Frontiers in Microbiology (Oct 2012)
Balance of XYL1 and XYL2 expression in different yeast chassis for improved xylose fermentation
Abstract
Reducing xylitol formation is an important step in engineering xylose reductase/xylitol dehydrogenase pathway for ethanol production from xylose in Saccharomyces cerevisiae. In this study, to balance the expression of XYL1 and mutant XYL2 encoding xylose reductase and NADP+-preferring xylitol dehydrogenase for reduced xylitol production, we utilized a strategy combining chassis selection and direct fine-tuning of XYL1 and XYL2 expression. A XYL1 gene under control of various promoters of ADH1, truncated ADH1 and PGK1, and a mutated XYL2 with different copy numbers were constructed into different xylose-utilizing modules, which were then expressed in two yeast chassis W303a and L2612. The strategy enabled us to achieve an improved L2612-derived recombinant strain with XYL1 controlled by promoter PGK1 and with two copies of XYL2. The strain exhibited 21.3% lower xylitol yield and 40.0% higher ethanol yield. The results demonstrate the feasibility of the combinatorial strategy for construction of efficient xylose-fermenting Saccharomyces cerevisiae.
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