Search results for " hydrolysis"

showing 10 items of 142 documents

Inhibition of aflatoxin B1, B2, G1 and G2 production by Aspergillus parasiticus in nuts using yellow and oriental mustard flours

2015

Abstract Aflatoxins (AFs) are naturally occurring mycotoxin compounds produced by several species of Aspergillus, as Aspergillus flavus and Aspergillus parasiticus and are mutagenic, teratogenic, and carcinogenic compounds that have been implicated as causative agents in human hepatic and extra hepatic carcinogenesis. In this study, the reduction of the AFs present in dried fruits (peanut, cashew, walnut, almond, hazelnut and pistachio), produced by A. parasiticus CECT 2681, by isothiocyanates (ITCs) generated by the enzymatic hydrolysis of the glucosinolates (GLCs) present in oriental and yellow mustard flours was evaluated. The AFs reduction activity through ITCs application in dried frui…

AspergillusAflatoxinDried fruitbiologyChemistryfood and beveragesAspergillus flavusbiology.organism_classificationAspergillus parasiticusHydrolysischemistry.chemical_compoundEnzymatic hydrolysisFood scienceMycotoxinFood ScienceBiotechnologyFood Control
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Is ATP Hydrolysis the Power Stroke in ABC Transporters?

2018

BiochemistryATP hydrolysisChemistryBiophysicsATP-binding cassette transporterPower strokeBiophysical Journal
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An enzyme caught in action: Direct imaging of hydrolytic function and domain formation of phospholipase A2 in phosphatidylcholine monolayers

1989

AbstractPhospholipase A2, a ubiquitous lipolytic enzyme that actively catalyses hydrolysis of phospholipids, has been studied as a model for enzyme-substrate reactions, as a membrane structural probe, and as a model for lipid-protein interactions. Its mechanism of action remains largely controversial. We report here for the first time direct microscopic observation of the lipolytic action of fluorescently marked phospholipase A2 (Naja naja naja) against phosphatidylcholine monolayers in the lipid phase transition region. Under these conditions, phospholipase A2 is shown to target and hydrolyse solid-phase lipid domains of L-α-dipalmitoylphosphatidylcholine. In addition, after a critical ext…

BiophysicsPhospholipid02 engineering and technologyBiochemistry03 medical and health scienceschemistry.chemical_compoundPhospholipase A2Structural BiologyPhospholipase A2PhosphatidylcholineEnzymatic hydrolysisGeneticsmedicineLipid bilayer phase behaviorMolecular BiologyDomain030304 developmental biologyFluorescence microscopy0303 health sciencesPhospholipase APhospholipase BbiologyChemistryMonolayerCell Biology021001 nanoscience & nanotechnologyPhospholipidBiochemistryMechanism of actionEnzymatic hydrolysisbiology.proteinmedicine.symptom0210 nano-technologyFEBS Letters
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Rate-retarding effects of mixed anionic/non-ionic micelles on the alkaline hydrolysis of the chloropentamminocobalt(III) complex - Role of the anioni…

2006

Rate data for the alkaline hydrolysis of the chloropentaamminecobalt(III) cation in the presence of mixed micelles composed of (i) anionic sodium decylsulphate (SDeS) and non-ionic dodecylpenta(oxyethylene glycol) monoether (C12E5) surfactants and (ii) anionic sodium perfluorooctanoate (SPFO) and non-ionic C12E5 surfactants has been obtained at T 298K and constant electrolyte concentration 0.08 mol dm−3 ([NaOH] = 0.01 mol dm−3, [NaClO4] = 0.07 mol dm−3) over a wide range of total surfactant concentration (Ct) and anionic mole fraction (χ). The critical micelle concentrations (c.m.c.s) of the mixed micelles have been determined over the entire χ range by means of surface tension measurements…

CHLOROPENTAAMMINECOBALT(III) CATIONSYSTEMSSODIUM DODECYL-SULFATEBASE HYDROLYSISMICELLIZATIONBINARY-MIXTURESSYNERGISM
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Design of enzyme-mediated controlled release systems based on silica mesoporous supports capped with ester-glycol groups

