4.7 Article

Improved production of 2′-fucosyllactose in engineered Saccharomyces cerevisiae expressing a putative α-1, 2-fucosyltransferase from Bacillus cereus

Journal

MICROBIAL CELL FACTORIES
Volume 20, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12934-021-01657-5

Keywords

2 '-fucosyllactose; alpha-1, 2-fucosyltransferase; Bacillus cereus; Saccharomyces cerevisiae; GDP-L-fucose

Funding

  1. National Key R&D Program of China [2019YFA0905700]
  2. National Natural Science Foundation of China [31800047, 31970071]
  3. Major Basic Research of Shandong Provincial Natural Science Foundation [ZR2019ZD19]
  4. Shandong Provincial Natural Science Foundation [ZR2018BC006]
  5. China Postdoctoral Science Foundation [2017M622186]
  6. Shandong Technology Innovation Center of Synthetic Biology [sdsynbio-2018PY-01]
  7. Shandong University
  8. Shandong University [2017TB0010]

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The research successfully constructed a microbial cell factory in Saccharomyces cerevisiae for cost-effective mass production of 2'-fucosyllactose by expressing an alpha-1, 2-fucosyltransferase from Bacillus cereus and enhancing de novo GDP-L-fucose biosynthesis. Through continuous optimization of engineering strategies, the production yield of 2'-FL was significantly increased.
Background: 2'-fucosyllactose (2'-FL) is one of the most abundant oligosaccharides in human milk. It constitutes an authorized functional additive to improve infant nutrition and health in manufactured infant formulations. As a result, a cost-effective method for mass production of 2'-FL is highly desirable. Results: A microbial cell factory for 2'-FL production was constructed in Saccharomyces cerevisiae by expressing a putative alpha-1, 2-fucosyltransferase from Bacillus cereus (FutBc) and enhancing the de novo GDP-L-fucose biosynthesis. When enabled lactose uptake, this system produced 2.54 g/L of 2'-FL with a batch flask cultivation using galactose as inducer and carbon source, representing a 1.8-fold increase compared with the commonly used alpha-1, 2-fucosyltransferase from Helicobacter pylori (FutC). The production of 2'-FL was further increased to 3.45 g/L by fortifying GDP-mannose synthesis. Further deleting gal80 enabled the engineered strain to produce 26.63 g/L of 2'-FL with a yield of 0.85 mol/mol from lactose with sucrose as a carbon source in a fed-batch fermentation. Conclusion: FutBc combined with the other reported engineering strategies holds great potential for developing commercial scale processes for economic 2'-FL production using a food-grade microbial cell factory.

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