Search results for "Electrophoresi"

showing 10 items of 1009 documents

Molecular devices for nanoelectronics and plasmonics

2009

This thesis is focused on fabrication and characterization of molecular devices. In connection with molecular electronics the dielectrophoresis based method for trapping and attaching nanoscale double-stranded DNA between nanoelectrodes was developed. Moreover, the method was extended to self-assembled DNA nanostructures. The method allowed to obtain valuable information about electrical and dielectrophoretic properties of DNA. In addition, two general approaches to the utilization of DNA origami structures for the assembly of materials are described and experimentally demonstrated. In context of molecular plasmonics, a novel lithographic fabrication method for positioning dye molecules on …

DNA self-assemblydielectrophoresissurface plasmonstechnology industry and agricultureDNAdyes
researchProduct

A Sensitive Method for Identification of DNA Dependent DNA Polymerases in Acrylamide Gels after Seperation by Micro Disc Electrophoresis

1973

Abstract DNA polymerase, disc electrophoresis, template affinity Two sensitive methods are described for detection of DNA dependent DNA polymerase activities in polyacrylamide gels after their fractionation by micro-disc electrophoresis. One technique is based on the increase in fluorescence of the ethidium bromide complex with template polydeoxyribonucleotides brought about by the action of the polymerases. The sensitivity of the previously described technique has been enhanced. Another method, 14 fold as sensitive, uses radioactive precursors in the enzyme assay after electrophoretic separation; washing, slicing and counting allows to evaluate incorporation into acid insoluble polymer, re…

DNA BacterialAcrylamidesbiologyDNA polymeraseElectrophoresis DiscTritiummedicine.disease_causeFluorescenceGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundBiochemistrychemistryDisc electrophoresisEthidiumAcrylamideDNA NucleotidyltransferasesEscherichia coliMethodsbiology.proteinmedicineGelsEscherichia coliDNA-directed DNA polymeraseDensitometryDNA NucleotidyltransferasesZeitschrift für Naturforschung C
researchProduct

Survival in extreme dryness and DNA-single-strand breaks.

1992

A wide variety of organisms (the so-called "anhydrobiotes') is able to survive long periods of time in a state of utmost dehydration and can thus survive in extremely dry environments including artificially imposed or space vacuum. Known strategies of survival include the accumulation of certain polyols, especially disaccharides, which help prevent damage to membranes and proteins. Here we report that DNA in vacuum-dried spores is damaged to a very substantial degree by processes leading to DNA strand breaks. Most of these lesions are obviously repaired during germination, but extensive damage to DNA and enzymes after long exposure times (months to years) finally diminish the chances of sur…

DNA BacterialAtmospheric ScienceDNA RepairVacuumDNA damageDNA repairAerospace EngineeringGerminationBiologyAgar gelchemistry.chemical_compoundmedicineDesiccationDNA single strandElectrophoresis Agar GelSpores BacterialAstronomy and AstrophysicsCell biologyGeophysicschemistrySpace and Planetary ScienceGeneral Earth and Planetary SciencesDrynessAutoradiographymedicine.symptomDesiccationDNABacillus subtilisDNA DamageAdvances in space research : the official journal of the Committee on Space Research (COSPAR)
researchProduct

Expression in Streptomyces lividans of Nonomuraea genes cloned in an artificial chromosome

2004

A bacterial artificial chromosomal library of Nonomuraea sp. ATCC39727 was constructed using Escherichia coli-Streptomyces artificial chromosome (ESAC) and screened for the presence of dbv genes known to be involved in the biosynthesis of the glycopeptide A40926. dbv genes were cloned as two large, partially overlapping, fragments and transferred into the host Streptomyces lividans, thus generating strains S. lividansColon, two colonsNmESAC50 and S. lividansColon, two colonsNmESAC57. The heterologous expression of Nonomuraea genes in S. lividans was successfully demonstrated by using combined RT-PCR and proteomic approaches. MALDI-TOF analysis revealed that a Nonomuraea ABC transporter is e…

DNA BacterialChromosomal library of Nonomuraea sp. ATCC39727Escherichia coli–Streptomyces artificial chromosome (ESAC)RT-PCRMolecular cloningApplied Microbiology and BiotechnologyStreptomycesGenetic analysisThiostreptonchemistry.chemical_compoundActinomycetalesChromosomes ArtificialCloning MolecularA40926GeneRegulator geneGeneticsGenomic LibrarybiologyMALDI-TOF mass spectrometryPromoterGeneral Medicinebiology.organism_classificationStreptomycesdbv gene cluster2D-PAGEchemistryGenes BacterialHeterologous expressionHeterologous expressionPulsed field gel electrophoresidalbavancinBiotechnologyApplied Microbiology and Biotechnology
researchProduct

Spatial and temporal changes in Actinobacterial dominance in experimental artificial groundwater recharge.

