Search results for "HYDROLYSIS"

showing 10 items of 632 documents

Pleiotropic Role of Recombinant Silaffin-Like Cationic Polypeptide P5S3: Peptide-Induced Silicic Acid Stabilization, Silica Formation and Inhibition …

2016

Silica-mineralizing organisms such as diatoms manage several aspects of silica chemistry when polymerizing monomeric silicic acid into amorphous silica. Silicic acid is undersaturated in the diatoms’ habitats and mechanisms of enrichment and prevention of uncontrolled mineralization are not well understood. Diatom-biosilica is associated with organic compounds, including polycationic, post-translationally modified peptides termed silaffins, which induce the condensation of silicic acid under supersaturated conditions. Here, we report the pleiotropic action of the designed silaffin-like peptide P5S3, which (i) stabilizes 4–8x silicic acid (in supersaturated conditions of 8.3 mm), (ii) decele…

chemistry.chemical_classificationPrecipitation (chemistry)Inorganic chemistryCationic polymerizationPeptide02 engineering and technologyGeneral Chemistryrespiratory system010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical sciencesAmino acidchemistry.chemical_compoundHydrolysischemistryBiomimetic synthesisPolymer chemistrySilicic acid0210 nano-technologyDissolutionChemistrySelect
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Protonation and rearrangement of the tricyclo[4.2.2.22,5]dodeca-3,7,9,11-tetraene scaffold

2006

The biplanemers 2a,b contain enol ether substructures, which permit facile protonations of the π electron system. The subsequent ether cleavage is characterized by rearrangements of the polycyclic scaffold of the carbenium ions or the electroneutral primary products. Apart from the expected products 3a and 5a, a series of unexpected ketones and diketones (4a′, 9b, 10b, 11b, and 12b) were obtained.

chemistry.chemical_classificationPrimary (chemistry)ChemistryStereochemistryOrganic ChemistryProtonationElectron systemBiochemistryMedicinal chemistryIonHydrolysisDrug DiscoveryEnol etherEther cleavageTetrahedron Letters
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Comparison of Water Adsorption Properties of Cellulose and Cellulose Nanocrystals Studied by Near-Infrared Spectroscopy and Gravimetry

2017

The adsorption properties of water molecules on cellulose and cellulose nanocrystals (CNCs), isolated from defatted rice bran (DRB) by 55% sulfuric acid hydrolysis under sonication were investigated. The powdered samples of cellulose and CNCs were analysed by using near infrared spectroscopy (NIR) and gravimetry at 38% and 55% humidities. Small amounts of samples were dried under vacuum at 120°C and the NIR spectra of the dry samples and their spectra during the adsorption water molecules were measured by using an NIR spectrometer equipped with a transflectance accessory and a DTGS detector. The quantitative adsorption of water molecules by the samples was determined by gravimetry. Second a…

chemistry.chemical_classificationProperties of waterMaterials scienceHydrogen bondMechanical EngineeringSonicationAnalytical chemistrySulfuric acid02 engineering and technologyPolymer010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences0104 chemical scienceschemistry.chemical_compoundHydrolysisAdsorptionchemistryMechanics of MaterialsGeneral Materials ScienceCellulose0210 nano-technologyNuclear chemistryKey Engineering Materials
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Controlled cleavage of KLH1 and KLH2 by the V8 protease from Staphylococcus aureus reassociation, electrophoretic and transmission electron microscop…

1999

The reassociation behaviour of protease V8-cleaved peptides from KLH1 and KLH2, the two hemocyanin isoforms from the giant keyhole limpet Megathura crenulata, has been studied by transmission electron microscopy of negatively stained specimens and SDS/PAGE. Reassociation of the complete mixture of protease cleavage products and of combinations of peptide fragments purified by HPLC was performed in the presence of 100 mm CaCl2 and 100 mm MgCl2 at pH 7.4, over a period of 1 to 4 weeks. The V8 protease splits KLH1 into peptide fragments containing the functional units abc, def, defg, defgh, g and h. This mixture of peptide fragments reassociated to form helical tubular polymers, with a diamete…

chemistry.chemical_classificationProteasebiologyStereochemistrymedicine.medical_treatmentProtein subunitHydrolysisSerine EndopeptidasesHemocyaninPeptideMegathura crenulatabiology.organism_classificationCleavage (embryo)BiochemistryPeptide FragmentsMicroscopy ElectronBiochemistrychemistryPolymerizationHemocyaninsmedicineProtein IsoformsElectrophoresis Polyacrylamide GelPolyacrylamide gel electrophoresisEuropean journal of biochemistry
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Two proteases from nuclei of rat testis cells. I. Isolation

1987

Abstract Two proteases, assayed with fluorogenic peptides and tentatively designated Rc and Kc, have been isolated from nuclei of rat testis cells by differential extraction with acetic acid, removal of some proteins at pH 4.5, and polyacrylamide gel electrophoresis followed by electroblotting onto nitrocellulose paper. Protease R hydrolyzes t‐Butyl‐oxycarbonyl‐Val‐Pro‐Arg‐7‐amino‐4‐methyl‐coumarin and other peptides in which arginine is joined to 7‐amino‐4‐methyl‐coumarin by amide linkage. Protease Kc has a preference for peptides terminating in lysine‐7‐amino‐4‐methylcoumarin amide. Neither of these proteases is active against Glu‐Phe‐7‐amino‐4‐methyl‐coumarin amide or Carbobenzoxy‐Arg‐7‐…

chemistry.chemical_classificationProteasesProteaseArgininemedicine.medical_treatmentBiologyMolecular biologychemistry.chemical_compoundHydrolysisEnzymechemistryBiochemistrymedicineAnimal Science and ZoologyTrichloroacetic acidPolyacrylamide gel electrophoresisElectroblottingBollettino di zoologia
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Enzyme molecular mechanism as a starting point to design new inhibitors: a theoretical study of O-GlcNAcase.

