Search results for "Neurospora"

showing 10 items of 24 documents

Sedimentation properties of chitosomal chitin synthetase from the wild-type strain and the 'slime' variant of Neurospora crassa.

1989

Marked differences in the pattern of sedimentation of cellular structures were observed after isopycnic centrifugation of crude cell-free preparations from the Neurospora crassa wall-less 'slime' variant and mycelial wild-type strain. Kinetic studies of particle sedimentation showed that the various types of subcellular components, as revealed by turbidity, UV absorption, polypeptide patterns, and chitin synthetase activity determinations, sediment independently of one another. An important feature was the finding that chitin synthetase from 'slime' peaked at a median specific gravity of 1.1201 +/- 0.0036, whereas that from wild-type strain sedimented at a higher buoyant density (specific g…

BiophysicsCentrifugation IsopycnicBiochemistryNeurospora crassaCell wallchemistry.chemical_compoundChitinCentrifugation Density GradientMolecular BiologyPolyacrylamide gel electrophoresisSpecific GravityDifferential centrifugationChitin SynthaseOrganellesbiologyStrain (chemistry)Neurospora crassafungiCrassaGenetic VariationSedimentationbiology.organism_classificationcarbohydrates (lipids)Molecular WeightKineticsMicroscopy ElectronNeurosporaBiochemistrychemistryGlucosyltransferasesElectrophoresis Polyacrylamide GelSpectrophotometry UltravioletBiochimica et biophysica acta
researchProduct

Separation of chitosomes and secretory vesicles from the ?slime? variant of Neurospora crassa

1987

Cells from the “slime” variant of Neurospora crassa were broken in isotonic conditions by use of triethanolamine buffer plus EDTA. After removal of large membranous structures by low-speed centrifugation, chitosomes and secretory vesicles were separated by means of gel filtration, precipitation of membranous contaminants with Concanavalin A, and centrifugation in sucrose or glycerol gradients. Polypeptidic composition of fractions enriched in secretory vesicles or chitosomes was found to be distinct. By these criteria we concluded that chitosomes and secretory vesicles represent different populations of microvesicles. Both microvesicular populations appeared free of endoplasmic reticulum an…

biologyEndoplasmic reticulumGeneral Medicinebiology.organism_classificationBiochemistryMicrobiologyNeurosporaSecretory VesicleMicrovesiclesNeurospora crassaInvertaseBiochemistryConcanavalin AGeneticsbiology.proteinCentrifugationMolecular BiologyArchives of Microbiology
researchProduct

Demonstration of dihydro-orotate dehydrogenase inNeurospora crassa hyphae with a cytochemical procedure

1971

Dihydro-orotate dehydrogenase activity was demonstrated in the hyphae of the fungusNeurospora crassa by a cytochemical technique. The activity was slightly stronger in the hyphal tips thus demonstrating the more intense metabolic activity in these parts of the mycelium. Several control reactions showed that the staining reaction was specific.

Orotic AcidMicroscopyFormatesStaining and LabelingbiologyHyphaHistocytochemistryChemistryfungiCrassaDehydrogenaseCell BiologyDihydro-orotate dehydrogenasebiology.organism_classificationStainingNeurosporaBiochemistryAnatomyOxidoreductasesMetabolic activityAzo CompoundsDevelopmental biologyMyceliumThe Histochemical Journal
researchProduct

Effects of acclimation time and epigenetic mechanisms on growth of Neurospora in fluctuating environments

2017

AbstractReaction norms or tolerance curves have often been used to predict how organisms deal with fluctuating environments. A potential drawback is that reaction norms measured in different constant environments may not capture all aspects of organismal responses to fluctuating environments. We examined growth of the filamentous fungusNeurospora crassain fluctuating temperatures and tested if growth in fluctuating temperatures can be explained simply by growth in different constant temperatures or if more complex models are needed. In addition, as previous studies on fluctuating environments have revealed that past temperatures that organisms have experienced can affect their response to c…

