is used for protein specie separation, detection, and relative quantification, whenever tandem MS is used to obtain peptide sequence information that is managed according to bioinformatic procedures to identify the differentially represented protein species. The proteomic results consist of a dynamic portray of over- and down-represented protein species that…

Bioinformatic0301 basic medicineGel electrophoresisfood.ingredientbiologyChemistryStreptomyces coelicolorComputational biologyRelative quantificationProteomicsbiology.organism_classificationTandem mass spectrometryPseudoalteromonas haloplanktis03 medical and health sciencesProtein separation030104 developmental biologyfoodMicrobisporaProtein purificationGenetics2D-DIGEProtein identificationMolecular BiologyPeptide sequenceNanoLC-ESI-LIT-MS/MS
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Sedimentation properties of chitosomal chitin synthetase from the wild-type strain and the 'slime' variant of Neurospora crassa.

1989

Marked differences in the pattern of sedimentation of cellular structures were observed after isopycnic centrifugation of crude cell-free preparations from the Neurospora crassa wall-less 'slime' variant and mycelial wild-type strain. Kinetic studies of particle sedimentation showed that the various types of subcellular components, as revealed by turbidity, UV absorption, polypeptide patterns, and chitin synthetase activity determinations, sediment independently of one another. An important feature was the finding that chitin synthetase from 'slime' peaked at a median specific gravity of 1.1201 +/- 0.0036, whereas that from wild-type strain sedimented at a higher buoyant density (specific g…

BiophysicsCentrifugation IsopycnicBiochemistryNeurospora crassaCell wallchemistry.chemical_compoundChitinCentrifugation Density GradientMolecular BiologyPolyacrylamide gel electrophoresisSpecific GravityDifferential centrifugationChitin SynthaseOrganellesbiologyStrain (chemistry)Neurospora crassafungiCrassaGenetic VariationSedimentationbiology.organism_classificationcarbohydrates (lipids)Molecular WeightKineticsMicroscopy ElectronNeurosporaBiochemistrychemistryGlucosyltransferasesElectrophoresis Polyacrylamide GelSpectrophotometry UltravioletBiochimica et biophysica acta
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Identifying human platelet glycoproteins IIb and IIIa by capillary electrophoresis.

1998

Glanzmann thrombasthenia (GT) is an inherited hemorrhagic defect due to a failure of the platelet membrane glycoprotein (GP) IIb–IIIa complex. Capillary electrophoresis (CE) analysis of solubilized platelet membranes from normal individuals showed the presence of two peaks with a migration time of 27 and 29 min, respectively. An excellent run-to-run and day-to-day reproducibility of the technique (< 1% variation of the retention time) was documented. Using an automated Ferguson method, the apparent molecular masses were 100.0 kDa and 138.5 kDa, respectively. Immunoprecipitation with monoclonal antibodies anti-GP IIIa (B59.2.1) and anti-IIb (61.9.1.3) showed the two peaks as IIIa and IIb, re…

Blood PlateletsMaleClinical BiochemistryPlatelet Glycoprotein GPIIb-IIIa ComplexPlatelet membrane glycoproteinBiochemistryAnalytical ChemistryCapillary electrophoresisThrombastheniamedicineHumansPlateletChildPolyacrylamide gel electrophoresischemistry.chemical_classificationMembrane GlycoproteinsGlanzmann's thrombastheniaCell MembraneElectrophoresis Capillarymedicine.diseaseFlow CytometryMolecular biologyPrecipitin TestsPlatelet Glycoprotein GPIIb-IIIa ComplexchemistryGlycoproteinThrombastheniaElectrophoresis
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Reaggregation and binding of cell wall proteins from Candida albicans to structural polysaccharides

1998

Urea or hot sodium dodecyl sulphate extracted a significant amount of the same proteins from the matrix of the cell wall of the yeast form and mycelial cells of Candida albicans. Gel filtration analysis of the urea-extracted proteins revealed that they occurred in the form of large complexes which were unaffected by up to 8 M urea. Among them, proteins en route to becoming covalently associated within the wall scaffold were identified by their reaction with specific antibodies. When urea was removed by dialysis, some of these proteins specifically reassociated into large aggregates which bound strongly with ConA, whereas others remained soluble in smaller associated products. The ability of…

Blotting WesternChitinPlasma protein bindingPolysaccharideBinding CompetitiveMicrobiologyFungal ProteinsCell wallchemistry.chemical_compoundChitinCell WallCandida albicansConcanavalin AUreaCandida albicansGlucansMolecular BiologyLaminaribiosePolyacrylamide gel electrophoresisAntibodies FungalGlucanchemistry.chemical_classificationbiologyMembrane ProteinsSodium Dodecyl SulfateGeneral Medicinebiology.organism_classificationMicroscopy ElectronMicroscopy FluorescenceSolubilitychemistryBiochemistryChromatography GelElectrophoresis Polyacrylamide GelProtein BindingResearch in Microbiology
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A new form of tumor and fetal collagen that binds laminin.

1993

Human breast and colon carcinoma tissues contain a form of collagen, not described before, composed of alpha 1 chains of similar size (approximately 100 kDa) but different charge. The three constitutive chains, separated by two-dimensional electrophoresis, are a unique acidic component, undetectable in other collagen types, with an apparent isoelectric point of 4-5, and two more basic components displaying the same electrophoretic behavior as alpha 1(III) and alpha 1(I), respectively. The acidic chain is structurally distinct from alpha 1(I) and displays a cyanogen bromide-derived fragment of similar size to CB5(III). This collagen in its native state is resistant to trypsin and metalloprot…

Breast NeoplasmsBiologyBiochemistryUmbilical Cordchemistry.chemical_compoundFetusLamininmedicineElectrochemistryAnimalsHumansTrypsinCyanogen BromideIsoelectric PointPolyacrylamide gel electrophoresisSkinchemistry.chemical_classificationMetalloproteinaseMetalloendopeptidasesTrypsinMolecular biologyPeptide FragmentsIntestinesMicroscopy ElectronIsoelectric pointchemistryImmunologyColonic Neoplasmsbiology.proteinCyanogen bromideCattleElectrophoresis Polyacrylamide GelCollagenLamininProtein AGlycoproteinmedicine.drugBiochemistry
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