Bioethanol production performance of five recombinant strains of laboratory and industrial xylose-fermenting Saccharomyces cerevisiae

Bioresour Technol. 2009 Apr;100(8):2392-8. doi: 10.1016/j.biortech.2008.11.047. Epub 2009 Jan 6.

Abstract

In this study, five recombinant Saccharomyces cerevisiae strains were compared for their xylose-fermenting ability. The most efficient xylose-to-ethanol fermentation was found by using the industrial strain MA-R4, in which the genes for xylose reductase and xylitol dehydrogenase from Pichia stipitis along with an endogenous xylulokinase gene were expressed by chromosomal integration of the flocculent yeast strain IR-2. The MA-R4 strain rapidly converted xylose to ethanol with a low xylitol yield. Furthermore, the MA-R4 strain had the highest ethanol production when fermenting not only a mixture of glucose and xylose, but also mixed sugars in the detoxified hydrolysate of wood chips. These results collectively suggest that MA-R4 may be a suitable recombinant strain for further study into large-scale ethanol production from mixed sugars present in lignocellulosic hydrolysates.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aerobiosis
  • Aldehyde Reductase / metabolism
  • D-Xylulose Reductase / metabolism
  • Ethanol / metabolism*
  • Fermentation*
  • Industrial Microbiology*
  • Laboratories*
  • Lignin / metabolism
  • Phosphotransferases (Alcohol Group Acceptor) / metabolism
  • Recombination, Genetic / genetics
  • Saccharomyces cerevisiae / enzymology
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae / isolation & purification*
  • Saccharomyces cerevisiae / metabolism*
  • Time Factors
  • Xylose / metabolism*

Substances

  • lignocellulose
  • Ethanol
  • Lignin
  • Xylose
  • Aldehyde Reductase
  • D-Xylulose Reductase
  • Phosphotransferases (Alcohol Group Acceptor)
  • xylulokinase