Search results for "Real-Time"

showing 10 items of 881 documents

Adaptive high-gain extended kalman filter and applications

2010

The work concerns the ``observability problem” --- the reconstruction of a dynamic process's full state from a partially measured state--- for nonlinear dynamic systems. The Extended Kalman Filter (EKF) is a widely-used observer for such nonlinear systems. However it suffers from a lack of theoretical justifications and displays poor performance when the estimated state is far from the real state, e.g. due to large perturbations, a poor initial state estimate, etc… We propose a solution to these problems, the Adaptive High-Gain (EKF). Observability theory reveals the existence of special representations characterizing nonlinear systems having the observability property. Such representations…

DC-motor: Multidisciplinaire généralités & autres [C99] [Ingénierie informatique & technologie]continuous-discrete observernonlinear observersreal-time implementation: Multidisciplinary general & others [C99] [Engineering computing & technology]extended Kalman filteradaptive high-gain observernonlinear systems
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Dynamic changes in the subcellular distribution of the tobacco ROS-producing enzyme RBOHD in response to the oomycete elicitor cryptogein.

2014

Highlight text The oomycete elicitor cryptogein triggers the relocation of RBOHD from intracellular compartments to the plasma membrane in tobacco cells. This suggests that intracellular trafficking is a potential determinant of RBOHD activity.

DETERGENT-RESISTANT MEMBRANESPhysiologyNicotiana tabacum[SDV]Life Sciences [q-bio]BY-2 cellsPlant SciencecryptogeinCell membranechemistry.chemical_compoundAPOPLASTIC OXIDATIVE BURSTCELL-SURFACEDISEASE RESISTANCE[MATH]Mathematics [math]Plant Proteinsreactive oxygen speciesFungal proteinNADPH oxidaseMicroscopy Confocalbiologyfood and beveragesElicitorCell biologymedicine.anatomical_structureBiochemistryprotein trafficking.[SDE]Environmental SciencessymbolsNADPH OXIDASE RBOHDprotein traffickingResearch PaperPhytophthoraCycloheximiderespiratory burst oxidase homolog D (RBOHD)Real-Time Polymerase Chain ReactionFungal Proteinssymbols.namesakeNICOTIANA-BENTHAMIANAMicroscopy Electron TransmissionTobaccomedicine[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[INFO]Computer Science [cs]NITRIC-OXIDENicotiana tabacumCell MembraneNADPH OxidasesGolgi apparatusbiology.organism_classificationSubcellular localizationLIPID RAFTSchemistryPLASMA-MEMBRANEbiology.proteinPLANT DEFENSE
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Aneuploid IMR90 cells induced by depletion of pRB, DNMT1 and MAD2 show a common gene expression signature

2019

Chromosome segregation defects lead to aneuploidy which is a major feature of solid tumors. How diploid cells face chromosome mis-segregation and how aneuploidy is tolerated in tumor cells are not completely defined yet. Thus, an important goal of cancer genetics is to identify gene networks that underlie aneuploidy and are involved in its tolerance. To this aim, we induced aneuploidy in IMR90 human primary cells by depleting pRB, DNMT1 and MAD2 and analyzed their gene expression profiles by microarray analysis. Bioinformatic analysis revealed a common gene expression profile of IMR90 cells that became aneuploid. Gene Set Enrichment Analysis (GSEA) also revealed gene-sets/pathways that are …

DNA (Cytosine-5-)-Methyltransferase 1AneuploidyBiologyMicroarrayReal-Time Polymerase Chain ReactionRetinoblastoma ProteinCell LineRNA interferenceGene expressionProtein Interaction MappingGeneticsmedicineHumansGeneOligonucleotide Array Sequence AnalysisMicroarray analysis techniquesGene Expression ProfilingBioinformatics analysiChromosomeFibroblastsmedicine.diseaseAneuploidyGene Expression RegulationRNAiMad2 ProteinsDNMT1Cancer researchKIF4ARNA InterferenceTranscriptomeIMR90 human fibroblast
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dltA overexpression: A strain-independent keystone of daptomycin resistance in methicillin-resistant Staphylococcus aureus

