Search results for " Liquid"

showing 10 items of 3037 documents

Analysis of kynurenine transaminase activity in Drosophila by high performance liquid chromatography

1991

Abstract A sensitive assay for kynurenine transaminase activity (E.C. 2.6.1.7) based on rapid separation of the reaction product by high performance liquid chromatography (HPLC) has been developed. Drosophila sordidula extracts have been assayed by this new method and this is the first time that kynurenine transaminase activity has been demonstrated in Drosophila . The method of assay developed can be extended to any other organism. Kynurenine and 3-hydroxykynurenine were both used as substrates, and they were transaminated to kynurenic acid and xanthruenic acid, respectively. HPLC is used to separate and quantitate these reaction products from all other components in the reaction mixture. …

chemistry.chemical_classificationChromatographybiologyBiochemistryHigh-performance liquid chromatographyEnzyme assayTransaminaseAmino acidchemistry.chemical_compoundKynurenic acidBiochemistrychemistryInsect Sciencebiology.proteinSpecific activityPyruvic acidMolecular BiologyKynurenineInsect Biochemistry
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Enzyme class identification in cleaning products by hydrolysis followed by derivatization with o-phthaldialdehyde, HPLC and linear discriminant analy…

2008

The enzymes present in raw materials of the cleaning industry (enzyme industrial concentrates) and in household cleaners were isolated by precipitation with acetone and hydrolyzed with HCl. The resulting amino acids were derivatized with o-phthaldialdehyde, and the derivatives were separated by HPLC. The peaks of 14 amino acids were observed using a C18 column and a multi-segmented gradient of acetonitrile-water in the presence of a 5 mM citric/citrate buffer of pH 6.5. Using either normalized peak areas (divided by the sum of the peak areas of the chromatogram) or ratios of pairs of peak areas as predictor variables, linear discriminant analysis models, capable of predicting the enzyme cla…

chemistry.chemical_classificationChromatographybiologyChemistryHydrolysisDetergentsDiscriminant AnalysisHousehold ProductsCellulaseHigh-performance liquid chromatographyAnalytical ChemistryEnzymeschemistry.chemical_compoundHydrolysisEnzymeArtificial IntelligenceAcetoneBy-productbiology.proteinAmylaseAmino AcidsDerivatizationChromatography High Pressure Liquido-PhthalaldehydeTalanta
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CHROMATOGRAPHIC DETECTION OF SESQUITERPENE LACTONES IN PARTHENIUM PLANTS FROM NORTHWEST ARGENTINA

1999

Several chloroformic extracts containing some sesquiterpene lactones from autochtonous plants of Parthenium hysterophorus, collected in the province of Salta (Argentina), were separated and identified by high performance reversed-phase liquid chromatography with C18 column and propanol-water mobile phases, using gradient elution and concentrations of propanol larger than 10% (v/v). Lactones previously purified and characterized by H1 RMN, C13 RMN, IR, and mass spectrometry, were used as standards. The objective of the study was to check if the nature of the lactones was modified according to the altitude of the region where the plants were grown. Among the lactones, five were already descri…

chemistry.chemical_classificationChromatographybiologyClinical BiochemistryPharmaceutical ScienceParthenium hysterophorusPharmacognosySesquiterpenebiology.organism_classificationBiochemistryHigh-performance liquid chromatographyTerpenoidAnalytical ChemistryPropanolPartheniumchemistry.chemical_compoundchemistryLactoneJournal of Liquid Chromatography & Related Technologies
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Evaluation of advanced silica packings for the separation of biopolymers by high-performance liquid chromatography

1987

Abstract The reversed-phase chromatography of proteins by gradient elution with acidic, low-ionic-strength aqueous—organic eluents is often associated with losses of the biological activity of the protein. In this study, the enzymatic activities of catalase, horseradish peroxidase and pepsin were examined under static and dynamic column conditions on non-porous, monodisperse 1.5-μm reversed-phase silicas with various n -alkyl ligands. Catalase readily lost its enzymatic activity under the influence of the acidic aqueous—organic eluents in the absence of the reversed-phase packing, whereas peroxidase was partially deactivated as a result of combined mobile phase and stationary phase effects …

chemistry.chemical_classificationChromatographybiologyElutionLigandOrganic ChemistryDispersityGeneral MedicineBiochemistryHorseradish peroxidaseHigh-performance liquid chromatographyAnalytical ChemistrychemistryPhase (matter)biology.proteinAlkylPeroxidaseJournal of Chromatography A
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Determination of polycyclic aromatic hydrocarbons in atmospheric particulate matter of Valencia city

1991

Polycyclic aromatic hydrocarbons (PAHs) were determined in atmospheric particulate matter in 11 sites of the Valencia area and at several times during the year. Sample analysis was carried out by ultrasonic acetonitrile extraction followed by reverse phase HPLC separation and fluorescence detection. The maximum concentration of total PAH developed in winter and spring. Mean values per sampling site varied from 0.193 to 1.668 μg/m3 of filtered air. Environmental noise and temperature were determined at those same 11 sites and correlated with PAH levels.

chemistry.chemical_classificationChromatographybiologyExtraction (chemistry)Polycyclic aromatic hydrocarbonReversed-phase chromatographyParticulatesbiology.organism_classificationBiochemistryHigh-performance liquid chromatographyHydrocarbonchemistryEnvironmental chemistryValenciaFresenius' Journal of Analytical Chemistry
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Purification and characterization of leucine aminopeptidase from kidney bean cotyledons

