Search results for "Fungal Genetics"

showing 10 items of 52 documents

Characterization of a glycosylphosphatidylinositol-bound cell-wall protein (GPI-CWP) in Yarrowia lipolytica.

2004

The structure and composition of the cell wall of yeast has so far been studied mainly in Saccharomyces cerevisiae. It is basically made up of three components: beta-glucans, chitin and mannose-containing glycoproteins, also called mannoproteins. Most covalently bound cell-wall mannoproteins belong to the so-called glycosylphosphatidylinositol cell-wall protein (GPI-CWP) family, cell-wall proteins that are bound through the remnant of a GPI residue to 1,6-beta-glucan. The non-conventional yeast Yarrowia lipolytica shares Generally Regarded As Safe (GRAS) status with S. cerevisiae, has some industrial applications and is increasingly being proposed as a host for the production of recombinant…

Signal peptideSaccharomyces cerevisiae ProteinsGlycosylphosphatidylinositolsSaccharomyces cerevisiaeGenes FungalMolecular Sequence DataYarrowiaSaccharomyces cerevisiaeBiologyMicrobiologyGene productFungal ProteinsSpecies SpecificityCell WallAmino Acid SequenceDNA FungalPeptide sequencechemistry.chemical_classificationMembrane GlycoproteinsBase SequenceSequence Homology Amino AcidFungal geneticsMembrane ProteinsYarrowiabiology.organism_classificationYeastcarbohydrates (lipids)BiochemistrychemistryGlycoproteinMicrobiology (Reading, England)
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Eukaryotic tRNAs(Pro): primary structure of the anticodon loop; presence of 5-carbamoylmethyluridine or inosine as the first nucleoside of the antico…

1990

The modified nucleoside U*, located in the first position of the anticodon of yeast, chicken liver and bovine liver tRNA(Pro) (anticodon U*GG), has been determined by means of TLC, HPLC, ultraviolet spectrum and gas chromatography-mass spectrometry. The structure was established as 5-carbamoylmethyluridine (ncm5U). In addition, we report on the primary structures of the above-mentioned tRNAs as well as those which have the IGG anticodon. In yeast, the two tRNA(Pro) (anticodons U*GG and IGG) differ by eight nucleotides, whereas in chicken and in bovine liver, both anticodons are carried by the same 'body tRNA' with one posttranscriptional exception at position 32, where pseudouridine is asso…

StereochemistryMolecular Sequence DataBiophysicsBiologyBiochemistryPseudouridinechemistry.chemical_compoundRNA Transfer ProRNA TransferStructural BiologyYeastsGeneticsmedicineAnticodonAnimalsNucleotideInosineUridinechemistry.chemical_classificationChromatographyBase SequenceMolecular StructureProtein primary structureFungal geneticsRNARNA FungalRNA Transfer Amino Acid-SpecificInosinechemistryBiochemistryTransfer RNANucleic Acid ConformationCattleSpectrophotometry UltravioletNucleosideChickensmedicine.drugBiochimica et biophysica acta
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The POT1 gene for yeast peroxisomal thiolase is subject to three different mechanisms of regulation

1992

The Saccharomyces cerevisiae POT1 gene is, as are other yeast peroxisomal protein genes, inducible by fatty acids and repressible by glucose. We have now found that it is also induced during the stationary phase of the culture. To investigate these three regulatory circuits, we have studied the mRNA levels of regulatory mutants as well as the changes in chromatin structure upon gene activation. We conclude that the regulation of transcriptional activity in glucose repression, oleate induction, and stationary phase induction follow different molecular mechanisms. We suggest that this multiplicity of regulatory mechanisms may represent a general rule for the yeast peroxisomal protein genes.

Transcriptional ActivationTranscription GeneticGenes FungalSaccharomyces cerevisiaeMutantOleic AcidsSaccharomyces cerevisiaeMicrobodiesMicrobiologyGene Expression Regulation FungalGene expressionRNA MessengerAcetyl-CoA C-AcetyltransferaseMolecular BiologyGeneRegulation of gene expressionbiologyCell CycleFungal geneticsRNA FungalPeroxisomebiology.organism_classificationChromatinChromatinGlucoseBiochemistryOleic AcidMolecular Microbiology
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Wickerhamomyces sylviae f.a., sp. nov., an ascomycetous yeast species isolated from migratory birds.

