Literature DB >> 16665677

Involvement of superoxide radical in extracellular ferric reduction by iron-deficient bean roots.

I Cakmak1, D A van de Wetering, H Marschner, H F Bienfait.   

Abstract

The recent proposal of Tipton and Thowsen (Plant Physiol 79: 432-435) that iron-deficient plants reduce ferric chelates in cell walls by a system dependent on the leakage of malate from root cells was tested. Results are presented showing that this mechanism could not be responsible for the high rates of ferric reduction shown by roots of iron-deficient bean (Phaseolus vulgaris L. var Prélude) plants. The role of O(2) in the reduction of ferric chelates by roots of iron-deficient bean plants was also tested. The rate of Fe(III) reduction was the same in the presence and in the absence of O(2). However, in the presence of O(2) the reaction was partially inhibited by superoxide dismutase (SOD), which indicates a role for the superoxide radical, O(2) ([unk]), as a facultative intermediate electron carrier. The inhibition by SOD increased with substrate pH and with decrease in concentration of the ferrous scavenger bathophenanthroline-disulfonate. The results are consistent with a mechanism for transmembrane electron transport in which a flavin or quinone is the final electron carrier in the plasma membrane. The results are discussed in relation to the ecological importance that O(2) ([unk]) may have in the acquisition of ferric iron by dicotyledonous plants.

Entities:  

Year:  1987        PMID: 16665677      PMCID: PMC1054247          DOI: 10.1104/pp.85.1.310

Source DB:  PubMed          Journal:  Plant Physiol        ISSN: 0032-0889            Impact factor:   8.340


  18 in total

1.  The oxidation of reduced flavin mononucleotide by molecular oxygen.

Authors:  Q H GIBSON; J W HASTINGS
Journal:  Biochem J       Date:  1962-05       Impact factor: 3.857

2.  Iron Nutrition of Nicotiana Tabacum L. in Relation to Riboflavin, Riboflavin-5-phosphate, and Flavin Adenine Dinucleotide Content.

Authors:  G W Welkie; G W Miller
Journal:  Plant Physiol       Date:  1960-07       Impact factor: 8.340

3.  Redox activity at the surface of oat root cells.

Authors:  B Rubinstein; A I Stern; R G Stout
Journal:  Plant Physiol       Date:  1984-10       Impact factor: 8.340

4.  Fe reduction in cell walls of soybean roots.

Authors:  C L Tipton; J Thowsen
Journal:  Plant Physiol       Date:  1985-10       Impact factor: 8.340

5.  Depolarization of Cell Membrane Potential during Trans-Plasma Membrane Electron Transfer to Extracellular Electron Acceptors in Iron-Deficient Roots of Phaseolus vulgaris L.

Authors:  P C Sijmons; F C Lanfermeijer; A H de Boer; H B Prins; H F Bienfait
Journal:  Plant Physiol       Date:  1984-12       Impact factor: 8.340

6.  Mechanism of iron uptake by peanut plants : I. Fe reduction, chelate splitting, and release of phenolics.

Authors:  V Römheld; H Marschner
Journal:  Plant Physiol       Date:  1983-04       Impact factor: 8.340

7.  Cytosolic NADPH is the electron donor for extracellular fe reduction in iron-deficient bean roots.

Authors:  P C Sijmons; W van den Briel; H F Bienfait
Journal:  Plant Physiol       Date:  1984-05       Impact factor: 8.340

8.  Localization and capacity of proton pumps in roots of intact sunflower plants.

Authors:  V Römheld; C Müller; H Marschner
Journal:  Plant Physiol       Date:  1984-11       Impact factor: 8.340

9.  A transplasmamembrane electron transport system in maize roots.

Authors:  R Federico; C E Giartosio
Journal:  Plant Physiol       Date:  1983-09       Impact factor: 8.340

10.  Obligatory reduction of ferric chelates in iron uptake by soybeans.

Authors:  R L Chaney; J C Brown; L O Tiffin
Journal:  Plant Physiol       Date:  1972-08       Impact factor: 8.340

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  15 in total

1.  Iron deficiency decreases the Fe(III)-chelate reducing activity of leaf protoplasts.

Authors:  E B González-Vallejo; F Morales; L Cistué; A Abadía; J Abadía
Journal:  Plant Physiol       Date:  2000-02       Impact factor: 8.340

2.  The pH Requirement for in Vivo Activity of the Iron-Deficiency-Induced "Turbo" Ferric Chelate Reductase (A Comparison of the Iron-Deficiency-Induced Iron Reductase Activities of Intact Plants and Isolated Plasma Membrane Fractions in Sugar Beet).

Authors:  S. Susin; A. Abadia; J. A. Gonzalez-Reyes; J. J. Lucena; J. Abadia
Journal:  Plant Physiol       Date:  1996-01       Impact factor: 8.340

3.  Response of plant-colonizing pseudomonads to hydrogen peroxide.

Authors:  J Katsuwon; A J Anderson
Journal:  Appl Environ Microbiol       Date:  1989-11       Impact factor: 4.792

4.  Wood Smoke Particle Sequesters Cell Iron to Impact a Biological Effect.

Authors:  Andrew J Ghio; Joleen M Soukup; Lisa A Dailey; Haiyan Tong; Matthew J Kesic; G R Scott Budinger; Gökhan M Mutlu
Journal:  Chem Res Toxicol       Date:  2015-10-22       Impact factor: 3.739

5.  Accumulation of apoplastic iron in plant roots : a factor in the resistance of soybeans to iron-deficiency induced chlorosis?

Authors:  N Longnecker; R M Welch
Journal:  Plant Physiol       Date:  1990-01       Impact factor: 8.340

6.  Physiological Characteristics of Fe Accumulation in the ;Bronze' Mutant of Pisum sativum L., cv ;Sparkle' E107 (brz brz).

Authors:  R M Welch; T A Larue
Journal:  Plant Physiol       Date:  1990-06       Impact factor: 8.340

7.  Iron-Stress Induced Redox Activity in Tomato (Lycopersicum esculentum Mill.) Is Localized on the Plasma Membrane.

Authors:  T J Buckhout; P F Bell; D G Luster; R L Chaney
Journal:  Plant Physiol       Date:  1989-05       Impact factor: 8.340

Review 8.  Air pollutants disrupt iron homeostasis to impact oxidant generation, biological effects, and tissue injury.

Authors:  Andrew J Ghio; Joleen M Soukup; Lisa A Dailey; Michael C Madden
Journal:  Free Radic Biol Med       Date:  2020-02-21       Impact factor: 7.376

Review 9.  Generation of superoxide anion and hydrogen peroxide at the surface of plant cells.

Authors:  A Vianello; F Macrì
Journal:  J Bioenerg Biomembr       Date:  1991-06       Impact factor: 2.945

10.  Membrane-bound guaiacol peroxidases from maize (Zea mays L.) roots are regulated by methyl jasmonate, salicylic acid, and pathogen elicitors.

Authors:  Angela Mika; Marike Johanne Boenisch; David Hopff; Sabine Lüthje
Journal:  J Exp Bot       Date:  2009-12-23       Impact factor: 6.992

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