News Release

Wine-making yeast shows promise for bioethanol production

Peer-Reviewed Publication

PLOS

Researchers from the Stanford University School of Medicine have identified a gene in the yeast Saccharomyces cerevisiae that might be important for ethanol production from plant material, providing insights into the bioethanol alternative to 'fossil fuels'. Combining new high-throughput genome sequencing technology with traditional genetic methods, this study highlights the previously unknown potential of natural S. cerevisiae strains to convert five-carbon sugars such as xylose into ethanol. Details are published May 13 in the open-access journal PLoS Genetics.

S. cerevisiae is the primary organism used in the fermentation process required for industrial bioethanol production. However, despite voraciously fermenting the six-carbon sugars, such as glucose, found in cornstarch or sugar cane, it was not thought to be able to ferment the five-carbon sugars that are abundant in agricultural wastes or dedicated crops like switchgrass. As the industry moves towards plant-based ethanol, a strain of yeast that can ferment both types of sugar equally well is highly desirable.

Therefore, Jared Wenger and Katja Schwartz sought to identify previously unstudied Saccharomyces yeast strains with some ability to ferment xylose. They found a number of strains, primarily used in wine-making, which could metabolize this important sugar in order to grow slowly. They studied one strain in particular, applying a new genome sequencing technology to determine the genetic basis of its growth – the presence of a single gene they named XDH1.

Although the ability of these naturally occurring yeasts to grow on this sugar is modest and they are still not as capable at using xylose as other, genetically-modified strains, this discovery may lead to the development of new, industrially-applicable strains of S. cerevisiae for use in large-scale bioethanol production.

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FINANCIAL DISCLOSURE: The authors wish to thank the Stanford Global Climate and Energy Project (GCEP) (grant # 33450), as well the NIH-NIGMS Genetics & Developmental Biology Training Program (grant # NIHGM007790) for funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

COMPETING INTERESTS: The authors have declared that no competing interests exist.

CITATION: Wenger JW, Schwartz K, Sherlock G (2010) Bulk Segregant Analysis by High-Throughput Sequencing Reveals a Novel Xylose Utilization Gene from Saccharomyces cerevisiae. PLoS Genet 6(5): e1000942. doi:10.1371/journal.pgen.1000942

IN YOUR COVERAGE, PLEASE USE THIS LINK TO PROVIDE ACCESS TO THE FREELY AVAILABLE ARTICLE (the link will go live when the embargo ends): http://www.plosgenetics.org/article/info:doi/10.1371/journal.pgen.1000942

Contact:
Jared Wenger
(+1) 650 498 5995
jwenger@stanford.edu

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