Search results for "MALHERBOLOGIE"

showing 10 items of 12 documents

Fitness of backcross six of hybrids between transgenic oilseed rape (Brassica napus) and wild radish (Raphanus raphanistrum

2002

The process of introgression between a transgenic crop modified for better agronomic characters and a wild relative could lead potentially to increased weediness and adaptation to the environment of the wild species. However, the formation of hybrid and hybrid progeny could be associated with functional imbalance and low fitness, which reduces the risk of gene escape and establishment of the wild species in the field. Our work compares the fitness components of parents and different types of backcross in the sixth generation of hybrids between transgenic oilseed rape (Brassica napus, AACC, 2n = 38) resistant to the herbicide glufosinate and wild radish (Raphanus raphanistrum, RrRr, 2n = 18)…

0106 biological sciencesFLUX DE GENEDrug ResistanceBrassicaIntrogressionGenes PlantRaphanus raphanistrum01 natural sciencesRaphanusGene flow03 medical and health scienceschemistry.chemical_compoundMALHERBOLOGIEGenetics[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyInbreeding[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyCOLZAEcology Evolution Behavior and SystematicsComputingMilieux_MISCELLANEOUS030304 developmental biologyHybridGenetics0303 health sciencesbiologyHerbicidesBrassica napusfood and beveragesAMELIORATION DES PLANTESPlants Genetically Modifiedbiology.organism_classificationAgronomyGlufosinatechemistrySeedlingsBackcrossingHybridization GeneticInbreeding010606 plant biology & botany
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Kinetic studies on protoporphyrinogen oxidase inhibition by diphenyl ether herbicides

1991

Diphenyl ethers (DPEs) and related herbicides are powerful inhibitors of protoporphyrinogen oxidase, an enzyme involved in the biosynthesis of haems and chlorophylls. The inhibition kinetics of protoporphyrinogen oxidase of various origins by four DPEs, (methyl)-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid (acifluorfen and its methyl ester, acifluorfen-methyl), methyl-5-[2-chloro-4-(trifluoromethyl) phenoxy]-2-chlorobenzoate (LS 820340) and methyl-5-[2-chloro-5-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid (RH 5348), were studied. The inhibitions of the enzymes from maize (Zea mays) mitochondrial and etiochloroplastic membranes and mouse liver mitochondrial membranes were com…

0106 biological sciencesOxidoreductases Acting on CH-CH Group DonorsStereochemistry[SDV]Life Sciences [q-bio]Carboxylic acidMitochondria LiverEtherSaccharomyces cerevisiaeAcifluorfen01 natural sciencesBiochemistryMitochondrial ProteinsMiceStructure-Activity Relationship03 medical and health scienceschemistry.chemical_compoundMALHERBOLOGIEPhenolsAnimalsProtoporphyrinogen OxidaseMolecular BiologyComputingMilieux_MISCELLANEOUS030304 developmental biologychemistry.chemical_classification0303 health sciencesTrifluoromethylFlavoproteinsHerbicidesDiphenyl etherIntracellular MembranesCell BiologyPlantsMitochondriaProtoporphyrinogen IX[SDV] Life Sciences [q-bio]KineticsEnzymechemistryProtoporphyrinogen oxidaseOxidoreductasesEthersResearch Article010606 plant biology & botanyBiochemical Journal
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Characterization of (3H) acifluorfen binding to purified pea etioplasts, and evidence that protoporphyrinogen oxidase specifically binds acifluorfen

1992

It is now generally accepted that protoporphyrinogen oxidase is the target-enzyme for diphenylether-type herbicides. Recent studies [Camadro, J-M., Matringe, M., Scalla, R. & Labbe, P. (1991) Biochem. J. 277, 17–21] have revealed that in maize, diphenyl ethers competitively inhibit protoporphyrinogen oxidase with respect to its substrate, protoporphyrinogen IX. In this study, we show that, in purified pea etioplast, [3H]acifluorfen specifically binds to a single class of high-affinity binding sites with an apparent dissociation constant of 6.2 ± 1.3 nM and a maximum density of 29 ± 5 nmol/g protein. [3H]Acifluorfen binding reaches equilibrium in about 1 min at 30°C. Half dissociation occurs…

