食品科学 ›› 2025, Vol. 46 ›› Issue (11): 87-93.doi: 10.7506/spkx1002-6630-20241222-185

• 生物工程 • 上一篇    

代谢工程改造大肠杆菌通过补救途径合成3-岩藻糖基乳糖

梁山泉,何滋,江正强,杨绍青   

  1. (中国农业大学食品科学与营养工程学院,中国轻工业食品生物工程重点实验室,北京 100083)
  • 发布日期:2025-05-14
  • 基金资助:
    国家自然科学基金重点项目(22338013);“十四五”国家重点研发计划重点专项(2022YFC2104902)

Metabolic Engineering of Escherichia coli to Synthesize 3-Fucosyllactose via the Salvage Pathway

LIANG Shanquan, HE Zi, JIANG Zhengqiang, YANG Shaoqing   

  1. (Key Laboratory of Food Bioengineering, China National Light Industry, College of Food Science and Nutritional Engineering, China Agricultural University, Beijing 100083, China)
  • Published:2025-05-14

摘要: 3-岩藻糖基乳糖(3-fucosyllactose,3-FL)是一种典型的人乳寡糖(human milk oligosaccharides,HMOs),在婴幼儿生长和大脑发育方面具有重要生理功能。本研究采用代谢工程的方法改造大肠杆菌BL21star(DE3),实现3-FL的高效生物合成。将幽门螺杆菌(Helicobacter pylori)来源的α-1,3-岩藻糖基转移酶基因futA和脆弱拟杆菌(Bacteroides fragilis)来源的L-岩藻糖激酶/二磷酸鸟苷-L-岩藻糖焦磷酸化酶基因fkp共同导入初始菌株BLW(Escherichia coli BL21star(DE3)ΔlacZΔwcaJ)中,摇瓶发酵3-FL的产量为1.01 g/L。利用CRISPR/Cas9基因编辑系统敲除L-岩藻糖代谢途径的相关基因,包括L-岩藻糖异构酶基因fucI、L-岩藻糖激酶基因fucK和鼠李糖异构酶基因rhaA,3-FL的产量增加到1.36 g/L。筛选到幽门螺杆菌NCTC11637来源的α-1,3-岩藻糖基转移酶FT1合成3-FL的效果最好,表达FT1重组菌BLWFR-T的3-FL产量提升到1.56 g/L。随后优化通路基因的表达水平,采用质粒pETDuet-1表达fkp,质粒pRSFDuet-1表达FT1得到重组菌BLWFR-T2的3-FL产量提高到2.58 g/L。增强辅因子三磷酸鸟苷的再生,过表达肌苷鸟苷激酶基因gsk和鸟苷酸激酶基因gmk的重组菌BLWFR-T7的3-FL产量最高,达3.01 g/L。BLWFA-T7在5 L发酵罐中分批补料发酵78 h后的3-FL产量达到最高,为27.82 g/L。该研究为微生物发酵法高效合成3-FL及其他HMOs提供了研究基础。

关键词: 3-岩藻糖基乳糖;大肠杆菌;补救途径;生物合成;代谢工程

Abstract: 3-Fucosyllactose (3-FL) is a typical human milk oligosaccharides (HMOs) and plays a significant physiological function in the growth and brain development of infants. In this study, efficient biosynthesis of 3-FL was achieved by metabolic engineering of Escherichia coli BL21star(DE3). The α-1,3-fucosyltransferase gene futA from Helicobacter pylori and the L-fucokinase/GDP-L-fucose pyrophosphorylase gene fkp from Bacteroides fragilis were co-introduced into the initial strain, E. coli BL21star(DE3)ΔlacZΔwcaJ, resulting in the production of 1.01 g/L of 3-FL in a shake flask. By using the CRISPR/Cas9 system to delete the genes related to the fucose metabolism pathway, including the L-fucose isomerase gene fucI, the L-fucose kinase gene fucK and the L-rhamnose isomerase gene rhaA, the yield of 3-FL increased to 1.36 g/L. The α-1,3-fucosyltransferase FT1 from H. pylori NCTC11637 was the most effective in 3-FL biosynthesis, and the recombinant strain BLWFA-T expressing FT1 produced 1.56 g/L of 3-FL. Subsequently, the expression level of the fucose metabolism pathway-related genes was optimized, and the recombinant strain BLWFR-T2 expressing fkp through plasmid pETDuet-1 and expressing FT1 through plasmid pRSFDuet-1 produced 2.58 g/L of 3-FL. Finally, the regeneration of the cofactor guanosine triphosphate (GTP) was enhanced, and the recombinant strain BLWFR-T7 overexpressing the guanylate kinase gene gmk and the inosine-guanosine kinase gene gsk produced the highest level of 3-FL (3.01 g/L). After fed-batch fermentation for 78 h, BLWFA-T7 produced the highest yield of 3-FL (27.82 g/L) in a 5 L fermentor. This study provides a research basis for efficient microbial synthesis of 3-FL and other HMOs.

Key words: 3-fucosyllactose; Escherichia coli; salvage pathway; biosynthesis; metabolic engineering

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