Genome-Scale Reconstruction of the Saccharomyces cerevisiae Metabolic Network

  1. Jochen Förster1,3,4,
  2. Iman Famili2,4,
  3. Patrick Fu2,
  4. Bernhard Ø. Palsson2, and
  5. Jens Nielsen1,5
  1. 1Center for Process Biotechnology, BioCentrum-DTU, Technical University of Denmark, DK-2800 Lyngby, Denmark; 2Department of Bioengineering, University of California San Diego, La Jolla, California 92093, USA

Abstract

The metabolic network in the yeast Saccharomyces cerevisiaewas reconstructed using currently available genomic, biochemical, and physiological information. The metabolic reactions were compartmentalized between the cytosol and the mitochondria, and transport steps between the compartments and the environment were included. A total of 708 structural open reading frames (ORFs) were accounted for in the reconstructed network, corresponding to 1035 metabolic reactions. Further, 140 reactions were included on the basis of biochemical evidence resulting in a genome-scale reconstructed metabolic network containing 1175 metabolic reactions and 584 metabolites. The number of gene functions included in the reconstructed network corresponds to ∼16% of all characterized ORFs in S. cerevisiae. Using the reconstructed network, the metabolic capabilities of S. cerevisiae were calculated and compared with Escherichia coli. The reconstructed metabolic network is the first comprehensive network for a eukaryotic organism, and it may be used as the basis for in silico analysis of phenotypic functions.

[Supplemental material is available online at www.genome.org. The detailed genome-scale reconstructed model ofSaccharomyces cerevisiae can be found athttp://www.cpb.dtu.dk/models/yeastmodel.html orhttp://geneticcircuits.ucsd.edu/organisms/yeast.html.]

Footnotes

  • 3 Present address: Fluxome Sciences A/S, Soltofts Plads, Building 223, Technical University of Denmark, DK-2800 Lyngby, Denmark

  • 4 These authors contributed equally to this work.

  • 5 Corresponding author.

  • E-MAIL jn{at}biocentrum.dtu.dk; FAX 45-45-88-41-48.

  • Article and publication are at http://www.genome.org/cgi/doi/10.1101/gr.234503.

    • Received March 3, 2002.
    • Accepted November 25, 2002.
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