Search results for "Transform"

showing 10 items of 3975 documents

Determination of DNA single strand breaks and selective DNA amplification by N-nitrodimethylamine and analogs, and estimation of the indicator cells'…

1986

N-nitrodimethylamine is metabolized oxidatively to N-nitrohydroxymethylmethylamine, which decomposes to yield formaldehyde and N-nitromethylamine. All four compounds and N-nitromethylamine were tested for their ability to induce DNA single strand breaks in hepatocytes and in SV 40-transformed Chinese hamster embryo cell lines. Only the two monoalkylnitramines were positive. They induced single strand breaks in hepatocytes, but were not effective in the other cells. Formaldehyde and N-nitrohydroxymethylmethylamine were toxic to the cells. None of the compounds tested was able to induce selective DNA amplification in the two transformed cell lines. Enzymes involved in drug metabolism were ass…

DNA ReplicationCancer ResearchHamsterDNA Single-StrandedSimian virus 40BiologyChinese hamsterCell Linechemistry.chemical_compoundCricetulusCricetinaeFormaldehydeAnimalsEpoxide hydrolaseCells Culturedchemistry.chemical_classificationDose-Response Relationship DrugDNA replicationGene AmplificationGeneral Medicinebiology.organism_classificationCell Transformation ViralEmbryo MammalianRatsEnzymeOncologychemistryBiochemistryLiverCell cultureDrug metabolismDNADimethylaminesJournal of cancer research and clinical oncology
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Alteration of nuclear (2'-5')oligoriboadenylate synthetase and nuclease activities preceding replication of human immunodeficiency virus in H9 cells.

1988

After infection of the respective target cells with the human immunodeficiency virus (HIV-1) viral progeny is produced only after a short temporary delay of some days, depending on cell type. After this period of time a sudden onset of HIV-1 protein synthesis with a dramatic increase in virus release occurs. (2'-5')Oligoriboadenylates [(2'-5')A], capable to activate a latent ribonuclease (RNase L) degrading both mRNA and rRNA, are known mediators involved in the early response of cells to virus infection. Here we show that the (2'-5')A-synthesizing (2'-5')A synthetase, which is inducible by interferon and activated by double-stranded RNA, as well as a (2'-5')A nuclease (2',3'-exoribonucleas…

DNA ReplicationRNase PNuclear EnvelopeVirus ReplicationBiochemistryVirusCell LineSubstrate SpecificityInterferonExoribonucleaseEndoribonucleasesmedicine2'5'-Oligoadenylate SynthetaseHumansRibonucleaseCell NucleusMessenger RNAbiologyChemistryNucleic Acid HybridizationCell Transformation ViralVirologyMolecular biologyVirus ReleaseKineticsbiology.proteinHIV-1Exoribonuclease activitymedicine.drugBiological chemistry Hoppe-Seyler
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Inhibition of human T-cell leukemia virus type I replication in primary human T cells that express antisense RNA

1989

The human T-cell leukemia virus type I is associated with adult T-cell leukemia-lymphoma in humans, a disease which is induced by a malignant transformation of T lymphocytes. Retrovirus vectors carrying human T-cell leukemia virus type I-derived sequences in reversed transcriptional orientation were used to express antisense RNA transcripts in primary human leukocytes. Human T-cell leukemia virus type I replication and virus-mediated immortalization were inhibited in cells harboring antisense constructs. This study suggests that retrovirus-mediated antisense RNA inhibition can be used to protect primary human T-lymphocytes from human T-cell leukemia virus type I-mediated cell transformation.

DNA ReplicationT-LymphocytesvirusesGenetic VectorsImmunologyViral transformationVirus ReplicationMicrobiologyVirusCell LineRetrovirushemic and lymphatic diseasesVirologymedicineHumansRNA AntisenseHuman T-lymphotropic virus 1biologyRNAbiology.organism_classificationmedicine.diseaseVirologyMolecular biologyAntisense RNALeukemiaGene Expression RegulationViral replicationInsect ScienceHuman T-lymphotropic virus 1RNACell DivisionResearch ArticleJournal of Virology
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Plasmonic nanosensor array for multiplexed DNA-based pathogen detection

2019

In this research we introduce a plasmonic nanoparticle based optical biosensor for monitoring of molecular binding events. The sensor utilizes spotted gold nanoparticle arrays as sensing platform. The nanoparticle spots are functionalized with capture DNA sequences complementary to the analyte (target) DNA. Upon incubation with the target sequence, it will bind on the respectively complementary functionalized particle spot. This binding changes the local refractive index, which is detected spectroscopically as the resulting changes of the localized surface plasmon resonance (LSPR) peak wavelength. In order to increase the signal, a small gold nanoparticle label is introduced. The binding ca…

