Search results for "thione"

showing 10 items of 865 documents

Characterization of the DNA-binding activity of the E1 and E2 proteins and the E1/E2 complex of human papillomavirus type 33.

1997

The E1 and E2 proteins of papillomaviruses are essential for the initiation of viral DNA replication. We have purified the E2 protein of human papillomavirus type 33 (HPV-33) by immunoaffinity chromatography. The purified E2 protein bound with high affinity to all four consensus binding sites of HPV-33 (Kd approximately equal to 2 x 10(-10)M). A putative E2 binding site differing at one position in the second stem of the palindrome was not bound by E2. The E1 protein of HPV-33 purified by affinity chromatography using glutathione S-transferase as tag displayed specific DNA-binding activity in footprint analyses protecting HPV-33 nucleotides 7896 to 7909/1 to 18 from DNasel digestion. Hypers…

chemistry.chemical_classificationBinding SitesPalindromeOncogene Proteins ViralGlutathioneBiologyVirologyMolecular biologyDNA-Binding ProteinsDNA binding sitechemistry.chemical_compoundViral Envelope ProteinschemistryAffinity chromatographyVirologySense (molecular biology)HumansNucleotideBinding siteDigestionPapillomaviridaeProtein BindingJournal of General Virology
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Semiquantitative bioluminescent assay of glutathione

1998

A novel technique has been developed for semiquantitative detection of glutathione (GSH) in small volumes of liquid samples. GSH is detected via enzymatic linkage to the NADP/NADPH + H+ redox system through glutathione reductase. Accumulated NADPH is measured via the bioluminescent FMN oxidoreductase bacterial luciferase reaction. A linear correlation is obtained between bioluminescence intensity of the luciferase reaction and the GSH content of the liquid sample. Possible applications of this procedure are discussed. © 1998 John Wiley & Sons, Ltd.

chemistry.chemical_classificationBioluminescent assayChemistryGlutathione reductaseBiophysicsGlutathioneRedoxchemistry.chemical_compoundEnzymeBiochemistryChemistry (miscellaneous)FMN reductaseBioluminescenceLuciferaseJournal of Bioluminescence and Chemiluminescence
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Conjugation reactions of polyaromatic quinones to mono- and bisglutathionyl adducts: Direct analysis by fast atom bombardment mass spectrometry

1988

The conjugation products of several reactive quinones with glutathione have been identified by fast atom bombardment mass spectrometry. Appropriate conditions have been developed which enabled the direct, dynamic mass spectral analysis of spontaneous, as well as glutathione transferase catalysed conjugation reactions. Applications to a series of quinones provided the direct detection and differentiation of the formation of mono- and bisglutathionyl adducts between regioisomeric quinone substrates in that only 1,4-quinones yielded bisglutathionyl adducts, which were not observed for the 1,2-isomers.

chemistry.chemical_classificationChemistryGlutathioneFast atom bombardmentMass spectrometryPhotochemistryQuinoneAdductchemistry.chemical_compoundHydrocarbonOrganic chemistrySpectral analysisDirect analysisSpectroscopyBiological Mass Spectrometry
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Sequiterpene-related compounds as endocrine disrupters in Oncopeltus fasciatus, and potential reduced glutathione synthesis modifiers

1999

Sesquiterpene lactones have been found to exhibit effects on insect growth and development. In this study, the bioactivity of natural lactones extracted from Centaurea mariolensis and some structurally related synthetic derivatives has been investigated. Assays have also been carried out in order to determine the potential of these lactones as modifiers of reduced glutathione (GSH) synthesis.

chemistry.chemical_classificationEnvironmental EngineeringChemical compoundStereochemistryChemical structureBiological activityGlutathioneBiologySesquiterpenePollutionchemistry.chemical_compoundMechanism of actionchemistryBiochemistryEndocrine disruptormedicineEnvironmental Chemistrymedicine.symptomWaste Management and DisposalLactoneScience of The Total Environment
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Purification of rat liver epoxide hydratase to apparent homogeneity.

1975

Epoxide hydratase (EC 4.2.1.63) is a microsomal enzyme which catalyses the conversion of epoxides to trans-dihydrodiols. Epoxides, produced by the action of microsomal monooxygenases (EC 1.14.1.1) from aromatic and olefinic compounds, are thought to be responsible for many of the harinful effects of polycyclic hydrocarbons and related compounds. Thus epoxide hydratase, together with glutathione 9transferases, (EC 2.5.1.18) may play an important role in the removal of carcinogenic and cytotoxic metabolites (for reviews see [l-3]). It has been reported [4,5] that dihydrodiols formed from some polycyclic hydrocarbons (benz(a)anthracene and benzo(a)pyrene) are reactivated by the microsomal mono…

chemistry.chemical_classificationEpoxide HydrolasesMaleAnthraceneBiophysicsCell BiologyGlutathioneMonooxygenaseBiochemistryRatsMolecular Weightchemistry.chemical_compoundEnzymechemistryBiochemistryStructural BiologyGeneticsMicrosomeMicrosomes LiverPyreneAnimalsPolycyclic HydrocarbonsMolecular BiologyCarcinogenHydro-LyasesFEBS letters
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Selenium supplementation improves antioxidant capacity in vitro and in vivo in patients with coronary artery disease

