Search results for " enzyme"

showing 10 items of 791 documents

Disassembling Papaver: a restriction site analysis of chloroplast DNA

1992

The results from a chloroplast DNA restriction site analysis of the genera Papaver and Roemeria of subf. Papaveroideae (Papaveraceae) and five outgroup taxa are presented. Papaver is represented by 14 species of eight of the 11 sections recognized, Roemeria by two of its three species. Hunnemannia fumariifolia (subf. Eschscholzioideae), Chelidonium majus (subf. Chelidonioideae), Romneya coulteri, Argemone munita and Stylomecon heterophyllum (all subf. Papaveroideae) were chosen as outgroups. DNAs were digested with 24 restriction enzymes. The major results from this analysis are: 1. Papaver, Roemeria and Stylomecon form a monophyletic group supported by at least 17 restriction site mutation…

Restriction siteMonophylyRestriction enzymeRestriction mapSister groupbiologyChloroplast DNAPapaverBotanyPapaveroideaePlant Sciencebiology.organism_classificationEcology Evolution Behavior and SystematicsNordic Journal of Botany
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Effects of garlic powders with varying alliin contents on hepatic drug metabolizing enzymes in rats

2003

International audience; The anticarcinogenic effect of garlic has been demonstrated in both epidemiologic and experimental studies. In this study, possible mechanisms involved in the anticarcinogenic effect of garlic consumption were assessed by determining its capacity to alter drug metabolizing enzymes, in relation with its alliin content. Rats were fed a diet for 2 weeks containing 5% garlic powders produced from bulbs grown on soils with different levels of sulfate fertilization and therefore containing differing amounts of alliin. Activities of several hepatic enzymes, which are important in carcinogen metabolism such cytochromes P450 (CYP) and phase II enzymes, were determined. Garlic…

S01 - Nutrition humaine - Considérations généralesMaleDiallyl disulfideAlliinPharmacognosyhttp://aims.fao.org/aos/agrovoc/c_11091chemistry.chemical_compound0302 clinical medicinehttp://aims.fao.org/aos/agrovoc/c_4395[SDV.IDA]Life Sciences [q-bio]/Food engineeringGlucuronosyltransferaseComputingMilieux_MISCELLANEOUSAilGlutathione Transferasechemistry.chemical_classification0303 health sciencesbiologyDiallyl disulfidehttp://aims.fao.org/aos/agrovoc/c_2603food and beveragesBiological activityCytochrome P-450 CYP2E1[SDV.IDA] Life Sciences [q-bio]/Food engineering3. Good healthBiochemistryLiver030220 oncology & carcinogenesisGeneral Agricultural and Biological SciencesAllium sativumDrug-metabolizing enzymesFoiehttp://aims.fao.org/aos/agrovoc/c_290Médicamenthttp://aims.fao.org/aos/agrovoc/c_25197Alliin03 medical and health scienceshttp://aims.fao.org/aos/agrovoc/c_2395Cytochrome P-450 CYP1A2Cytochrome P-450 CYP1A1AnimalsAnticarcinogenic AgentsCysteineRats WistarQ04 - Composition des produits alimentairesGarlic030304 developmental biologySantéCytochrome P450General ChemistryGlutathioneAllium sativumPropriété pharmacologiqueDietRatsEnzymechemistryEnzymebiology.proteinRAThttp://aims.fao.org/aos/agrovoc/c_3511http://aims.fao.org/aos/agrovoc/c_6464
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Sensitivity of three commercial tests for SARS-CoV-2 serology in children: an Italian multicentre prospective study

2022

Abstract Background US Food and Drug Administration has issued Emergency Use Authorizations for hundreds of serological assays to support Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) diagnosis. The aim of this study is to evaluate, for the first time in children, the performance of three widely utilized SARS-CoV-2 serology commercial assays, Diesse Diagnostics (IgG, IgA, IgM) and Roche Diagnostics, both Roche Nucleocapsid (N) IgG and Roche Spike (S) IgG assays. Methods Sensitivity and 95% confidence intervals (CIs) were estimated for each of the three different serological tests and mixed and direct comparison were performed. Univariate and multivariate Poisson regression mo…

SARS-CoV-2COVID-19; Children; Electrochemiluminescent immunoassay (ECLIA); Enzyme-linked immunosorbent assay (ELISA); SARS-CoV-2Electrochemiluminescent immunoassay (ECLIA)Enzyme-linked immunosorbent assay (ELISA)COVID-19General MedicineUnited StatesImmunoglobulin AImmunoglobulin MImmunoglobulin GCOVID-19 Children Electrochemiluminescent immunoassay (ECLIA) Enzyme-linked immunosorbent assay (ELISA) SARS-CoV-2HumansProspective StudiesChildChildren
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Expression of yeast but not human apurinic/apyrimidinic endonuclease renders Chinese hamster cells more resistant to DNA damaging agents.