0106 biological sciences0301 basic medicineAcclimatizationMutantEnvironmentMethylation010603 evolutionary biology01 natural sciencesAcclimatizationNeurosporaArticleEpigenesis GeneticNeurospora crassaHistones03 medical and health sciencesGeneticsEpigeneticsGenetics (clinical)030304 developmental biology0303 health sciencesbiologyCell CyclefungiTemperatureAcetylationDNA MethylationModels Theoreticalbiology.organism_classificationFilamentous fungusNeurospora030104 developmental biologyRNA Interference PathwayH3k4 methylationDNA methylationBiophysicsGene-Environment InteractionRNA Interference
researchProduct

Calcium, calmodulin-dependent protein phosphorylation in Neurospora crassa

1984

Abstract A calcium, calmodulin-dependent protein kinase activity has been partially purified by calmodulin-Sepharose affinity chromatography from the soluble fraction of Neurospora crassa . The phosphorylated peptide has an apparent molecular mass on SDS-polyacrylamide gel of 47 kDa. The apparent half maximal phosphorylation is obtained after 1.5 min at 30° C in the presence of calcium and calmodulin. The apparent half maximal activation of the phosphorylation is obtained at 1 μM calcium, and 0.1 or 0.2 μM calmodulin from bovine brain or Neurospora , respectively. The 32 P incorporation is enhanced about 10-fold by calmodulin.

[SDE] Environmental SciencesCalmodulin[SDV]Life Sciences [q-bio]Biophysicschemistry.chemical_elementCalciumBiochemistryNeurosporaProtein kinaseNeurospora crassa03 medical and health sciencesAffinity chromatographyCalmodulinStructural BiologyGenetics[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyProtein phosphorylation[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyProtein kinase AMolecular BiologyComputingMilieux_MISCELLANEOUS030304 developmental biology0303 health sciencesbiologyNeurospora crassa030306 microbiologyCell Biologybiology.organism_classification[SDV] Life Sciences [q-bio]chemistryBiochemistry[SDE]Environmental Sciencesbiology.proteinPhosphorylationCalcium
researchProduct

Molecular cloning of the RPS0 gene from Candida tropicalis.

2001

The Saccharomyces cerevisiae RPS0 A and B genes encode proteins essential for maturation of the 40S ribosomal subunit precursors. We have isolated a homologue of the RPS0 gene from Candida tropicalis, which we named CtRPS0. The C. tropicalisRPS0 encodes a protein of 261 amino acid residues with a predicted molecular weight of 28.65 kDa and an isoelectric point of 4.79. CtRps0p displays significant amino acid sequence homology with Rps0p from C. albicans, S. cerevisiae, Neurospora crassa, Schizosaccharomyces pombe, Pneumocystis carinii and higher organisms, such as human, mouse and rat. CtRPS0 on a high copy number vector can complement the lethal phenotype linked to the disruption of both R…

Ribosomal ProteinsSaccharomyces cerevisiaeGenes FungalMolecular Sequence DataBioengineeringSaccharomyces cerevisiaeBiologyApplied Microbiology and BiotechnologyBiochemistryNeurospora crassaCandida tropicalisFungal ProteinsRibosomal proteinGeneticsAmino Acid SequenceCloning MolecularGeneSouthern blotCandidaGeneticsBase SequenceSequence Homology Amino AcidGenetic Complementation TestNucleic acid sequencebiology.organism_classificationSchizosaccharomyces pombeProtein Processing Post-TranslationalBiotechnologyYeast (Chichester, England)
researchProduct

Self-assembly properties of the proteinaceous coat secreted by the ?slime? variant of Neurospora crassa

