Sunday, May 3, 2009
2-66
Development of Recombinant Yeast for L-arabinose fermentation
A lack of natural microorganisms that can convert all hexoses and pentoses to ethanol has been a major constraint. Most industrial ethanol fermentations now use the natural yeast Saccharomyces cerevisiae to rapidly and efficiently convert hexoses from starch and sugar to ethanol. However, the yeast is unable to ferment the pentose sugars (xylose and arabinose). Our laboratory altered the genetic structure of S. cerevisiae by cloning and overexpressing xylose reductase, xylitol dehydrogenase and xylulokinase, which make it possible to convert glucose and xylose to ethanol.
The focus of this work is to establish an arabinose fermentation pathway in our glucose/xylose co-fermenting yeast S. cerevisiae 424A(LNH-ST). We have cloned and overexpressed genes encoding L-arabinitol 4-dehydrogenase and L-xylulose reductase in 424A(LNH-ST). The newly constructed strain can grow on arabinose and ferment arabinose present in cellulosic biomass to ethanol. Our new strain is also capable of co-fermenting a mixture of all sugars (glucose, mannose, galactose, xylose and arabinose) present in hydrolysates from any types of cellulosic biomass to the ethanol.