Search results for "OXIDATION"

showing 10 items of 1913 documents

Inhibition of tumor lactate oxidation: consequences for the tumor microenvironment.

2011

Abstract Background and purpose Tumor cells are recognized as being highly glycolytic. However, recently it was suggested that lactate produced in hypoxic tumor areas may be taken up by the monocarboxylate transporter MCT1 and oxidized in well-oxygenated tumor parts. Furthermore, it was shown that inhibition of lactate oxidation using the MCT1 inhibitor α-cyano-hydroxycinnamate (CHC) can radio-sensitize tumors possibly by forcing a switch from lactate oxidization to glycolysis in oxygenated cells, which in turn improves tumor oxygenation and indirectly kills radio-resistant hypoxic tumor cells from glucose starvation. Material and methods To provide direct evidence for the existence of a ta…

Monocarboxylic Acid TransportersPasteur effectMice NudeUterine Cervical NeoplasmsImmunoenzyme Techniques03 medical and health sciencesMice0302 clinical medicineLactate oxidationFluorodeoxyglucose F18Cell Line TumorTumor MicroenvironmentPimonidazoleAnimalsRadiology Nuclear Medicine and imaging030304 developmental biologyMonocarboxylate transporter0303 health sciencesTumor microenvironmentbiologySymportersChemistryGlucose analogHematologyTumor OxygenationWarburg effectCell Hypoxia3. Good healthGlucoseOncologyCinnamatesHead and Neck NeoplasmsNitroimidazoles030220 oncology & carcinogenesisImmunologyLuminescent Measurementsbiology.proteinCancer researchCarcinoma Squamous CellLactatesLinear ModelsAutoradiographyFemaleGlycolysisOxidation-ReductionRadiotherapy and oncology : journal of the European Society for Therapeutic Radiology and Oncology
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Synthesis, structure and reactivity of trans-UO22+ complexes of OH-containing ligands †

2000

trans-Dioxouranium dinuclear complexes of a few OH-containing ligands possessing N-, O-binding sites were synthesized and characterised. Seven of these were also structurally characterised by single crystal X-ray diffraction. All these complexes exhibit symmetric U2O2 core structures in addition to having a seven-co-ordinated environment about each uranium centre. Even when the ligand possessed more than one CH2OH group, only one such group was found to be involved both in chelation as well as in bridging. These complexes exhibited facile transmetallation reactions with vanadium and molybdenum precursors. Though their core structures are alike, the complexes differ in their lattice arrangem…

Monooxovanadium(V)Hydrogen-PeroxideLigandStereochemistryVanadium HaloperoxidaseVanadiumchemistry.chemical_elementGeneral ChemistryBaseBindingCrystallographyTransmetalationchemistryModelsMolybdenumOxidationElectrochemistryChelationSingle crystalDerivativesSalicylaldehydeJournal of the Chemical Society, Dalton Transactions
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Reversible Dioxygen Binding and Phenol Oxygenation in a Tyrosinase Model System

2000

The complex [Cu2(L-66)]2+ (L-66 = a,a'-bis¿bis[2-(1'-methyl-2'-benzimidazolyl)ethyl]amino¿-m-xylene) undergoes fully reversible oxygenation at low temperature in acetone. The optical [lambda(max) = 362 (epsilon 15000), 455 (epsilon 2000), and 550 nm (epsilon 900M(-1)cm(-1))] and resonance Raman features (760 cm(-1), shifted to 719cm(-1)(-1) with 18O2) of the dioxygen adduct [Cu2(L-66)(O2)]2+ indicate that it is a mu-eta2:eta2-peroxodicopper(II) complex. The kinetics of dioxygen binding, studied at - 78 degrees C, gave the rate constant k1 = 1.1M(-1) 5(-1) for adduct formation, and k(-1) =7.8 x 10(-5)s(-1), for dioxygen release from the Cu2O2 complex. From these values, the O2 binding consta…

Monophenol MonooxygenaseChemistrySpectrophotometry AtomicTyrosinaseOrganic ChemistryKineticsGeneral ChemistryResonance (chemistry)PhotochemistryMedicinal chemistryBinding constantCatalysisQuinoneAdductOxygenchemistry.chemical_compoundReaction rate constantModels ChemicalPhenolsAcetoneOxidation-ReductionChemistry - A European Journal
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Influence of Laccase and Tyrosinase on the Antioxidant Capacity of Selected Phenolic Compounds on Human Cell Lines