DNA detectionplasmonic arrayFourier-transform-imaging spectroscopyLSPR sensingnanobiotekniikkananohiukkasetDNAbiosensoritplasmonic nanoparticles
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Investigating bacterial populations in styrene-degrading biofilters by 16S rDNA tag pyrosequencing

2014

Microbial biofilms are essential components in the elimination of pollutants within biofilters, yet still little is known regarding the complex relationships between microbial community structure and biodegradation function within these engineered ecosystems. To further explore this relationship, 16S rDNA tag pyrosequencing was applied to samples taken at four time points from a styrene-degrading biofilter undergoing variable operating conditions. Changes in microbial structure were observed between different stages of biofilter operation, and the level of styrene concentration was revealed to be a critical factor affecting these changes. Bacterial genera Azoarcus and Pseudomonas were among…

DNA BacterialAchromobacterTime FactorsBiofiltrationMolecular Sequence DataZoologyApplied Microbiology and BiotechnologyDNA RibosomalMicrobiologyEnvironmental BiotechnologyBioreactorsFISHRNA Ribosomal 16SHydrogenophagaCluster Analysis14. Life underwaterTaxonomic rankStyreneBiotransformationIn Situ Hybridization FluorescencePhylogenybiologyBacteriaBrevundimonasAzoarcusPyrosequencingGeneral MedicineSequence Analysis DNAbiology.organism_classification16S ribosomal RNABiotaMicrobial population biologyBiofilmsPyrosequencingFiltrationBiotechnologyApplied Microbiology and Biotechnology
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Genetic potential, diversity and activity of an atrazine-degrading community enriched from a herbicide factory effluent

2008

Aims:  To characterize an atrazine-degrading bacterial community enriched from the wastewater of a herbicide factory. Methods and Results:  The community mineralized 81·4 ± 1·9% of [14C-ring]atrazine and 31·0 ± 1·8% of [14C-ethyl]atrazine within 6 days of batch cultivation in mineral salts medium containing atrazine as the sole nitrogen source. Degradation activity of the community towards different chloro- and methylthio-substituted s-triazine compounds was also demonstrated. Restriction analysis of amplified 16S rDNA revealed high diversity of bacterial populations forming the community, with Pseudomonas species dominating in the clone library. Atrazine-degrading genetic potential of the …

DNA BacterialCOMMUNAUTE BACTERIENNEBioaugmentationWASTEWATERLibraryATRAZINEIndustrial WasteBACTERIAL COMMUNITYBIODEGRADATIONQUANTITATIVE PCRBiologyPolymerase Chain ReactionApplied Microbiology and Biotechnology03 medical and health scienceschemistry.chemical_compoundBiotransformationPseudomonasRNA Ribosomal 16STRZAtrazineGenetic variabilityFood science030304 developmental biology0303 health sciencesGenetic diversityBacteriaHerbicidesTriazines030306 microbiologybusiness.industryGeneral Medicine16S ribosomal RNAbiology.organism_classification6. Clean waterBiotechnology[SDV.MP]Life Sciences [q-bio]/Microbiology and Parasitologyatrazine ; biodegradation ; atz ; trz ; bacterial community ; wastewater ; quantitative PCRchemistryATZbusinessBacteriaPlasmidsBiotechnologyJournal of Applied Microbiology
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An improved protocol for electroporation ofOenococcus oeniATCC BAA-1163 using ethanol as immediate membrane fluidizing agent

2008

Aims:  To finalize an effective and reproducible electroporation procedure to transform Oenococcus oeni ATCC BAA-1163 strain. Methods and Results:  The vector pGID052 was selected to optimize the electroporation procedure. Transformation efficiency was 5·8 × 103 per μg of DNA. Transformation was improved when competent cells were prepared with exponential phase cultures; optimum electroporation parameters were an electric pulse of 12·5 kV cm−1, under a resistance of 200 Ω and the presence of 10% (v/v) ethanol in the electroporation buffer (EPB). Conclusions:  An effective protocol to transform O. oeni ATCC BAA-1163 strain by electroporation has been obtained by addition of ethanol to the EP…

