Search results for "Erich"

showing 10 items of 805 documents

Klīniski nozīmīgo gram negatīvo baktēriju rezistence pret antibakteriālajiem līdzekļiem

2015

Maģistra darba ietvaros ir apkopoti un izanalizēti materiāli no 2013. gada janvāra līdz 2013. gada decembrim. Izolāti tika iegūti no pacientu elpceļiem: bronhu atsūknējumiem, krēpām, pleiras šķidruma un biopsiju paraugiem. Šo izolātu rezistenci pret antibakteriālajiem līdzekļiem tika pārbaudīta ar beta laktāmu, hinolonu un aminoglikozīdu klases pretmikrobu līdzekļiem. Darba mērķis ir klīniski nozīmīgo Gram negatīvo baktēriju identifikācija un jutības pret antibakteriālajiem līdzekļiem noteikšana. Savukārt, lai no hemokultūras ātri identificētu baktēriju sugu, tika lietota molekulārbioloģiskā metode: GenoType BC gramnegative tests. Gram negatīvo mikroorganismu jutības noteikšanai pret antiba…

Beta laktāmiESBLantibakteriālā rezistenceEscherichia coliantibakteriālie līdzekļiFarmācija
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In vivo detection, RNA-binding properties and characterization of the RNA-binding domain of the p7 putative movement protein from carnation mottle ca…

1999

Biochemical and structural characterization studies on the p7 putative movement protein from a Spanish isolate of carnation mottle carmovirus (CarMV) have been conducted. The CarMV p7 gene was fused to a sequence coding for a six-histidine tag and expressed in bacteria, allowing the purification of CarMV p7 and the production of a specific antiserum. This antiserum led to the immunological identification of CarMV p7 in infected leaf tissue from the experimental host Chenopodium quinoa. Putative nucleic acid-binding properties of the CarMV p7 have been explored and demonstrated with both electrophoretic mobility shift and RNA-protein blot in vitro assays using digoxigenin-labeled riboprobes.…

Binding SitesCarmovirusRecombinant Fusion ProteinsMolecular Sequence DataCooperative bindingRNARNA-Binding ProteinsBiologybiology.organism_classificationMolecular biologyPlant Viral Movement ProteinsViral ProteinsBiochemistryVirologyNucleic acidEscherichia coliCarmovirusAmino Acid SequenceMovement proteinPeptide sequenceGeneBinding domainVirology
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Reactivity of anticancer metallodrugs with serum proteins: New insights from size exclusion chromatography-ICP-MS and ESI-MS

2010

International audience; A method based on the coupling of high resolution size-exclusion liquid chromatography using a polymer stationary phase with inductively coupled plasma mass spectrometry was developed to study the interactions of two metallodrugs - cisplatin and RAPTA-T - with the serum proteins albumin and transferrin. In contrast to previous approaches, the technique allowed the total recovery of the metals from the column and was able to discriminate between the different species of the metallodrugs and their complexes with the proteins at femtomolar detection levels. Metal binding was found to be dependent on the protein concentration and on the incubation time of the sample. Cis…

Binding-SitesElectrospray ionizationSize-exclusion chromatographyPeptidePlasma-Mass Spectrometry010402 general chemistry01 natural sciencesArticleAnalytical ChemistryOrganometallic Ruthenium CompoundCapillary electrophoresisComplexes[CHIM.ANAL]Chemical Sciences/Analytical chemistry[CHIM]Chemical SciencesInductively coupled plasma mass spectrometrySpectroscopychemistry.chemical_classificationChromatographyChemistry010401 analytical chemistryCisplatin BindingTransferrinAlbuminCapillary-ElectrophoresisMultidimensional Liquid-ChromatographyBlood proteins0104 chemical sciencesTransferrinPlatinum Antitumor ChemistryEscherichia-Coli
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Biogenic amines in fermented foods

2010

Food-fermenting lactic acid bacteria (LAB) are generally considered to be non-toxic and non-pathogenic. Some species of LAB, however, can produce biogenic amines (BAs). BAs are organic, basic, nitrogenous compounds, mainly formed through decarboxylation of amino acids. BAs are present in a wide range of foods, including dairy products, and can occasionally accumulate in high concentrations. The consumption of food containing large amounts of these amines can have toxicological consequences. Although there is no specific legislation regarding BA content in many fermented products, it is generally assumed that they should not be allowed to accumulate. The ability of microorganisms to decarbox…

