Search results for "specificity"

showing 10 items of 2234 documents

Medicago species affect the community composition of arbuscular mycorrhizal fungi associated with roots

2007

National audience; The symbiosis between plants and arbuscular mycorrhizal fungi (AMF) is ancient and involves 80% of terrestrial plant families. The symbiotic association between AMF and plants was described to be non specific. However, AMF were reported to influence plant community diversity and productivity. On the other way, the effect of plant genotypes belonging to closely related species on AMF diversity has not been explored so far. The aim of this work was to assess the impact of four different Medicago species, M. laciniata, M. murex, M. polymorpha and M. truncatula cv. Jemalong J5, on the composition of AM fungal community, when cultivated in a silty-thin clay soil (Mas d’Imbert,…

[SDE] Environmental SciencesGenotypeANNUAL MEDICSPhysiology[SDV]Life Sciences [q-bio]Bulk soilQUANTITATIVE POLYMERASE CHAIN REACTIONPlant ScienceBiologyMEDICAGODNA RibosomalPlant RootsLARGE RIBOSOMAL SUBINIT RIBOSOMAL DEOXYRIBONUCLEIC ACID (LSU RDNA)03 medical and health sciencesARBUSCULAR MYCORRHIZAL (AM) FUNGISpecies SpecificityMedicago laciniataMycorrhizaeLarge ribosomal subunitBotany[SDV.BV]Life Sciences [q-bio]/Vegetal BiologyMedicago polymorpha[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyPhylogenyGlomusDNA PrimersGene Library030304 developmental biology0303 health sciencesMedicagofungiGenetic Variationfood and beverages04 agricultural and veterinary sciences15. Life on landRIBOBOMAL DEOXYRIBONUCLEIC ACID (LSU RDNU)biology.organism_classificationMedicago truncatula[SDV.BV.PEP]Life Sciences [q-bio]/Vegetal Biology/Phytopathology and phytopharmacy[SDV] Life Sciences [q-bio]LARGE RIBOSOMAL SUBINIT[SDE]Environmental Sciences040103 agronomy & agriculture0401 agriculture forestry and fisheriesGENETIC DIVERSITYQUANTITATIVE POLYMERASCHAIN REACTIONMedicago murex
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Microbial Community Structure and Density Under Different Tree Species in an Acid Forest Soil (Morvan, France)

2005

Overexploitation of forests to increase wood production has led to the replacement of native forest by large areas of monospecific tree plantations. In the present study, the effects of different monospecific tree cover plantations on density and composition of the indigenous soil microbial community are described. The experimental site of "Breuil-Chenue" in the Morvan (France) was the site of a comparison of a similar mineral soil under Norway spruce (Picea abies), Douglas fir (Pseudotuga menziesii), oak (Quercus sessiflora), and native forest [mixed stand dominated by oak and beech (Fagus sylvatica)]. Sampling was performed during winter (February) at three depths (0-5, 5-10, and 10-15 cm…

[SDE] Environmental Sciences[SDV]Life Sciences [q-bio]Ribosomal Intergenic Spacer analysisSoil ScienceCHENE SESSILEStratification (vegetation)TreesDOUGLASSoilSpecies SpecificityFagus sylvaticaDNA Ribosomal SpacerHETRE COMMUNBiomassBeechSoil MicrobiologyEcology Evolution Behavior and SystematicsPrincipal Component AnalysisEPICEA COMMUNBiomass (ecology)BacteriaEcologybiologyEcologyFungiGenetic VariationPicea abiesForestryBiodiversitybiology.organism_classificationQUERCUS SESSIFLORACarbonFagaceae[SDV] Life Sciences [q-bio]Microbial population biology[SDE]Environmental SciencesFranceGENETIQUE DES POPULATIONSMicrobial Ecology
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Transcriptional response of Medicago truncatula sulphate transporters to arbuscular mycorrhizal symbiosis with and without sulphur stress

