Abstract

Iron (Fe) is an essential element for human nutrition, and its deficiency or low hemoglobin levels are a global health issue. Strategies aimed at increasing the amounts of essential elementals in agricultural products, as sprouts of adzuki bean (Vigna angularis), can be a way to minimize deficiencies, mainly in the populations of developing countries. Therefore, in this work was evaluated: production of Fe-enriched adzuki bean sprouts; Fe accumulation and translocation in plants in different culture media enriched with different Fe masses (500, 1000, 2000, and 3000 µg); and effects of the enrichment by means of 3000 µg FeIII-ethylenediaminetetraacetic acid (FeIII-EDTA): on the distribution of Ca, Cu, Fe, K, P, Mg, S, and Zn in different parts of the plant; on protein concentrations (albumins, globulins, prolamins, and glutelins) and their association with Fe in edible parts of the plant (stems); and on Fe bioaccessibility in the edible part of the plant (stems). The enrichment via FeIII-EDTA favored the translocation and increased Fe content of sprouts (75%), besides promoting interactions of Fe with albumins (141%), globulins (180%), and glutelins (93%). In the bioaccessibility assays, Fe was 83% bioaccessible in Fe-enriched sprouts.

Highlights

  • Iron (Fe) is an essential element for cellular homeostasis, oxygen transport, DNA synthesis, and energy metabolism as well as a cofactor for enzymes of the mitochondrial respiratory chain and nitrogen fixation

  • The Fe enrichment of adzuki bean sprouts depends on the chemical species used in the cultivation

  • The inclusion of adzuki bean sprouts enriched with Fe in the daily diet is a promising way to meet the daily intake recommendations of essential elements, especially Fe

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Summary

Introduction

Iron (Fe) is an essential element for cellular homeostasis, oxygen transport, DNA synthesis, and energy metabolism as well as a cofactor for enzymes of the mitochondrial respiratory chain and nitrogen fixation. For the Fe quantification in water, NaCl (1.0 mol L−1), ethanol (70% v/v) and NaOH (1.0 mol L−1) extracts, a ZEEnit 60 model atomic absorption spectrometer (Analytikjena AG, Germany) equipped with a transversely heated graphite atomizer, pyrolytically coated graphite tube, and transversal Zeeman-effect background correction were used. A solution containing 1.0 mg L−1 Mg (Merck, USA) was utilized to assess the robustness of the spectrometer.[23] Titrisol standard solutions of 1000 mg L−1 for Ca (CaCl2), Cu (CuCl2), Fe (FeCl3), K (KCl), Mg (MgCl2), P (H3PO4), S (H2SO4), and Zn (ZnCl2) (Merck, USA) were applied to prepare the reference analytical solutions, after dilution in HNO3 0.1% (v/v) for elemental analysis by inductively coupled plasma optical emission spectrometry (ICP OES) and FeCl3 for determining the Fe content by graphite furnace atomic absorption spectrometry (GF AAS). Fe salt solutions [FeCl3⋅6H2O, FeSO4⋅7H2O, or ethylenediaminetetraacetic acid ferric sodium (NaFeIII‐EDTA)] (Sigma-Aldrich, USA)] were prepared for the enrichment procedure

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