2013

In the present work, we investigated the phylogenetic position and phenotypic characteristics of eight yeast isolates collected from migratory birds on the island of Ustica, Italy. A phylogenetic analysis based on the D1/D2 region of the large-subunit rRNA gene showed that all isolates clustered as a single separate lineage within the Wickerhamomyces clade. They exhibited distinct morphological and physiological characteristics and were clearly separated from their closest relatives, Wickerhamomyces lynferdii, Wickerhamomyces anomalus and Wickerhamomyces subpelliculosus, in blastn searches. On the basis of the isolation source, physiological features and molecular strain typing carried out …

Wickerhamomyces anomalusLineage (evolution)Molecular Sequence DataWickerhamomyces; Birds; YeastZoologyMinisatellite RepeatsBiologyWickerhamomyceMicrobiologyBirdsWickerhamomycesBirdPhylogeneticsBotanyRibosome SubunitsAnimalsDNA FungalMycological Typing TechniquesEcology Evolution Behavior and SystematicsPhylogenyIslandsPhylogenetic treeFungal geneticsDNAGeneral MedicineSequence Analysis DNARibosomal RNARibosome Subunits Large EukaryoticDNA FingerprintingYeastRAPDRandom Amplified Polymorphic DNA TechniqueFungalAnimal Migration; Animals; Birds; DNA Fingerprinting; DNA Fungal; Islands; Italy; Minisatellite Repeats; Molecular Sequence Data; Mycological Typing Techniques; Random Amplified Polymorphic DNA Technique; Ribosome Subunits Large Eukaryotic; Saccharomycetales; Sequence Analysis DNA; PhylogenyItalySaccharomycetalesLargeEukaryoticAnimal MigrationSequence AnalysisSettore AGR/16 - Microbiologia AgrariaInternational journal of systematic and evolutionary microbiology
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Rapid identification of wine yeast species based on RFLP analysis of the ribosomal internal transcribed spacer (ITS) region

1998

In this study, we identified a total of 33 wine yeast species and strains using the restriction patterns generated from the region spanning the internal transcribed spacers (ITS 1 and 2) and the 5.8S rRNA gene. Polymerase chain reaction (PCR) products of this rDNA region showed a high length variation for the different species. The size of the PCR products and the restriction analyses with three restriction endonucleases (HinfI, CfoI, and HaeIII) yielded a specific restriction pattern for each species with the exception of the corresponding anamorph and teleomorph states, which presented identical patterns. This method was applied to analyze the diversity of wine yeast species during sponta…

WineBiologyDNA RibosomalBiochemistryMicrobiologyHaeIIIYeastsGeneticsmedicineInternal transcribed spacerDNA FungalMolecular BiologyGeneticsFungal geneticsfood and beveragesRNA FungalGeneral MedicineSpacer DNARibosomal RNARNA Ribosomal 5.8SRestriction enzymeYeast in winemakingFermentationRestriction fragment length polymorphismPolymorphism Restriction Fragment Lengthmedicine.drugArchives of Microbiology
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Two new species of the genus Ochroconis, O. lascauxensis and O. anomala isolated from black stains in Lascaux Cave, France

2012

In the year 2001, some conspicuous black stains appeared on the walls of Lascaux Cave in France, which progressively disseminated throughout the cave. These black stains were so evident by 2007 that they have become one of the cave's major problems. In a mycological study of the black stains, Ochroconis strains were abundant among the isolates and constituted the major group of melanised fungi. Two new species of the genus Ochroconis, O. lascauxensis and O. anomala, were isolated and described. The description is based on the morphology of the fungi and the phylogenetic relationships of two of its gene regions internal transcribed spacer (ITS) and RNA polymerase II subunit B (RPB2). In addi…

[SDV]Life Sciences [q-bio]Molecular Sequence DataDNA Ribosomal03 medical and health sciencesCaveAscomycotaPhylogeneticsBotanyDNA Ribosomal SpacerGeneticsInternal transcribed spacerAnomalaDNA FungalEcology Evolution Behavior and SystematicsPhylogeny[SDV.MP.MYC]Life Sciences [q-bio]/Microbiology and Parasitology/Mycology030304 developmental biologyBlack stains0303 health sciencesgeographygeography.geographical_feature_categorybiologyAscomycotaOchroconis anomala030306 microbiologyFungal geneticsLascaux CaveOchroconis lascauxensisbiology.organism_classification[SDV.MP.MYC] Life Sciences [q-bio]/Microbiology and Parasitology/Mycology3. Good healthCavesInfectious DiseasesOchroconis lascauxensisOchroconis anomala[SDE]Environmental SciencesPaintingsFrance
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The Largest Subunit of RNA Polymerase II as a New Marker Gene to Study Assemblages of Arbuscular Mycorrhizal Fungi in the Field

2014

Due to the potential of arbuscular mycorrhizal fungi (AMF, Glomeromycota) to improve plant growth and soil quality, the influence of agricultural practice on their diversity continues to be an important research question. Up to now studies of community diversity in AMF have exclusively been based on nuclear ribosomal gene regions, which in AMF show high intra-organism polymorphism, seriously complicating interpretation of these data. We designed specific PCR primers for 454 sequencing of a region of the largest subunit of RNA polymerase II gene, and established a new reference dataset comprising all major AMF lineages. This gene is known to be monomorphic within fungal isolates but shows an…

