Search results for "Cytochrome"

showing 10 items of 607 documents

Inducing properties of rifampicin and rifabutin for selected enzyme activities of the cytochrome P-450 and UDP-glucuronosyltransferase superfamilies …

1996

Important species differences have been reported concerning the induction properties of rifampicin towards enzymes of the P-450 superfamily. Mice, rabbits and humans are far more responsive than rats and guinea pigs. In the present study a strong induction of cytochrome P-450 3A-dependent enzyme activities was observed in female rat liver microsomes after high dose treatment (> or = 250 mg/kg/day for 9 days) with rifampicin, resulting in an up to 30-fold enhanced hydroxylation rate of testosterone in the 2 beta-, 6 beta- and 15 beta-position in vitro. Other cytochrome P-450 isozyme-selective reactions were not, or only marginally, affected. A steep increase in cytochrome P-450 3A activity o…

Microbiology (medical)RifabutinCYP3AGlucuronidation10050 Institute of Pharmacology and Toxicology610 Medicine & healthPharmacologyBiology2726 Microbiology (medical)Cytochrome P-450 Enzyme Systempolycyclic compoundsmedicineAnimals2736 Pharmacology (medical)TestosteronePharmacology (medical)GlucuronosyltransferaseRats WistarEnzyme inducerAntibiotics AntitubercularAntibacterial agentPharmacologyDose-Response Relationship DrugCytochrome P4502725 Infectious Diseasesbacterial infections and mycosesRatsInfectious Diseases3004 PharmacologyLiverRifabutinMicrosomebiology.protein570 Life sciences; biologyFemaleRifampinRifampicinmedicine.drug
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Phylogenomic evidence for the presence of a flagellum and cbb(3) oxidase in the free-living mitochondrial ancestor.

2011

The initiation of the intracellular symbiosis that would give rise to mitochondria and eukaryotes was a major event in the history of life on earth. Hypotheses to explain eukaryogenesis fall into two broad and competing categories: those proposing that the host was a phagocytotic proto-eukaryote that preyed upon the free-living mitochondrial ancestor (hereafter FMA), and those proposing that the host was an archaebacterium that engaged in syntrophy with the FMA. Of key importance to these hypotheses are whether the FMA was motile or nonmotile, and the atmospheric conditions under which the FMA thrived. Reconstructions of the FMA based on genome content of Rickettsiales representatives-gener…

Midichloria mitochondriiSequence analysiseukaryogenesiMidichloriaFlagellumGenomeOxidative PhosphorylationElectron Transport Complex IVEvolution MolecularPhylogeneticsGeneticsmitochondrionCytochrome c oxidaseSymbiosisMolecular BiologyGeneEcology Evolution Behavior and SystematicsPhylogenyRickettsieaeGeneticsbiologyBase SequencephylogenomicSequence Analysis DNAbiology.organism_classificationBiological EvolutionMitochondriaEukaryotic CellsFlagellabiology.proteinrickettsialeRickettsialesGenome BacterialMolecular biology and evolution
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Characterisation of Lymnaea cubensis, L. viatrix and L. neotropica n. sp., the main vectors of Fasciola hepatica in Latin America, by analysis of the…

2007

Although, in the endemic areas throughout the world, human fascioliasis presents varying patterns in its epidemiology, the species of lymnaeid snail that act as intermediate hosts and vectors are always crucial in the transmission of the causative parasites. Species in the Galba/Fossaria group of snails, such as Lymnaea cubensis, L. viatrix var. A ventricosa, L. viatrix var. B elongata and Galba truncatula, appear to be frequently involved in the transmission of Fasciola hepatica in Central and South America, although specific classification within this morphologically and anatomically confusing group is often very difficult. To explore the potential use of molecular analyses in the identif…

Mitochondrial DNA030231 tropical medicineSnailDisease VectorsDNA MitochondrialDNA Ribosomal030308 mycology & parasitology03 medical and health sciences0302 clinical medicinebiology.animalBotanyparasitic diseasesAnimalsRibosomal DNAGalba truncatulaLymnaea0303 health sciencesbiologyPhylogenetic tree[SDV.BID.EVO]Life Sciences [q-bio]/Biodiversity/Populations and Evolution [q-bio.PE]Cytochrome c oxidase subunit ICentral AmericaRibosomal RNAFasciola hepaticaSouth Americabiology.organism_classificationInfectious DiseasesParasitologyTrematoda
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The mitochondrial genome of fission yeast: inability of all introns to splice autocatalytically, and construction and characterization of an intronle…