2013

The mechanisms leading to reduced susceptibility to daptomycin (DAP) are multifactorial and have not been fully elucidated. We analysed, by sequencing and expression studies, the role of the major molecular targets (cell-envelope charge genes, dltA, mprF, cls2; cell-wall turnover and autolysis genes, sceD, atl) involved in the emergence of DAP resistance in three series of isogenic clinical methicillin-resistant Staphylococcus aureus (MRSA) in which DAP resistance emerged after a heterogeneous glycopeptide-intermediate S. aureus (hGISA) step under teicoplanin and DAP therapy. All of the isolates had different genotypes and were delta-haemolysin negative, reflecting a strain proclivity to ac…

DNA BacterialMethicillin-Resistant Staphylococcus aureusMicrobiology (medical)Settore MED/07 - Microbiologia E Microbiologia ClinicaGenotypemedicine.drug_classAntibioticsGene ExpressionBiologyReal-Time Polymerase Chain Reactionmedicine.disease_causeStaphylococcal infectionsMicrobiologyDaptomycinDrug Resistance BacterialmedicineHumansPharmacology (medical)Carbon-Oxygen LigasesGeneTeicoplaninSequence Analysis DNAGeneral MedicineStaphylococcal Infectionsmedicine.diseaseMethicillin-resistant Staphylococcus aureusGlycopeptideMRSA daptomycin resistanceAnti-Bacterial AgentsInfectious DiseasesStaphylococcus aureusMutationDaptomycinmedicine.drug
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Quantification of a novel group of nitrate-reducing bacteria in the environment by real-time PCR

2004

Abstract Nitrate reduction is performed by phylogenetically diverse bacteria. Analysis of narG (alpha subunit of the membrane bound nitrate reductase) trees constructed using environmental sequences revealed a new cluster that is not related to narG gene from known nitrate-reducing bacteria. In this study, primers targeting this as yet uncultivated nitrate-reducing group were designed and used to develop a real-time SYBR® Green PCR assay. The assay was tested with clones from distinct nitrate-reducing groups and applied to various environmental samples. narG copy number was high ranging between 5.08×108 and 1.12×1011 copies per gram of dry weight of environmental sample. Environmental real-…

DNA BacterialMicrobiology (medical)Geologic SedimentsMolecular Sequence DataGene DosageBiologyNitrate reductaseNitrate ReductasePolymerase Chain ReactionMicrobiologyDenitrifying bacteriaNitrate ReductasesRNA Ribosomal 16STaq Polymerase[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyMolecular BiologyGeneNitritesPhylogenySoil MicrobiologyGramGeneticsBacteriaBase SequencePhylogenetic treeSequence Analysis DNAbiology.organism_classification16S ribosomal RNA[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyReal-time polymerase chain reactionSequence AlignmentBacteriaJournal of Microbiological Methods
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pilF polymorphism-based real-time PCR to distinguish Vibrio vulnificus strains of human health relevance

2012

The Gram-negative bacterium Vibrio vulnificus is a common inhabitant of estuarine environments. Globally, V. vulnificus is a significant foodborne pathogen capable of causing necrotizing wound infections and primary septicemia, and is a leading cause of seafood-related mortality. Unfortunately, molecular methods for the detection and enumeration of pathogenic V. vulnificus are hampered by the genetically diverse nature of this pathogen, the range of different biotypes capable of infecting humans and aquatic animals, and the fact that V. vulnificus contains pathogenic as well as non-pathogenic variants. Here we report an alternative approach utilizing the development of a real-time PCR assay…

DNA BacterialSequence analysisMolecular Sequence DataColony Count MicrobialVirulenceMicrobiologiaFood ContaminationVibrio vulnificusReal-Time Polymerase Chain ReactionMicrobiologyBacterial geneticsMicrobiologyBacterial ProteinsGenePathogenVibrio vulnificusPolymorphism GeneticbiologyBase SequenceVirulenceintegumentary systemfungiSequence Analysis DNAbiology.organism_classificationbacterial infections and mycosesVirologyReal-time polymerase chain reactionSeafoodFood MicrobiologybacteriaBacteriaFood Science
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A TaqMan-based real-time PCR assay for the specific detection and quantification ofLeuconostoc mesenteroidesin meat products

2007

A new real-time PCR procedure was developed for the specific detection and quantification of Leuconostoc mesenteroides in meat products. It is a TaqMan assay based on 23S rRNA gene targeted primers and probe. Specificity was evaluated using purified DNA from 132 strains: 102 lactic acid bacteria (LAB), including 57 reference strains and 46 food isolates, belonging to genus Leuconostoc and related genera, and 30 non-LAB strains. Quantification was linear over at least 5 log units using both serial dilutions of purified DNA and calibrated cell suspensions from Leuconostoc mesenteroides ssp. dextranicum CECT 912T. This assay was able to detect at least five genomic equivalents, using purified …