2015

Polyphenolic compounds affect the color, odor and taste of numerous food products of plant origin. In addition to the visual and gustatory properties, they serve as radical scavengers and have antioxidant effects. Polyphenols, especially resveratrol in red wine, have gained increasing scientific and public interest due to their presumptive beneficial impact on human health. Enzymatic oxidation of phenolic compounds takes place under the influence of polyphenol oxidases (PPO), including tyrosinase and laccase. Several studies have demonstrated the radical scavenger effect of plants, food products and individual polyphenols in vitro, but, apart from resveratrol, such impact has not been prove…

Monophenol MonooxygenasePlant Extracts530 PhysicsoxidationDPPH•food and beveragesantioxidant activitytyrosinase530 Physikcell culturesArticleAntioxidantsCell LinelaccaseFungal Proteinslcsh:QD241-441lcsh:Organic chemistryHumansOxidation-ReductionpolyphenolsMolecules
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2016

AbstractAuthigenic carbonate build-ups develop at seafloor methane-seeps, where microbially mediated sulphate-dependent anaerobic oxidation of methane facilitates carbonate precipitation. Despite being valuable recorders of past methane seepage events, their role as archives of atmospheric processes has not been examined. Here we show that cyclic sedimentation pulses related to the Indian monsoon in concert with authigenic precipitation of methane-derived aragonite gave rise to a well-laminated carbonate build-up within the oxygen minimum zone off Pakistan (northern Arabian Sea). U–Th dating indicates that the build-up grew during past ~1,130 years, creating an exceptional high-resolution a…

Monsoon of South AsiaMultidisciplinary010504 meteorology & atmospheric sciencesAragoniteGeochemistryAuthigenicengineering.material010502 geochemistry & geophysicsOxygen minimum zone01 natural sciencesSeafloor spreadingchemistry.chemical_compoundchemistry13. Climate actionAnaerobic oxidation of methaneengineeringCarbonate14. Life underwaterPrecipitationGeology0105 earth and related environmental sciencesScientific Reports
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The prevalence of surface oxygen vacancies over the mobility of bulk oxygen in nanostructured ceria for the total toluene oxidation

2015

12 figures, 2 tables

MorphologyNanocubesMaterials scienceInorganic chemistryNanoparticlechemistry.chemical_elementOxygenHydrothermal circulationCatalysisCatalysisCrystalchemistry.chemical_compoundCeriaSurface oxygen vacanciesEnvironmental Science(all)General Environmental ScienceNanotubesProcess Chemistry and TechnologyTolueneToluene oxidationNanostructuresCrystal sizechemistryNanoparticlesNanorodNanorodsToluene
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Effect of C/N shock variation on the performances of a moving bed membrane bioreactor.

2015

Abstract The effect of a sharp variation of C/N ratio in a moving bed membrane bioreactor (MB-MBR) pilot plant treating high strength wastewater has been investigated. The experimental campaign was divided into two periods, each characterized by a different C/N ratio (namely, 2.5 and 15, Period 1 and Period 2, respectively). The MB-MBR system was analyzed in terms of organic carbon removal, nitrification efficiency, biokinetic activity and fouling behavior. The results showed that the nitrification process was severely affected by lower C/N value and by high concentration of ammonia. It was noticed an extensive stress effect on the autotrophic bacteria. Furthermore, it was observed an incre…

Moving bed membrane bioreactorEnvironmental EngineeringBiofoulingNitrogenOLRBioengineeringPilot ProjectsC/N ratio; Moving bed membrane bioreactor; Nitrification; OLR; Bioengineering; Environmental Engineering; Waste Management and DisposalMembrane bioreactorWaste Disposal FluidAmmoniachemistry.chemical_compoundExtracellular polymeric substanceBiopolymersBioreactorsAmmoniaBioreactorBiomassWaste Management and DisposalBiological Oxygen Demand AnalysisChromatographyFoulingBacteriaRenewable Energy Sustainability and the EnvironmentChemistryMembranes ArtificialGeneral MedicineC/N ratioNitrificationCarbonMembraneChemical engineeringBiofilmsNitrificationOxidation-ReductionParticle depositionBioresource technology
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The role of water in the photocatalytic degradation of acetonitrile and toluene in gas-solid and liquid-solid regimes

