Search results for " hydrolysis"

showing 10 items of 142 documents

Physicochemical and Rheological Characterization of Different Low Molecular Weight Gellan Gum Products and Derived Ionotropic Crosslinked Hydrogels

2021

A series of four different low molecular weight gellan gum products was obtained by alkaline hydrolysis with the aim to investigate the impact of the molecular weight on the rheological properties of the polysaccharide aqueous dispersions and on the physicochemical characteristics of derived ionotropic crosslinked hydrogels. In particular, thermo-rheological analysis was conducted on aqueous dispersions to study the influence of molecular weight on the thermogelation properties typical of the native polysaccharide while strain sweep experiments were conducted to establish if aqueous dispersion shows a viscoelastic behavior. The effect of different Ca2+ on the rheological properties of hydro…

Polymers and PlasticsSciencelow molecular weight gellan gumGeneral. Including alchemyBioengineering02 engineering and technologybasic hydrolysis010402 general chemistryPolysaccharide01 natural sciencesArticleViscoelasticityBiomaterialsHydrolysischemistry.chemical_compoundQD1-65RheologymedicineQD1-999Alkaline hydrolysisQD146-197chemistry.chemical_classificationQionotropic crosslinked gellan gum hydrogelOrganic Chemistrybasic hydrolysi021001 nanoscience & nanotechnologyGellan gum0104 chemical sciencesChemistrythermotropic behaviorChemical engineeringchemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoSelf-healing hydrogelsionotropic crosslinked gellan gum hydrogelsSwellingmedicine.symptom0210 nano-technologyInorganic chemistryGels
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Functional and bioactive properties of peptides derived from marine side streams

2021

In fish processing, a great amount of side streams, including skin, bones, heads and viscera, is wasted or downgraded as feed on a daily basis. These side streams are rich sources of bioactive nitrogenous compounds and protein, which can be converted into peptides through enzymatic hydrolysis as well as bacterial fermentation. Peptides are short or long chains of amino acids differing in structure and molecular weight. They can be considered as biologically active as they can contribute to physiological functions in organisms with applications in the food and pharmaceutical industries. In the food industry, such bioactive peptides can be used as preservatives or antioxidants to prevent food…

Preservative3309.03 Antioxidantes en Los AlimentosantioxidantDrug IndustryFood industry030309 nutrition & dieteticsFood spoilagePharmaceutical ScienceReviewAntioxidants03 medical and health sciencesIngredient0404 agricultural biotechnologyNutraceuticalRiversEnzymatic hydrolysisDrug DiscoveryAnimalsFood IndustryHumansFood scienceantihypertensivePharmacology Toxicology and Pharmaceutics (miscellaneous)lcsh:QH301-705.5Antihypertensive Agents3309.20 Propiedades de Los Alimentos2. Zero hungerchemistry.chemical_classificationnutraceuticals0303 health sciencesseafood side streamsfunctional propertiesbusiness.industryfungifood and beveragesBiological activity04 agricultural and veterinary sciences040401 food scienceAmino acidSeafoodSolubilitychemistrylcsh:Biology (General)Dietary SupplementsEmulsions2302.24 PéptidosPeptidesbusinessbioactive peptides
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Role of ΔpH in the mechanism of zeaxanthin-dependent amplification of qE

1995

Abstract The influence of zeaxanthin on the high-energy-state fluorescence quenching (qE) and the pH dependence of the maximum chlorophyll fluorescence yield (Fm) was examined in spinach thylakoids. High contents of zeaxanthin were achieved using different pretreatments. A pronounced, zeaxanthin-dependent amplification of non-photochemical quenching (NPQ) was exclusively found in thylakoids containing zeaxanthin, synthesized in the dark via the buildup of an artificial ΔpH. These thylakoids also showed a significant quenching of chlorophyll fluorescence in the range pH 5.5–6.3, where no or only slight quenching was visible in zeaxanthin-free thylakoids. Thylakoids containing high amounts of…

RadiationQuenching (fluorescence)Radiological and Ultrasound TechnologybiologyNon-photochemical quenchingBiophysicsfood and beveragesbiology.organism_classificationPhotochemistryeye diseasesZeaxanthinchemistry.chemical_compoundchemistryATP hydrolysisYield (chemistry)ThylakoidSpinachRadiology Nuclear Medicine and imagingChlorophyll fluorescenceJournal of Photochemistry and Photobiology B: Biology
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Structural dynamics in F1ATPase during the first reaction cycle of ATP hydrolysis

