Abstract:Abstract. The characteristics of flavin excretion from iron-deficient sugar-beet roots have been studied. Roots from iron-deficient sugar beet excreted flavins when plants were allowed to decrease the pH of the nutrient solution, but not when plants were grown in nutrient solutions buffered at high pH. As shown by reversedphase high-performance liquid chromatography, the two major flavins whose excretion was induced by iron deficiency were different from riboflavin, FMN and FAD. These flavins have been identif… Show more
“…In the case of H. niger root cultures, the minimum pH was between 4.4~4.6 [36]. In sugar beet [34], pH reached approximately 3.7 after 15days, and pH was maintained at 3.5~4.0 in muskmelon [10]. In H. albus hairy roots, the minimum pH was around 4.0 when a single root tip was subjected to iron deficiency and around 4.5 when propagated roots did.…”
Section: Discussionmentioning
confidence: 98%
“…It was also found that not all but some strategy I plants from Aizoceae to Umbelliferae, including tobacco, beet, sunflower and cucumber, excrete riboflavin [39], and also unique riboflavin sulfates in the case of sugar beet [33,34], in the rhizosphere under iron-deficient conditions. Recently, cultured roots of Hyoscyamus niger were also found to be able to secrete riboflavin without their aerial parts [36].…”
SummaryHyoscyamus albus hairy roots with/without an exogenous gene (11 clones) were established by inoculation of Agrobacterium rhizogenes. All clones cultured under iron deficient condition secreted riboflavin from root tips into the culture medium and the productivity depended on the number and size of root tips among the clones, although the addition of sucrose was essential for riboflavin production. A decline of pH was observed before riboflavin production and root development using either a root tip or propagated roots: propagated roots were employed for further work due to their lesser variation.Additions of proton-pump inhibitors, N,N'-dicyclohexylcarbodiimide (DCCD) at 100 and 10 μM and erythrosine B at 100 μM, suppressed the pH decline at 100 and 10 μM accompanied by inhibition of riboflavin secretion and root growth; at 10 μM of erythrosine B, pH decline occurred with a moderate delay, but both growth and riboflavin efflux were inhibited. Neither inhibition of the pH decline nor riboflavin production was observed at 1 μM. To examine the necessity of acidification and riboflavin secretion by the roots themselves, artificial pH reduction of culture medium with organic acids and the addition of exogenous riboflavin with/without pH reduction were performed. When hairy roots were cultured in iron-deficient medium acidified with citric acid (pH 4.0) or malic acid (pH 3.7), pH increased rapidly to around 5 overnight, following which riboflavin production and root growth occurred. Addition of riboflavin did not affect riboflavin secretion by the roots, but acidification with citric acid (pH 4.0) helped achiever greater riboflavin production and earlier pH elevation. These results indicate that riboflavin efflux does not directly connected to active pH reduction, and more significantly active riboflavin secretion occurs by internal requirement in H. albus hairy roots under iron deficiency.
“…In the case of H. niger root cultures, the minimum pH was between 4.4~4.6 [36]. In sugar beet [34], pH reached approximately 3.7 after 15days, and pH was maintained at 3.5~4.0 in muskmelon [10]. In H. albus hairy roots, the minimum pH was around 4.0 when a single root tip was subjected to iron deficiency and around 4.5 when propagated roots did.…”
Section: Discussionmentioning
confidence: 98%
“…It was also found that not all but some strategy I plants from Aizoceae to Umbelliferae, including tobacco, beet, sunflower and cucumber, excrete riboflavin [39], and also unique riboflavin sulfates in the case of sugar beet [33,34], in the rhizosphere under iron-deficient conditions. Recently, cultured roots of Hyoscyamus niger were also found to be able to secrete riboflavin without their aerial parts [36].…”
SummaryHyoscyamus albus hairy roots with/without an exogenous gene (11 clones) were established by inoculation of Agrobacterium rhizogenes. All clones cultured under iron deficient condition secreted riboflavin from root tips into the culture medium and the productivity depended on the number and size of root tips among the clones, although the addition of sucrose was essential for riboflavin production. A decline of pH was observed before riboflavin production and root development using either a root tip or propagated roots: propagated roots were employed for further work due to their lesser variation.Additions of proton-pump inhibitors, N,N'-dicyclohexylcarbodiimide (DCCD) at 100 and 10 μM and erythrosine B at 100 μM, suppressed the pH decline at 100 and 10 μM accompanied by inhibition of riboflavin secretion and root growth; at 10 μM of erythrosine B, pH decline occurred with a moderate delay, but both growth and riboflavin efflux were inhibited. Neither inhibition of the pH decline nor riboflavin production was observed at 1 μM. To examine the necessity of acidification and riboflavin secretion by the roots themselves, artificial pH reduction of culture medium with organic acids and the addition of exogenous riboflavin with/without pH reduction were performed. When hairy roots were cultured in iron-deficient medium acidified with citric acid (pH 4.0) or malic acid (pH 3.7), pH increased rapidly to around 5 overnight, following which riboflavin production and root growth occurred. Addition of riboflavin did not affect riboflavin secretion by the roots, but acidification with citric acid (pH 4.0) helped achiever greater riboflavin production and earlier pH elevation. These results indicate that riboflavin efflux does not directly connected to active pH reduction, and more significantly active riboflavin secretion occurs by internal requirement in H. albus hairy roots under iron deficiency.
