Search results for "plant root"

showing 10 items of 232 documents

Vigna mungo, V. radiata and V. unguiculata plants sampled in different agronomical-ecological-climatic regions of India are nodulated by Bradyrhizobi…

2009

International audience; Vigna mungo, Vigna radiata and Vigna unguiculata are important legume crops cultivated in India, but little is known about the genetic resources in native rhizobia that nodulate these species. To identify these bacteria, a core collection of 76 slow-growing isolates was built from root nodules of V. mungo, V. radiata and V. unguiculata plants grown at different sites within three agro-ecological-climatic regions of India. The genetic diversity of the bacterial collection was assessed by restriction fragment length polymorphism (RFLP) analysis of PCR-amplified DNA fragments of the 16S–23S rDNA intergenic spacer (IGS) region, and the symbiotic genes nifH and nodC. One …

Root noduleVigna spp.RadiataDIVERSITYApplied Microbiology and BiotechnologyPlant Root NodulationPolymerase Chain ReactionVignaSymbiotic genesCluster AnalysisBradyrhizobiumPhylogeny0303 health sciencesDiversitybiologyEcologyfood and beveragesFabaceae[SDV.MP]Life Sciences [q-bio]/Microbiology and ParasitologyRestriction fragment length polymorphismOxidoreductasesRoot Nodules PlantPolymorphism Restriction Fragment LengthDNA BacterialBradyrhizobium yuanmingensePHYLOGENYVIGNA SPP.Molecular Sequence DataIndiaN-AcetylglucosaminyltransferasesMicrobiologyBradyrhizobiumRhizobia03 medical and health sciencesVIGNA RADIATABacterial ProteinsBotanyDNA Ribosomal SpacerSYMBIOTIC GENESEcology Evolution Behavior and Systematics030304 developmental biologyRELATION HOTE-PARASITEGenetic diversity030306 microbiologyBRADYRHIZOBIUMSequence Analysis DNA15. Life on landVIGNA MUNGObiology.organism_classificationMULTI-LOCUS SEQUENCE ANALYSISMulti-locus sequence analysis
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Fungal Assemblages Associated with Roots of Halophytic and Non-halophytic Plant Species Vary Differentially Along a Salinity Gradient

2012

Structure of fungal communities is known to be influenced by host plants and environmental conditions. However, in most cases, the dynamics of these variation patterns are poorly understood. In this work, we compared richness, diversity, and composition between assemblages of endophytic and rhizospheric fungi associated to roots of two plants with different lifestyles: the halophyte Inula crithmoides and the non-halophyte I. viscosa (syn. Dittrichia viscosa L.), along a spatially short salinity gradient. Roots and rhizospheric soil from these plants were collected at three points between a salt marsh and a sand dune, and fungi were isolated and characterized by ITS rDNA sequencing. Isolates…

SalinitySoil salinityInula crithmoideSoil ScienceSodium ChlorideEndophyteDNA RibosomalPlant RootsPlant use of endophytic fungi in defenseSoilAscomycotaSpecies SpecificityHalophyteBotanyDNA Ribosomal SpacerDittrichia viscosaEndophytesLife ScienceOtusDNA FungalEcology Evolution Behavior and SystematicsPhylogenySoil Microbiologygeographygeography.geographical_feature_categoryEcologybiologyEcologyBasidiomycotaFungiSalt-Tolerant PlantsSequence Analysis DNAPlantsDittrichia viscosabiology.organism_classificationAscomycota; Basidiomycota; Dittrichia viscosa; Fungi; Inula; Inula crithmoides; OtusSalinitySalt marshInulaSpecies richness
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Cytotoxic Acacic Acid Glycosides from the Roots of Albizia coriaria

2009

Two new oleanane-type saponins, coriariosides A (1) and B (2), along with a known saponin, gummiferaoside C (3), were isolated from the roots of Albizia coriaria. Their structures were established by extensive analysis of 1D and 2D NMR experiments (COSY, ROESY, TOCSY, HSQC, and HMBC) and mass spectrometry. Compounds 1 and 3 when tested for cytotoxicity against two colorectal human cancer cells showed activity against the HCT 116 (IC50 4.2 microM for 1 and 2.7 microM for 3) and HT-29 (IC50 6.7 microM for 1 and 7.9 microM for 3) cell lines.

