TY - JOUR
T1 - Production of 2,3-butanediol from xylose by engineered Saccharomyces cerevisiae
AU - Kim, Soo Jung
AU - Seo, Seung Oh
AU - Park, Yong Cheol
AU - Jin, Yong Su
AU - Seo, Jin Ho
N1 - Publisher Copyright:
© 2014 Elsevier B.V.
PY - 2014/12/20
Y1 - 2014/12/20
N2 - 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.
AB - 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.
KW - 2,3-Butanediol (2,3-BD)
KW - Pyruvate decarboxylase-deficient mutant
KW - Saccharomyces cerevisiae
KW - Xylose
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U2 - 10.1016/j.jbiotec.2013.12.017
DO - 10.1016/j.jbiotec.2013.12.017
M3 - Article
C2 - 24480571
AN - SCOPUS:84923922989
SN - 0168-1656
VL - 192
SP - 376
EP - 382
JO - Journal of Biotechnology
JF - Journal of Biotechnology
ER -