2008

Abstract Artificial groundwater recharge (AGR) is used in the drinking water industry to supplement groundwater resources and to minimise the use of chemicals in water treatment. This study analysed the spatial and temporal changes of microbial communities in AGR using two test systems: a nutrient-amended fluidized-bed reactor (FBR) and a sand column. Structural changes in the feed lake water (Lake Roine), FBR, and sand column bacterial communities were determined by denaturing gradient gel electrophoresis (DGGE) and the length heterogeneity analysis of amplified 16S rRNA genes (LH-PCR). Two clone libraries were created to link the LH-PCR results to the dominant bacterial groups. The lake w…

DNA BacterialConservation of Natural ResourcesEnvironmental EngineeringFresh WaterBiologyPolymerase Chain ReactionWater SupplyRNA Ribosomal 16SDominance (ecology)Cloning MolecularWaste Management and DisposalFinlandPhylogenyWater Science and TechnologyCivil and Structural EngineeringDNA PrimersEcologyEcological ModelingCommunity structureGroundwater rechargePollutionActinobacteriaRNA BacterialMicrobial population biologyGenes BacterialbacteriaWater treatmentWater MicrobiologySurface waterGroundwaterTemperature gradient gel electrophoresisWater research
researchProduct

Characterization of Different Deoxyribonucleases in Human Lymphocytes

1975

Abstract Deoxyribonucleases, Disc Electrophoresis, Lymphocytes Four groups of deoxyribonuclease activities from human lymphocytes have been characterized by deoxyribonuclease assay in DNA-containing polyacrylamide gels following their separation by disc-electrophoresis. All activities hydrolyse DNA endonucleolytically. One neutral deoxyribo­ nuclease found in the cytoplasmic fraction prefers native or UV-irradiated DNA over denatured DNA as substrate and is a 5′-monoester former. Two groups of acid deoxyribonuclease activities are detectable in the nuclear fraction. Both are 3′-monoester formers. One is as well active with denatured DNA as with native DNA, the other one shows the same activ…

DNA BacterialCytoplasmUltraviolet RaysPolyacrylamideNucleic Acid DenaturationGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundHydrolysismedicineHumansLymphocytesCell NucleusDeoxyribonucleasesSubstrate (chemistry)DeoxyribonucleaseDNAHydrogen-Ion ConcentrationElectrophoresis DiscRadiation Effectsmedicine.anatomical_structurechemistryBiochemistryCytoplasmDeoxyribonucleasesNucleusDNAZeitschrift für Naturforschung C
researchProduct

PCR-DGGE fingerprints of microbial succession during a manufacture of traditional water buffalo mozzarella cheese.

2004

D . E R C O L I N I , G . M A U R I E L L O , G . B L A I O T T A , G . M O S C H E T T I A N D S . C O P P O L A . 2003. Aims: To monitor the process and the starter effectiveness recording a series of fingerprints of the microbial diversity occurring at different steps of mozzarella cheese manufacture and to investigate the involvement of the natural starter to the achievement of the final product. Methods and Results: Samples of raw milk, natural whey culture (NWC) used as starter, curd after ripening and final product were collected during a mozzarella cheese manufacture. Total microbial DNA was directly extracted from the dairy samples as well as bulk colonies collected from the plates…

