Search results for "spore"

showing 10 items of 252 documents

Aproximación a las comunidades de carófitos que existieron en la albufera de valencia a partir del estudio de las oósporas del sedimento

2009

14 páginas, 8 figuras, 3 tablas.

CarófitosTolypellaEspañaPlant ScienceValènciaNitellaCharaCharophytCarófitos; Oósporas; La Albufera; Valencia; España; Chara; Nitella; Tolypella; LamprothamniumAbundance (ecology)lcsh:BotanyBotany:CIENCIAS DE LA VIDA::Biología vegetal (Botánica) ::Biología marina [UNESCO]BalticaLamprothamniumNitellaEcology Evolution Behavior and SystematicsCharabiologyL’AlbuferaEcologySedimentLa AlbuferaVegetationOosporesOósporasbiology.organism_classificationlcsh:QK1-989SpainOosporeUNESCO::CIENCIAS DE LA VIDA::Biología vegetal (Botánica) ::Biología marinaValenciaCharophyteEutrophication
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Cytology of Thamnidium elegans Link. II. Distribution and behaviour of nuclei in hyphae, sporangiophores and sporangiospores.

1976

The resting nuclei in hyphae, sporangiophores and sporangiospores of sporangia and sporangiola of Thamnidium elegans consist of a large centrals nucleolus and a shell of chromatin surrounding the nucleolus. Division of the nucleus in hyphae and sporangiospores is achieved by elongation and constriction.

Cell NucleusHyphaNucleolusSporangiumFungiGeneral MedicineThamnidium elegansBiologySpores FungalBiochemistryMicrobiologyCell biologyNuclear divisionmedicine.anatomical_structureCytologyGeneticsmedicineMucoralesMolecular BiologyNucleusCell DivisionArchives of microbiology
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Hemin induces germ tube formation in Candida albicans.

1997

Hemin induced germination of Candida albicans blastoconidia when cells grown up to the early exponential phase were shifted from 28 to 37 degrees C (70 to 75% of cells exhibited germ tubes). N-Acetyl-D-glucosamine (GlcNAc), another inducer of myceliation in this fungus, caused a similar effect. The combination of hemin and GlcNAc resulted in a higher percentage (95%) of blastoconidial germination. These results suggest that in addition to temperature, hemin levels and carbon source may coordinately regulate the expression of subsets of genes involved in the yeast-to-mycelium transition in C. albicans.

Cellular differentiationImmunologyGerm tubeBiologyMicrobiologyBlastoconidiumMicrobiologyAcetylglucosaminechemistry.chemical_compoundCandida albicansInducerDrug InteractionsCandida albicansDose-Response Relationship DrugCell DifferentiationSpores Fungalbiology.organism_classificationYeastCorpus albicansInfectious DiseasesGlucosechemistryHeminParasitologyHeminResearch ArticleInfection and immunity
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Dimethylsulfoxide as carrier in enzyme cytochemistry.

1971

Addition of dimethylsulfoxide (DMSO) to the incubation medium of succinate dehydrogenase in a concentration of 10% enhances the staining reaction in the hyphae of the fungus Cercosporella herpotrichoides after an incubation period of 15 min. Controls without DMSO remain unstained. DMSO causes a rapid penetration of the components of the medium through the mucilage that covers the hyphae.

CercosporellaHistologyintegumentary systembiologyHyphaStaining and LabelingHistocytochemistryorganic chemicalsSuccinate dehydrogenasefungiCell BiologyStainingIncubation periodMedical Laboratory TechnologyBiochemistryMucilagebiology.proteinCytochemistryDimethyl SulfoxideMitosporic FungiMolecular BiologyIncubationHistochemie. Histochemistry. Histochimie
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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)
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Photobiology in space: An experiment on Spacelab I

1984

The joint European/US Spacelab Mission I, scheduled for October 1983 for a 9 day lasting Earth-orbiting flight, provides a laboratory system for various disciplines of science, including exobiology. On the pallet, in the experiment ES 029 "Microorganisms and Biomolecules in Space Hard Environment" 316 dry samples of Bacillus subtilis spores will be exposed to space vacuum and/or selected wavelenghs of solar UV radiation. After recovery action spectra of inactivation, mutation induction, reparability and photochemical damage in DNA and protein will be determined. The results will contribute to the understanding of the mechanism of the increased UV sensitivity of bacterial spores in vacuo and…

DNA BacterialSpores BacterialPhysicsRecovery - actionExtraterrestrial EnvironmentUltraviolet RaysGeneral MedicineSpace FlightAgricultural and Biological Sciences (miscellaneous)United StatesUv sensitivityAstrobiologyEuropeBacterial ProteinsPhotobiologySpace and Planetary ScienceMutationGeneral Earth and Planetary SciencesInterplanetary spaceflightEcology Evolution Behavior and SystematicsBacillus subtilisGeneral Environmental ScienceMutation inductionOrigins of Life
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Response ofBacillus subtilis spores to dehydration and UV irradiation at extremely low temperatures

