The race of ethanol production and the ethanol concentrations attained
by the most promising xylose-fermenting yeasts, Pichia stipitis, Cand
ida shehatae, and Pachysolen tannophilus, compare poorly with that of
commercial ethanol fermentation by non-xylose-fermenting Saccharomyces
cerevisiae using glucose-based substrates. The oxygen requirement for
efficient fermentation by the xylose-fermenting yeasts and the lack o
f such a general requirement by S. cerevisiae indicates basic underlyi
ng differences in their physiological relations to oxygen. The redox i
mbalance in the initial conversion of xylose to xylulose, sensitivity
to high concentrations of ethanol differences in the respiratory pathw
ay and sensitivity to microbial inhibitors, particularly those liberat
ed during pretreatment and hydrolysis of lignocellulose substrates, ha
ve been identified as major factors limiting ethanol fermentation by t
he xylose-fermenting yeasts. Recombinant S. cerevisiae, containing fun
ctional xylose reductase and xylitol dehydrogenase, grows on, but poor
ly ferments, xylose. The unfavorable kinetic properties of these enzym
es and an inadequate pentose phosphate pathway apparently limit the ab
ility of the recombinant yeast to ferment xylose.