1997

Abasic sites represent ubiquitous DNA lesions that arise spontaneously or are induced by DNA-damaging agents. They block DNA replication and are considered to be cytotoxic and mutagenic. The key enzymes involved in the repair of abasic sites are apurinic/apyrimidinic (AP) endonucleases which process these lesions in an error-free mechanism. To analyze the role of AP endonuclease in the protection of mammalian cells against DNA damaging agents, we have transfected both the human (APE) and the yeast (APN1) AP endonuclease in Chinese hamster cells and compared the effects of expression of these genes in stable transfectants as to survival of cells and formation of chromosomal aberrations. Alth…

Saccharomyces cerevisiae ProteinsDNA RepairDNA repairCell SurvivalBlotting WesternCarbon-Oxygen LyasesChromosome DisordersCHO CellsToxicologyTransfectionAP endonucleaseDNA repair ; Apurinic endonuclease ; cellular defense mechanismschemistry.chemical_compoundCricetinaeGeneticsDNA-(Apurinic or Apyrimidinic Site) LyaseAnimalsHumansAP siteRNA MessengerFluorescent Antibody Technique IndirectMolecular BiologyCell NucleusChromosome AberrationsEndodeoxyribonucleasesbiologyCell DeathfungiNuclear ProteinsBase excision repairHydrogen PeroxideBlotting NorthernMethyl MethanesulfonateMolecular biologyDNA-(apurinic or apyrimidinic site) lyaseDNA Repair EnzymeschemistryGene Expression Regulationbiology.proteinChromosome breakageDNANucleotide excision repairDNA DamagePlasmidsMutation research
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Effects of yeast proteolytic activity on Oenococcus oeni and malolactic fermentation

2006

International audience; Alcoholic fermentation of synthetic must was performed using either Saccharomyces cerevisiae or a mutant Delta pep4, which is deleted for the proteinase A gene. Fermentation with the mutant Delta pep4 resulted in 61% lower levels of free amino acids, and in 62% lower peptide concentrations at the end of alcoholic fermentation than in the control. Qualitative differences in amino acid composition were observed. Changes observed in amino acids in peptides were mainly quantitative. After alcoholic fermentation each medium was inoculated with Oenococcus oeni. Malolactic fermentation in the medium with the Delta pep4 strain took 10 days longer than the control. This diffe…

Saccharomyces cerevisiae ProteinsNitrogenMalatesWineSaccharomyces cerevisiaeEthanol fermentationMicrobiology03 medical and health sciencesMalate DehydrogenaseProteinase APEP4EndopeptidasesGeneticsMalolactic fermentationLactic acid bacteriaNitrogen metabolismAmino AcidsMolecular Biology030304 developmental biologyOenococcus oenichemistry.chemical_classification0303 health sciencesbiology030306 microbiologyProteolytic enzymesfood and beveragesFree amino nitrogenbiology.organism_classificationYeastYeastAmino acidGram-Positive Cocci[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryBiochemistryFermentationPeptideFermentation
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Evaluation of the genotoxic and cytochrome P450 monooxygenase‐inhibitory potential of dicuran on procaryotic and eucaryotic test systems

2000

The effect of the herbicide Dicuran 500 FL (formulated product) on the phenotypical and genotypical changes in procaryotic and eucaryotic organisms was investigated using short-term tests for detecting genotoxins. Since pesticides discharged in the water environment can modulate the mixed-function monooxygenases (MFO) detoxification system of water organisms, the in vivo and in vitro effects of Dicuran on hepatic cytochrome P450 (cyt P450) monooxygenase activities were also examined in juvenile carp (Cyprinus carpio L.). By measuring the activities of MFO in experimental carp exposed to Dicuran an attempt was made to establish whether Dicuran could be bioactivated by MFO into ultimate mutag…