1996

Spores of Bacillus subtilis have been exposed to the conditions of extreme dehydration (argon/silica gel; simulated space vacuum) for up to 12 weeks at 298 K and 80 K in the dark. The inactivation has been correlated with the production of DNA-double strand-breaks. The temperature-dependence of the rate constants for inactivation or production of DNA-double strand-breaks is surprisingly low. Controls kept in the frozen state at 250 K for the same period of time showed no sign of deterioration. In another series of experiments the spores have been UV irradiated (253.7 nm) at 298 K, 200 K and 80 K after exposure to dehydrating conditions for 3 days. Fluence-effect relationships for inactivati…

DNA BacterialVacuumUltraviolet Rayschemistry.chemical_elementBacillus subtilisPhotochemistrychemistry.chemical_compoundReaction rate constantmedicineDehydrationIrradiationEcology Evolution Behavior and SystematicsSpores BacterialBacteriological TechniquesArgonbiologyChemistrySilica gelGeneral Medicinemedicine.diseasebiology.organism_classificationSporeCold TemperatureBiochemistrySpace and Planetary ScienceBacillus subtilisDNA DamageOrigins of Life and Evolution of the Biosphere
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Identification of the mstE Gene Encoding a Glucose-inducible, Low Affinity Glucose Transporter in Aspergillus nidulans

2006

The mstE gene encoding a low affinity glucose transporter active during the germination of Aspergillus nidulans conidia on glucose medium has been identified. mstE expression also occurs in hyphae, is induced in the presence of other repressing carbon sources besides glucose, and is dependent on the function of the transcriptional repressor CreA. The expression of MstE and its subcellular distribution have been studied using a MstE-sGFP fusion protein. Concordant with data on mstE expression, MstE-sGFP is synthesized in the presence of repressing carbon sources, and fluorescence at the periphery of conidia and hyphae is consistent with MstE location in the plasma membrane. Deletion of mstE …

DNA ComplementaryDatabases FactualMonosaccharide Transport ProteinsRecombinant Fusion ProteinsGlucose uptakeGenes FungalGreen Fluorescent ProteinsMolecular Sequence DataHyphaeRepressorBiochemistryAspergillus nidulansSubstrate SpecificityFungal ProteinsCell membraneAspergillus nidulansGene Expression Regulation FungalmedicineAmino Acid SequenceMolecular BiologyGenePhylogenyExpressed Sequence TagsFungal proteinbiologyCell MembranefungiGlucose transporterCell BiologySpores FungalBlotting Northernbiology.organism_classificationFusion proteinRepressor ProteinsKineticsGlucosemedicine.anatomical_structureMicroscopy FluorescenceBiochemistryGene DeletionJournal of Biological Chemistry
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Lack of phosphoserine phosphatase activity alters pollen and tapetum development in Arabidopsis thaliana.

2015

Formation of mature pollen grain, an essential process for the reproduction of higher plants, is affected in lines that are deficient in the enzymes of the phosphorylated pathway of serine biosynthesis (PPSB). Mutants of phosphoserine phosphatase (PSP), the enzyme that catalyses the last step of PPSB, are embryo-lethal. When they are complemented with a construct carrying PSP1 cDNA under the control of the 35S promoter (psp1.1 35S:PSP1), which is poorly expressed in anther tissues, plants display a wild-type phenotype, but are male-sterile. The pollen from the psp1.1 35S:PSP1 lines are shrunken and unviable. Here we report the morphological alterations that appear in the psp1.1 35S:PSP1 lin…

DNA ComplementaryStamenArabidopsisPlant ScienceFlowersBiologymedicine.disease_causePollen coatMicrosporePollenGeneticsmedicineSerineArabidopsis thalianaPlant OilsPollinationPromoter Regions GeneticPlant ProteinsTapetumfood and beveragesPhosphoserine phosphataseGeneral Medicinebiology.organism_classificationPlants Genetically ModifiedPhosphoric Monoester HydrolasesBiochemistryPollenAgronomy and Crop SciencePollen wallPlant science : an international journal of experimental plant biology
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Evaluation of a Real-Time PCR Assay for the Detection and Quantification of Group Spores in Food

2010

A procedure based on quantitative real-time PCR was evaluated for the detection and quantification of Bacillus cereus spores. Several methods for DNA isolation, such as various heat treatments and germination solutions, were evaluated on spore suspensions of representative strains of the B. cereus group. Overall, the commercially available DNeasy tissue kit yielded the maximum amount of DNA. The procedure also was used to construct calibration curves for different food matrices, with a wide spore quantification range of 5 log units using serial dilutions of spore suspensions of B. cereus CECT 148T. The detection limit for B. cereus in artificially contaminated liquid egg and reconstituted i…

Detection limitChromatographySerial dilutionfungiBacillus cereusBiologybiology.organism_classificationMicrobiologyEndosporeDNA extractionMicrobiologySporeCereusGerminationFood ScienceJournal of Food Protection
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