DNA BacterialCell Membrane PermeabilityGram-Positive Asporogenous RodsBiologyApplied Microbiology and Biotechnologylaw.invention03 medical and health sciencesBacterial Proteinslaw030304 developmental biologyOenococcus oeniMEMBRANE FLUIDIZING AGENT0303 health sciencesEthanolStrain (chemistry)OENOCOCCUS OENI030306 microbiologyElectroporationCell Membranebiology.organism_classificationTransformation (genetics)[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyBiochemistryRecombinant DNAELECTROPORATIONHeterologous expressionBacteriaPlasmidsTransformation efficiencyLetters in Applied Microbiology
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Estimation of atrazine-degrading genetic potential and activity in three French agricultural soils

2004

The impact of organic amendment (sewage sludge or waste water) used to fertilize agricultural soils was estimated on the atrazine-degrading activity, the atrazine-degrading genetic potential and the bacterial community structure of soils continuously cropped with corn. Long-term application of organic amendment did not modify atrazine-mineralizing activity, which was found to essentially depend on the soil type. It also did not modify atrazine-degrading genetic potential estimated by quantitative PCR targeting atzA, B and C genes, which was shown to depend on soil type. The structure of soil bacterial community determined by RISA fingerprinting was significantly affected by organic amendmen…

DNA BacterialEAU USEEAmendment010501 environmental sciencesBiologyPolymerase Chain ReactionZea mayscomplex mixtures01 natural sciencesApplied Microbiology and BiotechnologyMicrobiologychemistry.chemical_compoundBacterial ProteinsAtrazine[SDV.MP] Life Sciences [q-bio]/Microbiology and ParasitologyBiotransformationSoil MicrobiologyComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciences2. Zero hungerBacteriaEcologybusiness.industryCommunity structureBiodiversity04 agricultural and veterinary sciences15. Life on landSoil typeDNA FingerprintingBiotechnology[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyAgronomyMicrobial population biologyWastewaterchemistrySoil water040103 agronomy & agriculture0401 agriculture forestry and fisheriesAtrazineFrancebusinessSludge
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Fitness drift of an atrazine-degrading population under atrazine selection pressure.

2008

International audience; Pseudomonas sp. ADP harbouring the atrazine catabolic plasmid ADP1 was subcultured in liquid medium containing atrazine as sole source of nitrogen. After approximately 320 generations, a new population evolved which replaced the initial population. This newly evolved population grew faster and degraded atrazine more rapidly than the initial population. Plasmid profiles and Southern blot analyses revealed that the evolved strain, unlike the ancestral strain, presented a tandem duplication of the atzB gene encoding the second enzyme of the atrazine catabolic pathway responsible for the transformation of hydroxyatrazine to N-isopropylammelide. This duplication resulted …

DNA BacterialPopulationBiologyMicrobiologyPSEUDOMONAS SP03 medical and health scienceschemistry.chemical_compoundPlasmidGene DuplicationPseudomonasGene duplicationELEMENTSDirect repeatAtrazineInsertion sequenceSelection GeneticADAPTATIONeducationEcology Evolution Behavior and Systematics030304 developmental biologyGenetics0303 health scienceseducation.field_of_study030306 microbiologySALMONELLA-TYPHIMURIUMSTRAIN ADPCATABOLISM GENESTransformation (genetics)Blotting Southern[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologychemistryGenes BacterialBACTERIADNA Transposable ElementsGROWTHAtrazineTandem exon duplicationPLASMIDRESISTANCEPlasmidsEnvironmental microbiology
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T-DNA insertion alters the terpenoid content composition and bioactivity of transgenic Artemisia annua.

2014

In this study, the interference of T-DNA insertion upon Agrobacterium-mediated transformation on the biochemical expression of the host genome is discussed. Plant extracts of transgenic Artemisia annua L. with or without an overexpressed farnesyl pyrophosphate synthase gene have been investigated for their bioactivity and metabolic profile in comparison with wild type A. annua. The highest antimicrobial activity against Staphylococcus aureus, Bacillus subtilis and Candida albicans was observed in the T253 transgenic lines. Moreover, the crude extract from T253 showed higher antimalarial activity against the Plasmodium faciparum K1 strain than those of the others. The terpenoid constituents…

DNA BacterialTransgeneArtemisia annuaPlant ScienceBacillus subtilisMicrobial Sensitivity TestsArtemisia annuaSqualenechemistry.chemical_compoundDrug DiscoveryBotanyPharmacologybiologyTerpenesfungiWild typeGeranyltranstransferaseGeneral Medicinebiology.organism_classificationAntimicrobialPlants Genetically ModifiedTerpenoidTransformation (genetics)Complementary and alternative medicinechemistryBiochemistryNatural product communications
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