Biogenic AminesDecarboxylationMedicine (miscellaneous)Food ContaminationWineBiologyLACTIC-ACID BACTERIADecarboxylationRisk AssessmentOENOCOCCUS-OENI03 medical and health scienceschemistry.chemical_compoundBiogenic amine[SDV.IDA]Life Sciences [q-bio]/Food engineeringFood microbiology[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringWINESfood fermentationLACTOCOCCUS-LACTISFermentation in food processing030304 developmental biology2. Zero hungerchemistry.chemical_classification0303 health sciencesNutrition and DieteticsTYROSINE DECARBOXYLASELACTOBACILLUS-BREVIS030306 microbiologyLactobacillus brevistoxicological effectsHISTAMINE-PRODUCING BACTERIAacid stressfood and beveragesbiology.organism_classificationLactic acidAmino acidlactic acid bacteriachemistryBiochemistryTYRAMINE PRODUCTIONESCHERICHIA-COLILactobacillaceaeFermentationFood MicrobiologyFermentationDairy ProductsMULTIPLEX PCR
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Molecular Cloning, Heterologous Expression, and Characterization of Ornithine Decarboxylase from Oenococcus oeni

2011

International audience; Ornithine decarboxylase (ODC) is responsible for the production of putrescine, the major biogenic amine found in wine. Oenococcus oeni is the most important lactic acid bacterium in the winemaking process and is involved in malolactic fermentation. We report here the characterization of ODC from an O. oeni strain isolated from wine. Screening of 263 strains isolated from wine and cider from all over the world revealed that the presence of the odc gene appears to be strain specific in O. oeni. After cloning, heterologous expression in Escherichia coli, and characterization, the enzyme was found to have a molecular mass of 85 kDa and a pI of 6.2 and revealed maximal ac…

Biogenic Aminesgenetic structuresWinemedicine.disease_causeMicrobiologyOrnithine decarboxylaseOrnithine decarboxylaseIndustrial Microbiology03 medical and health scienceschemistry.chemical_compoundmedicineMalolactic fermentationHumans[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyEscherichia coliOenococcus030304 developmental biologyOenococcus oeniWinemaking0303 health sciencesCadaverinebiology030306 microbiologyTemperaturefood and beveragesHydrogen-Ion Concentrationbiology.organism_classificationMolecular WeightKineticschemistryBiochemistryFermentationPutrescineHeterologous expressionOenococcus oeniFood ScienceJournal of Food Protection
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Gangliosides and sialic acid effects upon newborn pathogenic bacteria adhesion: An in vitro study

2012

The effect of the main gangliosides (GM(1), GM(3), GD(3)) and free sialic acid (Neu5Ac) upon the adhesion of pathogenic bacteria implicated in infant diarrhoea is assessed in vitro using the Caco-2 cell line. Concentrations of the bioactive compounds found in the bioaccessible (soluble) fraction of infant formula and human milk are employed. Bacterial adhesion behaviour included enterotoxigenic Escherichia coli (ETEC), enteropathogenic E.coli (EPEC), Listeria monocytogenes, Salmonella entericaserovartyphi, Shigella sonnei, Campylobacter jejuni and Helicobacter pylori. Three different approaches were assayed: pre-incubation of bacteria and compounds before addition to cells (competition); pr…

Biologymedicine.disease_causeModels BiologicalCampylobacter jejuniBacterial AdhesionAnalytical ChemistryMicrobiologychemistry.chemical_compoundListeria monocytogenesGangliosidesEnterotoxigenic Escherichia colimedicineHumansBacteriaInfant NewbornPathogenic bacteriaBacterial InfectionsGeneral Medicinebiology.organism_classificationN-Acetylneuraminic AcidIn vitroSialic acidchemistryCell cultureDiarrhea InfantileCaco-2 CellsBacteriaFood ScienceFood Chemistry
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Artificial chromosomes for antibiotic-producing actinomycetes.

2000

Bacteria belonging to the order Actinomycetales produce most microbial metabolites thus far described, several of which have found applications in medicine and agriculture. However, most strains were discovered by their ability to produce a given molecule and are, therefore, poorly characterized physiologically and genetically. Thus, methodologies for genetic manipulation of actinomycetes are not available and efficient tools have been developed for just a few strains. This constitutes a serious limitation to applying molecular genetics approaches to strain development and structural manipulation of microbial metabolites. To overcome this hurdle, we have developed bacterial artificial chrom…

Biomedical EngineeringBioengineeringHuman artificial chromosomeMolecular cloningApplied Microbiology and BiotechnologyStreptomycesPlasmidActinomycetalesEscherichia coliGenomic libraryGene LibraryGeneticsBacterial artificial chromosomebiologyModels GeneticStreptomyces coelicolorChromosomes Bacterialbiology.organism_classificationStreptomycesAnti-Bacterial AgentsBlotting SouthernMolecular MedicineActinomycetalesGenetic EngineeringBiotechnologyPlasmidsNature biotechnology
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Giant liposomes as model membranes for immunological studies: spontaneous insertion of purified K1-antigen (poly-alpha-2,8-NeuAc) of Escherichia coli.

