Search results for "PLASMID"

showing 10 items of 327 documents

Identification of SCP2165, a new SCP2-derived plasmid of Streptomyces coelicolor A3(2).

2005

Aims:  Characterization of SCP2165, a plasmid identified in the Gram-positive bacterium Streptomyces coelicolor A3(2). Methods and Results:  Pulsed-field gel electrophoresis (PFGE) of mycelia of a S. coelicolor strain embedded in low melting agarose revealed the presence of a plasmid. Restriction enzyme mapping and sequence analysis of a 2·1 kb fragment revealed that this plasmid could be SCP2. SCP2 and its spontaneous derivative SCP2* are self-transmissible plasmids and have chromosome mobilizing ability (c.m.a.). SCP2* has a c. 1000-fold increased c.m.a. compared with SCP2. Interestingly the plasmid, named SCP2165, shows a c.m.a. from 5 × 10−2 to 1 × 10−1 which is 50–100-fold higher than …

Gel electrophoresisPlasmid preparationRecombination GeneticbiologyGene Transfer HorizontalSequence analysisStreptomycetaceaeStreptomyces coelicolorCloning vectorStreptomyces coelicolorbiology.organism_classificationApplied Microbiology and BiotechnologyStreptomycesMolecular biologyElectrophoresis Gel Pulsed-FieldPlasmidConjugative plasmids Pulsed-field gel electrophoresis SCP2 SCP2 derived plasmids Streptomyces coelicolorConjugation GeneticCrosses GeneticPlasmidsLetters in applied microbiology
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Midbiotics: conjugative plasmids for genetic engineering of natural gut flora.

2019

ABSTRACT The possibility to modify gut bacterial flora has become an important goal, and various approaches are used to achieve desirable communities. However, the genetic engineering of existing microbes in the gut, which are already compatible with the rest of the community and host immune system, has not received much attention. Here, we discuss and experimentally evaluate the possibility to use modified and mobilizable CRISPR-Cas9-endocing plasmid as a tool to induce changes in bacterial communities. This plasmid system (briefly midbiotic) is delivered from bacterial vector into target bacteria via conjugation. Compared to, for example, bacteriophage-based applications, the benefits of …

Gene Editingantibiotic resistanceBrief Reportbeta-Lactam ResistanceAnti-Bacterial AgentsGastrointestinal Microbiomeconjugative plasmidConjugation GeneticGenetic engineeringEscherichia coliESBL carriageCRISPR-Cas SystemsCRISPR editingenterobacteriaPlasmidsRNA Guide KinetoplastidaGut microbes
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Phage-borne factors and host LexA regulate the lytic switch in phage GIL01.

2011

ABSTRACT The Bacillus thuringiensis temperate phage GIL01 does not integrate into the host chromosome but exists stably as an independent linear replicon within the cell. Similar to that of the lambdoid prophages, the lytic cycle of GIL01 is induced as part of the cellular SOS response to DNA damage. However, no CI-like maintenance repressor has been detected in the phage genome, suggesting that GIL01 uses a novel mechanism to maintain lysogeny. To gain insights into the GIL01 regulatory circuit, we isolated and characterized a set of 17 clear plaque ( cp ) mutants that are unable to lysogenize. Two phage-encoded proteins, gp1 and gp7, are required for stable lysogen formation. Analysis of …

Gene Expression Regulation ViralvirusesBacteriophages Transposons and PlasmidsBacillus thuringiensisBacillus PhagesBiologyMicrobiologyHost-Parasite InteractionsBacteriolysisLysogenBacterial ProteinsLysogenic cycleHost chromosomeSOS responseSOS Response GeneticsMolecular BiologyLysogenyGeneticsBinding SitesSerine Endopeptidasesbiochemical phenomena metabolism and nutritionBacillus PhageTemperatenessLytic cycleDNA ViralbacteriaVirus ActivationRepressor lexAProtein BindingJournal of bacteriology
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Phylogenomics of Enterococcus faecalis from wild birds: new insights into host‐associated differences in core and accessory genomes of the species

