2,3-Butanediol (2,3-BD) production from xylose that is abundant in lignocellulosic hydrolyzate would make the production of 2,3-BD more sustainable and economical. Saccharomyces cerevisiae can produce only trace amounts of 2,3-BD, but also cannot ferment xylose. Therefore, it is necessary to introduce both 2,3-BD production and xylose assimilation pathways into S. cerevisiae for producing 2,3-BD from xylose. A pyruvate decarboxylase (Pdc)-deficient mutant (SOS4) was used as a host in order to increase carbon flux toward 2,3-BD instead of ethanol. The XYL1, XYL2, and XYL3 genes coding for xylose assimilating enzymes derived from Scheffersomyces stipitis were introduced into the SOS4 strain to enable xylose utilization. Additionally, the alsS and alsD genes from Bacillus subtilis and endogenous BDH1 gene were overexpressed to increase 2,3-BD production from xylose. As a result, the resulting strain (BD4X) produced 20.7 g/L of 2,3-BD from xylose with a yield of 0.27 g 2,3-BD/g xylose. The titer of 2,3-BD from xylose increased up to 43.6 g/L under a fed-batch fermentation. The BD4X strain produced (R, R)-2,3-BD dominantly (>97% of the total 2,3-BD) with trace amounts of meso-2,3-BD. These results suggest that S. cerevisiae might be a promising host for producing 2,3-BD from lignocellulosic biomass for industrial applications.
Bibliographical noteFunding Information:
This research was supported by the Advanced Biomass R&D Center (ABC) of Korea Grant ( 2010-0029799 ) funded by the Ministry of Education, Science and Technology and Korea Research Council of Fundamental Science & Technology (KRCF) grant.
© 2014 Elsevier B.V.
- 2,3-Butanediol (2,3-BD)
- Pyruvate decarboxylase-deficient mutant
- Saccharomyces cerevisiae