Search results for "Fluorescence"

showing 10 items of 2463 documents

Influence of Feeding and Oviposition by Phytophagous Pentatomids on Photosynthesis of Herbaceous Plants

2010

Abstract Feeding by herbivorous insects may change photosynthetic activity of host plants. We studied how feeding and oviposition by herbivorous stink bugs, Murgantia histrionica and Nezara viridula (Heteroptera: Pentatomidae), affect photosynthetic parameters of Brassica oleracea (savoy cabbage) and Phaseolus vulgaris (French bean). First, we measured photosynthetic gas exchange, chlorophyll fluorescence imaging, and emission of induced volatile organic compounds (VOC) immediately after feeding and during a post-feeding period. Photosynthesis decreased rapidly and substantially in B. oleracea and P. vulgaris infested by feeding bugs. Stomatal conductance did not decrease proportionally wit…

ChlorophyllStomatal conductanceTime FactorsOvipositionBrassicaBiologyPhotosynthesisBiochemistryGas Chromatography-Mass SpectrometryHost-Parasite InteractionsHeteropteraTritrophic interactionschemistry.chemical_compoundPhotosynthesifoodPentatomidaeparasitic diseasesBotanyAnimalsPhotosynthesisChlorophyll fluorescenceEcology Evolution Behavior and SystematicsPhaseolusMurgantia histrionicaVolatile Organic CompoundsTerpenesFeedingSavoy cabbagefungiGreen leaf volatilesNezara viridulaFeeding BehaviorGeneral MedicinePentatomidaebiology.organism_classificationfood.foodPlant LeavesHeteroptera; Pentatomidae; Murgantia histrionica; Nezara viridula; Feeding; Oviposition; Photosynthesis; Tritrophic interactionsSettore AGR/11 - Entomologia Generale E ApplicatachemistryNezara viridulaChlorophyllFemaleSesquiterpenesJournal of Chemical Ecology
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Sun-induced fluorescence - a new probe of photosynthesis: First maps from the imaging spectrometer HyPlant.

2015

Variations in photosynthesis still cause substantial uncertainties in predicting photosynthetic CO2 uptake rates and monitoring plant stress. Changes in actual photosynthesis that are not related to greenness of vegetation are difficult to measure by reflectance based optical remote sensing techniques. Several activities are underway to evaluate the sun-induced fluorescence signal on the ground and on a coarse spatial scale using space-borne imaging spectrometers. Intermediate-scale observations using airborne-based imaging spectroscopy, which are critical to bridge the existing gap between small-scale field studies and global observations, are still insufficient. Here we present the first …

Chlorophyllinduced fluorescencesunImaging spectrometer2306 Global and Planetary ChangeFluorescence2300 General Environmental SciencePhotosynthesiEnvironmental ChemistryAirborne measurement910 Geography & travelSpectral resolutionPhotosynthesisAbsorption (electromagnetic radiation)Spectroscopyairborne measurementsChlorophyll fluorescenceGeneral Environmental ScienceRemote sensingGlobal and Planetary ChangeSpectrometerEcology2300Remote sensingImaging spectroscopyVegetation monitoringFLEXImaging spectroscopy10122 Institute of GeographyGEO/10 - GEOFISICA DELLA TERRA SOLIDASpectrometry FluorescenceSun-induced fluorescence2304 Environmental ChemistryHyPlantRemote Sensing TechnologySunlightEnvironmental scienceSpatial variabilityChlorophyll fluorescence2303 EcologyGlobal change biology
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Effects of elevated production of autochthonous dissolved organic matter on the freely dissolved concentration of cadmium

2018

Eutrophication enhances the production of autochthonous dissolved organic matter (DOM), which is a major driving factor behind the impairment of many aquatic ecosystems. In a mesocosm study, we investigated the effects of the abundance and composition of DOM on the potential bioavailability of cadmium (Cd) caused by eutrophication, using three-dimensional excitation-emission matrix fluorescence spectroscopy integrated with tangential flow ultrafiltration technology. The complexing capacity of DOM-Cd and the sorption distribution coefficient between DOM and the bulk solution was calculated based on a 1 : 1 complexation model. The fluorescent DOM was decomposed into three components (one prot…

Chlorophyllliuennut orgaaninen hiili0106 biological sciencesChlorophyll aautochthonous dissolved organic matterta1172UltrafiltrationBiological Availabilitychemistry.chemical_element010501 environmental sciencesManagement Monitoring Policy and Law01 natural sciencesFluorescenceMesocosmchemistry.chemical_compoundDissolved organic carbonEnvironmental ChemistryBiomassOrganic ChemicalsHumic Substanceskadmiumaquatic ecosystems0105 earth and related environmental sciencesCadmiumChlorophyll A010604 marine biology & hydrobiologyvesiekosysteemitPublic Health Environmental and Occupational HealthSorptionGeneral MedicineEutrophicationBioavailabilitySpectrometry FluorescencechemistryEnvironmental chemistryorgaaninen ainesEutrophicationCadmiumEnvironmental Science: Processes & Impacts
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Gliadin, zonulin and gut permeabilità: effects on celiac and non-celiac intestinal mucosa and intestinal cell lines.

