Search results for "Oxidation-Reduction"

showing 10 items of 689 documents

Superoxide Flux in Endothelial Cells via the Chloride Channel-3 Mediates Intracellular Signaling

2007

Reactive oxygen species (ROS) have been implicated in both cell signaling and pathology. A major source of ROS in endothelial cells is NADPH oxidase, which generates superoxide (O2.−) on the extracellular side of the plasma membrane but can result in intracellular signaling. To study possible transmembrane flux of O2.−, pulmonary microvascular endothelial cells were preloaded with the O2.−-sensitive fluorophore hydroethidine (HE). Application of an extracellular bolus of O2.−resulted in rapid and concentration-dependent transient HE oxidation that was followed by a progressive and nonreversible increase in nuclear HE fluorescence. These fluorescence changes were inhibited by superoxide dism…

ApoptosisMembrane PotentialsSuperoxide dismutasechemistry.chemical_compoundChloride ChannelsSuperoxidesExtracellularAnimalsHumansEnzyme InhibitorsRNA Small InterferingMolecular BiologyLungCells CulturedFluorescent Dyeschemistry.chemical_classificationReactive oxygen speciesNADPH oxidasebiologySuperoxideAngiotensin IIThrombinAcetophenonesEndothelial CellsNADPH OxidasesCell BiologyArticlesCell biologyMitochondriaPhenanthridinesOxygenchemistryDIDSbiology.proteinCalciumSignal transductionOxidation-ReductionIntracellularSignal Transduction
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Energetic coupling between plastids and mitochondria drives CO2 assimilation in diatoms.

2015

International audience; Diatoms are one of the most ecologically successful classes of photosynthetic marine eukaryotes in the contemporary oceans. Over the past 30 million years, they have helped to moderate Earth's climate by absorbing carbon dioxide from the atmosphere, sequestering it via the biological carbon pump and ultimately burying organic carbon in the lithosphere. The proportion of planetary primary production by diatoms in the modern oceans is roughly equivalent to that of terrestrial rainforests. In photosynthesis, the efficient conversion of carbon dioxide into organic matter requires a tight control of the ATP/NADPH ratio which, in other photosynthetic organisms, relies prin…

Aquatic Organismschemistry.chemical_compoundAdenosine TriphosphateSettore BIO/04 - Fisiologia VegetaleCYCLIC ELECTRON FLOWPlastidsPhotosynthesisPHAEODACTYLUM-TRICORNUTUMPlant Proteinschemistry.chemical_classificationMultidisciplinarymicroalgaeRespirationCarbon fixationEnergetic interactionsProton-Motive ForceMitochondriametabolic mutantPhenotypeATP/NADPH ratioOXYGEN PHOTOREDUCTIONCarbon dioxideOxidoreductasesOxidation-ReductionOceanOceans and SeasElectron flowMarine eukaryotesBiologyPhotosynthesisCHLAMYDOMONAS-REINHARDTIICarbon cycleCarbon CycleMitochondrial ProteinsEnergetic exchangesBotanyOrganic matterEcosystem[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular Biology14. Life underwaterPlastidEcosystemDiatomsChemiosmosisfungiECSCarbon Dioxidechemistry13. Climate actionNADP
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Proton coupled electron transfer of ubiquinone Q2 incorporated in a self-assembled monolayer.

2011

We present a complete study of the reduction of ubiquinone Q(2) (UQ(2)) in simpler aqueous medium, over a pH range of 2.5 to 12.5. The short isoprenic chain ubiquinones (UQ(2)) were incorporated in a self-assembled monolayer. Under these conditions, the global 2e(-) electrochemical reaction can be described on the basis of a nine-member square scheme. The thermodynamic constants of the system were determined. The global 2e(-) process is controlled by the uptake of the second electron. The elementary electrochemical rate constants obtained by fitting of the experimental rate constant were k(s4) = 1.5 s(-1) for QH˙(+)(2)↔ QH(2), k(s5) = 1.5 s(-1) for QH˙↔ QH(-) and k(s6) = 1 s(-1) for Q˙(-)↔ …

Aqueous mediumChemistrySurface PropertiesUbiquinoneAnalytical chemistryGeneral Physics and AstronomyWaterSelf-assembled monolayerElectronHydrogen-Ion ConcentrationElectrochemistryElectron TransportReaction rate constantCoenzyme Q – cytochrome c reductaseMonolayerElectrochemistryThermodynamicsGoldPhysical and Theoretical ChemistryProton-coupled electron transferProtonsOxidation-ReductionPhysical chemistry chemical physics : PCCP
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Voltammetric behavior of berenil.