SaponinPharmaceutical ScienceAlbizziaPharmacognosyPlant RootsAnalytical ChemistryTriterpeneCoriariaDrug DiscoveryBotanyHumansCameroonOleanolic AcidMedicinal plantsNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationPlants MedicinalMolecular StructurebiologyOrganic ChemistryGlycosideSaponinsHCT116 Cellsbiology.organism_classificationAlbiziaAntineoplastic Agents PhytogenicTriterpenesTerpenoidComplementary and alternative medicinechemistryMolecular MedicineDrug Screening Assays AntitumorHT29 CellsJournal of Natural Products
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New Acylated Triterpene Saponins from Silene fortunei that Modulate Lymphocyte Proliferation

2002

Three new acylated triterpene saponins 1-3, with a quillaic acid as aglycon, were isolated from the roots of Silene fortunei together with a known phytoecdysteroid (20-hydroxyecdysone). The compounds were characterized mainly by a combination of 2D NMR techniques, mass spectrometry, and chemical methods. Saponins 1-3, jenisseensosides C and D (4, 5), and 6 (deacylated form of 2/3 and 4/5) were found to stimulate the proliferation of the Jurkat tumor cell lines at low concentration. At high concentration, 2/3 and 4/5 inhibited the proliferation of the cells and suggested the induction of apoptosis.

SaponinPhytoecdysteroidPharmaceutical ScienceApoptosisLymphocyte proliferationPharmacognosyLymphocyte ActivationPlant RootsJurkat cellsAnalytical ChemistryJurkat CellsTriterpeneDrug DiscoveryHumansSileneNuclear Magnetic Resonance BiomolecularPharmacologychemistry.chemical_classificationSilenePlants MedicinalMolecular StructurebiologyHydrolysisOrganic ChemistryGlycosideAcetylationStereoisomerismSaponinsbiology.organism_classificationTriterpenesComplementary and alternative medicinechemistryBiochemistryMolecular MedicineJournal of Natural Products
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New triterpenoid estersaponins from the root barks of Pittosporum verticillatum subsp. verticillatum and evaluation of cytotoxicities

2013

The phytochemical investigation of the root barks of Pittosporum verticillatum Bojer subsp. verticillatum led to the isolation of three new triterpene saponins, 3-O-[β-D-glucopyranosyl-(1→2)]-[α-L-arabinopyranosyl-(1→3)]-[α-L-arabinofuranosyl-(1→4)]-β-D-glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-R1-barrigenol (1), 3-O-[β-D-glucopyranosyl-(1→2)]-[α-L-arabinopyranosyl-(1→3)]-[α-L-arabinofuranosyl-(1→4)]-β-D-glucuronopyranosyl-21-O-(2-acetoxy-2-methylbutanoyl)-28-O-acetyl-R1-barrigenol (2), 3-O-[β-D-glucopyranosyl-(1→2)]-[α-L-arabinopyranosyl-(1→3)]-[α-L-arabinofuranosyl-(1→4)]-β-D-glucuronopyranosyl-21-O-β,β-dimethylacryloyl-22-O-angeloyl-R1-barrigenol (3), and one known saponin sen…

Senaciapittoside BStereochemistrySaponinPlant RootsCell LineTerpeneTriterpenoidTriterpeneCell Line TumorNeoplasmsDrug DiscoveryAnimalsHumansRosalesPharmacologychemistry.chemical_classificationMolecular StructurebiologyPlant ExtractsGeneral MedicineSaponinsPittosporumbiology.organism_classificationTriterpenesRatschemistryPhytochemicalPlant BarkHuman cancerFitoterapia
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Enhanced Accumulation of Betulinic Acid in Transgenic Hairy Roots of Senna obtusifolia Growing in the Sprinkle Bioreactor and Evaluation of Their Bio…

