Search results for "ALBI"

showing 10 items of 440 documents

In Candida parapsilosis the ATC1 Gene Encodes for an Acid Trehalase Involved in Trehalose Hydrolysis, Stress Resistance and Virulence

2014

An ORF named CPAR2-208980 on contig 005809 was identified by screening a Candida parapsilosis genome data base. Its 67% identity with the acid trehalase sequence from C. albicans (ATC1) led us to designate it CpATC1. Homozygous mutants that lack acid trehalase activity were constructed by gene disruption at the two CpATC1 chromosomal alleles. Phenotypic characterization showed that atc1Δ null cells were unable to grow on exogenous trehalose as carbon source, and also displayed higher resistance to environmental challenges, such as saline exposure (1.2 M NaCl), heat shock (42°C) and both mild and severe oxidative stress (5 and 50 mM H2O2). Significant amounts of intracellular trehalose were …

Fungal PhysiologyMutantGlycobiologyTrehalase activitylcsh:MedicineMicrobiologiaPathogenesisPathology and Laboratory MedicineCandida parapsilosisBiochemistrychemistry.chemical_compoundNucleic AcidsMicrobial PhysiologyMedicine and Health SciencesTrehalaseTrehalaselcsh:ScienceFungal BiochemistryCandida albicansCandidaMultidisciplinaryVirulencebiologyOrganic CompoundsSalt ToleranceCatalaseEnzymesChemistryPhysical SciencesResearch ArticleGenes FungalMolecular Sequence DataCarbohydratesMycologyMicrobiologyMicrobiologyFungal ProteinsAmino Acid SequenceHeat shockGlycoproteinslcsh:ROrganismsFungiChemical CompoundsWild typeTrehaloseBiology and Life Sciencesbiology.organism_classificationTrehaloseYeastOxidative StressMetabolismchemistryProteolysisEnzymologylcsh:QHeat-Shock ResponsePLoS ONE
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Cell Wall and Secreted Proteins ofCandida albicans: Identification, Function, and Expression

1998

SUMMARYThe cell wall is essential to nearly every aspect of the biology and pathogenicity of Candida albicans. Although it was intially considered an almost inert cellular structure that protected the protoplast against osmotic offense, more recent studies have demonstrated that it is a dynamic organelle. The major components of the cell wall are glucan and chitin, which are associated with structural rigidity, and mannoproteins. The protein component, including both mannoprotein and nonmannoproteins, comprises some 40 or more moieties. Wall proteins may differ in their expression, secretion, or topological location within the wall structure. Proteins may be modified by glycosylation (prima…

Fungal proteinGlycosylationBiologyMicrobiologyArticleHsp70Fungal ProteinsCell wallchemistry.chemical_compoundInfectious DiseasesBiochemistrychemistryMembrane proteinCell WallCandida albicansOrganelleExtracellularSecretionMolecular BiologyMicrobiology and Molecular Biology Reviews
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Biofilm formation byCandida albicansmutants for genes coding fungal proteins exhibiting the eight-cysteine-containing CFEM domain

2006

Several features and functions of a Candida albicans gene, PGA10 (also designated as RBT51), coding for a putative polypeptide species belonging to a subset of fungal proteins containing an eight-cysteine domain referred as CFEM (Common in several Fungal Extracellular Membrane proteins), are described. The ORF of the gene (ORF19.5674) encoded a protein of 250 amino acids, with a predicted molecular mass of 25.17 kDa. The product of the PGA10 gene also exhibited some features reminiscent of a class II-type hydrophobin. Deletion of PGA10 resulted in a cascade of pleiotropic effects, mostly affecting cell-surface-related properties. Thus, the null pga10Delta mutant displayed an increased sensi…

Fungal proteinHydrophobinMutantBiofilmGeneral MedicineBiologybiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyCorpus albicansProtein Structure TertiaryMicrobiologyFungal ProteinsBiochemistryMembrane proteinBiofilmsCandida albicansMutationCloning MolecularCandida albicansGeneFEMS Yeast Research
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Changes in the cell wall glycoprotein composition of Candida albicans associated to the inhibition of germ tube formation by EDTA.

