Search results for "Amidase"

showing 10 items of 81 documents

Effects of photodynamic processes and ultraviolet light on duck and hen egg-white lysozymes.

1973

— The photochemical yields for inactivation and amino acid destruction in hen and duck egg-white lysozyme are presented. Duck lysozyme II is devoid of histidine but it has two more tyrosine residues than does hen lysozyme. The data indicate that sensitized oxidation of the single histidine residue of hen lysozyme is of no significance for the inactivation of this lysozyme. The ultraviolet destruction of tryptophan and cystine residues appears to be equally related with the loss in enzymatic activity of hen lysozyme. In the case of duck lysozyme, however, the ultraviolet inactivation appears to be predominantly governed by the destruction of cystine residues.

LightPhotochemistryUltraviolet RaysCystineBiochemistrychemistry.chemical_compoundEgg WhiteSpecies SpecificityUltraviolet lightAnimalsPhysical and Theoretical ChemistryTyrosineAmino AcidsHistidinechemistry.chemical_classificationTryptophanGeneral MedicineAmino acidRadiation EffectsEnzymeDuckschemistryBiochemistryFemaleMuramidaseLysozymeChickensPhotochemistry and photobiology
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Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans.

2011

One major expectation from the transcriptome in humans is to characterize the biological basis of associations identified by genome-wide association studies. So far, few cis expression quantitative trait loci (eQTLs) have been reliably related to disease susceptibility. Trans-regulating mechanisms may play a more prominent role in disease susceptibility. We analyzed 12,808 genes detected in at least 5% of circulating monocyte samples from a population-based sample of 1,490 European unrelated subjects. We applied a method of extraction of expression patterns—independent component analysis—to identify sets of co-regulated genes. These patterns were then related to 675,350 SNPs to identify maj…

MaleCancer ResearchGene ExpressionGenome-wide association studyGenetic NetworksCoronary Artery Disease[SDV.GEN] Life Sciences [q-bio]/GeneticsCardiovascularMESH: MonocytesMonocytesMESH: HypertensionTranscriptomes0302 clinical medicineMESH: ProteinsMESH: Genetic VariationGenetics (clinical)GeneticsMESH: Aged0303 health scienceseducation.field_of_studyMESH: Middle AgedMESH: Polymorphism Single NucleotideIntracellular Signaling Peptides and ProteinsMESH: Genetic Predisposition to DiseaseGenomicsMESH: Transcription FactorsMiddle AgedMESH: Ribosomal ProteinsMESH: Gene Expression Regulation3. Good healthHypertensionMedicineFemaleMESH: Diabetes Mellitus Type 1Research ArticleAdultRibosomal Proteinslcsh:QH426-470PopulationQuantitative Trait LociLocus (genetics)Single-nucleotide polymorphismBiologyQuantitative trait locusPolymorphism Single Nucleotide03 medical and health sciencesMESH: Gene Expression ProfilingGenome Analysis ToolsGeneticsGenome-Wide Association StudiesHumansGenetic Predisposition to DiseaseGene NetworkseducationMolecular BiologyBiologyEcology Evolution Behavior and SystematicsMESH: Genome Human030304 developmental biologyGenetic associationAdaptor Proteins Signal TransducingAged[SDV.GEN]Life Sciences [q-bio]/GeneticsMESH: HumansGenome HumanGene Expression ProfilingGenetic VariationProteinsHuman GeneticsMESH: AdultAtherosclerosisMESH: MaleMESH: Quantitative Trait LociGene expression profilingCeliac Diseaselcsh:GeneticsDiabetes Mellitus Type 1Gene Expression RegulationExpression quantitative trait lociGenetics of DiseaseMESH: Genome-Wide Association StudyMESH: MuramidaseMuramidaseGenome Expression AnalysisMESH: Female030217 neurology & neurosurgeryMESH: Celiac DiseaseGenome-Wide Association StudyTranscription Factors
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A novel compound heterozygous mutation in GALC associated with adult-onset Krabbe disease: case report and literature review

2021

Krabbe disease (KD) is a rare autosomal recessive lipid storage leukodystrophy. It is caused by deficient enzyme activity resulting from mutations of the β-galactocerebrosidase (GALC) gene. KD is distinguished into subtypes based on the age of onset; these are early infantile, late infantile, juvenile, and adult-onset. We report a case of a 47-year-old Caucasian man with a 2-year history of muscle atrophy and weakness in both hands associated with pyramidal signs and mild spasticity in the lower limbs. An extensive work-up led this motor neuron disease-like disorder to be diagnosed as adult-onset KD. The patient was found to be compound heterozygous for two GALC mutations (p.G286D and p.Y49…