2006

Objective. Little is known about the interaction of gliadin with intestinal epithelial cells and the mechanism(s) through which gliadin crosses the intestinal epithelial barrier. We investigated whether gliadin has any immediate effect on zonulin release and signaling. Material and methods. Both ex vivo human small intestines and intestinal cell monolayers were exposed to gliadin, and zonulin release and changes in paracellular permeability were monitored in the presence and absence of zonulin antagonism. Zonulin binding, cytoskeletal rearrangement, and zonula occludens-1 (ZO-1) redistribution were evaluated by immunofluorescence microscopy. Tight junction occludin and ZO-1 gene expression …

Cholera ToxinGene ExpressionEnzyme-Linked Immunosorbent AssayOccludindigestive systemCoeliac diseaseGliadinPermeabilityTight JunctionsIntestinal mucosaOccludinIntestine SmallmedicineAnimalsHumansIntestinal MucosaProtein PrecursorsCells CulturedIntestinal permeabilitybiologyTight junctionHaptoglobinsGastroenterologynutritional and metabolic diseasesZonulinMembrane ProteinsEpithelial Cellsmedicine.diseasePhosphoproteinsMolecular biologydigestive system diseasesRatsCeliac DiseaseMicroscopy FluorescenceParacellular transportImmunologybiology.proteinZonula Occludens-1 ProteinGliadin
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TFIIH Operates through an Expanded Proximal Promoter To Fine-Tune c-myc Expression

2004

A continuous stream of activating and repressing signals is processed by the transcription complex paused at the promoter of the c-myc proto-oncogene. The general transcription factor IIH (TFIIH) is held at promoters prior to promoter escape and so is well situated to channel the input of activators and repressors to modulate c-myc expression. We have compared cells expressing only a mutated p89 (xeroderma pigmentosum complementation group B [XPB]), the largest TFIIH subunit, with the same cells functionally complemented with the wild-type protein (XPB/wt-p89). Here, we show structural, compositional, and functional differences in transcription complexes between XPB and XPB/wt-89 cells at t…

Chromatin ImmunoprecipitationDNA ComplementaryCell SurvivalUltraviolet RaysBlotting WesternGreen Fluorescent ProteinsGene ExpressionRepressorCellular homeostasisBiologyTransfectionModels BiologicalProto-Oncogene MasProto-Oncogene Proteins c-mycTranscription Factors TFIIRibonucleasesPotassium PermanganateTranscription (biology)HumansRNA MessengerPromoter Regions GeneticMolecular BiologyModels GeneticGeneral transcription factorCell CycleGenetic Complementation TestDNA HelicasesPromoterCell BiologyFibroblastsFlow CytometryMolecular biologyDNA-Binding ProteinsKineticsTranscription Factor TFIIHMicroscopy FluorescenceMutationTranscription preinitiation complexTranscription factor II HTranscription Factor TFIIHPlasmidsMolecular and Cellular Biology
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The Saccharomyces cerevisiae Hot1p regulated gene YHR087W (HGI1) has a role in translation upon high glucose concentration stress.

2012

Abstract Background While growing in natural environments yeasts can be affected by osmotic stress provoked by high glucose concentrations. The response to this adverse condition requires the HOG pathway and involves transcriptional and posttranscriptional mechanisms initiated by the phosphorylation of this protein, its translocation to the nucleus and activation of transcription factors. One of the genes induced to respond to this injury is YHR087W. It encodes for a protein structurally similar to the N-terminal region of human SBDS whose expression is also induced under other forms of stress and whose deletion determines growth defects at high glucose concentrations. Results In this work …