1991

In this paper we report the inability of four group I introns in the gene encoding subunit I of cytochrome c oxidase (cox1) and the group II intron in the apocytochrome b gene (cob) to splice autocatalytically. Furthermore we present the characterization of the first cox1 intron in the mutator strain anar-14 and the construction and characterization of strains with intronless mitochondrial genomes. We provide evidence that removal of introns at the DNA level (termed DNA splicing) is dependent on an active RNA maturase. Finally we demonstrate that the absence of introns does not abolish homologous mitochondrial recombination.

Mitochondrial DNARNA MitochondrialRNA SplicingMolecular Sequence DataBiologyDNA MitochondrialGenomeElectron Transport Complex IVConsensus SequenceSchizosaccharomycesGeneticsGroup I catalytic intronAmino Acid SequenceCloning MolecularMolecular BiologyGeneGeneticsBase SequenceIntronRNAGroup II intronCytochromes bCytochrome b GroupIntronsMitochondriaRNA splicingNucleic Acid ConformationRNAApoproteinsMolecular and General Genetics MGG
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Phylogeny of the Drosophila obscura species group deduced from mitochondrial DNA sequences

1994

Approximately 2 kb corresponding to different regions of the mtDNA of 14 different species of the obscura group of Drosophila have been sequenced. In spite of the uncertainties arising in the phylogenetic reconstruction due to a restrictive selection toward a high mtDNA A+T content, all the phylogenetic analysis carried out clearly indicate that the obscura group is formed by, at least, four well-defined lineages that would have appeared as the consequence of a rapid phyletic radiation. Two of the lineages correspond to monophyletic subgroups (i.e., affinis and pseudoobscura), whereas the obscura subgroup remains heterogeneous assemblage that could be reasonably subdivided into at least two…

Mitochondrial DNARNA Transfer LeuRNA Mitochondrialmedia_common.quotation_subjectMolecular Sequence DataBiologyDNA MitochondrialMonophylySpecies SpecificityPhylogeneticsRNA Ribosomal 16SGeneticsAnimalsDrosophila (subgenus)Phyletic gradualismMolecular BiologyPhylogenyRNA Transfer SerEcology Evolution Behavior and Systematicsmedia_commonGene RearrangementGeneticsBase CompositionBase SequencePhylogenetic treeNADH DehydrogenaseSequence Analysis DNACytochrome b Groupbiology.organism_classificationMolecular phylogeneticsRNADrosophilaDrosophila obscura
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Genetic divergence between morphological forms of brown troutSalmo truttaL. in the Balkan region of Macedonia

2010

The objective of this study was to characterize the genetic structure of two Balkan brown trout morphotypes, Salmo macedonicus and Salmo pelagonicus, and to test whether molecular traits support the species’ status proposed by traditional morphological identification. The mitochondrial DNA 12S-rDNA, cyt b and control region genes were sequenced in 15 specimens collected from three localities in the Former Yugoslav Republic of Macedonia. The results of these markers did not support the taxonomic category of species but confirmed the existence of two morphotypes, Salmo trutta macedonicus and Salmo trutta pelagonicus, in the Aegean–Adriatic lineages of the Salmo trutta species complex.

Mitochondrial DNASpecies complexTroutanimal diseasesSettore BIO/05 - ZoologiaZoologyAquatic ScienceDNA MitochondrialBrown troutSalmo truttaAnimalsCluster AnalysisSalmomorphotypemtDNA.PhylogenyEcology Evolution Behavior and SystematicsbiologyEcologyCytochrome bGenetic VariationSequence Analysis DNAbiology.organism_classificationSalmo macedonicusEuropeGenetic divergenceGenetics PopulationFormer Yugoslav Republic of Macedonia (FYRM)HaplotypesGenetic structureJournal of Fish Biology
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Statistical Validation of the Identification of Tuna Species:  Bootstrap Analysis of Mitochondrial DNA Sequences

