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Updated: Jun 20, 2026

Site-Specific Lysine Lactylation via Genetic Code Expansion in E. coli and Mammalian Cells
Published on: February 24, 2026
High-Efficiency Production of N-Acetyllactosamine (LacNAc) Using a Cell-Coupled Biocatalytic Strategy with Engineered
Cheng Han1,2, Huanle Gao1,2, Zimeng Zhang1,2
1Key Laboratory of Carbohydrate Chemisty and Biotechnology, Ministry of Education, Jiangnan University, 1800 Lihu Avenue, Wuxi, Jiangsu 214122, China.
Abstract:
N-Acetyllactosamine (LacNAc) serves as a key intermediate in the biosynthesis of 6'-sialyl-N-acetyllactosamine (6'-SLN) and 3'-sialyl-N-acetyllactosamine (3'-SLN), which are the predominant components of sialylated milk oligosaccharides (SMOs) in goat milk. Therefore, methods for high-efficiency and low-cost production of LacNAc are necessary for 6'-SLN and 3'-SLN production. In this study, a new strategy for LacNAc production through a whole-cell coupled fermentation approach using sucrose and N-acetylglucosamine (GlcNAc) as substrates was explored. First, the enzymatic activities of β-1,4-galactosyltransferase (Hpβ4GalT and HpGalT), which were involved in LacNAc biosynthesis, were evaluated; the results indicated that Hpβ4GalT exhibits a higher LacNAc synthesis capacity than HpGalT. Subsequently, LacNAc was synthesized using a whole-cell catalytic system based on multistrain coupling. Then, to further enhance the titer, Saccharomyces cerevisiae cells were introduced to enable energy regeneration, and a coexpression strategy was employed to minimize the cell density. Following the optimization of induction and coupled fermentation conditions, LacNAc production increased 6-fold. Finally, the fermentation optimization conditions were validated in a 5-L bioreactor, achieving a maximum LacNAc titer of 32.38 g/L and a substrate GlcNAc molar yield of 84.46%.
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