1991

Abstract The velocity of ATP hydrolysis, catalyzed by purified F 1 ATPase from Micrococcus luteus , was decelerated on decreasing the temperature. At 13′C one reaction cycle is completed after 20 s. Hydrolysis was triggered upon rapid mixing of the enzyme with ATP. During the first reaction cycle, succeeding structural alterations of the F 1 ATPase were traced by time resolved X-ray scattering. The scattering spectra obtained from consecutive intervals of 1 s, revealed the F 1 ATPase to pass a conformational state exhibiting an expanded (6%) molecular shape. The expanded state was observed between 45% and 65% of the time required to complete the reaction cycle. This pointx out a conformatio…

Reaction mechanismProtein ConformationStereochemistryATPaseBiophysicsTime resolved X-ray scatteringBiochemistryMicrococcusCatalysisF1ATPaseHydrolysisMolecular dynamicsAdenosine TriphosphateStructural BiologyATP hydrolysisGeneticsMolecular Biologychemistry.chemical_classificationbiologyHydrolysisX-RaysReaction cycleCell Biologybiology.organism_classificationKineticsProton-Translocating ATPasesEnzymechemistryDynamic structure transitionbiology.proteinMicrococcus luteusFEBS Letters
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Theoretical study of phosphodiester hydrolysis in nucleotide pyrophosphatase/phosphodiesterase. Environmental effects on the reaction mechanism.

2010

We here present a theoretical study of the alkaline hydrolysis of methyl p-nitrophenyl phosphate (MpNPP(-)) in aqueous solution and in the active site of nucleotide pyrophosphatase/phosphodiesterase (NPP). The analysis of our simulations, carried out by means of hybrid quantum mechanics/molecular mechanics (QM/MM) methods, shows that the reaction takes place through different reaction mechanisms depending on the environment. Thus, while in aqueous solution the reaction occurs by means of an A(N)D(N) mechanism, the enzymatic process takes place through a D(N)A(N) mechanism. In the first case, we found associative transition-state (TS) structures, while in the enzyme TS structures have dissoc…

Reaction mechanismStereochemistrydnaNAlkaline hydrolysis (body disposal)Molecular Dynamics SimulationBiochemistryCatalysisHydrolysisColloid and Surface ChemistryCatalytic DomainPyrophosphatasesAqueous solutionbiologyChemistryNucleotidesPhosphoric Diester HydrolasesHydrolysisActive sitePhosphodiesteraseWaterGeneral ChemistryAlkaline PhosphataseSolutionsZincPhosphodiester bondbiology.proteinXanthomonas axonopodisThermodynamicsJournal of the American Chemical Society
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A PLE-based resolution of cocaine, pseudococaine, and 6- and 7-methoxylated cocaine analogues

1996

Abstract The enzymatic hydrolysis of racemic cocaine and cocaine analogues using pig liver esterase (PLE) is shown to afford a practical means for achieving their chemical resolution. This reaction was found to proceed not only with good enantioselectivity, but with an interesting chemoselectivity as well.

Resolution (mass spectrometry)ChemistryOrganic ChemistryClinical BiochemistryPharmaceutical ScienceBiochemistryEsterasePseudococaineEnzymatic hydrolysisDrug DiscoveryMolecular MedicineOrganic chemistryChemoselectivityMolecular BiologyPig liverBioorganic & Medicinal Chemistry Letters
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Stereoselective synthesis and transformation of pinane-based 2-amino-1,3-diols

2021

A library of pinane-based 2-amino-1,3-diols was synthesised in a stereoselective manner. Isopinocarveol prepared from (−)-α-pinene was converted into condensed oxazolidin-2-one in two steps by carbamate formation followed by a stereoselective aminohydroxylation process. The relative stereochemistry of the pinane-fused oxazolidin-2-one was determined by 2D NMR and X-ray spectroscopic techniques. The regioisomeric spiro-oxazolidin-2-one was prepared in a similar way starting from the commercially available (1R)-(−)-myrtenol (10). The reduction or alkaline hydrolysis of the oxazolidines, followed by reductive alkylation resulted in primary and secondary 2-amino-1,3-diols, which underwent a reg…