2012

[EN] An ethylene glycol-capped hybrid material for the controlled release of molecules in the presence of esterase enzyme has been prepared. The final organic-inorganic hybrid solid S1 was synthesized by a two-step procedure. In the first step, the pores of an inorganic MCM-41 support (in the form of nanoparticles) were loaded with [Ru(bipy) 3]Cl 2 complex, and then, in the second step, the pore outlets were functionalized with ester glycol moieties that acted as molecular caps. In the absence of an enzyme, release of the complex from aqueous suspensions of S1 at pH 8.0 is inhibited due to the steric hindrance imposed by the bulky ester glycol moieties. Upon addition of esterase enzyme, del…

Cell viabilityINGENIERIA DE LA CONSTRUCCIONEthyleneRuthenium complexesMCM-41 supportsCytotoxicityGlycol derivativesEsteraseFunctionalizedOrganic-inorganic hybrid solidsGlycolschemistry.chemical_compoundQUIMICA ORGANICATumor Cells CulturedElectrochemistryControlled release systemsOrganic chemistryControlled releaseGeneral Materials ScienceSteric hindrancesMCF-7 cellsSpectroscopyHydrolysisEsterasesSilicaEstersSurfaces and InterfacesSilicon DioxideCondensed Matter PhysicsControlled releaseChlorine compoundsEster bondsBody fluidsHybrid materialsHybrid materialPorosityCell deathCell SurvivalSurface PropertiesCytotoxic drugsRutheniumHydrolysisEnzymatic hydrolysisEsterase enzymesPolymer chemistryHumansCamptothecin (CPT)Molecular capSize reductionsTherapeutic ApplicationEthylene glycolTwo-step procedureEsterificationSuspensions (fluids)Ruthenium compoundsQUIMICA INORGANICAMesoporous supportOligo(ethylene glycol)Cell internalizationMolecular gatesConfocal microscopychemistryEnzymatic hydrolysisEnzyme-mediated hydrolysisNanoparticlesCamptothecinCell cultureMesoporous materialAqueous suspensionsEthylene glycolHeLa Cells
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Speciation of Al3+ in fairly concentrated solutions (20 to 200 mmol L-1) at I = 1 mol L-1 (NaNO3), in the acidic pH range, at different temperatures.

2011

AbstractThe hydrolysis of Al3+ was studied in aqueous 1 mol L−1 NaNO3 solution at different concentrations (20–200 mmol L−1) and temperatures (283.15–343.15 K) by potentiometry (ISE-H+, glass electrode). Many different speciation models were considered in the calculations and it was found that the best model is represented by the following species: Al(OH)2+, Al(OH)45+, Al13(OH)327+. Hydrolysis constants and enthalpy changes at different temperatures are reported.

Chemical Health and SafetyAqueous solutionChemistryHealth Toxicology and Mutagenesismedia_common.quotation_subjectEnthalpyInorganic chemistryToxicologyGlass electrodelaw.inventionSpeciationHydrolysislawMolePh rangealuminium(III) speciation hydrolysis constants hydrolysis enthalpy changesSettore CHIM/01 - Chimica Analiticamedia_commonAluminium(III) speciation; Hydrolysis constants; Hydrolysis enthalpy changes
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Chemical and catalytical properties of thermal polymers of amino acids (proteinoids)

1974

The significance of thermal polyamino acids (proteinoids) as abiotic predecessors of proteins is reviewed on the basis of new experimental results. Most proteinoids yield only 50% to 80% amino acid upon acid hydrolysis. They contain 40% to 60% less peptide links than typical proteins, whereas their average nitrogen content is like that of proteins. The arrangement of amino acid residues is nonrandom. The degree of nonrandomness is difficult to determine because unusual crosslinks disturb most of the sequencing methods typically applied in protein chemistry. The products obtained in a polymerization experiment are heterogeneous. They can be separated into a limited number of related fraction…

