TY - JOUR
T1 - Efficient succinic acid production from lignocellulosic biomass by simultaneous utilization of glucose and xylose in engineered Escherichia coli
AU - Liu, Rongming
AU - Liang, Liya
AU - Li, Feng
AU - Wu, Mingke
AU - Chen, Kequan
AU - Ma, Jiangfeng
AU - Jiang, Min
AU - Wei, Ping
AU - Ouyang, Pingkai
PY - 2013/12
Y1 - 2013/12
N2 - To enhance succinic acid formation during xylose fermentation in Escherichia coli, overexpression of ATP-forming phosphoenolpyruvate carboxykinase (PEPCK) from Bacillus subtilis 168 in an ldhA, pflB, and ppc deletion strain resulted in a significant increase in cell mass and succinic acid production. However, BA204 displays a low yield of glucose fermentation and sequential glucose-xylose utilization under regulation by the phosphotransferase system (PTS). To improve the capability of glucose fermentation and simultaneously consume sugar mixture for succinic acid production, a pflB, ldhA, ppc, and ptsG deletion strain overexpressing ATP-forming PEPCK, named E. coli BA305, was constructed. As a result, after 120h fed-batch fermentation of sugarcane bagasse hydrolysate, the dry cell weight and succinic acid concentration in BA305 were 4.58gL-1 and 39.3gL-1, respectively.
AB - To enhance succinic acid formation during xylose fermentation in Escherichia coli, overexpression of ATP-forming phosphoenolpyruvate carboxykinase (PEPCK) from Bacillus subtilis 168 in an ldhA, pflB, and ppc deletion strain resulted in a significant increase in cell mass and succinic acid production. However, BA204 displays a low yield of glucose fermentation and sequential glucose-xylose utilization under regulation by the phosphotransferase system (PTS). To improve the capability of glucose fermentation and simultaneously consume sugar mixture for succinic acid production, a pflB, ldhA, ppc, and ptsG deletion strain overexpressing ATP-forming PEPCK, named E. coli BA305, was constructed. As a result, after 120h fed-batch fermentation of sugarcane bagasse hydrolysate, the dry cell weight and succinic acid concentration in BA305 were 4.58gL-1 and 39.3gL-1, respectively.
KW - ATP
KW - Escherichia coli
KW - Lignocellulosic hydrolysate
KW - Simultaneous utilization
KW - Succinic acid
UR - http://www.scopus.com/inward/record.url?scp=84885058877&partnerID=8YFLogxK
U2 - 10.1016/j.biortech.2013.09.052
DO - 10.1016/j.biortech.2013.09.052
M3 - 文章
C2 - 24096277
AN - SCOPUS:84885058877
SN - 0960-8524
VL - 149
SP - 84
EP - 91
JO - Bioresource Technology
JF - Bioresource Technology
ER -