1990

A flow chamber has been constructed to use giant liposomes (diameter 5-50 microns) as model membranes for immunological studies and other experiments involving the interaction with water-soluble compounds. As an example of immunological importance, the insertion of purified K-antigen from Escherichia coli K1 has been studied. Despite its large hydrophilic part (poly-alpha-2,8-NeuAc), which is capped at its potential reducing end with phosphatidic acid acting as a lipid anchor group, this water-soluble material is readily incorporated into liposomal membranes of dimyristoylphosphatidylcholine (DMPC). The incorporation has been proven by immunofluorescence using a FITC-labeled monoclonal anti…

BiophysicsFluorescent Antibody TechniqueNeuraminidaseBiologymedicine.disease_causeBiochemistryModels BiologicalResidue (chemistry)chemistry.chemical_compoundMembrane LipidsmedicineEscherichia coliMicroscopy Phase-ContrastEscherichia coliHEPESchemistry.chemical_classificationLiposomeAntigens BacterialAntibodies MonoclonalWaterCell BiologyPhosphatidic acidbiology.organism_classificationEnterobacteriaceaeEnzymeMembranechemistryBiochemistrySolubilityImmunoglobulin GAntigens SurfaceLiposomesDimyristoylphosphatidylcholineBiochimica et biophysica acta
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Double-spanning Plant Viral Movement Protein Integration into the Endoplasmic Reticulum Membrane Is Signal Recognition Particle-dependent, Translocon…

2005

The current model for cell-to-cell movement of plant viruses holds that transport requires virus-encoded movement proteins that intimately associate with endoplasmic reticulum membranes. We have examined the early stages of the integration into endoplasmic reticulum membranes of a double-spanning viral movement protein using photocross-linking. We have discovered that this process is cotranslational and proceeds in a signal recognition particle-dependent manner. In addition, nascent chain photocross-linking to Sec61alpha and translocating chain-associated membrane protein reveal that viral membrane protein insertion takes place via the translocon, as with most eukaryotic membrane proteins, …

BioquímicaSec61Vesicle-associated membrane protein 8Receptors PeptideLipid BilayersReceptors Cytoplasmic and NuclearBiologyEndoplasmic ReticulumBiochemistryViral ProteinsMembranes (Biologia)Escherichia coliMolecular BiologySignal recognition particle receptorSignal recognition particleMembrane GlycoproteinsEndoplasmic reticulumCalcium-Binding ProteinsMembrane ProteinsSTIM1Cell BiologyTransloconTransmembrane proteinCell biologyPlant Viral Movement ProteinsCross-Linking ReagentsMutagenesisRNA ViralCarmovirusSignal Recognition ParticleSEC Translocation Channels
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Variable presence of 5-methylcytosine in commercial RNA and DNA

2015

Nucleoside methylations and other nucleic acid modifications have recently encountered a surge in interest, prompted, among other things, by the detection of methylation and active demethylation of DNA and mRNA by similar mechanisms. In DNA, deoxycytidine methylation by Dnmt enzymes generates 5-methyldeoxycytidine,1 an important epigenetic mark that typically causes inactivation of transcription of the methylated promoter region. Recent exciting developments have shown that these marks are not concrete-cast, but can be actively removed by the oxidative action of TET enzymes,2 which generate, through a series of 2-electron oxidations, first hydroxymethylcytidine (hm5C), then formyldeoxycytid…

Bisulfite sequencingSaccharomyces cerevisiaeBiologyMass Spectrometrychemistry.chemical_compoundTranscription (biology)Escherichia coliMethylated DNA immunoprecipitationmodified nucleosideMolecular BiologyOligonucleotideRNADNACell BiologyRNA modificationMolecular biology5-MethylcytosinechemistryBiochemistry5-MethylcytosineNucleic acidRNADNA modificationDNAResearch PapermethylcytosineChromatography LiquidRNA Biology
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