Biosynthesis of Sialyllacto-N-tetraose c in Engineered Escherichia coli

被引:2
|
作者
Li, Chenchen [1 ]
Li, Mengli [1 ]
Gao, Wei [1 ]
Zhang, Tao [1 ,2 ]
Liu, Zhu [3 ]
Miao, Ming [1 ,2 ]
机构
[1] Jiangnan Univ, State Key Lab Food Sci & Resources, Wuxi 214122, Jiangsu, Peoples R China
[2] Jiangnan Univ, Sch Food Sci & Technol, Wuxi 214122, Jiangsu, Peoples R China
[3] Zhejiang Inst Food & Drug Control, Hangzhou 310052, Zhejiang, Peoples R China
关键词
sialyllacto-<italic>N</italic>-tetraose c; metabolicengineering; Escherichia coli; CTP cofactor regeneration; HUMAN-MILK; OLIGOSACCHARIDES; SIALYLTRANSFERASE; GLYCANS; ACID;
D O I
10.1021/acs.jafc.4c08711
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Human milk oligosaccharides (HMOs) have attracted considerable interest for their vital role in supporting infant health. Among these, sialyllacto-N-tetraose c (LST c), a pentasaccharide with the structure Neu5Ac(alpha 2,6)Gal(beta 1,4)GlcNAc(beta 1,3)Gal(beta 1,4)Glc, stands out due to its critical importance in the development and application of complex HMOs. In this study, we employed multivariate modular metabolic engineering (MMME) to screen for efficient sialyltransferases and balance metabolic fluxes, successfully constructing strains capable of LST c biosynthesis. Additionally, by blocking competing pathway genes, enhancing the supply of UDP-GlcNAc and UDP-Gal precursors, and establishing a CTP cofactor regeneration system, we developed a high-yielding Escherichia coli strain, W15. This strain achieved an LST c titer of 220.9 mg/L in shake flask cultures. In a 3-L fed-batch fermentation, the LST c concentration reached 922.2 mg/L, with a productivity of 10.25 mg/L/h and a specific yield of 38.70 mg/g DCW. This research provides an effective strategy for producing LST c in microbial cell factories.
引用
收藏
页码:25836 / 25846
页数:11
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