ScienceAlkaline hydrolysis (body disposal)Alkylation2-amino-12-diol010402 general chemistryRing (chemistry)01 natural sciencesFull Research PaperBenzaldehydechemistry.chemical_compoundQD241-441monoterpeenitOrganic chemistryorgaaniset yhdisteetkemiallinen synteesistereoselective010405 organic chemistryQOrganic ChemistryRegioselectivityTautomer0104 chemical sciencesChemistrytautomerismchemistryoxazolidin-2-oneStereoselectivityTwo-dimensional nuclear magnetic resonance spectroscopytautomeriamonoterpeneBeilstein Journal of Organic Chemistry
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Production of vegetable oil-based biofuels—Thermochemical behavior of fatty acid sodium salts during pyrolysis

2009

Abstract To develop an advanced pyrolysis process for various biomass-derived feedstocks and improve product quality and yield, in-depth investigations into the reaction mechanisms are needed. This paper reports on pyrolysis experiments (Py-GC/MSD and FID) with model compounds including the sodium salts of stearic (C18), oleic (C18:1), and linoleic (C18:2) acids principally obtained from alkaline hydrolysis of vegetable oils. Of the parameters studied – temperature (450–750 °C), time (20 s and 80 s), and the degree of unsaturation (i.e., saturated and mono- and dienoic C18-hydrocarbon chains) – the latter had the most significant effect on the formation of volatile compounds detected in pyr…

Sodiumchemistry.chemical_elementAnalytical ChemistryOleic acidchemistry.chemical_compoundHomologous seriesFuel TechnologyVegetable oilchemistryOrganic chemistrylipids (amino acids peptides and proteins)Sodium stearateStearic acidAlkaline hydrolysisPyrolysisJournal of Analytical and Applied Pyrolysis
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Direct infusion mass spectrometry as a fingerprint of protein-binding media used in works of art

2005

A direct infusion mass spectrometry method for the characterization of proteinaceous glues from binding media used in pictorial works of art prior to conservation or restoration treatment is proposed. Amino acids are released by acid hydrolysis and dissolved in a mixture of acidic water and ethanol. This mixture is directly infused into a mass spectrometer without any derivatization. The mass spectrometer is operated in positive ion electrospray mode (ESI-MS) to yield [M+H]+ ions for the amino acids. Relative amounts of each amino acid are calculated for each protein (beef and porcine gelatines, albumin, casein and egg). The analyzed proteins were satisfactorily distinguished. The method is…

Spectrometry Mass Electrospray IonizationElectrosprayResolution (mass spectrometry)Protein mass spectrometrySwineMass spectrometryPeptide MappingSensitivity and SpecificitySample preparation in mass spectrometryAnalytical Chemistrychemistry.chemical_compoundAdhesivesAnimalsAmino AcidsDerivatizationSpectroscopychemistry.chemical_classificationChromatographyHydrolysisOrganic ChemistryProteinsReproducibility of ResultsAmino acidchemistryCattlePaintingsAcid hydrolysisProtein BindingRapid Communications in Mass Spectrometry
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Regioselective substitution of 6,7-dichloroquinoline-5,8-dione: synthesis and X-ray crystal structure of 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dion…

2003

6,7-Dichloroquinoline-5,8-dione (1) was reacted with a number of 2-aminopyridine derivatives. Of the several possible products of this reaction, 4a,10,11-triazabenzo[3,2-a]fluorene-5,6-dione (6), produced by condensation and rearrangement, was obtained as the major product, and its structure was subsequently unambigously determined by X-ray crystallographic study. Ortho-quinones were produced via nucleophilic substitution at position C7, which was unexpected, considering that para-quinones were produced via C6 substitution in the reaction between compound 1 and ethyl acetoacetate in our previous work. Such unexpected nucleophilic substitution at C7 provides an effective, yet simple route, t…

StereochemistryClinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsCrystallography X-RayBiochemistryMedicinal chemistryChemical synthesisInhibitory Concentration 50chemistry.chemical_compoundNucleophilic aromatic substitutionDrug DiscoveryTumor Cells CulturedNucleophilic substitutionHumansMolecular BiologySubstitution reactionFluorenesMolecular StructureOrganic ChemistryQuinonesRegioselectivityStereoisomerismQuinonechemistryDoxorubicinEthyl acetoacetateQuinolinesMolecular MedicineAcid hydrolysisDrug Screening Assays AntitumorBioorganic & Medicinal Chemistry
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