2019

Wild birds have been suggested to be reservoirs of antimicrobial resistant and/or pathogenic Enterococcus faecalis (Efs) strains, but the scarcity of studies and available sequences limit our understanding of the population structure of the species in these hosts. Here, we analysed the clonal and plasmid diversity of 97 Efs isolates from wild migratory birds. We found a high diversity, with most sequence types (STs) being firstly described here, while others were found in other hosts including some predominant in poultry. We found that pheromone‐responsive plasmids predominate in wild bird Efs while 35% of the isolates entirely lack plasmids. Then, to better understand the ecology of the sp…

Gene Transfer HorizontalPopulation structureAnimals WildBiologyMicrobiologyGenomeEnterococcus faecalisHost SpecificityBirds03 medical and health sciencesPlasmidPhylogeneticsPhylogenomicsEnterococcus faecalisAnimalsEcology Evolution Behavior and SystematicsPhylogeny030304 developmental biology0303 health sciences030306 microbiologyHost (biology)Gene Expression Regulation Bacterialbiology.organism_classificationEvolutionary biologyHorizontal gene transferGenome Bacterial
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DNA delivery to 'ex vivo' human liver segments.

2011

Hydrodynamic injection is an efficient procedure for liver gene therapy in rodents but with limited efficacy in large animals, using an 'in vivo' adapted regional hydrodynamic gene delivery system. We study the ability of this procedure to mediate gene delivery in human liver segments obtained by surgical resection. Watertight liver segments were retrogradely injected from hepatic vein with a saline solution containing a plasmid bearing the enhanced green fluorescent protein (eGFP) gene, under different conditions of flow rate (1, 10 and 20 ml s(-1)) and final perfused volume. Samples were cultured for 1 to 2 days and used for microscopy and molecular analysis of gene expression. The fluore…

Genetic enhancementGreen Fluorescent ProteinsGene Transfer TechniquesGenetic TherapyBiologyGene deliveryHepatic VeinsMolecular biologyGreen fluorescent proteinCatheterizationLiverIn vivoTranscription (biology)Gene expressionInjections IntravenousGeneticsHydrodynamicsMolecular MedicineHumansMolecular BiologyGeneEx vivoPlasmidsGene therapy
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Clostridium difficile IStron CdISt1: Discovery of a Variant Encoding Two Complete Transposase-Like Proteins

2004

ABSTRACT Screening a Clostridium difficile strain collection for the chimeric element Cd ISt1 , we identified two additional variants, designated Cd ISt1 -0 and Cd ISt1 -III. In in vitro assays, we could prove the self-splicing ribozyme activity of these variants. Structural comparison of all known Cd ISt1 variants led us to define four types of IStrons that we designated Cd ISt1 -0 through Cd ISt1 -III. Since Cd ISt1 -0 encodes two complete transposase-like proteins (TlpA and TlpB), we suggest that it represents the original genetic element, hypothesized before to have originated by fusion of a group I intron and an insertion sequence element.

Genetics0303 health sciencesbiology030306 microbiologyClostridioides difficileStrain (biology)Bacteriophages Transposons and PlasmidsMolecular Sequence DataRibozymeIntronTransposasesClostridium difficilebiology.organism_classificationMicrobiologyIntrons03 medical and health sciencesGenes Bacterialbiology.proteinBacteriologyDNA Transposable ElementsClostridiaceaeInsertion sequenceMolecular BiologyTransposase030304 developmental biology
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Simulating the Influence of Conjugative Plasmids Kinetic Values on the Multilevel Dynamics of Antimicrobial Resistance in a Membrane Computing Model