1994

Hyphal development in Candida albicans was blocked by EDTA. This effect was not due to a general growth inhibition since the chelator did not affect protein and DNA synthesis. Recovery of mycelial growth was observed when EDTA-grown cells were incubated at 37 degrees C in EDTA-free medium. High-molecular-weight mannoproteins (HMWM) that are mycelium-specific wall components, and particularly a 260-kDa species (HMWM-260), were absent in the wall of cells grown under germination conditions in the presence of EDTA. Synthesis of the HMWM-260 species was not inhibited but its incorporation (secretion) into the wall structure seemed to be blocked in EDTA-treated cells.

Fungal proteinMembrane GlycoproteinsHyphaDNA synthesisProtoplastsGerm tubeGeneral MedicineBiologybiology.organism_classificationBiochemistryMicrobiologyCell wallFungal ProteinsMolecular Weightchemistry.chemical_compoundBiochemistrychemistryCell WallCandida albicansGeneticsSecretionGrowth inhibitionCandida albicansMolecular BiologyEdetic AcidArchives of microbiology
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Some biological features of Candida albicans mutants for genes coding fungal proteins containing the CFEM domain

2011

Several biological features of Candida albicans genes (PGA10, RBT5 and CSA1) coding for putative polypeptide species belonging to a subset of fungal proteins containing an eight-cysteine domain referred as common in several fungal extracellular membrane (CFEM) are described. The deletion of these genes resulted in a cascade of pleiotropic effects. Thus, mutant strains exhibited higher cell surface hydrophobicity levels and an increased ability to bind to inert or biological substrates. Confocal scanning laser microscopy using concanavalin A-Alexafluor 488 (which binds to mannose and glucose residues) and FUN-1 (a cytoplasmic fluorescent probe for cell viability) dyes showed that mutant stra…

Fungal proteinMutantBiofilmGeneral MedicineBiologybiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyCorpus albicansCell biologyGene expressionExtracellularCandida albicansGeneFEMS Yeast Research
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Rapid PCR-based test for identifying Candida albicans by using primers derived from the pH-regulated KER1 gene.

2006

A PCR-based method in combination with a simple, reliable and inexpensive DNA extraction procedure for rapid detection of Candida albicans clinical isolates is described here. The extraction protocol is based on a combination of chemical (NaOH and detergents) and physical (boiling) treatments, thus avoiding many of the problems inherent in the currently available DNA extraction protocols (basically the use of expensive and/or toxic chemical reagents), and may be useful for daily clinical routine. The PCR-based system described here uses a single pair of primers (SC1F and SC1R) deduced from the C. albicans-specific KER1 gene sequence. These primers amplify a 670-bp fragment of the KER1 gene.…

Fungal proteinbiologyInverse polymerase chain reactionLysineGenes FungalMultiple displacement amplificationGlutamic AcidMembrane ProteinsGeneral MedicineAmpliconHydrogen-Ion Concentrationbiology.organism_classificationApplied Microbiology and BiotechnologyMicrobiologyDNA extractionMolecular biologyPolymerase Chain ReactionCorpus albicanslaw.inventionFungal ProteinslawCandida albicansCandida albicansPolymerase chain reactionDNA PrimersFEMS yeast research
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Isolation and characterization of extracellular vesicles in Candida albicans

2020

Background : The occurrence of systemic infections due to C. albicans has increased especially in critically ill patients. In fungal infections, secretory mechanisms are key events for disease establishment. Recent findings demonstrate that fungal organisms release many molecular components to the extracellular space in extracellular vesicles. Aims: We develop a method to obtain exosomes from yeast cultures of the Candida albicans . Methods : Yeast strains used in this work were C. albicans SC5314, C. parapsilosis (ATCC 22019) and C. krusei (ATCC 6258). Yeasts were grown at 37.º in liquid YPD medium. The cell cultures were centrifuged and the supernatant filtered through sterile nitrocellul…

Future studiesbiologyCritically illChemistry3108.05 HongosProtein compositionbiology.organism_classificationExosomesExtracellular vesiclesMolecular biologyCorpus albicansExosomasCandida albicansCandida albicans
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Ontogeny of the human amygdala.