MaleCellular and Molecular NeuroscienceHeterozygoteMutationGeneticsHumansSettore MED/26 - NeurologiaMiddle AgedGenetics (clinical)Compound heterozygous mutation GALC Adult-onset Krabbe disease Peripheral neuropathyGalactosylceramidaseLeukodystrophy Globoid Cell
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Gaucher's disease: therapy by intravenous infusions of modified glucocerebrosidase

1993

MaleGaucher Diseasebusiness.industryGeneral MedicineIntravenous InfusionsPharmacologymedicine.diseaseMolecular medicineHuman geneticsGlucosylceramidaseGaucher's diseaseDrug DiscoverymedicineGlucosylceramidaseHumansMolecular MedicineChildInfusions IntravenousbusinessGlucocerebrosidaseGenetics (clinical)The Clinical Investigator
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The role of juvenile hormone in immune function and pheromone production trade-offs: a test of the immunocompetence handicap principle

2003

The immunocompetence handicap hypothesis postulates that secondary sexual traits are honest signals of mate quality because the hormones (e.g. testosterone) needed to develop secondary sexual traits have immunosuppressive effects. The best support for predictions arising from the immunocompetence handicap hypothesis so far comes from studies of insects, although they lack male-specific hormones such as testosterone. In our previous studies, we found that female mealworm beetles prefer pheromones of immunocompetent males. Here, we tested how juvenile hormone (JH) affects male investment in secondary sexual characteristics and immune functions in the mealworm beetle, Tenebrio molitor. We inje…

MaleMealwormmedicine.medical_specialtySecondary sex characteristicZoologyPheromonesGeneral Biochemistry Genetics and Molecular BiologyInternal medicinemedicineAnimalsTenebrioGeneral Environmental ScienceSex CharacteristicsGeneral Immunology and MicrobiologybiologyMonophenol MonooxygenaseHandicap principleGeneral Medicinebiology.organism_classificationJuvenile HormonesEndocrinologySexual selectionSex pheromoneJuvenile hormonePheromoneFemaleMuramidaseImmunocompetenceGeneral Agricultural and Biological SciencesImmunocompetenceResearch ArticleProceedings of the Royal Society of London. Series B: Biological Sciences
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Discovery and SAR Evolution of Pyrazole Azabicyclo[3.2.1]octane Sulfonamides as a Novel Class of Non-Covalent N-Acylethanolamine-Hydrolyzing Acid Ami…

2021

Inhibition of intracellular N-acylethanolamine-hydrolyzing acid amidase (NAAA) activity is a promising approach to manage the inflammatory response under disabling conditions. In fact, NAAA inhibition preserves endogenous palmitoylethanolamide (PEA) from degradation, thus increasing and prolonging its anti-inflammatory and analgesic efficacy at the inflamed site. In the present work, we report the identification of a potent, systemically available, novel class of NAAA inhibitors, featuring a pyrazole azabicyclo[3.2.1]octane structural core. After an initial screening campaign, a careful structure–activity relationship study led to the discovery of endo-ethoxymethyl-pyrazinyloxy-8-azabicyclo…

MaleStereochemistryAnti-Inflammatory AgentsPeptides and proteinsPyrazoleArticleAmidohydrolasesAmidaseRats Sprague-DawleyStructure-Activity Relationshipchemistry.chemical_compoundIn vivoN-AcylethanolamineDrug DiscoverymedicineAnimalsHumansSulfonesEnzyme InhibitorsIC50InhibitionInflammationchemistry.chemical_classificationPalmitoylethanolamideMolecular StructureInhibitorsSulfonamideMice Inbred C57BLMolecular Docking SimulationMechanism of actionchemistryMicrosomes LiverInhibitorsInhibitionSulfonesPeptides and proteinsInflammationPyrazolesMolecular Medicinemedicine.symptomProtein BindingTropanesJournal of Medicinal Chemistry
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Crystalloid Lysozyme Inclusions in Paneth Cells of Vitamin A-Deficient Rats

1992

The effect of vitamin A-deficiency on jejunal Paneth cells in rats was investigated. Crystalloid particles were observed in secretion granules of Paneth cells from 6 out of 8 rats with vitamin A-deficiency. The particles were similar to those found in Paneth cells under other experimental conditions. Using an immuno-electron-microscopic technique we demonstrated a clear lysozyme immunoreactivity of these particles. In 2 vitamin A-deficient rats tubular structures have been detected in addition to the crystalloid particles. Crystalloid particles or tubular structures were not detectable in a control group of 8 vitamin A-supplemented rats. The morphological alterations of Paneth cells may be …

