Alteration of citrate metabolism in cluster roots of white lupin [Lupinus albus]

Organic acid excretion plays a key role in the superior Pi-acquisition of barely soluble inorganic P sources from soils. Seedlings of white lupin (Lupinus albus L.) grown for 37 d in -P nutrient solution showed typical -P symptoms, such as low P content, increased root/shoot ratio and the developmen...

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Published inPlant and cell physiology Vol. 44; no. 9; pp. 901 - 908
Main Authors Kihara, T. (Gifu Univ. (Japan). Faculty of Agriculture), Wada, T, Suzuki, Y, Hara, T, Koyama, H
Format Journal Article
LanguageEnglish
Published Japan Oxford University Press 01.09.2003
Oxford Publishing Limited (England)
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Summary:Organic acid excretion plays a key role in the superior Pi-acquisition of barely soluble inorganic P sources from soils. Seedlings of white lupin (Lupinus albus L.) grown for 37 d in -P nutrient solution showed typical -P symptoms, such as low P content, increased root/shoot ratio and the development of cluster roots which released large amounts of citrate. Citrate concentration in the cluster roots was 21.5 micromol (g FW)**-1, which corresponded to a 4.3- and 2.6-fold increase of +P and -P root apexes, respectively. Cluster roots possessed higher phosphoenolpyruvate carboxylase and phosphoenolpyruvate phosphatase activity than those in +P root apexes, which could result in increasing the supply of substrate for citrate synthase. On the other hand, the cytosolic pathway which converts citrate to 2-oxoglutarate consists of aconitase and NADP-specific isocitrate dehydrogenase activity that was lower in the cluster roots than in +P root apexes, and may contribute to citrate accumulation. Thus, metabolic balance with these alterations would play an important role in increasing citrate concentration in the cluster roots. The molecular characterization of NADP-specific isocitrate dehydrogenase indicated that the cytosolic isoenzyme functions as a hetero-dimer, and that the activity would be regulated by the transcript levels for both isoforms.
Bibliography:F61
F60
2004006129
local:pcg115
Received May 19, 2003; Accepted July 7, 2003
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content type line 23
ISSN:0032-0781
1471-9053
DOI:10.1093/pcp/pcg115