Search results for "pH dependence"

showing 5 items of 5 documents

Chromatographic retention–activity relationships for prediction of the toxicity pH-dependence of phenols

2007

Abstract An investigation of the use of the chromatographic retention (log  k ) as an in vitro approach for modeling the pH-dependence of the toxicity to Guppy of phenols is developed. A data set of 19 phenols with available experimental toxicity–pH data was used. The importance of the mechanism of toxic action (MOA) of phenols was studied. log  k data at three pH values were used for the phenols classification and two groups or ‘MODEs’ were identified. For one ‘MODE’ a quantitative retention–activity relationship (QRAR) model was calculated. Finally, the model was used to assess the toxicity to Guppy of phenols at different pH values. The results of this investigation suggest that chromato…

Environmental EngineeringHealth Toxicology and MutagenesisQuantitative Structure-Activity RelationshipModels BiologicalLethal Dose 50chemistry.chemical_compoundPhenolsPh dependenceAnimalsEnvironmental ChemistryOrganic chemistryEcotoxicologyPhenolsChromatographyPoeciliaChromatographyChemistryPublic Health Environmental and Occupational HealthGeneral MedicineGeneral ChemistryHydrogen-Ion ConcentrationPollutionToxicityPh rangeFish <Actinopterygii>ForecastingChemosphere
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Introduction of histidine residues into avidin subunit interfaces allows pH-dependent regulation of quaternary structure and biotin binding

2003

AbstractIn order to turn the subunit association and biotin binding of avidin into pH-sensitive phenomena, we have replaced individually three amino acid residues in avidin (Met96, Val115 and Ile117) with histidines in the 1–3 interface, and in combination with a histidine conversion in the 1–2 interface (Trp110). The single replacements Met96His and Val115His in the 1–3 interface were found to have a clear effect on the quaternary structure of avidin, since subunit associations of these mutants became pH-dependent. The histidine replacement in the 1–2 interface affected the biotin-binding properties of the mutants, in particular reversibility of binding and protein–ligand complex formation…

Models MolecularBiotin bindingInsectaProtein subunitBiophysicsBiotinBiosensing TechniquesBiochemistryCell LineProtein structureStructural BiologyGeneticsAnimalsHistidinepH dependenceProtein Structure QuaternaryMolecular BiologyHistidinebiologyChemistryCell BiologyProtein engineeringHydrogen-Ion ConcentrationAvidinRecombinant ProteinsMolecular WeightProtein SubunitsSpectrometry FluorescenceAmino Acid SubstitutionBiochemistryBiotinylationBiophysicsbiology.proteinProtein quaternary structureProtein engineeringBaculoviridaeProtein BindingAvidinFEBS Letters
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Luminescence Efficiency of Si/SiO 2 Nanoparticles Produced by Laser Ablation

2019

Photoluminescence properties of Si(core)/SiO 2 (shell) nanoparticles produced by pulsed laser ablation in aqueous solution are investigated with the purpose to highlight the microscopic processes that govern the emission brightness and stability. Time resolved spectra evidence that these systems emit a µs decaying band centered around 1.95 eV, that is associated with the radiative recombination of quantum-confined excitons generated in the Si nanocrystalline core. Both the quantum efficiency and the stability of this emission are strongly dependent on the pH level of the solution, that is changed after the laser ablation is performed. They enhance in acid environment because of the H + pass…

PhotoluminescenceLaser ablationMaterials scienceSi/SiO2 nanoparticles pulsed laser ablation quantum confinement luminescence IR absorption pH dependencebusiness.industry2Surfaces and InterfacesCondensed Matter Physicslaser ablation; pH dependence; photoluminescence; quantum confinement; Si/SiO ; 2; nanoparticlesquantum confinementSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsQuantum dotSio2 nanoparticleslaser ablationMaterials ChemistryPh dependenceOptoelectronicsphotoluminescencenanoparticlespH dependenceElectrical and Electronic EngineeringLuminescencebusinessSi/SiOphysica status solidi (a)
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Voltammetric Investigation on Uranyl Sorption by Alginate Based Material. Influence of Hydrolysis and pH Dependence

2015

The removal of U(VI) as uranyl (UO22+) from aqueous solutions was investigated by sorption onto alginate based material. The hydrolysis of uranyl ion was always taken into account in the calculations of free (22UO) ion in aqueous solution, in the experimental pH range considered, as well as the acid-base properties of alginate polymer. The sorption process follows a pseudo-second order kinetic model and the sorption rate decreases when the pH value increases. In addition to the classical Langmuir and Freundlich models, the equilibrium data were fitted by using a modified multi-component equilibrium model, never tested before. Differential Pulse Voltammetry (DPV) and Inductively Coupled Plas…

U(VI) adsorption; pH dependence; low cost biosorption material; kinetic and equilibrium studies; Differential Pulse Voltammetry; ICP-OES measurementsDifferential Pulse Voltammetrylow cost biosorption materialpH dependencekinetic and equilibrium studieU(VI) adsorptionICP-OES measurements
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Temperature and pH Dependence of Gd-DOTA and Gd-DTPA Complexes Dissociation Studied by EXAFS

1997

The Gd L3-edge of Gd(DTPA) 2- and Gd(DOTA) - complexes, in crystalline state and aqueous solutions presenting various pH (0.15-8) at different temperatures (25-90 °C), are investigated by XAFS experiments. For the Gd(DTPA) 2- . complexes we observe a strong pH (0.15-1.5) dependence of XAFS signals. On the other hand, the XAFS signals of Gd(DOTA) - complexes exhibit a light pH (1-1.5) dependence and for pH<1 we observe a ligand decomposition. Conceming both complexes, we note just a light temperature dependence. To obtain information about the short and medium range order (up to 5 A), multiple scattering calculation is performed. For the first coordination shell, we apply multi-shell fitting…

chemistry.chemical_compoundAqueous solutionchemistryExtended X-ray absorption fine structureScatteringMedium rangeAnalytical chemistryPh dependenceGeneral Physics and AstronomyDOTADissociation (chemistry)X-ray absorption fine structureLe Journal de Physique IV
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