TY - JOUR
T1 - Succinic acid production from sucrose and sugarcane molasses by metabolically engineered Escherichia coli
AU - Li, Feng
AU - Ma, Jiangfeng
AU - Wu, Mingke
AU - Ji, Yaliang
AU - Chen, Wufang
AU - Ren, Xinyi
AU - Jiang, Min
N1 - Publisher Copyright:
© 2015 Chin J Biotech, All rights reserved.
PY - 2015/4/25
Y1 - 2015/4/25
N2 - Sugarcane molasses containing large amounts of sucrose is an economical substrate for succinic acid production. However, Escherichia coli AFP111 cannot metabolize sucrose although it is a promising candidate for succinic acid production. To achieve sucrose utilizing ability, we cloned and expressed cscBKA genes encoding sucrose permease, fructokinase and invertase of non-PTS sucrose-utilization system from E. coli W in E. coli AFP111 to generate a recombinant strain AFP111/pMD19T-cscBKA. After 72 h of anaerobic fermentation of the recombinant in serum bottles, 20 g/L sucrose was consumed and 12 g/L succinic acid was produced. During dual-phase fermentation comprised of initial aerobic growth phase followed by anaerobic fermentation phase, the concentration of succinic acid from sucrose and sugarcane molasses was 34 g/L and 30 g/L, respectively, at 30 h of anaerobic phase in a 3 L fermentor. The results show that the introduction of non-PTS sucrose-utilization system has sucrose-metabolizing capability for cell growth and succinic acid production, and can use cheap sugarcane molasses to produce succinic acid.
AB - Sugarcane molasses containing large amounts of sucrose is an economical substrate for succinic acid production. However, Escherichia coli AFP111 cannot metabolize sucrose although it is a promising candidate for succinic acid production. To achieve sucrose utilizing ability, we cloned and expressed cscBKA genes encoding sucrose permease, fructokinase and invertase of non-PTS sucrose-utilization system from E. coli W in E. coli AFP111 to generate a recombinant strain AFP111/pMD19T-cscBKA. After 72 h of anaerobic fermentation of the recombinant in serum bottles, 20 g/L sucrose was consumed and 12 g/L succinic acid was produced. During dual-phase fermentation comprised of initial aerobic growth phase followed by anaerobic fermentation phase, the concentration of succinic acid from sucrose and sugarcane molasses was 34 g/L and 30 g/L, respectively, at 30 h of anaerobic phase in a 3 L fermentor. The results show that the introduction of non-PTS sucrose-utilization system has sucrose-metabolizing capability for cell growth and succinic acid production, and can use cheap sugarcane molasses to produce succinic acid.
KW - Escherichia coli AFP111
KW - Non-PTS sucrose-utilization system
KW - Succinic acid
KW - Sucrose
KW - Sugarcane molasses
UR - http://www.scopus.com/inward/record.url?scp=84929623814&partnerID=8YFLogxK
U2 - 10.13345/j.cjb.140364
DO - 10.13345/j.cjb.140364
M3 - 文章
C2 - 26380410
AN - SCOPUS:84929623814
SN - 1000-3061
VL - 31
SP - 534
EP - 541
JO - Shengwu Gongcheng Xuebao/Chinese Journal of Biotechnology
JF - Shengwu Gongcheng Xuebao/Chinese Journal of Biotechnology
IS - 4
ER -