1989

The proteinaceous extracellular material (PEM) synthesized by the cells of the ‘slime” strain of Neurospora crassa (see Martinez et al. 1989) was solubilized by treatment with urea or guanidine. Removal of these chemicals by dialysis, caused reassembly of the solubilized proteins into material with the same microscopic appearance as the original PEM. Polypeptide patterns from both native and reassembled structures were identical. Dialysis-mediated reassembly of the solubilized proteins appeared to be dependent on both concentration of the soluble macromolecules and time. Gel chromatography of PEM solubilized with different agents revealed two discrete populations of complexes with molecular…

chemistry.chemical_classificationGel electrophoresisbiologyGeneral Medicinebiology.organism_classificationBiochemistryMicrobiologyIn vitroNeurospora crassaGel permeation chromatographychemistry.chemical_compoundchemistryBiochemistryGeneticsExtracellularGuanidineGlycoproteinMolecular BiologyMacromoleculeArchives of Microbiology
researchProduct

Further characterization of the histidine gene cluster of Streptomyces coelicolor A3(2): nucleotide sequence and transcriptional analysis of hisD.

1992

We have further characterized the genomic region of Streptomyces coelicolor A3(2) that contains genes involved in the biosynthesis of histidine. A 2,357-base pair fragment contained in plasmid pSCH3328 that complemented hisD mutations has been sequenced. Computer analysis revealed an open reading frame that encodes a protein with significant homology to the Escherichia coli, Salmonella typhimurium and Mycobacterium smegmatis hisD product, Saccharomyces cerevisiae HIS4C, and Neurospora crassa his3 gene products. Two other contiguous open reading frames oriented divergently with respect to hisD did not show significant similarity with any of the his genes or to other sequences included in the…

GeneticsDNA BacterialbiologyBase SequenceTranscription GeneticStreptomyces coelicolorMolecular Sequence DataRestriction MappingNucleic acid sequenceGeneral MedicineIn Vitro Techniquesbiology.organism_classificationMicrobiologyPrimer extensionStreptomycesNeurospora crassaOpen reading frameOpen Reading FramesCistronGenes BacterialGene clusterHistidineMolecular BiologyGene
researchProduct

Separation of chitosomal chitin synthetase from cell-free extracts ofNeurospora crassa “Slime” variant agglutinated with concanavalin A

1989

Cell-free extracts of the wall-less slime variant ofNeurospora crassa were treated with concanavalin A (Con A); this treatment caused a massive agglutination of the particulate structures in the cell-free homogenate, although most (73%) of the chitin synthetase initially present in the cell-free extract remained in the supernatant obtained after sedimentation of the lectin-flocculated material. This chitin synthetase showed the sedimentation properties of chitosomes (unique microvesicular structures) and failed to bind [3H]Con A. A significant percentage (42%) of the chitin synthetase activity associated with the Con A-flocculated material probably corresponds to mechanically trapped chitos…

chemistry.chemical_classificationbiologyfungiGeneral MedicineChitin synthasebiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyNeurospora crassaCell wallAgglutination (biology)chemistry.chemical_compoundEnzymeBiochemistryChitinchemistryConcanavalin Abiology.proteinUltracentrifugeCurrent Microbiology
researchProduct

Analysis of the polypeptide composition of the cell walls of Neurospora crassa. Similarities with the proteinaceous material secreted by the slime va…

1991

The polypeptide composition of cell walls from the wild-type strain of Neurospora crassa is compared with that of the proteinaceous extracellular coat (PEM) secreted by the slime strain of this fungus. Analyses included determination of the polypeptide pattern by polyacrylamide gel electrophoresis and blotting followed by staining with Concanavalin A and antibodies raised against the overall antigenic components present in either (whole cell walls or PEM) structure. A complex protein assortment was found associated to the walls of the wild type strain. The similarities observed between the polypeptide patterns of the cell walls and PEM, in addition to the immunological cross-reactivity exhi…

Strain (chemistry)biologyPlant Sciencebiology.organism_classificationNeurospora crassaStainingCell wallBiochemistryConcanavalin AGeneticsbiology.proteinExtracellularSecretionPolyacrylamide gel electrophoresisEcology Evolution Behavior and SystematicsBiotechnologyMycological Research
researchProduct