2′-Fucosyllactose (2′-FL) is vital for
the growth
and development of newborns. In this study, we developed a synthesis
pathway for 2′-FL in Escherichia coli BL21 (DE3). Then, we optimized the solubility of α-1,2-fucosyltransferase,
thereby enhancing the production yield of 2′-FL. Based on this
finding, we further enhanced the expression of guanosine inosine kinase
Gsk and knocked out the isocitrate lyase regulator gene iclR. This strategy reduced the formation of byproduct acetate during
the metabolic process and alleviated carbon source overflow effects
in the strain, resulting in further improvement of the yield of 2′-FL.
In a 3 L bioreactor, employing fed-batch fermentation with glycerol
and glucose as substrates, the engineered strain BWLAI-RSZL exhibited
impressive 2′-FL titers of 121.9 and 111.56 g/L, along with
productivity levels of 1.57 and 1.31 g/L/h, respectively. The reported
2′-FL titers reached a groundbreaking level, irrespective of
the carbon source employed (glycerol or glucose), highlighting the
significant potential for large-scale industrial synthesis of 2′-FL