2003

Data on the fetal development of the human amygdala is reviewed with special reference to major ontogenetic events. In the fifth gestational month, the inferior portion of the amygdala reveals cell-dense columns merging with the ganglionic eminence (proliferative zone) in Nissl-stained sections. These columns contain vimentin-positive fibers and can therefore be regarded as migrational routes. In the sixth and seventh months, distinct reorganization of the cytoarchitectonics takes place. The sequential occurrence of afferens can be visualized using anti-GAP-43; moreover, outgrowing axons appear to reach the periphery of the ganglionic eminence. The latter may thus represent an intermediate …

Ganglionic eminenceGeneral NeuroscienceGlutamate receptorGestational AgeNerve Tissue ProteinsAnatomyBiologyAmygdalaCalbindinAmygdalaGeneral Biochemistry Genetics and Molecular BiologyEmbryonic and Fetal Developmentmedicine.anatomical_structurenervous systemHistory and Philosophy of ScienceCytoarchitecturePostsynaptic potentialmedicineHumansCalretininNeuroscienceImmunostainingBiomarkersAnnals of the New York Academy of Sciences
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Molecular typing of clinical Candida strains using random amplified polymorphic DNA and contour-clamped homogenous electric fields electrophoresis.

2009

Aims:  This report describes an investigation into the genetic profiles of 38 Candida albicans and 19 Candida glabrata strains collected from a dental hospital of Monastir (Tunisia) and the Laboratory of Parasitology, Farhat Hached Hospital of Sousse (Tunisia), using two typing methods: random amplified polymorphic DNA (RAPD) and contour-clamped homogenous electric fields (CHEF). Methods and Results:  The two methods (RAPD and CHEF electrophoresis) were able to identify clonal-related isolates from different patients. RAPD method using two primers (CA1 and CA2) exhibited the highest discriminatory power by discriminating 22 genotypes for C. albicans with CA1 oligonucleotides and 19 genotype…

GeneticsElectrophoresisPolymorphism GeneticTunisiaCandida glabratabiologyCandidiasisCandida glabrataGeneral Medicinebacterial infections and mycosesbiology.organism_classificationApplied Microbiology and BiotechnologyGenetic analysisRAPDRandom Amplified Polymorphic DNA TechniqueDNA profilingParasitologyGenotypeCandida albicansHumansTypingCandida albicansBiotechnologyDNA PrimersJournal of applied microbiology
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BRG1 and NRG1 form a novel feedback circuit regulating Candida albicans hypha formation and virulence

2012

In the opportunistic fungal pathogen Candida albicans both cellular morphology and the capacity to cause disease are regulated by the transcriptional repressor Nrg1p. One of the genes repressed by Nrg1p is BRG1, which encodes a putative GATA family transcription factor. Deletion of both copies of this gene prevents hypha formation. We discovered that BRG1 over-expression is sufficient to overcome Nrg1p-mediated repression and drive the morphogenetic shift from yeast to hyphae even in the absence of environmental stimuli. We further observed that expression of BRG1 influences the stability of the NRG1 transcript, thus controlling filamentation through a feedback loop. Analysis of this phenom…

GeneticsFungal proteinHyphaRepressorGATA transcription factorVirulenceBiologyCandida albicansbiology.organism_classificationMolecular BiologyMicrobiologyTranscription factorCorpus albicansMolecular Microbiology
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