2021

Betulinic acid, which is found in transgenic roots of Senna obtusifolia (L.) H.S.Irwin & Barneby, is a pentacyclic triterpene with distinctive pharmacological activities. In this study, we report the differences in the content of betulinic acid and selected anthraquinones in transgenic S. obtusifolia hairy roots with overexpression of the PgSS1 gene (SOPSS2 line) and in transformed hairy roots without this genetic construct (SOA41 line). Both hairy root lines grew in 10 L sprinkle bioreactor. Additionally, the extracts obtained from this plant material were used for biological tests. Our results demonstrated that the SOPSS2 hairy root cultures from the bioreactor showed an increase in the c…

Senna PlantTransgeneBioengineeringAnthraquinonesApoptosisMicrobial Sensitivity TestsGram-Positive BacteriaBiochemistryModels BiologicalPlant Rootschemistry.chemical_compoundBioreactorsTriterpeneGene Expression Regulation PlantBetulinic acidCell Line TumorAnthraquinonesGene expressionGram-Negative BacteriaBioreactorHumansAntiviral activityBetulinic AcidMolecular BiologyCell ProliferationPlant Proteinsbcl-2-Associated X Proteinchemistry.chemical_classificationbiologyPlant ExtractsSprinkle bioreactorGeneral ChemistryGeneral Medicinebiology.organism_classificationAntimicrobialPlants Genetically ModifiedBiodiversitatAnticancerchemistryBiochemistryGlucosyltransferasesTransgenic hairy rootsMolecular MedicineAntimicrobialGene expressionTumor Suppressor Protein p53Senna obtusifoliaPentacyclic TriterpenesChemistrybiodiversity
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Lulwoana sp., a dark septate endophyte (DSE) in roots of Posidonia oceanica (L.) Delile seagrass

2014

Posidonia oceanica is the most common, widespread and important monocotyledon seagrass in the Mediterranean Basin, and hosts a large biodiversity of species, including microorganisms with key roles in the marine environment. In this study, we ascertain the presence of a fungal endophyte in the roots of P. oceanica growing on different substrata (rock, sand and matte) in two Sicilian marine meadows. Staining techniques on root fragments and sections, in combination with microscope observations, were used to visualise the fungal presence and determine the percentage of fungal colonisation (FC) in this tissue. In root fragments, statistical analysis of the FC showed a higher mean in roots anch…

SeptateSettore BIO/07 - EcologiaMolecular Sequence DataPlant ScienceDark septate endophytePlant RootsLulwoanaDark septate mycelium; Lulwoana; Posidonia oceanica; rootSettore BIO/01 - Botanica GeneraleAscomycotaBotanyEndophytesMediterranean SeaInternal transcribed spacerEcology Evolution Behavior and SystematicsMyceliumDark septate myceliumAlismatalesbiologySettore BIO/02 - Botanica SistematicaPosidonia oceanicaSettore AGR/12 - Patologia VegetaleGeneral Medicinebiology.organism_classificationrootRhizodermisColonisationSeagrassItalyPosidonia oceanica
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Essential oils composition of Periploca laevigata Aiton subsp. angustifolia (Labill.) Markgraf (Apocynaceae – Periplocoideae)

2012

The essential oil of roots, branches, leaves, flowers and fruits of Periploca laevigata Aiton subsp. angustifolia (Apocynaceae) from Lampedusa Island has been obtained by hydrodistillation and its composition analysed. The analyses allowed the identification and quantification of 86 volatile compounds. Branches showed the higher diversity with 57 compounds followed by fruits with 33, roots with 23, flowers with 16 and leaves with six compounds, respectively. In the matrices examined three constituents, heneicosane, docosane and tricosane are in common, although with different percentages. At least the most abundant compounds found in the matrices have been reported to have several biologica…