Chemical PhenomenaMacromolecular SubstancesPolymersOrigin of LifePeptideCatalysisChromatography DEAE-CelluloseProteinoidOrganic chemistryAmino Acid SequenceAmino AcidsMolecular BiologyEcology Evolution Behavior and SystematicsGeneral Environmental Sciencechemistry.chemical_classificationMolecular massHydrolysisProteinsGeneral MedicinePolymerHydrogen-Ion ConcentrationElectrophoresis DiscBiological EvolutionAgricultural and Biological Sciences (miscellaneous)Amino acidMolecular WeightChemistrySolubilitychemistryPolymerizationSpace and Planetary ScienceYield (chemistry)ThermodynamicsGeneral Earth and Planetary SciencesAcid hydrolysisOrigins of Life
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Mixed monolayers of natural and polymeric phospholipids: structural characterization by physical and enzymatic methods

1990

This study has focused on physical characterization and enzymatic hydrolysis of mixed monolayers of a natural phospholipid substrate and a polymerizable phospholipid analogue. Such a mixed system presents the possibility to stabilize model biomembranes, vary the molecular environment within the layer through polymerization and simultaneously examine these influences on monolayer structure. Phospholipase A2 was used here as a sensitive probe of the molecular environment within these mixed, polymerizable monolayers to complement information obtained from isotherm and isobar data. The results clearly show a strong influence of molecular environment on phospholipase A2 activity, even if differe…

Chemical PhenomenaPolymersBiophysicsPhospholipidBiochemistryPhospholipases Achemistry.chemical_compoundPhosphatidylcholineEnzymatic hydrolysisMonolayerOrganic chemistryPhospholipidsPhospholipase AMolecular StructureChemistry PhysicalHydrolysisTemperaturetechnology industry and agricultureSubstrate (chemistry)Membranes ArtificialCell BiologyPhospholipases A2MonomerchemistryPolymerizationPhosphatidylcholinesBiophysicsDimyristoylphosphatidylcholineBiochimica et Biophysica Acta (BBA) - Biomembranes
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Catalytic treatment of rapeseed straw for enhanced production of furfural and glucose for bioethanol production

2021

Abstract Ethanol produced from renewable biomass, such as lignocellulosic feedstock, is one of the most promising future biofuels. In this paper, rapeseed straw was tested as an abundant and cost-effective renewable resource material for the production of cellulosic glucose. Pre-treatment of this material is an important step to improve the efficiency of subsequent cellulose hydrolysis. In this study, we used two pre-treatment methods – hydrothermochemical and ultrasound. Studies have shown that, in the initial hydrothermal pre-treatment of rapeseed straw, Al2(SO4)3 may be used as an efficient catalyst, at least in procedures for obtaining glucose. An increase in the amount of this catalyst…

ChemistryBioengineeringStrawRaw materialPulp and paper industryFurfuralApplied Microbiology and BiotechnologyBiochemistryHydrolysischemistry.chemical_compoundCellulosic ethanolBiofuelEnzymatic hydrolysisRenewable resourceProcess Biochemistry
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Reactions of Carbonyl Compounds in Basic Solutions. Part 351: The Alkaline Hydrolysis and Reactivity – Structure – Spectra Correlations of (Z)-4-(Sub…

2002

The kinetics of the alkaline hydrolysis and the configuration, conformation and electronic structure were studied using IR, NMR spectroscopy, X-ray analysis and AM1 theoretical calculations for a series of (Z)-4-(substituted benzylidene)-2-phenyl-4H-oxazol-5-ones (1) and compared with analogous results reported for (E)-4-benzylidene-2-phenyl-4H-furan-5-ones (5) and related compounds.

ChemistryKineticsOrganic chemistryReactivity (chemistry)General ChemistryElectronic structureNuclear magnetic resonance spectroscopyAlkaline hydrolysis (body disposal)Medicinal chemistrySpectral lineJournal of Chemical Research
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