2002

Sequencing of the mitochondrial cytochrome b gene has been used to differentiate three tuna species: Thunnus albacares (yellowfin tuna), Thunnus obesus (bigeye tuna), and Katsuwonus pelamis (skipjack). A PCR amplified 528 bp fragment from 30 frozen samples and a 171 bp fragment from 26 canned samples of the three species were analyzed to determine the intraspecific variation and the positions with diagnostic value. Polymorphic sites between the species that did not present intraspecific variation were given a diagnostic value. The genetic distance between the sequences was calculated, and a phylogenetic tree was constructed, showing that the sequences belonging to the same species clustered…

Mitochondrial DNAYellowfin tunaMeatMolecular Sequence DataZoologyBigeye tunaDNA MitochondrialSpecies SpecificityAnimalsPhylogenyPolymorphism GeneticBase SequenceSequence Homology Amino AcidPhylogenetic treebiologyTunaCytochrome bReproducibility of ResultsGeneral Chemistrybiology.organism_classificationGenetic distanceEvolutionary biologyGeneral Agricultural and Biological SciencesTunaSequence Alignmenthuman activitiesThunnusJournal of Agricultural and Food Chemistry
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Identification and potential origin of invasive clawed frogsXenopus(Anura: Pipidae) in Sicily based on mitochondrial and nuclear DNA

2013

African clawed frogs of the widespread polytypic species Xenopus laevis Daudin, 1802 (ranging large parts of sub-Saharan Africa) have been spreading since the 1940s, and have established reproductive populations in Europe, Asia and the Americas, where they can have negative impact as competitors of native amphibians and as disease vectors for chytridomycosis or ranaviruses. Here we use two mitochondrial (cytochrome b, 16S rDNA) and one nuclear (RAG 1: Recombination Associated Gene 1) DNA markers to infer the potential origin of invasive clawed frogs from Sicily that represent the largest invasive population in Europe. Identical mtDNA haplotypes match with those of Xenopus laevis, and Sicili…

Mitochondrial DNAeducation.field_of_studybiologyEcologyCytochrome bPipidaeHaplotypePopulationXenopus laeviXenopusZoologyIntroduced speciesbiology.organism_classificationNuclear DNASouth Africainvasive specieAnimal Science and ZoologyeducationPhylogenetic assignmentSicilyItalian Journal of Zoology
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The origin of Swedish and Norwegian populations of the Eurasian harvest mouse (Micromys minutus).

2012

The harvest mouse (Micromys minutus) occurs throughout most of continental Europe. There are also two isolated and recently discovered populations on the Scandinavian peninsula, in Sweden and Norway. Here, we investigate the origin of these populations through analyses of mitochondrial DNA. We found that the two populations on the Scandinavian peninsula have different mtDNA haplotypes. A comparison of our haplotypes to published sequences from most of Europe showed that all Swedish and Norwegian haplotypes are most closely related to the haplotypes in harvest mice from Denmark. Hence, the two populations seem to represent independent colonisations but originate from the same geographical ar…

Mitochondrial DNAgeographygeography.geographical_feature_categoryCytochrome bEcologyHaplotypeZoologyNorwegianBiologybiology.organism_classificationlanguage.human_languagePhylogeographyAnimal ecologyPeninsulalanguageAnimal Science and ZoologyMicromys minutusEcology Evolution Behavior and Systematics
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Mutations of mitochondrial DNA and human death.

1990

In the skeletal muscle of patients with mitochondrial myopathies (Kearns-Sayre syndrome and chronic progressive external ophthalmoplegia) and in the heart and skeletal muscle of healthy persons cells lacking cytochrome c oxidase are found. The respiratory-defective cells have the following features in common: onset of the defect at juvenile or adult age; progressive character of the defect with increasing age; and focal pattern of respiratory-deficient cells (fibers). A statistic mutation of mtDNA in affected cells is suggested to cause the defect of mitochondrial function. It is postulated that the continuous accumulation of respiratory-deficient cells, mainly in the human heart with incre…

Mitochondrial DNAmedicine.medical_specialtyCytochrome-c Oxidase DeficiencyMitochondrionBiologyHuman mitochondrial geneticsDNA MitochondrialMitochondria HeartKearns–Sayre syndromeElectron Transport Complex IVMitochondrial myopathyMuscular DiseasesReference ValuesInternal medicinemedicineAnimalsHumansEcology Evolution Behavior and SystematicsGeneticsMammalsHomoplasmySkeletal muscleGeneral Medicinemedicine.diseaseMitochondria MuscleDeathEndocrinologymedicine.anatomical_structureMutationChronic progressive external ophthalmoplegiaDie Naturwissenschaften
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