[SDV]Life Sciences [q-bio]lcsh:MedicineDNA barcodinglaw.inventionGlomeromycotaPlant MicrobiologylawMycorrhizaeCommunity Assemblylcsh:SciencePolymerase chain reactionPhylogenyGeneticsPrincipal Component AnalysisMultidisciplinaryEcologycroissance des plantesFungal geneticsAgricultureBiodiversityExonsSoil EcologyCommunity Ecology[SDE]Environmental SciencesRNA Polymerase IIResearch ArticleSequence analysisGenes FungalMolecular Sequence DataSoil ScienceMycologyBiologychampignon mycorhizienMarker geneMicrobiologyZea mayspcrMutualismBotany[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyDNA Barcoding TaxonomicGlomeromycotalcsh:RfungiEcology and Environmental SciencesBiology and Life SciencesRibosomal RNAbiology.organism_classificationSpecies InteractionsProtein SubunitsPyrosequencinglcsh:QMycorrhizaAgronomic Ecologyqualité du solAgroecologyPLoS ONE
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Glucose uptake in germinating Aspergillus nidulans conidia: involvement of the creA and sorA genes

2003

d-Glucose uptake in germinating wild-typeAspergillus nidulansconidia is an energy-requiring process mediated by at least two transport systems of differing affinities for glucose: a low-affinity system (Km∼1·4 mM) and a high-affinity system (Km∼16 μM). The low-affinity system is inducible by glucose; the high-affinity system is subject to glucose repression effected by the carbon catabolite repressor CreA and is absent insorA3mutant conidia, which exhibit resistance tol-sorbose toxicity. An intermediate-affinity system (Km∼400 μM) is present insorA3conidia germinating in derepressing conditions.creAderepressed mutants show enhanced sensitivity tol-sorbose. The high-affinity uptake system ap…

biologyGlucose uptakeGenes FungalMutantFungal geneticsCatabolite repressionBiological Transport ActiveRepressorCarbohydrate metabolismbiology.organism_classificationMicrobiologyAspergillus nidulansConidiumFungal ProteinsRepressor ProteinsKineticsGlucoseBiochemistryDrug Resistance FungalAspergillus nidulansMutationSorboseMicrobiology
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ERA-experiment “space biochemistry”

1995

Abstract The general goal of the experiment was to study the response of anhydrobiotic (metabolically dormant) microorganisms (spores of Bacillus subtilis, cells of Deinococcus radiodurans, conidia of Aspergillus species) and cellular constituents (plasmid DNA, proteins, purple membranes, amino acids, urea) to the extremely dehydrating conditions of open space, in some cases in combination with irradiation by solar UV-light. Methods of investigation included viability tests, analysis of DNA damages (strand breaks, DNA-protein cross-links) and analysis of chemical effects by spectroscopic, electrophoretic and chromatographic methods. The decrease in viability of the microorganisms was as exp…

chemistry.chemical_classificationAtmospheric SciencebiologyDNA damageChemistryMicroorganismFungal geneticsAerospace EngineeringAstronomy and AstrophysicsDeinococcus radioduransBacillus subtilisbiology.organism_classificationAmino acidchemistry.chemical_compoundGeophysicsBiochemistrySpace and Planetary ScienceUreaGeneral Earth and Planetary SciencesDNAAdvances in Space Research
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Validation and application of a PCR primer set to quantify fungal communities in the soil environment by real-time quantitative PCR

2011

Fungi constitute an important group in soil biological diversity and functioning. However, characterization and knowledge of fungal communities is hampered because few primer sets are available to quantify fungal abundance by real-time quantitative PCR (real-time Q-PCR). The aim in this study was to quantify fungal abundance in soils by incorporating, into a real-time Q-PCR using the SYBRGreen (R) method, a primer set already used to study the genetic structure of soil fungal communities. To satisfy the real-time Q-PCR requirements to enhance the accuracy and reproducibility of the detection technique, this study focused on the 18S rRNA gene conserved regions. These regions are little affec…

fungal abundance organic carbon content real-time Q-PCR length polymorphism SYBRGreen method type de sol[SDV]Life Sciences [q-bio]lcsh:MedicinePlant SciencePlant Roots18S ribosomal RNASYBRGreen methodtype de sol[ SDE ] Environmental SciencesSoilFungal Reproductionlcsh:ScienceDNA FungalPhylogenyorganic carbon content2. Zero hunger0303 health sciencesDiversityMultidisciplinaryfungal abundanceEcologyEcologyRevealsFungal geneticsPolymerase-chain-reactionAgricultureBiodiversityAmpliconSoil Ecologysoil texture amplification enzymatique de l'adnBacterial communitiesSamplesreal-time Q-PCRCommunity Ecology[SDE]Environmental SciencesRhizosphereResearch ArticleSoil textureIn silicoMolecular Sequence DataSoil ScienceComputational biologyMycologyBiologyReal-Time Polymerase Chain ReactionMicrobiologyMicrobial Ecology03 medical and health sciencesSpecies SpecificityMedicago truncatulaMicrobial communityRNA Ribosomal 18SSoil ecologyBiology030304 developmental biologyDNA PrimersRibosomal-Rna genes[ SDV ] Life Sciences [q-bio]030306 microbiologylcsh:RFungiBotanyReproducibility of Resultslength polymorphismsoil textureSequence Analysis DNADna15. Life on landamplification enzymatique de l'adnDNA extractionlcsh:QPrimer (molecular biology)
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