1993

Abstract Berenil is reduced on mercury drops electrode in buffered aqueous media. The reduction of —N=N— group is controlled by diffusion. Polarographie waves are of analytical usefulness. The hydrogen discharge is favored by the basic centers of the molecule in Co(ll)/ammonia-buffered media.

Aqueous mediumHydrogenAnalytical chemistryPharmaceutical Sciencechemistry.chemical_elementHydrogen-Ion ConcentrationTrypanocidal AgentsMercury (element)chemistryElectrodeElectrochemistryMoleculeVoltammetryDiminazeneElectrodesOxidation-ReductionPolarographyJournal of pharmaceutical sciences
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Microheterogeneous electrocatalytic chiral recognition at monoclinic vanadium-doped zirconias: enantioselective detection of glucose.

2007

Synthetic tetragonal and monoclinic vanadium-doped zirconias (t- and m-VxZr1-xO2, 0.005x0.150) exert an effective catalytic effect toward the electrochemical oxidation of glucose in aqueous alkaline media. The catalytic effect of monoclinic specimens attached to carbon and fluorine-doped tin oxide electrodes exhibits a remarkable enantioselectivity, so that catalytic currents for the oxidation of L-glucose at +0.92 V vs AgCl/Ag are considerably larger than those obtained for the oxidation of D-glucose. This enantioselectivity can be associated with the existence of a noncentrosymmetric coordination of vanadium centers in the monoclinic crystalline form of zirconia. From the electrochemical …

Aqueous solutionMolecular StructureChemistryInorganic chemistryVanadiumchemistry.chemical_elementElectronsStereoisomerismVanadiumElectrocatalystTin oxideElectrochemistryCatalysisAnalytical ChemistryCatalysisGlucoseMicroscopy Electron TransmissionCalibrationElectrochemistryMicroscopy Electron ScanningCubic zirconiaZirconiumOxidation-ReductionMonoclinic crystal systemAnalytical chemistry
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Dioxygen reduction by cobalt(II) octaethylporphyrin at liquid|liquid interfaces.

2010

Oxygen reduction catalyzed by cobalt(II) (2,3,7,8,12,13,17,18-octaethylporphyrin) [Co(OEP)] at soft interfaces is studied by voltammetry and biphasic reactions. When Co(OEP) is present in a solution of 1,2-dichloroethane in contact with an aqueous acidic solution, oxygen is reduced if the interface is positively polarized (water phase versus organic phase). This reduction reaction is facilitated when an additional electron donor, here ferrocene, is present in excess in the organic phase.

Aqueous solutionPorphyrinsSurface PropertiesInorganic chemistrychemistry.chemical_elementElectron donorOxygenRedoxAtomic and Molecular Physics and OpticsCatalysisCatalysisOxygenchemistry.chemical_compoundchemistryPhase (matter)Organometallic CompoundsPhysical and Theoretical ChemistryCobaltVoltammetryOxidation-ReductionChemphyschem : a European journal of chemical physics and physical chemistry
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Reaction pathways of glucose oxidation by ozone under acidic conditions.

2009

The ozonation of d-glucose-1-(13)C, 2-(13)C, and 6-(13)C was carried out at pH 2.5 in a semi-batch reactor at room temperature. The products present in the liquid phase were analyzed by GC-MS, HPAEC-PAD, and (13)C NMR spectroscopy. Common oxidation products of glucose have also been submitted to identical ozonation conditions. For the first time, a pentaric acid was identified and its formation quantitatively correlated to the loss of C-6 of glucose in the form of carbon dioxide. Potential mechanisms for the formation of this pentaric acid are discussed. The well-accepted pathway involving the anomeric position in glucose, gluconic acid, arabinose, and carbon dioxide is reinvestigated. The …

ArabinoseOzoneDecarboxylationInorganic chemistry02 engineering and technologyUronic acidoxidation -mechanism01 natural sciencesBiochemistryGluconatesMass SpectrometryAnalytical Chemistrychemistry.chemical_compoundOzoneD-Glucose[ CHIM.OTHE ] Chemical Sciences/OtherOrganic chemistrydecarboxylationComputingMilieux_MISCELLANEOUS010405 organic chemistryOrganic ChemistryGeneral MedicineCarbon-13 NMRCarbon DioxideHydrogen-Ion Concentration021001 nanoscience & nanotechnologyArabinoseketo acidCarbon0104 chemical sciencesuronic acidGlucosechemistryCarbon dioxideGluconic acid0210 nano-technology[CHIM.OTHE]Chemical Sciences/OtherOxidation-Reductionpectic acidCarbohydrate research
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Sulfur isotope's signal of nanopyrites enclosed in 2.7 Ga stromatolitic organic remains reveal microbial sulfate reduction.

