Search results for " activity"

showing 10 items of 4540 documents

High pressure processing of food-grade emulsion systems: Antimicrobial activity, and effect on the physicochemical properties

2019

Abstract The use of high pressure processing (HPP) for development of stable emulsion-based delivery systems has been recently increased. Under adequate conditions, application of high pressures modifies the functionality of protein and polysaccharide molecules and significantly promotes the emulsifying activities. Application of high pressures also modulates the emulsion microstructure without any destabilization and gelation of protein molecules. The lipid oxidation in HPP-treated emulsions can be accelerated, particularly with higher pressure levels, while the HPP utilization on emulsions in acidic conditions can highly inhibit the growth of spoilage and pathogenic microorganisms. In thi…

chemistry.chemical_classification010304 chemical physicsChemistryGeneral Chemical EngineeringFood spoilageFood grade04 agricultural and veterinary sciencesGeneral ChemistryAntimicrobialPolysaccharide040401 food science01 natural scienceshigh pressure processing ; emulsion delivery systems ; emulsifying activity ; stability ; rheology ; antibacterial activityPascalization0404 agricultural biotechnologyLipid oxidationRheologyChemical engineering0103 physical sciencesEmulsionFood ScienceFood Hydrocolloids
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Engineering faster transglycosidases and their acceptor specificity

2019

Transglycosidases are enzymes that have the potential to catalyze the synthesis of a wide range of high-value compounds starting from biomass-derived feedstocks. Improving their activity and broadening the substrate range are important goals to enable the widespread application of this family of biocatalysts. In this work, we engineered 20 mutants of the rice transglycosidase Os9BGlu31 and evaluated their catalysis in 462 reactions over 18 different substrates. This allowed us to identify mutants that expanded their substrate range and showed high activity, including W243L and W243N. We also developed double mutants that show very high activity on certain substrates and exceptional specific…

chemistry.chemical_classification010405 organic chemistryExternal validationSubstrate (chemistry)010402 general chemistry01 natural sciencesPollutionAcceptorCombinatorial chemistry0104 chemical sciencesCatalysisEnzymechemistryCheminformaticsEnvironmental ChemistryHigh activityGreen Chemistry
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Evidence for essential primary amino groups in a bacterial coupling factor F1ATPase.

1980

Abstract We have found that the binding of pyridoxal-5′-phosphate to 6 primary amino groups leads to the inactivation of the enzyme. A preferential reaction of pyridoxal-5′-phosphate with the α-subunits of this enzyme can be demonstrated. The reactivity of the amino groups is influenced by various effectors. In the presence of ATP the inhibition of the ATPase activity is noncompetitive.

chemistry.chemical_classificationAdenosine TriphosphatasesPrimary (chemistry)Binding SitesChemistryStereochemistryEffectorCell MembraneBiophysicsCell BiologyBiochemistryMicrococcusCoupling (electronics)Structure-Activity RelationshipEnzymeBiochemistrySolubilityPyridoxal PhosphateAtpase activityReactivity (chemistry)Amino AcidsMolecular BiologyBiochemical and biophysical research communications
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Transport, stability, and biological activity of resveratrol

2011

Numerous studies have reported interesting properties of trans-resveratrol, a phytoalexin, as a preventive agent of several important pathologies: vascular diseases, cancers, viral infections, and neurodegenerative processes. These beneficial effects of resveratrol have been supported by observations at the cellular and molecular levels in both cellular and in vivo models, but the cellular fate of resveratrol remains unclear. We suggest here that resveratrol uptake, metabolism, and stability of the parent molecule could influence the biological effects of resveratrol. It appears that resveratrol stability involves redox reactions and biotransformation that influence its antioxidant properti…

chemistry.chemical_classificationAntioxidantendocrine system diseasesMembrane transport proteinorganic chemicalsGeneral NeurosciencePhytoalexinmedicine.medical_treatmentfood and beveragesBiological activityMetabolismBiologyResveratrolGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundHistory and Philosophy of SciencechemistryBiotransformationBiochemistryIn vivobiology.proteinmedicineskin and connective tissue diseaseshormones hormone substitutes and hormone antagonistsAnnals of the New York Academy of Sciences
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Acetogenins from Annonaceae