Settore BIO/07 - EcologiaAllomoneFlowersPlant ScienceBiologyPlant RootsBiochemistryessential oilPheromonesAnalytical Chemistrylaw.inventionIngredientlawBotanyOils VolatileMedicinal plantsEssential oilsemiochemicals visitorsApocynaceaeHost (biology)Organic ChemistrySettore CHIM/06 - Chimica Organicabiology.organism_classificationApocynaceaePlant LeavesSettore AGR/11 - Entomologia Generale E ApplicataFruitKairomoneSettore BIO/03 - Botanica Ambientale E ApplicatantimicrobialPeriplocoideaeNatural Product Research
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Involvement of nitrate reductase and pyoverdine in competitiveness of Pseudomonas fluorescens strain C7R12 in soil

2001

ABSTRACT Involvement of nitrate reductase and pyoverdine in the competitiveness of the biocontrol strain Pseudomonas fluorescens C7R12 was determined, under gnotobiotic conditions, in two soil compartments (bulk and rhizosphere soil), with the soil being kept at two different values of matric potential (−1 and −10 kPa). Three mutants affected in the synthesis of either the nitrate reductase (Nar − ), the pyoverdine (Pvd − ), or both (Nar − Pvd − ) were used. The Nar − and Nar − Pvd − mutants were obtained by site-directed mutagenesis of the wild-type strain and of the Pvd − mutant, respectively. The selective advantage given by nitrate reductase and pyoverdine to the wild-type strain was as…

SiderophorePseudomonas fluorescensNitrate reductasePseudomonas fluorescensApplied Microbiology and BiotechnologyNitrate ReductasePlant Roots03 medical and health scienceschemistry.chemical_compoundPlant MicrobiologySolanum lycopersicumNitrate ReductasesSelection GeneticSoil MicrobiologyComputingMilieux_MISCELLANEOUS030304 developmental biology[SDV.EE]Life Sciences [q-bio]/Ecology environment0303 health sciencesRhizospherePyoverdineEcologybiology030306 microbiologyPigments Biologicalbiology.organism_classification[SDV.EE] Life Sciences [q-bio]/Ecology environmentBiochemistrychemistryPseudomonadalesCommunicable Disease ControlMutationSoil microbiologyOligopeptidesFood ScienceBiotechnologyPseudomonadaceae
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LC–ESI–FT–MSn Metabolite Profiling of Symphytum officinale L. Roots Leads to Isolation of Comfreyn A, an Unusual Arylnaphthalene Lignan

2020

Preparations of comfrey (Symphytum officinale L.) roots are used topically to reduce inflammation. Comfrey anti-inflammatory and analgesic properties have been proven in clinical studies. However, the bioactive compounds associated with these therapeutic activities are yet to be identified. An LC&ndash

Spectrometry Mass Electrospray Ionizationcomfrey rootsMetaboliteAnti-Inflammatory AgentsComfreySymphytum officinalePlant Roots01 natural sciencescomfreyn AArticleCatalysisUmbilical veinInorganic Chemistrylcsh:Chemistrychemistry.chemical_compoundLC–ESI–Orbitrap–MSComfreyHuman Umbilical Vein Endothelial CellsSymphytum officinaleHumans<i>Symphytum officinale</i>Physical and Theoretical ChemistryGloboidnan AMolecular Biologylcsh:QH301-705.5SpectroscopyLignanPlants MedicinalChromatographyMolecular StructurebiologyChemistry010401 analytical chemistryOrganic ChemistryComfrey roots; Comfreyn A; LC–ESI–Orbitrap–MS; Phenylpropanoids; Symphytum officinaleGeneral Medicinebiology.organism_classification0104 chemical sciencesComputer Science Applications010404 medicinal & biomolecular chemistrylcsh:Biology (General)lcsh:QD1-999Metabolite profilingTwo-dimensional nuclear magnetic resonance spectroscopyChromatography LiquidphenylpropanoidsInternational Journal of Molecular Sciences
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