1992

A leucine aminopeptidase (EC 3,4,11.1) was purified from cotyledons of resting kidney beans (Phaseolus vulgaris L. cv. Processor) by acidic extraction, ammonium sulfate fractionation and chromatography on DEAE-Sephacel, Sephacryl S-300, Mono Q HPLC and Superose HPLC columns. The yield of the 317-fold purified enzyme was 9%. On gel filtrations on Sephacryl S-300 and Superose HPLC the elution volumes of the enzyme corresponded to an M, of 360 000. The enzyme gave one band on native gel electrophoresis and an electrophoretic titration in an immobilized pH gradient gave a single curve with a pI of 4.8. Two bands were observed in an SDS-gel electrophoresis with Mr values of 58 000 and 60 000 bot…

chemistry.chemical_classificationChromatographybiologyPhysiologyCell BiologyPlant ScienceGeneral MedicineAminopeptidaseHigh-performance liquid chromatographyEnzyme assayDithiothreitolSuperosechemistry.chemical_compoundEnzymechemistryBiochemistryGeneticsbiology.proteinImmobilized pH gradientLeucinePhysiologia Plantarum
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Analysis of amino acids using serially coupled columns.

2017

Single conventional columns in reversed-phase LC are insufficient for analysing the isoindoles of primary amino acids, due to their limited functionality. An interesting possibility for increasing the separation power is the combination of several columns of different nature, where the length is modified by coupling small segments. This approach may require a considerable investment to have multiple lengths for each stationary phase. However, the combination of only two columns of fixed length can be enough to resolve satisfactorily relatively complex mixtures, provided that an optimised gradient program is applied. In this work, a mixture of 19 primary amino acid isoindoles found in protei…

chemistry.chemical_classificationCouplingWork (thermodynamics)Chromatography Reverse-PhaseIndolesIsoindoles010401 analytical chemistryAnalytical chemistryProteinsFiltration and SeparationReversed-phase chromatography010402 general chemistry01 natural sciences0104 chemical sciencesAnalytical ChemistryAmino acidPrimary amino acidsSolventColumn (typography)chemistryAmino AcidsChromatography High Pressure LiquidJournal of separation science
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Structure and Dynamics of Liquid Crystalline Polymers from Deuteron NMR

1983

The molecular structures of thermotropic liquid crystalline polymers, which have been synthesized systematically in recent years, are described according to the model of decoupling the molecular motions of the mesogenic groups and the polymer chain by inserting a flexible spacer. The molecular structure is related to the properties of these systems, e.g., phase transition temperatures, mesophases formed, etc. The structure and mobility of a specific side chain, liquid crystalline polyacrylate with phenyl benzoate as a mesogenic group is investigated by deuteron NMR and compared with the behaviour of low molecular weight analogues selectively deuterated at equivalent positions, i.e., at the …

chemistry.chemical_classificationCrystallographyChemistryLiquid crystalMesogenPolymer chemistrySide chainGeneral ChemistryPolymerGlass transitionThermotropic crystalAlkylPolymeric liquid crystalIsrael Journal of Chemistry
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Assays of Proteasome-Dependent Cleavage Products

2005

The degradation of misfolded, aged, or no longer needed cytosolic proteins depends largely on the ubiquitin-proteasome system. Proteasomes degrade their substrates into fragments of 3-20 amino acids. Human 20S proteasomes can be purified from human erythrocytes by batch adsorption to DEAE-cellulose, ammonium sulfate precipitation, anion-exchange fast protein liquid chromatography (FPLC), and glycerol density gradient ultracentrifugation. 20S proteasomes purified by this method are suitable for the in vitro digestion of synthetic peptides as well as full-length proteins. The degradation products produced by proteasomes are separated by reversed-phase HPLC using an acetonitrile gradient. The …

chemistry.chemical_classificationCytosolChromatographychemistryProteasomeEdman degradationFast protein liquid chromatographyDensity gradient ultracentrifugationHigh-performance liquid chromatographyAmmonium sulfate precipitationAmino acid
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Method for evaluating the bioconversion of radioactive polyunsaturated fatty acids by use of reversed-phase liquid chromatography

1988

Abstract Reversed-phase high-performance liquid chromatography on a thermostatted octadecylsilyl column was used to separate mixtures of labelled polyunsaturated fatty acids (as their methyl esters) formed by successive desaturations and elongations of labelled linoleic (18:2 n - 6) or linolenic (18:3 n -3) acid by rat liver microsomes. Acetonitrile-water mixtures were used for elution of the esters. Unsaturated and saturated esters were detected by their refractive indices. The order of elution of fatty acid methyl esters in complex mixtures varies as a function of the chain length and unsaturation, analysis temperature, water concentration and solvent flow-rate. The peak areas vary as a f…

chemistry.chemical_classificationDegree of unsaturationChromatography GasChromatographyElutionChemistryOrganic ChemistryTemperatureFatty acidEstersGeneral MedicineReversed-phase chromatographyMetabolismFatty Acids NonesterifiedBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySolventsUnsaturated fatty acidChromatography LiquidPolyunsaturated fatty acidJournal of Chromatography A
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