Search results for "Fluorescence"

showing 10 items of 2463 documents

Study of Bacillus subtilis spore's : characterication of stuctures implied in its resistance

2013

The bacterial spore is a multilayer microbial form which is extremely resistant to environmental perturbations. This resistance is especially due to its unique structure which is particularly compact and weakly permeable. This work aims to identify and characterize the spore structures involved in these properties. Overall investigation methods, such as NMR and fluorescence anisotropy, have shown that the cortex of Bacillus subtilis spores is modified by temperature for level similar to that of the activation of germination. This will result in changes to the access to the inner membrane. A tool at the spore’s scale, the fluorescence lifetime imaging microscopy (FLIM) in conjunction with th…

Spores de Bacillus subtilisEthanolMembrane interneCortexInner membraneBacillus subtilis sporesImagerie en temps de vie de fluorescence[SDV.MP.BAC] Life Sciences [q-bio]/Microbiology and Parasitology/BacteriologyFluorescence lifetime imaging[SDV.BIO] Life Sciences [q-bio]/Biotechnology
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Common and form-specific cell wall antigens of Candida albicans as released by chemical and enzymatic treatments.

1996

In order to investigate the antigenic properties of the proteins and mannoproteins present in the cell surface of Candida albicans, and to identify individual antigenic moieties and their distribution, a number of polyclonal antisera were obtained by immunizing rabbits with chemical and enzymatic cell wall extracts obtained from intact cells from both growth forms (yeast and mycelium) of the fungus. Prior to injection, wall moieties present in the extracts were subjected to different treatments and/or purification procedures such as adsorption onto polystyrenelatex microbeads or electrophoretic separation. When used as probes in indirect immunofluorescence assays, the different antisera gav…

SporesVeterinary (miscellaneous)Blotting WesternGerm tubeImmunofluorescenceApplied Microbiology and BiotechnologyMicrobiologyCell wallFungal ProteinsCell WallCandida albicansmedicineCandida albicansFluorescent Antibody Technique IndirectAntibodies FungalAntiserumMembrane Glycoproteinsbiologymedicine.diagnostic_testbiology.organism_classificationMolecular biologyYeastCorpus albicansBiochemistryPolyclonal antibodiesbiology.proteinElectrophoresis Polyacrylamide GelAgronomy and Crop ScienceMycopathologia
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Determination of ammonia and primary amine compounds and Kjeldahl nitrogen in water samples with a modified Roth's fluorimetric method.

2005

Abstract A method for the simultaneous determination of primary amino groups and ammonium ion has been proposed. The method is based in solution derivatization with o-Phthaldialdehyde/N-acetyl-cisteine (OPA/NAC) and fluorescence measurement of the formed isoindols. Analytical characteristics and description of the developed procedure have been provided. The calibration graphs for ammonium (up to 1.44 mg L−1 of N) and methylamine as primary amino model compound (up to 0.282 mg L−1 of N), were obtained. Bivariate and multivariate calibration models have been tested. The limits of detection were 0.07 mg L−1 of N and 0.004 mg L−1 of N for ammonium and amine, respectively. The procedure was firs…

Standard curveAmmoniachemistry.chemical_compoundChromatographyChemistryMethylamineFluorescence spectrometryAmmoniumStandard solutionDerivatizationKjeldahl methodAnalytical ChemistryTalanta
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Quantitative analysis of chromite ores using glass discs in moderate dilutions of lithium tetraborate by x-ray fluorescence spectrometry

2006

A method for the quantitative analysis of chromite ores by x-ray fluorescence spectrometry using beads is proposed. The work concerned the serious problems caused by the refractory nature of these materials which prevents the use of glass discs in x-ray fluorescence. An in-depth study was done to optimise the variables which influence the glass disc formation process. Sufficiently homogeneous glass discs were obtained under the following experimental conditions: lithium tetraborate as flux with moderate sample dilution (1:40), with the addition of one or two drops of LiBr solution(250 g l−1), at a temperature of 1200 °C for 30 min. The qualitative and semiquantitative results for the chromi…

Standard curvechemistryCalibration curveAnalytical chemistryFluorescence spectrometryX-ray fluorescencechemistry.chemical_elementLithiumChromiteQuantitative analysis (chemistry)SpectroscopyDilutionX-Ray Spectrometry
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Discovery and structure-activity relationship studies of irreversible benzisothiazolinone-based inhibitors against Staphylococcus aureus sortase A tr…