DNA BacterialSerial dilutionMolecular Sequence DataSensitivity and SpecificityMicrobiologychemistry.chemical_compound23S ribosomal RNAGeneticsTaqManAnimalsMolecular BiologyDNA PrimersChromatographybiologyReverse Transcriptase Polymerase Chain Reactionfood and beveragesSequence Analysis DNARibosomal RNAbiology.organism_classificationMolecular biologyLactic acidMeat ProductsRNA Ribosomal 23SReal-time polymerase chain reactionchemistryLactobacillaceaeLeuconostoc mesenteroidesBacteriaFEMS Microbiology Letters
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Real-time quantitative PCR of Staphylococcus aureus and application in restaurant meals.

2006

Staphylococcus aureus is considered the second most common pathogen to cause outbreaks of food poisoning, exceeded only by Campylobacter. Consumption of foods containing this microorganism is often identified as the cause of illness. In this study, a rapid, reliable, and sensitive real-time quantitative PCR was developed and compared with conventional culture methods. Real-time quantitative PCR was carried out by purifying DNA extracts of S. aureus with a Staphylococcus sample preparation kit and quantifying it in the LightCycler system with hybridization probes. The assay was linear from a range of 10 to 10(6) S. aureus cells (r2 > 0.997). The PCR reaction presented an efficiency of >85%. …

DNA BacterialStaphylococcus aureusMicrococcaceaeRestaurantsCoefficient of variationColony Count MicrobialFood Contaminationmedicine.disease_causeMicrobiologyPolymerase Chain ReactionSensitivity and SpecificityMicrobiologylaw.inventionlawmedicineFood microbiologyHumansFood sciencePolymerase chain reactionbiologyCampylobacterReproducibility of Resultsbiology.organism_classificationReal-time polymerase chain reactionStaphylococcus aureusConsumer Product SafetySpainFood MicrobiologyStaphylococcusFood AnalysisFood ScienceJournal of food protection
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Impact of maize mucilage on atrazine mineralization andatzC abundance

2005

Soil was amended with maize mucilage, a major rhizodeposit, to study its role on the number of culturable soil micro-organisms, the structure of the bacterial community, atrazine mineralization and atzC abundance. The maximal percentage of atrazine mineralization was lower for mucilage-amended than for water-amended soil. Total culturable soil bacteria and 16S rDNA copy number, measured by RT-PCR, presented similar values and were not significantly (P < 0.05) different among treatments. Mucilage applied at a rate of 70 mu g C g(-1) dry soil day(-1) over two weeks did not modify the abundance of the total soil microflora. Global structure of soil bacterial communities revealed by RISA analys…

DNA Bacterial[SDV]Life Sciences [q-bio]AmendmentBiologyZea mayscomplex mixturesAmidohydrolaseschemistry.chemical_compoundBacterial ProteinsAdhesivesSoil PollutantsPoaceaeAtrazinereal-time pcrSoil MicrobiologymucilageBacteriaHerbicidesPesticide ResiduesBiodiversityGeneral MedicineMineralization (soil science)Biodegradation EnvironmentalMucilagechemistryAgronomyatzc geneInsect Science[SDE]Environmental SciencesSoil waterSoil PollutantsAgronomy and Crop ScienceSoil microbiologyatrazinePest Management Science
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A real-time PCR assay for detection and quantification of 2-branched (1,3)-β-D–glucan producing lactic acid bacteria in cider

2010

28 p.-1 fig.-4 tab.

DNA Bacterialbeta-GlucansFood spoilageMicrobiologyMelting curve analysisMicrobiologyPolysaccharidesLactobacillus(13)(12)--D-glucanLactic acid bacteriaFood sciencePediococcusOenococcusOenococcus oeniDNA PrimersbiologyBacteriaSpoilageReverse Transcriptase Polymerase Chain ReactionAlcoholic BeveragesGeneral MedicineAmpliconbiology.organism_classificationBacterial Typing TechniquesLactobacillusCidersGenes BacterialGlucosyltransferasesFood MicrobiologyPediococcusProteoglycansOenococcusBacteriaFood ScienceReal-time PCR
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