Intracellular fluxes in a recombinant xylose-utilizing Saccharomyces cerevisiae cultivated anaerobically at different dilution rates and feed concentrations

Authors

  • C. Fredrik Wahlbom,

    1. Department of Applied Microbiology, Lund University, P.O. Box 124, SE-221 00 Lund, Sweden; telephone: +46-46-222-8428; fax: +46-46-222-4203
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  • Anna Eliasson,

    1. Department of Applied Microbiology, Lund University, P.O. Box 124, SE-221 00 Lund, Sweden; telephone: +46-46-222-8428; fax: +46-46-222-4203
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  • Bärbel Hahn-Hägerdal

    Corresponding author
    1. Department of Applied Microbiology, Lund University, P.O. Box 124, SE-221 00 Lund, Sweden; telephone: +46-46-222-8428; fax: +46-46-222-4203
    • Department of Applied Microbiology, Lund University, P.O. Box 124, SE-221 00 Lund, Sweden; telephone: +46-46-222-8428; fax: +46-46-222-4203
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Abstract

A metabolic flux model was constructed for the yeast Saccharomyces cerevisiae comprising the most important reactions during anaerobic metabolism of xylose and glucose. The model was used to calculate the intracellular fluxes in a recombinant, xylose-utilizing strain of S. cerevisiae (TMB 3001) grown anaerobically in a defined medium at dilution rates of 0.03, 0.06, and 0.18 h−1. The feed concentration was varied from 0 g/L xylose and 20 g/L glucose to a mixture of 15 g/L xylose and 5 g/L glucose, so that the total concentration of carbon source was kept at 20 g/L. The specific uptake of xylose increased with the xylose concentration in the feed and with increasing dilution rate. The excreted xylitol was less than half of the xylose consumed. With increasing xylose concentration in the feed, the fluxes in the pentose phosphate pathway increased, whereas the flux through glycolysis decreased. Under all cultivation conditions, nicotinamide adenine dinucleotide (NADH) was the preferred cofactor for xylose reductase. The model showed that the flux through the reaction from ribulose 5-phosphate to xylulose 5-phosphate was very low under all cultivation conditions. © 2001 John Wiley & Sons, Inc. Biotechnol Bioeng 72: 289–296, 2001.

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