Search results for "Concentration."

showing 10 items of 1849 documents

Simulated solar UV-irradiation of endocrine disrupting chemical octylphenol.

2009

The photolysis of octylphenol (OP) was investigated using a solar simulator in the absence/presence of dissolved natural organic matter (DNOM), HCO(3)(-), NO(3)(-) and Fe(III) ions. The effects of different parameters such as initial pH, initial concentration of substrate, temperature, and the effect of hydrogen peroxide concentration on photodegradation of octylphenol in aqueous solution have been assessed. The results indicate that the oxidation rate increases in the presence of H(2)O(2), nitrate and DNOM. Phenol, 1,4-dihydroxylbenzene and 1,4-benzoquinone were identified as intermediate products of photodegradation of octylphenol, through an HPLC method. In addition, the disappearance of…

Environmental EngineeringUltraviolet RaysHealth Toxicology and MutagenesisInorganic chemistryEndocrine DisruptorsWater Purificationchemistry.chemical_compoundPhenolsEnvironmental ChemistryPhenolOrganic matterIrradiationPhenolsPhotodegradationHydrogen peroxideWaste Management and DisposalHumic Substanceschemistry.chemical_classificationIonsAqueous solutionPhotolysisChemistryTemperatureSubstrate (chemistry)Hydrogen PeroxideHydrogen-Ion ConcentrationPollutionSunlightWater Pollutants ChemicalJournal of hazardous materials
researchProduct

Producing high-strength liquor from mesophilic batch acidification of chicken manure.

2015

This report describes the results from anaerobic batch acidification of chicken manure as a mono-substrate studied under mesophilic conditions. The manure was diluted with tap water to prevent methane formation during acidification and to improve mixing conditions by reducing fluid viscosity; no anaerobic digester sludge has been added as an inoculum. Highest acidification rates were measured at concentrations of 10 gVS L−1 and 20 gVS L−1; the pH value remained high (pH 6.9–7.9) throughout the test duration and unexpected fast methane formation was observed in every single batch. At substrate concentrations of 10 gVS L−1 there was a remarkable methane formation representing a value of 82% …

Environmental EngineeringWaste managementChemistryHydrogen-Ion ConcentrationPulp and paper industryFatty Acids VolatilePollutionManureManureAnaerobic digestionBioreactorsTap waterBiogasWaste ManagementBiofuelBiofuelsAnimalsChicken manureAnaerobic exerciseChickensMethaneMesophileWaste managementresearch : the journal of the International Solid Wastes and Public Cleansing Association, ISWA
researchProduct

Characterization of an isoproturon mineralizing bacterial culture enriched from a French agricultural soil.

2009

The phenylurea herbicide isoproturon, 3-(4-isopropylphenyl)-1,1-dimethylurea (IPU), was found to be rapidly mineralized by a bacterial culture isolated from an agricultural soil regularly exposed to IPU. Molecular analysis of the bacterial culture by DNA fingerprinting, cloning and sequencing of the 16S rRNA genes revealed that it consisted of six different members among whom the dominant was related to Sphingomonas sp. Six bacterial strains belonging to genera Ancylobacter, Pseudomonas, Stenotrophomonas, Methylobacterium, Variovorax and Agrobacterium were isolated from the IPU-degrading culture. None of these were able to degrade IPU in pure culture and only the intact culture sustained th…

Environmental Engineeringfood.ingredientAgrobacteriumHealth Toxicology and Mutagenesis[SDE.MCG]Environmental Sciences/Global ChangesISOPROPURONMETABOLITESAncylobacterMicrobiologyfoodRNA Ribosomal 16SEnvironmental ChemistryBACTERIAL CULTUREMINERALIZATIONPhylogenySoil MicrobiologyMineralsbiologyBacteriaHerbicidesPhenylurea CompoundsPseudomonasPublic Health Environmental and Occupational HealthAgricultureGeneral MedicineGeneral ChemistryVariovoraxHydrogen-Ion Concentrationbiology.organism_classificationPollutionPH REGULATIONKineticsRNA BacterialBiodegradation EnvironmentalMethylobacteriumStenotrophomonasFranceSoil microbiologyBacteriaChemosphere
researchProduct

The role of intact oleosin for stabilization and function of oleosomes.