2013

Sulphur is an essential macronutrient for plant growth, development and response to various abiotic and biotic stresses due to its key role in the biosynthesis of many S-containing compounds. Sulphate represents a very small portion of soil S pull and it is the only form that plant roots can uptake and mobilize through H(+)-dependent co-transport processes implying sulphate transporters. Unlike the other organically bound forms of S, sulphate is normally leached from soils due to its solubility in water, thus reducing its availability to plants. Although our knowledge of plant sulphate transporters has been growing significantly in the past decades, little is still known about the effect of…

[SDE] Environmental SciencesmycorhizesTranscription Genetic[SDV]Life Sciences [q-bio]Anion Transport Proteinschemistry.chemical_elementmycorrhizaPlant Sciencesulfatechemistry.chemical_compoundBiosynthesisGene Expression Regulation PlantStress PhysiologicalMycorrhizaeBotanyGenetics[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyRNA MessengerSymbiosisGeneMedicagiPhylogenyAbiotic componentMedicagobiologyarbuscular mycorrhiza ; glomus intraradices ; medicago truncatula ; sulphate ; transportersGene Expression ProfilingfungiComputational Biologyfood and beveragesTransportermedicago truncatulabiology.organism_classificationSulfurMedicago truncatulaArbuscular mycorrhiza[SDV] Life Sciences [q-bio]chemistryOrgan Specificitytransportertransport[SDE]Environmental SciencessulphurSulfur
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A mathematical method for determining genome divergence and species delineation using AFLP.

2002

The delineation of bacterial species is presently achieved using direct DNA-DNA relatedness studies of whole genomes. It would be helpful to obtain the same genomically based delineation by indirect methods, provided that descriptions of individual genome composition of bacterial genomes are obtained and included in species descriptions. The amplified fragment length polymorphism (AFLP) technique could provide the necessary data if the nucleotides involved in restriction and amplification are fundamental to the description of genomic divergences. Firstly, in order to verify that AFLP analysis permits a realistic exploration of bacterial genome composition, the strong correspondence between …

[SDV.SA]Life Sciences [q-bio]/Agricultural sciences[SDV.OT]Life Sciences [q-bio]/Other [q-bio.OT]AgrobacteriumMolecular Sequence DataBacterial genome sizeBiologyMicrobiologyGenome03 medical and health sciencesPlasmidSpecies SpecificityGenetic variationDNA Ribosomal SpacerEcology Evolution Behavior and SystematicsComputingMilieux_MISCELLANEOUS030304 developmental biologyGenetics0303 health sciences[SDV.SA] Life Sciences [q-bio]/Agricultural sciencesPhylogenetic tree030306 microbiologyStrain (biology)Genetic VariationGeneral Medicinebiology.organism_classificationBiological EvolutionDNA FingerprintingEvolutionary biologyAmplified fragment length polymorphismGenome BacterialMathematicsPolymorphism Restriction Fragment LengthRhizobiumInternational journal of systematic and evolutionary microbiology
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Terminal tendon cell differentiation requires the glide/gcm complex.

2004

International audience; Locomotion relies on stable attachment of muscle fibres to their target sites, a process that allows for muscle contraction to generate movement. Here, we show that glide/gcm and glide2/gcm2, the fly glial cell determinants, are expressed in a subpopulation of embryonic tendon cells and required for their terminal differentiation. By using loss-of-function approaches, we show that in the absence of both genes, muscle attachment to tendon cells is altered, even though the molecular cascade induced by stripe, the tendon cell determinant, is normal. Moreover, we show that glide/gcm activates a new tendon cell gene independently of stripe. Finally, we show that segment p…