2018

18 pages; International audience; Microbial sulfate reduction (MSR) is thought to have operated very early on Earth and is often invoked to explain the occurrence of sedimentary sulfides in the rock record. Sedimentary sulfides can also form from sulfides produced abiotically during late diagenesis or metamorphism. As both biotic and abiotic processes contribute to the bulk of sedimentary sulfides, tracing back the original microbial signature from the earliest Earth record is challenging. We present in situ sulfur isotope data from nanopyrites occurring in carbonaceous remains lining the domical shape of stromatolite knobs of the 2.7-Gyr-old Tumbiana Formation (Western Australia). The anal…

ArcheanBiogeochemical cycleGeologic Sediments010504 meteorology & atmospheric sciencesIronGeochemistrychemistry.chemical_elementSulfides010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundδ34S[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/Geochemistry[ SDV.MP ] Life Sciences [q-bio]/Microbiology and ParasitologySulfur IsotopesMicrobial matAnaerobiosisstromatoliteSulfateEcology Evolution Behavior and Systematics0105 earth and related environmental sciencesGeneral Environmental SciencebiologyChemistrySulfatessulfur biogeochemical cycleWestern Australiabiology.organism_classification[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/GeochemistrySulfurDiagenesisTumbiana FormationStromatolite13. Climate actionAnaerobic oxidation of methaneGeneral Earth and Planetary SciencesOxidation-Reductionmicrobial sulfate reduction
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Speciation and oxidation kinetics of arsenic in the thermal springs of Wiesbaden spa, Germany.

2001

Since 1886 arsenic has been known to be present as a trace component in the Wiesbaden thermal waters at concentrations of over 100 microg L(-1). In this study for the first time molecular level speciation of arsenic was measured both in the water (by HG-AAS) and in wellstone scale deposits (by XANES). Most of the arsenic in the anoxic NaCl-type waters is in the reduced arsenite form. Hydrous ferric oxide (HFO) precipitates in the scale deposits scavenge only the minor dissolved arsenate portion which is, however, accumulated up to 3% w/w. Isothermal precipitation experiments at in-situ temperatures showed a difference between the progress of both arsenic and iron oxidation and precipitation…

ArsenitesInorganic chemistrychemistry.chemical_elementengineering.materialBiochemistryFerric CompoundsArsenicHydrous ferric oxideschemistry.chemical_compoundAdsorptionWater SupplyGermanyChemical PrecipitationArsenicArseniteAqueous solutionPrecipitation (chemistry)Spectrum AnalysisX-RaysArsenateAnoxic watersKineticschemistrySolubilityEnvironmental chemistryengineeringMicroscopy Electron ScanningOxidation-ReductionWater Pollutants ChemicalFresenius' journal of analytical chemistry
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Oxidative stress response of tumor cells: microarray-based comparison between artemisinins and anthracyclines

2004

The antimalarial artemisinins also reveal profound cytotoxic activity against tumor cells. Artemisinins harbor an endoperoxide bridge whose cleavage results in the generation of reactive oxygen species (ROS) and/or artemisinin carbon-centered free radicals. Established cancer drugs such as anthracyclines also form ROS and free radicals that are responsible for the cardiotoxicity of anthracyclines. In contrast, artemisinins do not reveal cardiotoxicity. In the present investigation, we compared the cytotoxic activities of different artemisinins (artemisinin, artesunate, arteether, artemether, artemisitene, dihydroartemisinylester stereoisomers) in 60 cell lines of the National Cancer Institu…

ArtemisininsDaunorubicinAntineoplastic AgentsPharmacologyBiologymedicine.disease_causeBiochemistryAntimalarialsInhibitory Concentration 50parasitic diseasesTumor Cells CulturedmedicineAnimalsCluster AnalysisHumansIdarubicinAnthracyclinesDoxorubicinRNA MessengerArtemisininOligonucleotide Array Sequence AnalysisPharmacologyCardiotoxicityGene Expression ProfilingArtemisininsGene expression profilingOxidative StressDrug Screening Assays AntitumorOxidation-ReductionSesquiterpenesOxidative stressmedicine.drugBiochemical Pharmacology
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