2014

Gram-positive bacteria, in general, and staphylococci, in particular, are the widespread cause of nosocomial and community-acquired infections. The rapid evolvement of strains resistant to antibiotics currently in use is a serious challenge. Novel antimicrobial compounds have to be developed to fight these resistant bacteria, and sortase A, a bacterial cell wall enzyme, is a promising target for novel therapies. As a transpeptidase that covalently attaches various virulence factors to the cell surface, this enzyme plays a crucial role in the ability of bacteria to invade the host's tissues and to escape the immune response. In this study we have screened a small molecule library against rec…

Staphylococcus aureusClinical BiochemistryPharmaceutical ScienceVirulenceStaphylococcal infectionsmedicine.disease_causeBiochemistryBacterial cell structureMicrobiologyStructure-Activity RelationshipBacterial ProteinsSortaseDrug DiscoverymedicineFluorescence Resonance Energy TransferHumansEnzyme InhibitorsMolecular BiologybiologyChemistryOrganic ChemistryStaphylococcal InfectionsAntimicrobialmedicine.diseasebiology.organism_classificationAminoacyltransferasesHigh-Throughput Screening AssaysMolecular Docking SimulationCysteine EndopeptidasesThiazolesBiochemistryStaphylococcus aureusSortase AMolecular MedicineBacteriaBioorganicmedicinal chemistry
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Lipid and phase specificity of α-toxin from S. aureus

2013

AbstractThe pore forming toxin Hla (α-toxin) from Staphylococcus aureus is an important pathogenic factor of the bacterium S. aureus and also a model system for the process of membrane-induced protein oligomerisation and pore formation. It has been shown that binding to lipid membranes at neutral or basic pH requires the presence of a phosphocholine-headgroup. Thus, sphingomyelin and phosphatidylcholine may serve as interaction partners in cellular membranes. Based on earlier studies it has been suggested that rafts of sphingomyelin are particularly efficient in toxin binding. In this study we compared the oligomerisation of Hla on liposomes of various lipid compositions in order to identif…

Staphylococcus aureusPore formationLiquid ordered phaseBacterial ToxinsLipid BilayersBiophysicsBiologyBiochemistryPhase Transitionchemistry.chemical_compoundHemolysin ProteinsMembrane LipidsMembrane MicrodomainsPhosphatidylcholineBinding siteLipid raftUnilamellar LiposomesPore-forming toxinLiposomeArtificial membranesBinding SitesCell MembraneOligomerisationCell BiologyS. aureusSphingomyelinsMembraneBiochemistrychemistryMicroscopy FluorescenceMutationPhosphatidylcholineslipids (amino acids peptides and proteins)Protein MultimerizationToxinSphingomyelinBiochimica et Biophysica Acta (BBA) - Biomembranes
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Staphylococcal alpha-toxin: formation of the heptameric pore is partially cooperative and proceeds through multiple intermediate stages.

1997

Staphylococcal alpha-toxin is a 293 residue polypeptide that assembles into pore-forming heptamers, residues 118-140, thereby inserting to form an amphipathic beta-barrel in the lipid bilayer. Fluorometric analyses were here conducted using cysteine-substitution mutants site-specifically-labeled at positions 35 or 130 with the environmentally-sensitive fluorophore acrylodan. In conjunction with functional assays, three conformational states of the heptamer were defined, which may represent transitional configurations of the toxin molecule along its way to membrane insertion and pore formation. The first was the freshly assembled, SDS-sensitive heptamer alpha7*a, where a minor alteration in …

Staphylococcus aureusProtein ConformationMutantBacterial ToxinsLipid BilayersExotoxinsSequence (biology)ProtomerBiochemistryResidue (chemistry)Hemolysin ProteinsProtein structureBacterial Proteins2-NaphthylamineAmphiphileAnimalsAmino Acid SequenceLipid bilayerFluorescent DyesChemistryErythrocyte MembraneMembraneSpectrometry FluorescenceBiophysicsMutagenesis Site-DirectedRabbitsBiochemistry
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Control of biofilm formation by poly-ethylene-co-vinyl acetate films incorporating nisin.

