Biosynthesis of a Functional Human Milk Oligosaccharide, 2′-Fucosyllactose, and L-Fucose Using Engineered Saccharomyces cerevisiae

被引:54
作者
Liu, Jing-Jing [1 ]
Kwak, Suryang [1 ,2 ]
Pathanibul, Panchalee [2 ]
Lee, Jae Won [2 ]
Yu, Sora [3 ]
Yun, Eun Ju [1 ,3 ]
Lim, Hayoon [1 ]
Kim, Kyoung Heon [3 ]
Jin, Yong-Su [1 ,2 ,4 ]
机构
[1] Univ Illinois, Carl R Woose Inst Genom Biol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Food Sci & Human Nutr, Urbana, IL 61801 USA
[3] Korea Univ, Grad Sch, Dept Biotechnol, Seoul 02841, South Korea
[4] 1206 West Gregory Dr, Urbana, IL 61801 USA
基金
新加坡国家研究基金会;
关键词
Saccharomyces cerevisiae; de novo pathway; 2 '-fucosyllactose; alpha-L-fucosidase; L-fucose; GDP-L-FUCOSE; ESCHERICHIA-COLI; BIOTECHNOLOGICAL PRODUCTION; EXPRESSION; FERMENTATION; PATHWAY; GENE; 3-FUCOSYLLACTOSE; ENZYMES; SUGARS;
D O I
10.1021/acssynbio.8b00134
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
2'-fucosyllactose (2-FL), one of the most abundant human milk oligosaccharides (HMOs), has received much attention due to its health-promoting activities, such as stimulating the growth of beneficial gut microorganisms, inhibiting pathogen infection, and enhancing the host immune system. Consequently, large quantities of 2-FL are on demand for food applications as well as in-depth investigation of its biological properties. Biosynthesis of 2-FL has been attempted primarily in Escherichia coli, which might not be the best option to produce food and cosmetic ingredients due to the presence of endotoxins on the cell surface. In this study, an alternative route to produce 2-FL via a de novo pathway using a food-grade microorganism, Saccharomyces cerevisiae, has been devised. Specifically, heterologous genes, which are necessary to achieve the production of 2-FL from a mixture of glucose and lactose, were introduced into S. cerevisiae. When the lactose transporter (Lac12), de novo GDP-L-fucose pathway (consisting of GDP-D-mannose-4,6-dehydratase (Gmd) and GDP-4-keto-6-deoxymannose-3,5-epimerase-4-reductase (WcaG)), and alpha 1,2-fucosyl-transferase (FucT2) were introduced, the resulting engineered strain (D452L-gwf) produced 0.51 g/L of 2-FL from a batch fermentation. In addition, 0.41 g/L of L-fucose was produced when a-L-fucosidase was additionally expressed in the 2-FL producing strain (D452L-gwf). To our knowledge, this is the first report of 2-FL and L-fucose production in engineered S. cerevisiae via the de novo pathway. This study provides the possibility of producing HMOs by a food-grade microorganism S. cerevisiae and paves the way for more HMO production in the future.
引用
收藏
页码:2529 / 2536
页数:15
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