[SDV]Life Sciences [q-bio]Cellglide/gcmBiologyMotor ActivityTendonsglide2/gcm203 medical and health sciencesTendon cellMuscle attachmentmedicineMuscle attachmentAnimalsDrosophila ProteinsRNA MessengerMolecular BiologyIn Situ Hybridization030304 developmental biology0303 health sciencesMuscles030302 biochemistry & molecular biologyNeuropeptidesTendon cell differentiationGene Expression Regulation DevelopmentalCell DifferentiationEpistasis GeneticAnatomyTendon cell differentiationEmbryonic stem cellCell biologyTendonDNA-Binding ProteinsMicroscopy ElectronDrosophila melanogasterSegment polarity genemedicine.anatomical_structureEpidermal CellsOrgan SpecificityTrans-ActivatorsDrosophilamedicine.symptomEpidermisLocomotionDevelopmental BiologyMuscle contractionProtein BindingSignal TransductionTranscription FactorsDevelopment (Cambridge, England)
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Cyclopropane Fatty Acid Synthase from Oenococcus oeni: Expression in Lactococcus lactis subsp. Cremoris and Biochemical Characterization

2015

Bacterial cyclopropane fatty acid synthases (CFA synthases) catalyze the transfer of a methyl group from S-adenosyl-L-methionine (AdoMet) to the double bond of a lipid chain, thereby forming a cyclopropane ring. CFAs contribute to resistance to acidity, dryness, and osmotic imbalance in many bacteria. This work describes the first biochemical characterization of a lactic acid bacterium CFA synthase. We have overexpressed Oenococcus oeni CFA synthase in E. coli in order to purify the enzyme. The optimum cyclopropanation activity was obtained at pH 5.6 and 35.8 °C. The high K(m) (AdoMet) value obtained (2.26 mM) demonstrates the low affinity of O. oeni enzyme toward the L. lactis subsp. cremo…

[SDV]Life Sciences [q-bio]medicine.disease_causeBiochemistryMicrobiologySubstrate SpecificityMicrobiology03 medical and health scienceschemistry.chemical_compoundEscherichia coliGeneticsmedicineCyclopropane fatty acidMolecular BiologyEscherichia coliOenococcusPhospholipidsComputingMilieux_MISCELLANEOUS030304 developmental biologyOenococcus oenichemistry.chemical_classification0303 health sciences[ SDV ] Life Sciences [q-bio]biologyATP synthase030306 microbiologyLactococcus lactis subsp cremorisFatty AcidsLactococcus lactisGene Expression Regulation BacterialMethyltransferasesGeneral Medicinebiology.organism_classification[SDV] Life Sciences [q-bio]Lactococcus lactisEnzymechemistryBiochemistryMutationbiology.proteinOenococcus
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Biochemical and structural features of a novel cyclodextrinase from cow rumen metagenome.

2007

A novel enzyme, RA.04, belonging to the alpha-amylase family was obtained after expression of metagenomic DNA from rumen fluid (Ferrer et al.: Environ. Microbiol. 2005, 7, 1996-2010). The purified RA.04 has a tetrameric structure (280 kDa) and exhibited maximum activity (5000 U/mg protein) at 70 degrees C and was active within an unusually broad pH range from 5.5 to 9.0. It maintained 80% activity at pH 5.0 and 9.5 and 75 degrees C. The enzyme hydrolyzed alpha-D-(1,4) bonds 13-fold faster than alpha-D-(1,6) bonds to yield maltose and glucose as the main products, and it exhibited transglycosylation activity. Its preferred substrates, in the descending order, were maltooligosaccharides (C3-C…

alpha-CyclodextrinsRumenGlycoside HydrolasesStarchAmylopectinOligosaccharidesApplied Microbiology and BiotechnologyCatalysisSubstrate Specificitychemistry.chemical_compoundBacterial ProteinsAmyloseCyclomaltodextrinaseAnimalsMaltoseGlucansChromatography High Pressure Liquidchemistry.chemical_classificationBinding Sitesbiologybeta-CyclodextrinsTemperatureActive sitePullulanStarchGeneral MedicineMaltoseHydrogen-Ion ConcentrationEnzymechemistryBiochemistryAmylopectinbiology.proteinMolecular MedicineCattleElectrophoresis Polyacrylamide GelAmylosegamma-CyclodextrinsBiotechnology journal
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Failure to differentiate Cryptosporidium parvum from C. meleagridis based on PCR amplification of eight DNA sequences.

