Cloning of Glucuronokinase from Arabidopsis thaliana, the Last Missing Enzyme of the myo-Inositol Oxygenase Pathway to Nucleotide Sugars*

  1. Raimund Tenhaken1
  1. From the Department of Cell Biology, Plant Physiology, University of Salzburg, Hellbrunnerstrasse 34, 5020 Salzburg, Austria
  1. 1 To whom correspondence should be addressed. Tel.: 43-662-8044-5551; Fax: 43-662-8044-619; E-mail: raimund.tenhaken{at}sbg.ac.at.

Abstract

Nucleotide sugars are building blocks for carbohydrate polymers in plant cell walls. They are synthesized from sugar-1-phosphates or epimerized as nucleotide sugars. The main precursor for primary cell walls is UDP-glucuronic acid, which can be synthesized via two independent pathways. One starts with the ring cleavage of myo-inositol into glucuronic acid, which requires a glucuronokinase and a pyrophosphorylase for activation into UDP-glucuronate. Here we report on the purification of glucuronokinase from Lilium pollen. A 40-kDa protein was purified combining six chromatographic steps and peptides were de novo sequenced. This allowed the cloning of the gene from Arabidopsis thaliana and the expression of the recombinant protein in Escherichia coli for biochemical characterization. Glucuronokinase is a novel member of the GHMP-kinase superfamily having an unique substrate specificity for d-glucuronic acid with a Km of 0.7 mm. It requires ATP as phosphate donor (Km 0.56 mm). In Arabidopsis, the gene is expressed in all plant tissues with a preference for pollen. Genes for glucuronokinase are present in (all) plants, some algae, and a few bacteria as well as in some lower animals.

Footnotes

  • * This work was supported in part by grants of the German Research Foundation (Deutsche Forschungsgemeinschaft, Bonn) and Austrian Science Fund Grant FWF P20297-B16 (Vienna).

  • 3 S. Endres and R. Tenhaken, unpublished results.

  • 2 The abbreviations used are:

    UGD
    UDP-glucose dehydrogenase
    GlcAK
    glucuronokinase
    UDP-GlcA
    UDP-D-glucuronic acid
    UDP-Glc
    UDP-d-glucose
    MIOX
    myo-inositol oxygenase
    USP
    UDP-sugar pyrophosphorylase
    HPLC
    high pressure liquid chromatography
    MOPS
    4-morpholinepropanesulfonic acid.

    • Received September 23, 2009.
    • Revision received November 10, 2009.
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    1. The Journal of Biological Chemistry 285, 2902-2910.
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