2020

AbstractPlasmids harboring antibiotic resistance genes differ in their kinetic values as plasmid conjugation rate, segregation rate by incompatibility with related plasmids, rate of stochastic loss during replication, cost reducing the host-cell fitness, and frequency of compensatory mutations to reduce plasmid cost, depending on the cell mutation frequency. How variation in these values influence the success of a plasmid and their resistance genes in complex ecosystems, as the microbiota? Genes are located in plasmids, plasmids in cells, cells in populations. These populations are embedded in ensembles of species in different human hosts, are able to exchange between them bacterial ensembl…

Genetics0303 health scienceseducation.field_of_study030306 microbiologyPopulationAntibiotic exposureBiology03 medical and health sciencesAntibiotic resistancePlasmidMutation frequencyeducationGeneMembrane computing030304 developmental biologyAntibiotic resistance genes
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A classification scheme for mobilization regions of bacterial plasmids

2003

Transmissible plasmids can be classified according to their mobilization ability, as being conjugative (self-transmissible) or mobilizable (transmissible only in the presence of additional conjugative functions). Naturally occurring mobilizable plasmids carry the genetic information necessary for relaxosome formation and processing, but lack the functions required for mating pair formation. Mobilizable plasmids have a tremendous impact in horizontal gene transfer in nature, including the spread of antibiotic resistance. However, analysis of their promiscuity and diversity has attracted less attention than that of conjugative plasmids. This review will focus on the analysis of the diversity …

GeneticsBacteriaPhylogenetic treeBacterial conjugationMolecular Sequence DataBiologyRelaxaseRelaxosomeMicrobiologyInfectious DiseasesPlasmidHorizontal gene transferAmino Acid SequenceGene poolTransfer techniquePlasmidsFEMS Microbiology Reviews
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Long-range translational coupling in single-stranded RNA bacteriophages: an evolutionary analysis

1998

In coliphage MS2 RNA a long-distance interaction (LDI) between an internal segment of the upstream coat gene and the start region of the replicase gene prevents initiation of replicase synthesis in the absence of coat gene translation. Elongating ribosomes break up the repressor LDI and thus activate the hidden initiation site. Expression studies on partial MS2 cDNA clones identified base pairing between 1427-1433 and 1738-1744, the so-called Min Jou (MJ) interaction, as the molecular basis for the long-range coupling mechanism. Here, we examine the biological significance of this interaction for the control of replicase gene translation. The LDI was disrupted by mutations in the 3'-side an…

GeneticsBase SequenceBase pairRNARepressorRNA-dependent RNA polymeraseTranslation (biology)RNA PhagesBiologyRNA-Dependent RNA PolymeraseRibosomeEvolution MolecularProtein BiosynthesisGeneticsProtein biosynthesisNucleic Acid ConformationRNA ViralGeneResearch ArticlePlasmidsNucleic Acids Research
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A Gene-Specific Requirement for FACT during Transcription Is Related to the Chromatin Organization of the Transcribed Region

2006

The FACT complex stimulates transcription elongation on nucleosomal templates. In vivo experiments also involve FACT in the reassembly of nucleosomes traversed by RNA polymerase II. Since several features of chromatin organization vary throughout the genome, we wondered whether FACT is equally required for all genes. We show in this study that the in vivo depletion of Spt16, one of the subunits of Saccharomyces cerevisiae FACT, strongly affects transcription of three genes, GAL1, PHO5, and Kluyveromyces lactis LAC4, which exhibit positioned nucleosomes at their transcribed regions. In contrast, showing a random nucleosome structure, YAT1 and Escherichia coli lacZ are only mildly influenced …

GeneticsChromatin ImmunoprecipitationSaccharomyces cerevisiae ProteinsTranscription GeneticbiologyHigh Mobility Group ProteinsRNA polymerase IIPromoterArticlesSaccharomyces cerevisiaeCell BiologyFACT complexChromatinChromatin remodelingChromatinDNA-Binding ProteinsHistone methylationProtein FACTEscherichia colibiology.proteinTranscriptional Elongation FactorsTranscription factor II DMolecular BiologyRNA polymerase II holoenzymePlasmidsMolecular and Cellular Biology
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