1998

ABSTRACT In order to determine the specificities of PCR-based assays used for detecting Cryptosporidium parvum DNA, eight pairs of previously described PCR primers targeting six distinct regions of the Cryptosporidium genome were evaluated for the detection of C. parvum , the agent of human cryptosporidiosis, and C. muris , C. baileyi , and C. meleagridis , three Cryptosporidium species that infect birds or mammals but are not considered to be human pathogens. The four Cryptosporidium species were divided into two groups: C. parvum and C. meleagridis , which gave the same-sized fragments with all the reactions, and C. muris and C. baileyi , which gave positive results with primer pairs targ…

animal diseases030231 tropical medicineGenes ProtozoanCryptosporidiumApplied Microbiology and BiotechnologyGenomePolymerase Chain ReactionSensitivity and SpecificityDNA sequencing18S ribosomal RNAMicrobiologylaw.invention03 medical and health sciences0302 clinical medicineSpecies Specificitylawparasitic diseasesTECHNIQUE PCRAnimalsHumansGenePolymerase chain reactionComputingMilieux_MISCELLANEOUSDNA Primers[SDV.EE]Life Sciences [q-bio]/Ecology environmentCryptosporidium parvum0303 health sciencesEcologybiologyBase Sequence030306 microbiologyCryptosporidiumDNA Protozoanbiology.organism_classificationVirologyBacterial Typing Techniques[SDV.EE] Life Sciences [q-bio]/Ecology environmentCryptosporidium parvumEnvironmental and Public Health MicrobiologyPrimer (molecular biology)Water MicrobiologyFood ScienceBiotechnologyApplied and environmental microbiology
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Evidence for differential and redundant function of the Sox genes Dichaete and SoxN during CNS development in Drosophila.

2002

Group B Sox-domain proteins encompass a class of conserved DNA-binding proteins expressed from the earliest stages of metazoan CNS development. In all higher organisms studied to date, related Group B Sox proteins are co-expressed in the developing CNS; in vertebrates there are three (Sox1, Sox2 and Sox3) and in Drosophila there are two (SoxNeuro and Dichaete). It has been suggested there may be a degree of functional redundancy in Sox function during CNS development. We describe the CNS phenotype of a null mutation in the Drosophila SoxNeuro gene and provide the first direct evidence for both redundant and differential Sox function during CNS development in Drosophila. In the lateral neuro…

animal structuresEmbryo NonmammalianMutantBiologyNervous SystemSOX Transcription FactorsSOX1NeuroblastSOX2Species SpecificityEctodermAnimalsDrosophila ProteinsMolecular BiologySOX Transcription FactorsGeneticsNeuroectodermHigh Mobility Group ProteinsGene Expression Regulation DevelopmentalPhenotypeNull alleleDNA-Binding ProteinsDrosophila melanogasterMutagenesisembryonic structuresVertebratesDevelopmental BiologyTranscription FactorsDevelopment (Cambridge, England)
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Neuroglobin, cytoglobin, and a novel, eye-specific globin from chicken

2004

Neuroglobin and cytoglobin are two recently discovered respiratory proteins of vertebrates. Here we report the first identification and expression analyses of these proteins in bird species. Neuroglobin from the domestic chicken Gallus gallus differs in approximately 30% from the mammalian proteins, but its genome structure shows the conservation of the B12.2, E11.0, and G7.0 intron positions. The chicken cytoglobin protein is shorter than the mammalian orthologs, from which it differs overall by approximately 25%, due to the absence of the C-terminal exon in the gene. Comparison of chicken and mammalian gene order shows that neuroglobin and cytoglobin are located on conserved syntenic chro…

animal structuresMolecular Sequence DataBiophysicsNeuroglobinNerve Tissue ProteinsBiologyBiochemistryRetinaEvolution MolecularExonSpecies SpecificitySequence Analysis ProteinGene duplicationAnimalsHumansAmino Acid SequenceGlobinMolecular BiologyGeneConserved SequencePhylogenyGeneticsSequence Homology Amino AcidCytoglobinIntronRNACell BiologyGlobinsNeuroglobinVertebratesChickensBiochemical and Biophysical Research Communications
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