DNA BacterialElectrophoresisfood.ingredientFood HandlingMicroorganismColony Count MicrobialApplied Microbiology and BiotechnologyPolymerase Chain Reactionchemistry.chemical_compoundfoodStarterCheeseAgarFood microbiologyAnimalsFood scienceLactic AcidPCR-DGGEbiologyChemistrymeshophilic bacteriafood and beveragesStreptococcusGeneral MedicineBiodiversityRaw milkbiology.organism_classificationDNA FingerprintingLactic acidCulture Mediamozzarella cheeseMilkmicrobial diversity natural whey culture PCR–DGGE analysis product identity quality controlstarter effectiveness tracing system water buffalo mozzarella cheeseFood MicrobiologyBacteriaBiotechnologyMesophileSettore AGR/16 - Microbiologia AgrariaJournal of applied microbiology
researchProduct

Pulsed-field gel electrophoresis for the discrimination of Oenococcus oeni isolates from different wine-growing regions in Germany

2008

Reliable techniques are needed for the identification individual Oenococcus oeni strains with desirable flavor characteristics and to monitor the survival and contribution of inoculated and indigenous bacteria. Therefore, we investigated the suitability of pulsed-field gel electrophoresis (PFGE) for the discrimination of 65 O. oeni isolates from six different wine-producing regions in Germany. Among the restriction enzymes tested, genomic DNA digestions with Sfi I were most effective by displaying 56 (86%) different banding profiles. Our results underline the high capacity of PFGE for strain identification and differentiation. Cluster analysis of the DNA restriction patterns revealed no dis…

DNA BacterialGel electrophoresisWineStrain (biology)WineHigh capacityGeneral MedicineBiologybiology.organism_classificationMicrobiologyElectrophoresis Gel Pulsed-FieldMicrobiologyGram-Positive CocciRestriction enzymegenomic DNASpecies SpecificityGermanyFermentationPulsed-field gel electrophoresisCluster AnalysisFood scienceDeoxyribonucleases Type II Site-SpecificPhylogenyFood ScienceOenococcus oeniInternational Journal of Food Microbiology
researchProduct

Evidence of Genomic Instability in Campylobacter jejuni Isolated from Poultry

1998

ABSTRACT Poultry isolates of Campylobacter jejuni derived from a survey of meat processing batches were genotyped by pulsed-field gel electrophoresis (PFGE) of chromosomal DNA to establish the clonal relationships between single-colony isolates. In the majority of batches studied, one or two genotype patterns predominated. However, in one batch (batch A), 21 single-colony isolates gave 14 different PFGE genotypes. The banding patterns obtained with Sma I were sufficiently different to distinguish between genotypes, although the patterns also produced many common bands. The question of whether these isolates represented different clones or had a common clonal ancestry was addressed by additi…

DNA BacterialGenotypeGenetics and Molecular BiologyBiologyApplied Microbiology and BiotechnologyCampylobacter jejuniPoultrySmaIMicrobiologyCampylobacter jejuniGenotypePulsed-field gel electrophoresisAnimalsTypingGenomic organizationGeneticsEcologyGenetic Variationbiology.organism_classificationElectrophoresis Gel Pulsed-Fieldbiology.proteinRestriction fragment length polymorphismChickensGenome BacterialFlagellinFood ScienceBiotechnologyApplied and Environmental Microbiology
researchProduct

Developmental control of the heat-shock stress regulon in Streptomyces coelicolor

1995

In the differentiating eubacterium Streptomyces coelicolor, nutritional imbalances activate a developmental programme which involves the heat-shock stress regulon. In liquid batch cultures, the growth curve could be separated into four components: rapid growth 1 (RG1), transition (T), rapid growth 2 (RG2) and stationary (S). Patterns of gene expression in cultures subjected to heat shock in various phases were recorded on two-dimensional gels and analysed using advanced statistical methods. The responses of all heat-shock proteins (HSPs) were highly dependent upon the growth phase, thus demonstrating that the four phases of growth were physiologically distinct. For many HSPs, the levels of …

DNA BacterialGrowth phaseBlotting WesternRegulonMicrobiologyMicrobiologyBacterial ProteinsHeat shock stressGene expressionElectrophoresis Gel Two-DimensionalEubacteriumIsoelectric PointMolecular BiologyGenebiologyStreptomyces coelicolorCell DifferentiationGene Expression Regulation BacterialGrowth curve (biology)Reference Standardsbiology.organism_classificationStreptomycesCell biologyMolecular WeightRegulonHeat-Shock ResponseMolecular Microbiology
researchProduct