Salmonella typhimuriumOxygenaseCarpsBiologymedicine.disease_causeMixed Function OxygenasesAmes testCytochrome P-450 Enzyme SystemmedicineWater environmentAnimalsCytochrome P-450 Enzyme InhibitorsCarpCytotoxinsHerbicidesMutagenicity Testsbusiness.industryPhenylurea CompoundsCytochrome P450General MedicineMonooxygenasebiology.organism_classificationPollutionBiotechnologyLiverBiochemistryMicronucleus testbiology.proteinbusinessWater Pollutants ChemicalGenotoxicityMutagensFood ScienceJournal of Environmental Science and Health, Part B
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Carbohydrate-Mediated Biomolecular Recognition and Gating of Synthetic Ion Channels

2013

Nanochannel-based biosensing devices have been proposed for selective detection of protein analyte molecules. However, the design and miniaturization of reusable channel-based biosensors is still a challenge in nanoscience and biotechnology. We present here a reusable nanofluidic biosensor based on reversible lectin-carbohydrate interactions. The nanochannels are fabricated in heavy ion tracked polymer membranes. The channel walls are functionalized with p-aminophenyl alpha-D-mannopyranoside (APMP) monolayers through carbodiimide coupling chemistry. The chemical (mannopyranoside) groups on the inner channel walls serve as binding sites and interact with specific protein molecules. The bindi…

Self assembled monolayersAnalyteCell recognitionSolid state nanoporesChemistrySelf-assembled monolayerNanotechnologyGatingSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergyNanofluidic diodeSaccharide binding siteFISICA APLICADASynthetic ion channelsMiniaturizationDna analysisConcanavalin AMannose labeled enzymesAsymmetric nanoporesPhysical and Theoretical ChemistryBiosensor
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ABO genotyping by PCR-RFLP and cloning and sequencing

2005

A refined PCR-RFLP based method was established to genotype ABO blood groups. The main objective of this study was to make the techniques also suitable for working with degraded DNA. Specific primer design was carried out to choose fragments shorter than 200 bp as necessary in forensic and archaeological applications. Four fragments of exon 6 and 7 of the ABO gene were amplified and digested by in total 7 restriction endonucleases. Particular attention was paid to the base changes at nucleotide positions 261(delG), 297, 526, 703, 721, 771, 796 and 1060(delC) in order to distinguish the six common alleles A101, A201, B, O01, O02 and O03. Furthermore, this method also enables determination of…

Sequence analysisBiologyPolymerase Chain ReactionABO Blood-Group Systemlaw.inventionlawABO blood group systemGenotypeHumansCloning MolecularGenotypingAllelesHistory AncientEcology Evolution Behavior and SystematicsPolymerase chain reactionGeneticsReproducibility of ResultsSequence Analysis DNAGeneral MedicineForensic MedicineRestriction enzymePhenotypeAncient DNAArchaeologyBlood StainsPostmortem ChangesAnthropologyDNA Transposable ElementsAnimal Science and ZoologyChromosome DeletionRestriction fragment length polymorphismToothPolymorphism Restriction Fragment LengthAnthropologischer Anzeiger
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Genetic organization of the mle locus and identification of a mleR-like gene from Leuconostoc oenos

1996

Characterization of the mle locus harboring the malolactic enzyme gene mleA and malate permease gene mleP from Leuconostoc oenos was completed in this study by mRNA analysis. Northern (RNA) blot experiments revealed a 2.6-kb transcript, suggesting an operon structure harboring mleA and mleP genes. Primer extension analysis showed that the mle operon has a single transcription start site located 17 nucleotides upstream of the ATG translation start site for the mleA gene. We found sequences, TTGACT and TATGAT (which are separated by 18 bp), that are closely related to the gram-positive and Escherichia coli consensus promoter sequences. Upstream of the mleA gene, an 894-bp open reading frame t…

Sequence analysisOperonMolecular Sequence DataLeuconostoc oenosMalatesLocus (genetics)BiologyApplied Microbiology and BiotechnologyOpen Reading FramesOperon[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyAmino Acid SequenceLactic AcidGenemalolactic enzymeGeneticsRegulation of gene expressionmalateBase SequenceEcologyLactococcus lactisNucleic acid sequenceChromosome MappingregulationBlotting Northernbiology.organism_classificationMolecular biologyOpen reading frameGenes BacterialLeuconostocResearch ArticleFood ScienceBiotechnologyApplied and Environmental Microbiology
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Use of microbial enzyme on brewing

2015

Settore AGR/01 - Economia Ed Estimo RuraleBREWING PROCESS BARLEY GRAIN EXOGENOUS ENZYMES GLUCANASES
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