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Plant Physiol, October 2000, Vol. 124, pp. 885-898

Responses of Sugar Beet Roots to Iron Deficiency. Changes in Carbon Assimilation and Oxygen Use1

Ana Flor López-Millán, Fermín Morales, Sofía Andaluz, Yolanda Gogorcena, Anunciación Abadía, Javier De Las Rivas, and Javier Abadía*

Department of Plant Nutrition, Aula Dei Experimental Station-Consejo Superior de Investigaciones Científicas, Apartado 202, E-50080 Zaragoza, Spain (A.F.L.-M., F.M., S.A., Y.G., A.A., J.A.); and Instituto de Recursos Naturales y Agrobiología de Salamanca-Consejo Superior de Investigaciones Científicas, Cordel de Merinas, E-37071 Salamanca, Spain (J.D.L.R.)

Different root parts with or without increased iron-reducing activities have been studied in iron-deficient and iron-sufficient control sugar beet (Beta vulgaris L. Monohil hybrid). The distal root parts of iron-deficient plants, 0 to 5 mm from the root apex, were capable to reduce Fe(III)-chelates and contained concentrations of flavins near 700 µM, two characteristics absent in the 5 to 10 mm sections of iron-deficient plants and the whole root of iron-sufficient plants. Flavin-containing root tips had large pools of carboxylic acids and high activities of enzymes involved in organic acid metabolism. In iron-deficient yellow root tips there was a large increase in carbon fixation associated to an increase in phosphoenolpyruvate carboxylase activity. Part of this carbon was used, through an increase in mitochondrial activity, to increase the capacity to produce reducing power, whereas another part was exported via xylem. Root respiration was increased by iron deficiency. In sugar beet iron-deficient roots flavins would provide a suitable link between the increased capacity to produce reduced nucleotides and the plasma membrane associated ferric chelate reductase enzyme(s). Iron-deficient roots had a large oxygen consumption rate in the presence of cyanide and hydroxisalycilic acid, suggesting that the ferric chelate reductase enzyme is able to reduce oxygen in the absence of Fe(III)-chelates.


1 This work was supported by the Comisión Interministerial de Ciencia y Tecnología (grant no. AGR97-1177 to A.A.), the Dirección General de Investigación Científica y Técnica (grant no. PB97-1176 to J.A.), and the Commission of European Communities (grant nos. AIR3-CT94-1973 and PL971176 to J.A.). A.F.L.-M. was supported by a fellowship from the Spanish Ministry of Science and Education. F.M. and Y.G. were scientists on contracts from the Spanish Ministry of Education and Culture and the Spanish Council of Scientific Research, respectively.

* Corresponding author; e-mail jabadia{at}eead.csic.es; fax 34-976-575620.

© 2000 American Society of Plant Physiologists



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