Chromatin ImmunoprecipitationTranslation<it>Saccharomyces cerevisiae</it>Saccharomyces cerevisiae Proteinslcsh:QH426-470Monosaccharide Transport ProteinsSaccharomyces cerevisiaeSaccharomyces cerevisiaeBiologyGene YHR087WHog1pTranscripció genèticaEukaryotic translationStress PhysiologicalPolysomeGene Expression Regulation FungalGene expressionProtein biosynthesisHigh glucose osmotic stresslcsh:QH573-671Transcription factorMolecular BiologyRegulation of gene expressionGenetic transcriptionlcsh:CytologyComputational BiologyTranslation (biology)biology.organism_classificationBlotting NorthernExpressió gènicaYeastlcsh:GeneticsGlucoseBiochemistryMicroscopy FluorescencePolyribosomesProtein BiosynthesisPolysomesGene <it>YHR087W</it>Gene expressionLlevatsMitogen-Activated Protein KinasesHot1pTranscription FactorsResearch ArticleBMC molecular biology
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Photochemical Derivatization and Fluorimetric Determination of Promethazine in a FIA Assembly

1992

Abstract The flow injection fluorimetric determination of promethazine is carried out by on-line photoderivatization. The PTFE tubing is helically coiled around the lamp. An analytical procedure is proposed by using aqueous solution as carrier stream: the calibration graph is linear over the range 0.05 - 20 ppm. The influence of foreign compounds is studied and the method is applied to promethazine determination in pharmaceutical formulations.

ChromatographyAqueous solutionCalibration curveBiochemistry (medical)Clinical BiochemistryBiochemistryDosage formFluorescence spectroscopyAnalytical ChemistryPromethazinechemistry.chemical_compoundchemistryElectrochemistrymedicineDerivatizationSpectroscopymedicine.drugAnalytical Letters
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Simultaneous Determination of Pyridoxine and Riboflavin in Energy Drinks by High-Performance Liquid Chromatography with Fluorescence Detection

2015

Energy drinks, as familiar consumer products, have been widely used in laboratory courses to help promote student interest, as well as to connect lecture concepts with laboratory work. Energy drinks contain B vitamins: pyridoxine (vitamin B6) and riboflavin (vitamin B2) of which amounts are high enough to be of concern. In this work, a fast and inexpensive high-performance liquid chromatography (HPLC) coupled with fluorescence detection method for determining pyridoxine and riboflavin simultaneously in energy drinks is developed. It takes advantage of the native fluorescence of B vitamins and provides high selectivity and sensitivity with low background noise. The method is suitable for und…

ChromatographyChemistryAnalytical chemistryRiboflavinGeneral ChemistryPyridoxineFluorescenceHigh-performance liquid chromatographyFluorescence spectroscopyEducationB vitaminsGraduate levelmedicinemedicine.drugVitamin b2Journal of Chemical Education
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Spectrofluorimetric determination of emetine by flow injection using barium peroxide and UV derivatization

1993

Abstract The flow-injection spectrofluorimetric determination of emetine was carried out by photoderivatization in the presence of barium peroxide, in a flow-injection assembly in which the PTFE tubing in the injection valve is helically coiled around the lamp. The sample solution merges with a barium peroxidephosphoric acid solution and then the resulting mixture is irradiated; pure distilled water is used as a carrier stream. The calibration graph is linear over the range 0.05–50 μ g ml −1 of emetine dihydrochloride. The influence of foreign compounds was studied and the method was applied to the determination of emetine in injection and human urine samples.

ChromatographyChemistryCalibration curveEmetine HydrochlorideFluorescence spectrometrychemistry.chemical_elementBariumBiochemistryAnalytical Chemistrychemistry.chemical_compoundDistilled waterBarium peroxideEnvironmental ChemistryDerivatizationQuantitative analysis (chemistry)SpectroscopyAnalytica Chimica Acta
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Determination of busulfan in human plasma using high-performance liquid chromatography with pre-column derivatization and fluorescence detection.

1999

A rapid, sensitive and reproducible high-performance liquid chromatographic assay for busulfan in human plasma was developed. After extraction of plasma samples with acetonitrile and methylene chloride, busulfan and the internal standard [1,5-bis(methanesulfonyloxy)pentane] were derivatized with 8-mercaptoquinoline to yield fluorescent compounds which were detected with a fluorescence detector equipped with filters of 360 nm (excitation) and 425 nm (emission). Calibration graphs showed a linear correlation (r>0.9990) over the concentration range of 20-2000 ng/ml. The recovery of busulfan from plasma standards was 70+/-5%. The detection and quantification limits for busulfan in plasma sample…

ChromatographyChemistryExtraction (chemistry)Reproducibility of ResultsGeneral ChemistryReference StandardsHigh-performance liquid chromatographyFluorescenceSensitivity and SpecificityFluorescence spectroscopyPentanechemistry.chemical_compoundSpectrometry FluorescenceCalibrationmedicineHumansDerivatizationQuantitative analysis (chemistry)Antineoplastic Agents AlkylatingBusulfanBusulfanChromatography High Pressure Liquidmedicine.drugJournal of chromatography. B, Biomedical sciences and applications
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