1997

In 1982, Jolad et al. isolated uvaricin, a new antitumor agent, from the roots of Uvaria acuminata (Annonaceae), a bis-tetrahydrofuranoid fatty acid lactone (1) related to polyketides or acetogenins. However, it contained a number of original structural characteristics, particularly a linear acetogenin, a bis-tetrahydrofuran pattern flanked by hydroxyls and a terminal unsaturated lactone. Two years later, Dabrah and Sneden (2, 3 and Cortes et al. (4) described four new products presenting the same structural characteristics. Because these products formed a new class of natural compounds, and are only found in species belonging to the family of Annonaceae, they are commonly called acetogenin…

chemistry.chemical_classificationAntitumor activitybiologyStereochemistryAbsolute configurationFatty acidbiology.organism_classificationUvaria acuminataUvaricinchemistry.chemical_compoundchemistryAnnonaceaeAcetogeninLactone
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Water-soluble polysaccharides from Opuntia stricta Haw. fruit peels: Recovery, identification and evaluation of their antioxidant activities

2015

Abstract Opuntia stricta Haw. is considered as one of the most common cactus plant growing in Tunisia. Extracting valuable compounds from its fruit peel, considered as by-product, is drawing more and more attention, making it on the verge of commercialization. Water-soluble polysaccharides were extracted from Opuntia stricta Haw. peels, and their chemical composition assessed using thin layer chromatography. The antioxidant activities of the extracted polysaccharides were assessed using 2,2-diphenyl-1-picrylhydrazyl free radical scavenging activity, total antioxidant activity and reducing power capacity. The extraction yield of water-soluble polysaccharides was 7.53±0.86%. The chemical comp…

chemistry.chemical_classificationArabinoseAntioxidant[SDV.BIO]Life Sciences [q-bio]/BiotechnologyRhamnoseOpuntia stricta Haw. peelsmedicine.medical_treatment[SDV]Life Sciences [q-bio]Extraction (chemistry)antioxidant activityPolysaccharideAscorbic acidThin-layer chromatographychemistry.chemical_compoundchemistrywater-soluble polysaccharidesGalactoseBotanymedicinepolysaccharide extraction[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringFood science[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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Peroxisomes and Hepatotoxicity

1995

Peroxisomes are ubiquitous organelles of eukaryotic cells and are present in significant amounts in hepatic liver cells. Peroxisomal enzymes contribute to several metabolic pathways including fatty acid, purine and amino acid catabolism or bile acid synthesis. The peroxisomal oxidative reactions produce hydrogen peroxide, mostly degraded by catalase which prevents oxidative stress. Moreover, peroxisomes are involved in arylderivative drug detoxification through its epoxide hydrolase activity.

chemistry.chemical_classificationCatabolismHematologyOxidative phosphorylationBiologyPeroxisomePathology and Forensic MedicineAmino acidEpoxide hydrolase activityMetabolic pathwayBiochemistrychemistryCatalaseGlyoxysomebiology.proteinAnatomyComparative Haematology International
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Epoxide Hydrolases: Structure, Function, Mechanism, and Assay

2005

Epoxide hydrolases are a class of enzymes important in the detoxification of genotoxic compounds, as well as in the control of physiological signaling molecules. This chapter gives an overview on the function, structure, and enzymatic mechanism of structurally characterized epoxide hydrolases and describes selected assays for the quantification of epoxide hydrolase activity.

chemistry.chemical_classificationCell signaling1303 BiochemistryStereochemistry10050 Institute of Pharmacology and Toxicology610 Medicine & healthEpoxide hydrolase activityEnzymeBiochemistrychemistryDetoxificationEpoxide Hydrolases1312 Molecular Biology570 Life sciences; biologyProtein foldingEpoxide hydrolaseFunction (biology)
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Brain Nucleotides and Excitatory Processes

1971

The trivial analogy in the structure of barbiturates and pyrimidines has suggested a series of studies, which were undertaken in our Laboratory since 1961 (Bonavita et al., 1960 to investigate on the role of some free nucleotides in cerebral activity.

chemistry.chemical_classificationCerebral activityChemistryExcitatory postsynaptic potentialNucleotideNeuroscience
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Crystal structure of the chalcone (E)-3-(furan-2-yl)-1-phenylprop-2-en-1-one

2015

The crystal packing of the compound is described by an inter­molecular arrangement with the mol­ecules as inter­laced layers in a zigzag fashion, denoting inter­acting self-complementary dimers mainly by the localization of weak hydrogen bonds in a head-to-tail arrangement.

chemistry.chemical_classificationChalconecrystal structureCrystallographyDouble bondHydrogen bondChemistryStereochemistryClaisen–Schmidt reactionbiological activityGeneral ChemistryCrystal structureCondensed Matter PhysicsRing (chemistry)hydrogen bondingAcceptorResearch CommunicationsCrystalchemistry.chemical_compoundCrystallographychalcone derivativezigzag fashion.QD901-999FuranGeneral Materials ScienceActa Crystallographica Section E: Crystallographic Communications
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