2011

O-Glycoprotein 2-acetamino-2-deoxy-β-d-glucopyranosidase (O-GlcNAcase) hydrolyzes O-linked 2-acetamido-2-deoxy-β-d-glucopyranoside (O-GlcNAc) residues from post-translationally modified serine/threonine residues of nucleocytoplasmic protein. The chemical process involves substrate-assisted catalysis, where two aspartate residues have been identified as the two key catalytic residues of O-GlcNAcase. In this report, the first step of the catalytic mechanism used by O-GlcNAcase involving substrate-assisted catalysis has been studied using a hybrid quantum mechanical/molecular mechanical (QM/MM) Molecular Dynamics (MD) calculations. The free energy profile shows that the formation of the oxazol…

chemistry.chemical_classificationProtonStereochemistryClostridium perfringensOxazolineMolecular Dynamics Simulationbeta-N-AcetylhexosaminidasesSurfaces Coatings and FilmsCatalysisSubstrate SpecificitySerinechemistry.chemical_compoundHydrolysisMolecular dynamicsEnzymechemistryMaterials ChemistryQuantum TheoryThermodynamicsPhysical and Theoretical ChemistryThreonineEnzyme InhibitorsOxazolesThe journal of physical chemistry. B
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On the Nature of the Enzyme–Substrate Complex and the Reaction Mechanism in Human Arginase I. A Combined Molecular Dynamics and QM/MM Study

2020

We present here a detailed theoretical analysis of L-arginine hydrolysis catalyzed by Human Arginase I (HARGI). Our study combines classical molecular dynamic simulations of different model for the...

chemistry.chemical_classificationReaction mechanism010405 organic chemistryChemistrySubstrate (chemistry)General Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisArginaseQM/MMMolecular dynamicsHydrolysisEnzymeACS Catalysis
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On the Dichotomic Behavior of the Z-2,4-Dinitrophenylhydrazone of 5-Amino-3-benzoyl-1,2,4-oxadiazole with Acids in Toluene and in Dioxane/Water:  Rea…

2004

The mononuclear rearrangement (MRH) of the Z-2,4-dinitrophenylhydrazone (4a) and of the Z-phenylhydrazone (4b) of 5-amino-3-benzoyl-1,2,4-oxadiazole into the relevant triazoles 5a and 5b in toluene has been quantitatively investigated in the presence of trichloroacetic acid (TCA) and of piperidine at 313.1 K. While the behavior in the presence of piperidine recalls the one previously evidenced for some Z-hydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole, the study of the reactivity in the presence of TCA has most interestingly evidenced a general-acid-catalyzed rearrangement for “both” 4a and 4b. Thus, 4a offers the first example of a solvent-dependent dichotomic behavior in MRH processes o…

chemistry.chemical_classificationReaction mechanismOrganic Chemistryacid catalysiOxadiazoleHydrazoneMedicinal chemistryToluenechemistry.chemical_compoundHydrolysisAcid catalysischemistryOrganic chemistrymononuclear rearrangement of heterocycleReactivity (chemistry)Piperidinebase catalysisThe Journal of Organic Chemistry
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Classification of vegetable oils according to their botanical origin using amino acid profiles established by High Performance Liquid Chromatography …

2010

Abstract A preliminary study using amino acid profiles to classify oils according to their botanical origin has been performed. Amino acid profiles were obtained from hydrolysis of proteins present in vegetable oils, and established by High Performance Liquid Chromatography (HPLC) with UV–vis detection. Proteins present in hazelnut, corn, soybean, olive, avocado, peanut and grapeseed oils were precipitated with acetone, and the residue was hydrolysed in acid medium. The amino acids obtained were derivatized with o -phthaldialdehyde and separated by HPLC. Peaks corresponding to 18 amino acids were observed using a C18 column and a gradient of acetonitrile–water in the presence of a 5 mM citr…

chemistry.chemical_classificationResidue (complex analysis)ChromatographyGeneral MedicineHigh-performance liquid chromatographyCitrate bufferAnalytical ChemistryAmino acidchemistry.chemical_compoundHydrolysisVegetable oilUltraviolet visible spectroscopychemistryAcetoneFood ScienceFood Chemistry
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Pig liver esterase (PLE)-mediated resolution of N-substituted 4-benzoyloxy-3-carbomethoxypiperidines: A convenient preparation of 4-hydroxy- and 4-be…

2000

Abstract Pig liver esterase (PLE) afforded smooth chemical resolution of racemic N -substituted 4-(benzoyloxy)-3-carbomethoxypiperidines. The enzyme showed good chemo- and enantioselective properties, thus allowing discrimination between the carbomethoxy and benzoate ester groups, the latter being more easily hydrolyzed. The proposed methodology also represents a practical means for the procurement of N -substituted 4-hydroxy-3-carbomethoxypiperidines in enantiomerically pure form.

chemistry.chemical_classificationResolution (mass spectrometry)StereochemistryOrganic ChemistryEnantioselective synthesisEsteraseCatalysisInorganic ChemistryHydrolysisEnzymechemistryOrganic chemistryPhysical and Theoretical ChemistryPig liver
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