2008

Background Selenium is a central determinant of antioxidative glutathione peroxidase 1 (GPx-1) expression and activity. The relevance of selenium supplementation on GPx-1 in coronary artery disease (CAD) needs to be established. We assessed the effect of selenium supplementation on GPx-1 in cell culture and on endothelial function in a prospective clinical trial. Methods Human coronary artery endothelial cells were incubated with 5.78 to 578 nmol/L sodium selenite, Se-methyl-selenocysteine hydrochloride, or seleno-l-methionine. Glutathione peroxidase 1 mRNA and protein expression and activity were measured. Coronary artery disease patients (n = 465) with impaired endothelial function (flow-…

chemistry.chemical_classificationGPX1medicine.medical_specialtyEndotheliumbusiness.industryGlutathione peroxidasechemistry.chemical_elementVasodilationPharmacologymedicine.diseaseSurgeryCoronary artery diseasemedicine.anatomical_structurechemistryIn vivomedicineCardiology and Cardiovascular MedicinebusinessSeleniumArteryAmerican Heart Journal
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Environmentally relevant precursors of carbonyl sulfide in aquatic systems

1997

Seawater solutions of environmentally relevant organosulfur compounds, commercial humic acid (HA), and natural dissolved organic matter (DOM) were incubated with and without UV light in order to determine the carbonyl sulfide (COS) producing capabilities of these compounds. COS dark- and photo-production rate constants were determined for dilute solutions of the organosulfur compounds (μmol l−1) and HA/DOM (mg l−1). Dissolved COS was determined using a purge and cryogenic trap method followed by GC/FPD detection. COS was produced in considerable amounts both non-photochemically and photochemically from the reduced form of free acid of glutathione (GSH) and photochemically from cysteine (CYS…

chemistry.chemical_classificationGeneral ChemistryGlutathioneOceanographychemistry.chemical_compoundReaction rate constantchemistryDissolved organic carbonEnvironmental ChemistryOrganic chemistryHumic acidSeawaterOrganosulfur compoundsWater Science and TechnologyCysteineCarbonyl sulfideMarine Chemistry
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Determination of Plasma Lipid Hydroperoxides by an NADPH/NADP + Coupled Enzyme Reaction System. Evaluation of a Method

1998

Summary: Several techniques based on different principles have been proposed to measure lipid hydroperoxides. Enzymatic methods are sensitive and can be quite specific but they are subject to interference by inhibitors and not all are stoichiometric. The present work proposes some modifications of the Heath & Tappel (Anal Biochem 1976; 7:184—91) enzymatic method of determination of lipid hydroperoxides in order to standardize and automate it and to meet the analytical criteria required for a biological assay. The proposed new protocol and the automated assay give acceptable within-run and between-run precisions, with coefficients of variation of 3.34% and 5.80%, respectively, at the usual p…

chemistry.chemical_classificationGlutathione PeroxidaseLipid PeroxidesChromatographyChemistryBiochemistry (medical)Clinical BiochemistryReproducibility of ResultsSystem evaluationGeneral MedicineBiological fluidAutomationKineticsGlutathione ReductaseInvestigation methodsEnzymeBiochemistrySpectrophotometryNadph nadpPlasma lipidsHumansQuantitative analysis (chemistry)NADPcclm
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Glutathione metabolism and heavy metal detoxification in Schizosaccharomyces pombe

1991

Sixty glutathione-deficient mutants (gsh −) of Schizosaccharomyces pombe have been isolated by their resistance towards the mutagen N-methyl-N′-nitro-N-nitrosoguanidine (MNNG) and their sensitivity to the heavy metal Cadmium (Cd). fifty-three mutants show glutathione contents of less than 5% compared with the wild-type. The residual glutathione contents correlate with the resistance to MNNG, with the sensitivity to Cd and with the growth rate in minimal medium. The gsh −, Cd-sensitive (Cd s) mutants also show sensitivity to other heavy metals. Wild-type strains, but not the gsh − mutants, are able to excrete the heavy metal, very likely as a sulfide-containing compound. This inability of th…

chemistry.chemical_classificationMutantMutagenGeneral MedicineGlutathioneMetabolismBiologymedicine.disease_causebiology.organism_classificationGlutathione synthetasechemistry.chemical_compoundEnzymechemistryBiochemistrySchizosaccharomyces pombeGeneticsmedicineHeavy metal detoxificationCurrent Genetics
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The Effect of Phosphinothricin (Glufosinate) on Glutathione Synthesis in Plants

1990

The inhibitory effect of DL-phosphinothricin (glufosinate) on glutathione synthesis was studied in vivo and in vitro. The influence of phosphinothricin on γ-glutamylcysteine synthetase was compared with the already known effects of l-buthionine sulfoximine and l-methionine sulfoximine. The results showed that phosphinothricin and buthionine sulfoximine are inhibitors of γ-glutamylcysteine synthetase of plants. With both substances the enzyme was inhibited by 50 % at a concentration of 7 . 10−4M (pI50 = 3.15). Methionine sulfoximine reduced the enzyme activity by 50% at 5 . 10−2 M (pI50 = 1.30). It is discussed that the target enzyme of phosphinothricin is the glutamine synthetase whereas th…

chemistry.chemical_classificationPlant ScienceMetabolismGlutathioneBiologyEnzyme assaychemistry.chemical_compoundEnzymechemistryBiosynthesisBiochemistryGlufosinateGlutamine synthetasebiology.proteinButhionine sulfoximineBotanica Acta
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