2013

Lipid storage in plants is achieved among all plant species by formation of oleosomes, enclosing oil (triacylglycerides) in small subcellular droplets. Seeds are rich in this pre-emulsified oil to provide a sufficient energy reservoir for growing. The triacylglyceride core of the oleosomes is surrounded by a phospholipid monolayer containing densely packed proteins called oleosins. They are anchored in the triacylglycerides core with a hydrophobic domain, while the hydrophilic termini remain on the surface. These specialized proteins are expressed during seed development and maturation. Particularly, they play a major role in the stabilization and function of oleosomes. To better understand…

Enzymatic digestionChemistryAirCircular DichroismPhospholipidWaterHydrogen-Ion ConcentrationLipid storageSurfaces Coatings and Filmschemistry.chemical_compoundBiochemistrySpectroscopy Fourier Transform InfraredMaterials ChemistryPlant speciesWater chemistryHelianthusPlant OilsEmulsionsSoybeansPhysical and Theoretical ChemistryOleosinFunction (biology)Plant ProteinsThe journal of physical chemistry. B
researchProduct

Synthesis and Structure-Activity Relationships of Amino Acid Conjugates of Cholanic Acid as Antagonists of the EphA2 Receptor

2013

The Eph–ephrin system plays a critical role in tumor growth and vascular functions during carcinogenesis. We had previously identified cholanic acid as a competitive and reversible EphA2 antagonist able to disrupt EphA2-ephrinA1 interaction and to inhibit EphA2 activation in prostate cancer cells. Herein, we report the synthesis and biological evaluation of a set of cholanic acid derivatives obtained by conjugation of its carboxyl group with a panel of naturally occurring amino acids with the aim to improve EphA2 receptor inhibition. Structure-activity relationships indicate that conjugation of cholanic acid with linear amino acids of small size leads to effective EphA2 antagonists whereas …

EphA2 antagonistsStereochemistryStructure-activity relationship studiesPharmaceutical Sciencemedicine.disease_causeArticleProtein Structure SecondaryAnalytical Chemistrylcsh:QD241-441Inhibitory Concentration 50Structure-Activity Relationshipchemistry.chemical_compoundamino acid conjugateslcsh:Organic chemistryEphA2 anatgonistscholanic acid; amino acid conjugates; EphA2 antagonists; structure-activity relationshipsCell Line TumorDrug DiscoveryAromatic amino acidsmedicineHumansPhosphorylationPhysical and Theoretical ChemistryReceptorbile acids; EphA2 anatgonists; Structure-activity relationship studies; amino acid conjugatesbile acidschemistry.chemical_classificationBinding SitesReceptor EphA1Receptor EphA2structure-activity relationshipsOrganic ChemistryAntagonistCholic AcidsHydrogen BondingEPH receptor A2Amino acidMolecular Docking SimulationCholanic acidcholanic acidchemistryBiochemistryChemistry (miscellaneous)Molecular MedicineCarcinogenesisProtein Processing Post-TranslationalProtein BindingConjugateMolecules
researchProduct

Further development of the β-lactamase MutaGen assay and evaluation by comparison with Ames fluctuation tests and theumu test

2005

A rapid, high-throughput bacterial mutagenicity test system has been developed (MutaGen test) that detects reversions of inactivating base-pair substitutions and frameshifts in a TEM-1 class A β-lactamase (ampicillinase) gene. To quickly and sensitively detect mutagens, the system utilises a series of plasmids that contain the mutated ampicillinase gene and the mucAB operon. Inactivating mutations in the ampicillinase gene include frameshifts integrated into repetitive GC-sequences and G-runs known to be mutagenic hot-spots, and base-pair substitutions inserted in or around the β-lactamase active site. Frameshift mutations completely inactivated the enzyme only when located downstream of th…

EpidemiologyOperonHealth Toxicology and Mutagenesislac operonMutagenBiologymedicine.disease_causebeta-LactamasesAmes testPlasmidAmp resistanceBromcresol PurplemedicineNitrocefinGenetics (clinical)GeneticsReporter geneBacteriaMutagenicity TestsfungiHydrogen-Ion ConcentrationMolecular biologyCephalosporinsMutationBiological AssayEnvironmental MonitoringPlasmidsEnvironmental and Molecular Mutagenesis
researchProduct

Isolation of a Putative Hydroxyacyl Enzyme Intermediate of an Epoxide Hydrolase

1994

A putative covalent, alpha-hydroxyacyl intermediate was isolated by the brief exposure of murine soluble epoxide hydrolase to its substrate. The reaction was reversed by time and blocked by competitive inhibitors. The formation of the intermediate was dependent upon the concentration of the enzyme and was increased by incubation under acidic conditions. The structure of the intermediate was supported by microchemical methods.

