International Journal of Molecular Sciences (Nov 2021)

<span style="font-variant: small-caps">D</span>-Xylose Sensing in <i>Saccharomyces cerevisiae</i>: Insights from <span style="font-variant: small-caps">D</span>-Glucose Signaling and Native <span style="font-variant: small-caps">D</span>-Xylose Utilizers

  • Daniel P. Brink,
  • Celina Borgström,
  • Viktor C. Persson,
  • Karen Ofuji Osiro,
  • Marie F. Gorwa-Grauslund

DOI
https://doi.org/10.3390/ijms222212410
Journal volume & issue
Vol. 22, no. 22
p. 12410

Abstract

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Extension of the substrate range is among one of the metabolic engineering goals for microorganisms used in biotechnological processes because it enables the use of a wide range of raw materials as substrates. One of the most prominent examples is the engineering of baker’s yeast Saccharomyces cerevisiae for the utilization of d-xylose, a five-carbon sugar found in high abundance in lignocellulosic biomass and a key substrate to achieve good process economy in chemical production from renewable and non-edible plant feedstocks. Despite many excellent engineering strategies that have allowed recombinant S. cerevisiae to ferment d-xylose to ethanol at high yields, the consumption rate of d-xylose is still significantly lower than that of its preferred sugar d-glucose. In mixed d-glucose/d-xylose cultivations, d-xylose is only utilized after d-glucose depletion, which leads to prolonged process times and added costs. Due to this limitation, the response on d-xylose in the native sugar signaling pathways has emerged as a promising next-level engineering target. Here we review the current status of the knowledge of the response of S. cerevisiae signaling pathways to d-xylose. To do this, we first summarize the response of the native sensing and signaling pathways in S. cerevisiae to d-glucose (the preferred sugar of the yeast). Using the d-glucose case as a point of reference, we then proceed to discuss the known signaling response to d-xylose in S. cerevisiae and current attempts of improving the response by signaling engineering using native targets and synthetic (non-native) regulatory circuits.

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