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Understanding the mechanisms that allow plants to respond to variable and reduced availability of inorganic phosphate is of increasing agricultural importance because of the continuing depletion of the rock phosphate reserves that are used to combat inadequate phosphate levels in the soil. Changes in gene expression, protein levels, enzyme activities and metabolite levels all point to a reconfiguration of the central metabolic network in response to reduced availability of inorganic phosphate, but the metabolic significance of these changes can only be assessed in terms of the fluxes supported by the network. Steady-state metabolic flux analysis was used to define the metabolic phenotype of a heterotrophic Arabidopsis thaliana cell culture grown on a Murashige and Skoog medium containing 0, 1.25 or 5 mm inorganic phosphate. Fluxes through the central metabolic network were deduced from the redistribution of (13) C into metabolic intermediates and end products when cells were labelled with [1-(13) C], [2-(13) C], or [(13) C6 ]glucose, in combination with (14) C measurements of the rates of biomass accumulation. Analysis of the flux maps showed that reduced levels of phosphate in the growth medium stimulated flux through phosphoenolpyruvate carboxylase and malic enzyme, altered the balance between cytosolic and plastidic carbohydrate oxidation in favour of the plastid, and increased cell maintenance costs. We argue that plant cells respond to phosphate deprivation by reconfiguring the flux distribution through the pathways of carbohydrate oxidation to take advantage of better phosphate homeostasis in the plastid.

Original publication

DOI

10.1111/tpj.12522

Type

Journal article

Journal

Plant J

Publication Date

06/2014

Volume

78

Pages

964 - 977

Keywords

Arabidopsis thaliana, Pi homeostasis, carbon conversion efficiency, heterotrophic metabolism, metabolic flux analysis, phosphate availability, phosphate stress, plastid metabolism, pyruvate kinase, subcellular compartmentation, Arabidopsis, Carbohydrate Metabolism, Cells, Cultured, Cytosol, Homeostasis, Oxidation-Reduction, Phenotype, Phosphates, Plastids, Pyruvate Kinase