“…Under Fe deficiency, the Arabidopsis plants secrete Fe-mobilizing phenolic compounds such as coumarins to acquire Fe by chelation and/ or reduction of Fe 3+ (Fourcroy et al 2014). Besides phenolics, some plant species such as sugar beet, spinach and alfalfa can synthesize and release abundant flavins that play redox and/or metal-complexing roles in augmenting Fe mobilization in the rhizosphere (Susín et al 1993(Susín et al , 1994Rodríguez-Celma et al 2011). Importantly, some PGPR strains such as Azospirillum brasilense and P. polymyxa BFKC01 can enhance Fe acquisition by increasing root-secreted phenolics (Pii et al 2015;Zhou et al 2016).…”
Soil bacteria can assist plant growth and increase uptake of nutrient elements, the question arises as to whether beneficial soil microbes confer augmented iron (Fe) content of host plants under Fe limited conditions. Herein, a novel strain of Burkholderia cepacia (strain JFW16) was isolated from rhziospheric soils of Astragalus sinicus grown under alkaline conditions. Inoculation of plants with B. cepacia JFW16 displayed increased endogenous Fe content compared with non-inoculated plants. Growth promotion and enhanced photosynthetic capacity were also observed for the inoculated plants. The inoculation with JFW16 significantly increased the rhizospheric acidification, and up-regulated the transcription of some Fe acquisition-associated genes in Astragalus sinicus. Moreover, the metabolic pathways of flavins were remarkably enhanced in the inoculated plants, showing the increased biosynthesis and release of flavins in roots. Collectively, these findings demonstrated the potential of B. cepacia JFW16 to improve Fe assimilation in agricultural crops.
ARTICLE HISTORY
“…It is known that iron deficiency promotes the excretion of phenolic compounds, organic acids, and flavins, which also contribute to Fe reduction and solubility (Welkie and Miller, 1988;Susín et al, 1994). The FRO gene, is a key enzyme in Fe acquisition, and the first FRO2 gene was identified in the model plant Arabidopsis thaliana (Robinson et al, 1999).…”
ABSTRACT. Iron (Fe) is an essential element for plant growth. Commonly, this element is found in an oxidized form in soil, which is poorly available for plants. Therefore, plants have evolved ferric-chelate reductase enzymes (FRO) to reduce iron into a more soluble ferrous form. Fe scarcity in plants induce the FRO enzyme activity. Although the legume Medicago truncatula has been employed as a model for FRO activity studies, only one copy of the M. truncatula MtFRO1 gene has been characterized so far. In this study, we identified multiple gene copies of the MtFRO gene in the genome of M. truncatula by an in silico search, using BLAST analysis in the database of the M. truncatula Genome Sequencing Project and the National Center for Biotechnology Information, and also determined whether they are functional. We identified five genes apart from MtFRO1, which had been already characterized. All of the MtFRO genes exhibited high identity with homologous FRO genes from Lycopersicon esculentum, Citrus junos and Arabidopsis thaliana. The gene copies also presented characteristic conserved FAD and NADPH motifs, transmembrane regions and oxidoreductase signature motifs. We also detected expression in five of the putative MtFRO sequences by semiquantitative RT-PCR analysis,
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