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Induction of the Root Cell Plasma Membrane Ferric Reductase (An Exclusive Role for Fe and Cu)

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Journal Plant Physiol
Specialty Physiology
Date 1997 Jul 1
PMID 12223760
Citations 7
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Abstract

Induction of ferric reductase activity in dicots and nongrass monocots is a well-recognized response to Fe deficiency. Recent evidence has shown that Cu deficiency also induces plasma membrane Fe reduction. In this study we investigated whether other nutrient deficiencies could also induce ferric reductase activity in roots of pea (Pisum sativum L. cv Sparkle) seedlings. Of the nutrient deficiencies tested (K, Mg, Ca, Mn, Zn, Fe, and Cu), only Cu and Fe deficiencies elicited a response. Cu deficiency induced an activity intermediate between Fe-deficient and control plant activities. To ascertain whether the same reductase is induced by Fe and Cu deficiency, concentration- and pH-dependent kinetics of root ferric reduction were compared in plants grown under control, -Fe, and -Cu conditions. Additionally, rhizosphere acidification, another process induced by Fe deficiency, was quantified in pea seedlings grown under the three regimes. Control, Fe-deficient, and Cu-deficient plants exhibited no major differences in pH optima or Km for the kinetics of ferric reduction. However, the Vmax for ferric reduction was dramatically influenced by plant nutrient status, increasing 16- to 38-fold under Fe deficiency and 1.5- to 4-fold under Cu deficiency, compared with that of control plants. These results are consistent with a model in which varying amounts of the same enzyme are deployed on the plasma membrane in response to plant Fe or Cu status. Rhizosphere acidification rates in the Cu-deficient plants were similarly intermediate between those of the control and Fe-deficient plants. These results suggest that Cu deficiency induces the same responses induced by Fe deficiency in peas.

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References
1.
Watkins J, Altazan J, Elder P, Li C, Nunez M, Cui X . Kinetic characterization of reductant dependent processes of iron mobilization from endocytic vesicles. Biochemistry. 1992; 31(25):5820-30. DOI: 10.1021/bi00140a018. View

2.
Fox T, Shaff J, Grusak M, Norvell W, Chen Y, Chaney R . Direct Measurement of 59Fe-Labeled Fe2+ Influx in Roots of Pea Using a Chelator Buffer System to Control Free Fe2+ in Solution. Plant Physiol. 1996; 111(1):93-100. PMC: 157815. DOI: 10.1104/pp.111.1.93. View

3.
Yi Y, Guerinot M . Genetic evidence that induction of root Fe(III) chelate reductase activity is necessary for iron uptake under iron deficiency. Plant J. 1996; 10(5):835-44. DOI: 10.1046/j.1365-313x.1996.10050835.x. View

4.
Yuan D, Stearman R, Dancis A, Dunn T, Beeler T, Klausner R . The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase required for iron uptake. Proc Natl Acad Sci U S A. 1995; 92(7):2632-6. PMC: 42272. DOI: 10.1073/pnas.92.7.2632. View

5.
Askwith C, Eide D, Van Ho A, Bernard P, Li L, Sipe D . The FET3 gene of S. cerevisiae encodes a multicopper oxidase required for ferrous iron uptake. Cell. 1994; 76(2):403-10. DOI: 10.1016/0092-8674(94)90346-8. View