代谢工程
发酵
生产(经济)
生化工程
焊剂(冶金)
生物技术
生物合成
合成生物学
化学
生物化学
工厂(面向对象编程)
代谢途径
基因
食品科学
生物
拉伤
微生物代谢
蛋白质工程
工业微生物学
蛋白质生物合成
化学合成
计算生物学
生物反应器
人类健康
下游加工
细菌
工业发酵
微生物
作者
Guocong Luo,Maiqi Chen,Yunqi Zhu,Mian Sheng,Wenbo Zhang,Wenbo Zhang,Yingying Zhu,Wenli Zhang,Wenli Zhang,Wanmeng Mu
标识
DOI:10.1021/acs.jafc.5c14521
摘要
The biosynthetic production of human milk oligosaccharides through metabolic engineering has gained increasing attention in recent years. Yet, limited research has focused on the microbial synthesis of 3'-sialyllactosamine (3'-SLN), a critical intermediate for assembling sialyl Lewis X (sLex). In this work, a pathway enabling 3'-SLN biosynthesis was constructed in Escherichia coli BL21(DE3). A key α2,3sialyltransferase (α2,3SiaT) from Bibersteinia trehalosi was identified and utilized to enhance the sialylation step toward 3'-SLN formation. To improve flux through the N-acetyllactosamine branch, essential genes were chromosomally integrated and overexpressed, while a CMP-N-acetylneuraminic acid synthesis module was coexpressed to secure an adequate donor supply. Furthermore, the expression balance was optimized through combinatorial adjustment of gene copy numbers and translational strength across modules. The engineered E. coli strain produced 0.78 g/L of 3'-SLN in shake-flask cultivation and further accumulated up to 7.75 g/L during 5-L fed-batch fermentation conditions, confirming the feasibility of microbial synthesis of 3'-SLN.
科研通智能强力驱动
Strongly Powered by AbleSci AI