Epoxide HydrolasesEpoxide hydrolase 2chemistry.chemical_classificationReaction mechanismStereochemistryAcylationBiophysicsSubstrate (chemistry)Cell BiologyReaction intermediateHydrogen-Ion ConcentrationTritiumBiochemistryRecombinant ProteinsKineticsMiceEnzymechemistryBiochemistryCovalent bondAnimalsHumansEpoxide hydrolaseMolecular BiologyIncubationBiochemical and Biophysical Research Communications
researchProduct

Properties and amino acid composition of pure epoxide hydratase

1975

1. Introduction Rat liver epoxide hydratase [EC 4.2.1.631 which catalyses the conversion of epoxides to trurans-dihydro- diols has been purified to apparent homogeneity as determined by three independent criteria [l] . The preparation obtained was capable of catalysing the hydration of both styrene oxide and the 4,5- (K- region)epoxide of benzo(a)pyrene [ 11. Epoxides of polycyclic hydrocarbons have been implicated as the agents responsible for the cytotoxic and carcinogenic properties of such compounds (for reviews see [2-41). A detailed knowledge of the properties of epoxide hydratase may, therefore, contribute towards an understanding of the mechanisms of cytotoxicity and carcinogenesis.…

Epoxide Hydrolaseschemistry.chemical_classificationPerformic acidSpectrum AnalysisCarboxypeptidase PBiophysicsTryptophanEpoxideCell BiologyHydrogen-Ion ConcentrationBiochemistryAmino acidKineticschemistry.chemical_compoundHydrolysischemistryStructural BiologyStyrene oxideGeneticsOrganic chemistryThioglycolic acidAmino AcidsMolecular BiologyHydro-LyasesNuclear chemistryFEBS Letters
researchProduct

Markers of Anemia in Children with Type 1 Diabetes

2018

Aim. The aim of the study was to assess markers of anemia in type 1 diabetes (T1D) children, compare them to results obtained in the control group, and estimate their relation to BMI SDS. Methods. 94 (59% ♀) T1D children without other autoimmune disorders, aged 12.5 ± 4.1 years, T1D duration: 4.2 ± 3.6 years, HbA1c 7.3 ± 1.5% (57 ± 12.6 mmol/mol). Sex- and age-matched controls (43 children). In all children, anthropometric measurements, the blood count, iron turnover parameters, and vitamin B12 concentration were taken. Results. T1DM children had significantly higher red cell distribution width (RDW) (13.6 versus 12.6%; p<0.001), hepcidin (0.25 versus 0.12 ng/ml; p<0.001), and vitamin…

Erythrocyte IndicesMalemedicine.medical_specialtyArticle SubjectAdolescentAnemiaEndocrinology Diabetes and Metabolism030209 endocrinology & metabolismLogistic regressionlcsh:Diseases of the endocrine glands. Clinical endocrinologyGastroenterologyBody Mass IndexYoung Adult03 medical and health sciences0302 clinical medicineEndocrinologyHepcidinsHepcidin030225 pediatricsInternal medicinemedicineHumansVitamin B12ChildGlycated HemoglobinType 1 diabeteslcsh:RC648-665biologyMean corpuscular hemoglobin concentrationmedicine.diagnostic_testbusiness.industrynutritional and metabolic diseasesAnemiaRed blood cell distribution widthAnthropometrymedicine.diseaseBlood Cell CountVitamin B 12Diabetes Mellitus Type 1Child Preschoolbiology.proteinFemalebusinessBiomarkersResearch ArticleJournal of Diabetes Research
researchProduct

Naturally occurring hemolysins in the coelomic fluid of Holothuria polii delle chiaie (Echinodermata).

1979

Abstract The coelomic fluid of Holothuria polii D.Ch contains hemolytic activity against erythrocytes of several vertebrate species. The hemolytic potency depends upon calcium ion concentration and varies according to erythrocyte source and cell number in the reaction mixture. Absorption experiments with formalinized rabbit erythrocytes suggest that hemolytic activity is not specific. Its heat lability, water insolubility at low pH values, and sensitivity to proteolytic enzymes suggest that hemolytic activity resides in protein molecules. The activity, maximal in alkaline media, appears to depend up time and temperature.

ErythrocytesCations DivalentSea CucumbersImmunologyDose-Response Relationship Immunologicchemistry.chemical_elementCalciumHemolysisHemolysin ProteinsPotencyAnimalsbiologyLabilityProteolytic enzymesTemperatureHemolysinExudates and TransudatesHydrogen-Ion Concentrationbiology.organism_classificationKineticschemistryBiochemistryCoelomAbsorption (chemistry)HolothuriaDevelopmental BiologyEchinodermataDevelopmental and comparative immunology
researchProduct