MaleVitaminmedicine.medical_specialtyBiologydigestive systemEpitheliumGeneral Biochemistry Genetics and Molecular Biologylaw.inventionRats Sprague-Dawleychemistry.chemical_compoundHistory and Philosophy of SciencelawInternal medicinemedicineAnimalsSecretionMicroscopy ImmunoelectronVitamin A DeficiencyGeneral Neurosciencemedicine.diseaseRatsVitamin A deficiencyMicroscopy ElectronZincJejunumEndocrinologyBiochemistrychemistryVacuolesMuramidaseLocal immunityElectron microscopeLysozymeElectron Probe MicroanalysisAnnals of the New York Academy of Sciences
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A muramidase from Acremonium alcalophilum hydrolyse peptidoglycan found in the gastrointestinal tract of broiler chickens

2021

Abstract This study evaluates peptidoglycan hydrolysis by a microbial muramidase from the fungus Acremonium alcalophilum in vitro and in the gastrointestinal tract of broiler chickens. Peptidoglycan used for in vitro studies was derived from 5 gram-positive chicken gut isolate type strains. In vitro peptidoglycan hydrolysis was studied by three approaches: (a) helium ion microscopy to identify visual phenotypes of hydrolysis, (b) reducing end assay to quantify solubilization of peptidoglycan fragments, and (c) mass spectroscopy to estimate relative abundances of soluble substrates and reaction products. Visual effects of peptidoglycan hydrolysis could be observed by helium ion microscopy an…

MalehydrolyysientsyymitsuolistomikrobistoBioengineeringPeptidoglycanMuramic acidApplied Microbiology and BiotechnologyCaecumchemistry.chemical_compoundHydrolysisAnimalsMuramidaseantimikrobiset yhdisteetGastrointestinal tractbiologyHydrolysisBroilerbiology.organism_classificationIn vitroAcremoniumGastrointestinal TracthomesienetchemistryBiochemistryMuramidasePeptidoglycanChickensbroileritBiotechnologyJournal of Industrial Microbiology and Biotechnology
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In vitrouptake of lysozyme-loaded liposomes coated with chitosan biopolymer as model immunoadjuvants

2009

Chitosan binds to negatively charged soy lecithin liposomes by an electrostatic interaction driven by its cationic amino group. This interaction allows developing stable coated vesicles suitable as a targeted carrier and controlled release system for drugs and vaccines. In this work, we studied the effect of chitosan-coated liposomes on the uptake and antigen presentation of hen egg-white lysozyme (HEL) in Peyer's patches peritoneal macrophages isolated from mice. Chitosan-coated liposomes were characterized according to size, zeta potential, and antigen-loading and release properties. Results showed an increase in the positive net charge and size of the liposomes as the concentration of ch…

Materials sciencePolymersCoated vesiclePharmaceutical Scienceengineering.materialChitosanchemistry.chemical_compoundMicePeyer's PatchesBiopolymersDrug Delivery SystemsAdjuvants ImmunologicCationsZeta potentialFluorescence microscopeAnimalsLiposomeChitosanChromatographyMicroscopy Confocaltechnology industry and agricultureControlled releasechemistryMicroscopy FluorescenceLiposomesengineeringInterleukin-2FemaleMuramidaseBiopolymerLysozymeJournal of Liposome Research
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Multifunctional clickable and protein-repellent magnetic silica nanoparticles

2016

Silica nanoparticles are versatile materials whose physicochemical surface properties can be precisely adjusted. Because it is possible to combine several functionalities in a single carrier, silica-based materials are excellent candidates for biomedical applications. However, the functionality of the nanoparticles can get lost upon exposure to biological media due to uncontrolled biomolecule adsorption. Therefore, it is important to develop strategies that reduce non-specific protein-particle interactions without losing the introduced surface functionality. Herein, organosilane chemistry is employed to produce magnetic silica nanoparticles bearing differing amounts of amino and alkene func…

Materials scienceSurface PropertiesSilicon dioxideNanoparticleNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesMagneticschemistry.chemical_compoundAdsorptionDynamic light scatteringAnimalsGeneral Materials Sciencechemistry.chemical_classificationBiomoleculeSerum Albumin BovineSilicon Dioxide021001 nanoscience & nanotechnologyDynamic Light ScatteringFerrosoferric Oxide0104 chemical sciencesElectrophoresischemistryCovalent bondThermogravimetryNanoparticlesPolystyrenesCattleElectrophoresis Polyacrylamide GelMuramidaseAdsorption0210 nano-technologyProtein adsorptionNanoscale
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