Literature DB >> 7768910

Quantification of compartmented metabolic fluxes in maize root tips using isotope distribution from 13C- or 14C-labeled glucose.

M Dieuaide-Noubhani1, G Raffard, P Canioni, A Pradet, P Raymond.   

Abstract

Metabolic pathways of the intermediate metabolism of maize root tips were identified and quantified after labeling to isotopic and metabolic steady state using glucose labeled on carbon-1, -2, or -6 with 14C or 13C. The specific radioactivity of amino acids and the 13C-specific enrichment of specific carbons of free glucose, sucrose, alanine and glutamate were measured and used to calculate metabolic fluxes. The non-triose pathways, including synthesis of polysaccharides, accumulation of free hexoses, and to a lesser extent starch synthesis, were found to consume 75% of the glucose entering the root tips. The cycle of synthesis and hydrolysis of sucrose was found to consume about 70% of the ATP produced by respiration. The comparison of the specific radioactivities of amino acids and phospholipid glycerol phosphate after labeling with [1-(14)C] or [6-(14)C]glucose revealed the operation of the pentose phosphate pathway. The transfer of label from [2-(14)C]glucose to carbon-1 of starch glucosyl units confirmed the operation of this pathway and indicated that it is located in plastids. It was found to consume 32% of the hexose phosphates entering the triose pathways. The remaining 68% were consumed by glycolysis. The determination of the specific enrichment of carbohydrate carbons -1 and -6 after labeling with [1-(13)C]glucose indicated that both the conversion of triose phosphates back to hexose phosphates and the transaldolase exchange contributed to this randomization. Of the triose phosphates produced by glycolysis and the pentose phosphate pathway, about 60% were found to be recycled to hexose phosphates, and 28% were directed to the tricarboxylic acid cycle. Of this 28%, two-thirds were found to be directed through the pyruvate kinase branch and one-third through the phosphoenolpyruvate branch. The latter essentially has an anaplerotic function since little malate was found to be converted to pyruvate (malic enzyme reaction).

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Year:  1995        PMID: 7768910     DOI: 10.1074/jbc.270.22.13147

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  28 in total

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Journal:  Plant Mol Biol       Date:  2002-01       Impact factor: 4.076

2.  Starch biosynthesis and intermediary metabolism in maize kernels. Quantitative analysis of metabolite flux by nuclear magnetic resonance.

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3.  A Combined Metabolomics and Fluxomics Analysis Identifies Steps Limiting Oil Synthesis in Maize Embryos.

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4.  Carbon uptake and the metabolism and transport of lipids in an arbuscular mycorrhiza

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Journal:  Plant Physiol       Date:  1999-06       Impact factor: 8.340

5.  Sucrose cycling in heterotrophic plant cell metabolism: first step towards an experimental model.

Authors:  Claude Roby; Sandra Cortès; Marina Gromova; Jean-Luc Le Bail; Justin K M Roberts
Journal:  Mol Biol Rep       Date:  2002       Impact factor: 2.316

6.  Sugar-Starvation-Induced Changes of Carbon Metabolism in Excised Maize Root Tips.

Authors:  M. Dieuaide-Noubhani; P. Canioni; P. Raymond
Journal:  Plant Physiol       Date:  1997-12       Impact factor: 8.340

7.  Subcellular flux analysis of central metabolism in a heterotrophic Arabidopsis cell suspension using steady-state stable isotope labeling.

Authors:  Shyam K Masakapalli; Pascaline Le Lay; Joanna E Huddleston; Naomi L Pollock; Nicholas J Kruger; R George Ratcliffe
Journal:  Plant Physiol       Date:  2009-11-25       Impact factor: 8.340

8.  Maize cytosolic NADP-malic enzyme (ZmCytNADP-ME): a phylogenetically distant isoform specifically expressed in embryo and emerging roots.

Authors:  Enrique Detarsio; Verónica G Maurino; Clarisa E Alvarez; Gabriela L Müller; Carlos S Andreo; María F Drincovich
Journal:  Plant Mol Biol       Date:  2008-07-13       Impact factor: 4.076

9.  Quantification of compartmented metabolic fluxes in developing soybean embryos by employing biosynthetically directed fractional (13)C labeling, two-dimensional [(13)C, (1)H] nuclear magnetic resonance, and comprehensive isotopomer balancing.

Authors:  Ganesh Sriram; D Bruce Fulton; Vidya V Iyer; Joan Marie Peterson; Ruilian Zhou; Mark E Westgate; Martin H Spalding; Jacqueline V Shanks
Journal:  Plant Physiol       Date:  2004-10-01       Impact factor: 8.340

10.  Co-localization of carbonic anhydrase and phosphoenol-pyruvate carboxylase and localization of pyruvate kinase in roots and hypocotyls of etiolated Glycine max seedlings.

Authors:  Maria Dimou; Anca Paunescu; Georgios Aivalakis; Emmanouil Flemetakis; Panagiotis Katinakis
Journal:  Int J Mol Sci       Date:  2009-06-29       Impact factor: 6.208

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