0106 biological sciencesOxidoreductases Acting on CH-CH Group DonorsStereochemistry[SDV]Life Sciences [q-bio]PhthalimidesAcifluorfen01 natural sciencesBiochemistrySubstrate Specificity03 medical and health scienceschemistry.chemical_compoundMALHERBOLOGIEEtioplastProtoporphyrinogen OxidaseBinding siteComputingMilieux_MISCELLANEOUS030304 developmental biologychemistry.chemical_classificationOrganelles0303 health sciencesOxidase testBinding SitesPlants MedicinalProtoporphyrin IXMolecular StructureBIOCHIMIEHerbicidesFabaceaeProtoporphyrinogen IX[SDV] Life Sciences [q-bio]KineticsEnzymechemistryBiochemistryNitrobenzoatesProtoporphyrinogen oxidaseOxidoreductases010606 plant biology & botany
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A pollen test to detect ACCase target-site resistance within Alopecurus myosuroides populations

2000

International audience

MALHERBOLOGIE[SDV.BV]Life Sciences [q-bio]/Vegetal Biology[SDV.BV] Life Sciences [q-bio]/Vegetal BiologyComputingMilieux_MISCELLANEOUSMETHODOLOGIE
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Synthesis of tritiated derivatives of the diphenylether herbicides acifluorfen and acifluorfen methyl

1992

Acifluorfen 1 and acifluorfen methyl 2, two herbicides of the diphenylether family, are inhibitors of protoporphyrinogen oxidases. Two tritiated derivatives of these compounds, namely 3-[3H]-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid [3H]-1, and methyl 3-[3H]-5-[2-chloro-4-(trifluoromethyl)phenoxy]-2-nitrobenzoic acid [3H]-2, have been synthesised from 3-[3H]-5-hydroxybenzoic acid, in order to probe their interactions with the target enzymes.

Stereochemistry[SDV]Life Sciences [q-bio]Nitro compoundEtherAcifluorfenBiochemistryAnalytical Chemistry03 medical and health scienceschemistry.chemical_compoundMALHERBOLOGIEDrug DiscoveryPIPHENYL ETHERRadiology Nuclear Medicine and imagingSYNTHESESpectroscopyComputingMilieux_MISCELLANEOUS030304 developmental biologychemistry.chemical_classification0303 health sciencesTrifluoromethyl030302 biochemistry & molecular biologyOrganic Chemistry3. Good health[SDV] Life Sciences [q-bio]Enzyme inhibitionEnzymeAcifluorfen-methylchemistryProtoporphyrinogen oxidaseCHIMIE ORGANIQUE
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Recherches sur les herbicides: etat des connaissances et perspectives

1991

National audience

[SDV] Life Sciences [q-bio]BIOTECHNOLOGIEMALHERBOLOGIE[SDV]Life Sciences [q-bio]ComputingMilieux_MISCELLANEOUSRESISTANCE
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Localization within chloroplasts of protoporphyrinogen oxidase, the target enzyme for diphenylether-like herbicides

1992

International audience

[SDV] Life Sciences [q-bio]MALHERBOLOGIE[SDV]Life Sciences [q-bio]ComputingMilieux_MISCELLANEOUS
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Les herbicides. Mode d'action et principes d'utilisation

1992

National audience

[SDV] Life Sciences [q-bio]MALHERBOLOGIE[SDV]Life Sciences [q-bio]ComputingMilieux_MISCELLANEOUSRESISTANCE
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Weed and corn recognition using 2D and 3D data fusion

2001

National audience

[SDV] Life Sciences [q-bio][SDE] Environmental SciencesMALHERBOLOGIE[SDV]Life Sciences [q-bio][SDE]Environmental SciencesRECONNAISSANCE DES FORMESComputingMilieux_MISCELLANEOUS
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A method for recognizing vegetal species from multispectral images

1999

International audience

[SDV] Life Sciences [q-bio][SDE] Environmental SciencesMALHERBOLOGIE[SDV]Life Sciences [q-bio][SDE]Environmental SciencesRECONNAISSANCE DES FORMESComputingMilieux_MISCELLANEOUS
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