National Basic Research Program of China (973 Program) (No. 2013CB733901), National High Technology Research and Development Program of China (863 Program) (No. 2011AA02A203), the Priority Academic Program Development of Jiangsu Higher Education Institutions, Program for New Century Excellent Talents in University.
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.
李凤,马江锋,吴明科,冀亚亮,陈吴方,任心怡,姜岷. 重组大肠杆菌利用蔗糖及糖蜜发酵生产丁二酸[J]. Chinese Journal of Biotechnology, 2015, 31(4): 534-541
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