2006

Photocatalytic degradation of acetonitrile and toluene was carried out both in gas-solid and in liquid-solid regimes by using commercialTiO2samples (Merck and Degussa P25). The investigation was mainly aimed to study the influence of water present in the reaction environment on the mechanism and degradation rate of two probe molecules. In gas-solid regime, the reacting mixture consisted of toluene or acetonitrile, oxygen, nitrogen, and water vapour. The main degradation product of toluene wasCO2with small amounts of benzaldehyde. In the presence of water vapour, the activity ofTiO2Merck remained stable but greatly decreased if water was absent.TiO2Degussa P25 continuously deactivated, even …

Muconic acidADSORPTIONBENZENEInorganic chemistrylcsh:TJ807-830lcsh:Renewable energy sourcesHUMIDIFIED AIRANATASE TIO2 CATALYSTOXIDATIONCH3CNBenzaldehydechemistry.chemical_compoundGeneral Materials ScienceFORMALDEHYDEBenzenePhotodegradationAcetonitrileBenzoic acidTITANIUM-DIOXIDERenewable Energy Sustainability and the EnvironmentGeneral ChemistryVAPOR-PHASETolueneAtomic and Molecular Physics and OpticsANATASE TIO2 CATALYST; TITANIUM-DIOXIDE; HUMIDIFIED AIR; VAPOR-PHASE; OXIDATION; ADSORPTION; BENZENE; CH3CN; FORMALDEHYDE; BEHAVIORchemistryBenzyl alcoholBEHAVIORInternational Journal of Photoenergy
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Ethanol cycle in an ethanologenic bacterium

2002

AbstractA novel redox cycle is suggested, performing interconversion between acetaldehyde and ethanol in aerobically growing ethanologenic bacterium Zymomonas mobilis. It is formed by the two alcohol dehydrogenase (ADH) isoenzymes simultaneously catalyzing opposite reactions. ADH I is catalyzing acetaldehyde reduction. The local reactant ratio at its active site probably is shifted towards ethanol synthesis due to direct channeling of NADH from glycolysis. ADH II is oxidizing ethanol. The net result of the cycle operation is NADH shuttling from glycolysis to the membrane respiratory chain, and ensuring flexible distribution of reducing equivalents between the ADH reaction and respiration.

NADH channelingBiophysicsRespiratory chainBiochemistryZymomonas mobilischemistry.chemical_compoundStructural BiologyGeneticsGlycolysisEthanol metabolismMolecular BiologyAlcohol dehydrogenaseZymomonasEthanolEthanolbiologyFutile cycleRespirationZymomonas mobilisAlcohol dehydrogenaseAcetaldehydeCell BiologyNADbiology.organism_classificationAerobiosisIsoenzymeschemistryBiochemistryFutile cycleChemostatbiology.proteinOxidation-Reductionhormones hormone substitutes and hormone antagonistsFEBS Letters
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Fullerene as a Platform for Recyclable TEMPO Organocatalysts for the Oxidation of Alcohols

2014

[60]Fullerene has been employed successfully as a molecular platform to anchor 12 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) moieties. Such an octahedrally substituted C60-derivative has been employed as an organocatalyst for the oxidation of primary and secondary alcohols using the Anelli protocol. The reaction showed a general applicability to various alcohols, and the catalyst was recovered easily and could be recycled for at least seven cycles with no loss in catalytic activity. EPR spectroscopy studies revealed that the amount of radicals decreases during the catalytic cycles, even if the recovered material still displays unchanged catalytic activity. This new approach paves the way …

NITROXIDEFullerenePrimary (chemistry)alcoholoxidationChemistryCATALYSISRadicalOrganic ChemistrySettore CHIM/06 - Chimica Organicaorganocatalysiorganic oxidationlaw.inventionCatalysisInorganic ChemistrylawAlcohol oxidationOrganocatalysisOrganic chemistryPhysical and Theoretical ChemistryTEMPOElectron paramagnetic resonanceFULLERENEEPR spectroscopyESR
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