6533b83afe1ef96bd12a7141

RESEARCH PRODUCT

Flux of protons released by wild type and ferritin over-expressor tobacco plants : effect of phosphorus and iron nutrition

G. VansuytBenoît JaillardA. StraczekJean-françois BriatG. Souche

subject

PhysiologyNicotiana tabacumATPasePlant ScienceREDUCTASE03 medical and health scienceschemistry.chemical_compoundProton transport[SDV.BBM] Life Sciences [q-bio]/Biochemistry Molecular BiologyGeneticsStorage protein[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyFerric-chelate reductaseIron deficiency (plant disorder)ComputingMilieux_MISCELLANEOUS030304 developmental biologychemistry.chemical_classification0303 health sciencesbiology04 agricultural and veterinary sciencesbiology.organism_classificationFerritinchemistryBiochemistryChlorophyll040103 agronomy & agriculturebiology.protein0401 agriculture forestry and fisheries

description

Abstract Tobacco ( Nicotiana tabacum ) plants over-expressing the iron storage protein ferritin, either in the cytoplasm or in the plastids, were grown under various P and Fe conditions. The crossed effects of both the genotypes and the environmental conditions on iron and chlorophyll concentrations in leaves, ferric reductase (EC 1.6.99.13) and plasmalemma H + -ATPase (EC 3.6.3.6) activities in roots, and fluxes of H + released by roots were determined. The increase in leaf Fe concentration observed in plants over-expressing ferritin was accompanied by an increase in root ferric reductase and H + -ATPase activities. Iron deficient conditions induced a decrease in Fe and chlorophyll concentrations in leaves, an increase in ferric reductase and H + -ATPase activities in roots and an increase in H + -flux released by roots in all genotypes. Phosphorus abundant conditions induced also an increase in ferric reductase and H + -ATPase activities in roots in all genotypes, and an increase in H + -flux released by roots in the genotype over-expressing ferritin in the cytoplasm. These results suggest that P could regulate the root Fe uptake system, at the gene expression level, as already reported for Zn in barley. Moreover, they show that H + -flux was not always consistent with H + -ATPase activity, revealing that the global measurement of root plasmalemma H + -ATPase activity has some limits compared to the localized determination of the H + -flux. These limits could be due to the fact that part of the H + -flux is not directly linked to H + -ATPase activity in roots.

https://hal.inrae.fr/hal-02677163