2010

The aim of this study was to evaluate the effect of poly-ethylene-co-vinyl acetate (EVA) films incorporating different concentrations (0.1%, 0.5% and 1%) of nisin on the biofilm-forming ability of Listeria monocytogenes ATCC 7644, Staphylococcus aureus 815 and Staphylococ-cus epidermidis ATCC 35984. Nisin was incorporated into two grades of EVA (EVA14 and EVA28) in the melt during a common film-blowing operation. The efficacy of EVA/nisin films was evaluated by biofilm biomass measurements and Live/Dead staining in combination with fluorescence microscopy. In order to evaluate whether the nisin incorporation could modify the film surface properties, contact angle measurements and scanning e…

Staphylococcusmedicine.disease_causeApplied Microbiology and BiotechnologyBacterial AdhesionNisin polymeric film biofilmMicrobiologyContact anglechemistry.chemical_compoundListeria monocytogenesStaphylococcus epidermidisStaphylococcus epidermidispolycyclic compoundsFluorescence microscopemedicineVinyl acetateNisinNisinListeria monocytogeneNisin; Polymeric film; Biofilm; Listeria monocytogenes; Staphylococcus aureus; Staphylococcus epidermidisbiologyBiofilmBiofilmFood PackagingGeneral Medicinebiochemical phenomena metabolism and nutritionbiology.organism_classificationListeria monocytogenesAnti-Bacterial AgentsSettore ING-IND/22 - Scienza E Tecnologia Dei MaterialiPolymeric filmchemistryStaphylococcus aureusBiofilmsStaphylococcus aureuPolyvinylsBiotechnologyNuclear chemistryApplied microbiology and biotechnology
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Visualization of RNA-Quadruplexes in Live Cells

2015

Visualization of DNA and RNA quadruplex formation in human cells was demonstrated recently with different quadruplex-specific antibodies. Despite the significant interest in these immunodetection approaches, dynamic detection of quadruplex in live cells remains elusive. Here, we report on NaphthoTASQ (N-TASQ), a next-generation quadruplex ligand that acts as a multiphoton turn-on fluorescent probe. Single-step incubation of human and mouse cells with N-TASQ enables the direct detection of RNA-quadruplexes in untreated cells (no fixation, permeabilization or mounting steps), thus offering a unique, unbiased visualization of quadruplexes in live cells.

Static ElectricityMelanoma ExperimentalLigands010402 general chemistryG-quadruplex01 natural sciencesBiochemistryCatalysisMice03 medical and health scienceschemistry.chemical_compoundColloid and Surface ChemistryBiomimeticsCationsCell Line TumorFluorescence Resonance Energy TransferAnimalsHumans[CHIM]Chemical Sciences[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biologyheterocyclic compoundsComputingMilieux_MISCELLANEOUSChelating AgentsFluorescent Dyes030304 developmental biologyPhotons[SDV.GEN]Life Sciences [q-bio]/Genetics0303 health sciencesbiologyChemistryRNADNAGeneral ChemistryFluorescenceMolecular biology3. Good health0104 chemical sciencesCell biologyVisualizationG-QuadruplexesFörster resonance energy transferMicroscopy FluorescenceCell cultureMCF-7 Cellsbiology.proteinRNAAntibodyDNAJournal of the American Chemical Society
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Comparative Study of Human and Automated Screening for Antinuclear Antibodies by Immunofluorescence on HEp-2 Cells

2015

Background : Several automated systems had been developed in order to reduce inter-observer variability in indirect immunofluorescence (IIF) interpretation. We aimed to evaluate the performance of a processing system in antinuclear antibodies (ANA) screening on HEp-2 cells. Patients and Methods : This study included 64 ANA-positive sera and 107 ANA-negative sera that underwent IIF on two commercial kits of HEp-2 cells (BioSystems® and Euroimmun®). IIF results were compared with a novel automated interpretation system, the “ Cyclopus CADImmuno®” (CAD). Results : All ANA-positive sera images were recognized as positive by CAD (sensitivity = 100%), while 17 (15.9%) of the ANA-negative sera ima…

Statistics and ProbabilityPathologymedicine.medical_specialtyIndirect immunofluorescenceAnti-nuclear antibodymedicine.diagnostic_testbusiness.industryConcordanceHealth InformaticsIIfImmunofluorescenceHealth Professions (miscellaneous)Settore FIS/07 - Fisica Applicata(Beni Culturali Ambientali Biol.e Medicin)Continuous integrationPattern identificationAutoantibodies HEp-2 Immunofluorescence autoimmune diseases automated screening standardization.Health Information ManagementMedicineFine speckledbusinessInternational Journal of Statistics in Medical Research
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