Literature DB >> 24347170

Ascorbate efflux as a new strategy for iron reduction and transport in plants.

Louis Grillet1, Laurent Ouerdane, Paulina Flis, Minh Thi Thanh Hoang, Marie-Pierre Isaure, Ryszard Lobinski, Catherine Curie, Stéphane Mari.   

Abstract

Iron (Fe) is essential for virtually all living organisms. The identification of the chemical forms of iron (the speciation) circulating in and between cells is crucial to further understand the mechanisms of iron delivery to its final targets. Here we analyzed how iron is transported to the seeds by the chemical identification of iron complexes that are delivered to embryos, followed by the biochemical characterization of the transport of these complexes by the embryo, using the pea (Pisum sativum) as a model species. We have found that iron circulates as ferric complexes with citrate and malate (Fe(III)3Cit2Mal2, Fe(III)3Cit3Mal1, Fe(III)Cit2). Because dicotyledonous plants only transport ferrous iron, we checked whether embryos were capable of reducing iron of these complexes. Indeed, embryos did express a constitutively high ferric reduction activity. Surprisingly, iron(III) reduction is not catalyzed by the expected membrane-bound ferric reductase. Instead, embryos efflux high amounts of ascorbate that chemically reduce iron(III) from citrate-malate complexes. In vitro transport experiments on isolated embryos using radiolabeled (55)Fe demonstrated that this ascorbate-mediated reduction is an obligatory step for the uptake of iron(II). Moreover, the ascorbate efflux activity was also measured in Arabidopsis embryos, suggesting that this new iron transport system may be generic to dicotyledonous plants. Finally, in embryos of the ascorbate-deficient mutants vtc2-4, vtc5-1, and vtc5-2, the reducing activity and the iron concentration were reduced significantly. Taken together, our results identified a new iron transport mechanism in plants that could play a major role to control iron loading in seeds.

Entities:  

Keywords:  Arabidopsis; Ascorbic Acid; Citrate; Iron; Malate; Membrane Transport; Reductase; vtc2–4

Mesh:

Substances:

Year:  2013        PMID: 24347170      PMCID: PMC3908387          DOI: 10.1074/jbc.M113.514828

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  47 in total

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Review 10.  Local and systemic signaling of iron status and its interactions with homeostasis of other essential elements.

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