Engineering Escherichia coli for Highly Efficient Biosynthesis of Lacto-N-difucohexaose II through De Novo GDP-<sc>l</sc>-fucose Pathway

被引:2
|
作者
Wang, Liang [1 ]
Zhu, Yingying [1 ]
Zhao, Chunhua [2 ]
Zhao, Mingli [1 ]
Li, Zeyu [1 ]
Xu, Wei [1 ]
Mu, Wanmeng [1 ]
机构
[1] Jiangnan Univ, State Key Lab Food Sci & Resources, Wuxi 214122, Jiangsu, Peoples R China
[2] Bloomature Biotechnol Corp Ltd, Beijing 102629, Peoples R China
关键词
alpha 1,3/4-fucosyltransferase; lacto-N-difucohexaose II; lacto-N-tetraose; human milk oligossaccharide; HUMAN-MILK OLIGOSACCHARIDES; LARGE-SCALE SYNTHESIS; HELICOBACTER-PYLORI; MOLECULAR-CLONING; TETRAOSE; NEOTETRAOSE; EXPRESSION;
D O I
10.1021/acs.jafc.4c01264
中图分类号
S [农业科学];
学科分类号
09 ;
摘要
Lacto-N-difucohexaose II (LNDFH II) is a typical fucosylated human milk oligosaccharide and can be enzymatically produced from lacto-N-tetraose (LNT) by a specific alpha 1,3/4-fucosyltransferase from Helicobacter pylori DMS 6709, referred to as FucT14. Previously, we constructed an engineered Escherichia coli BL21(DE3) with a single plasmid for highly efficient biosynthesis of LNT. In this study, two additional plasmids harboring the de novo GDP-L-fucose pathway module and FucT14, respectively, were further introduced to construct the strain for successful biosynthesis of LNDFH II. FucT14 was actively expressed, and the engineered strain produced LNDFH II as the major product, lacto-N-fucopentaose (LNFP) V as the minor product, and a trace amount of LNFP II and 3-fucosyllactose as very minor products. Additional expression of the alpha 1,3-fucosyltransferase FutM1 from a Bacteroidaceae bacterium from the gut metagenome could obviously enhance the LNDFH II biosynthesis. After optimization of induction conditions, the maximum titer reached 3.011 g/L by shake-flask cultivation. During the fed-batch cultivation, LNDFH II was highly efficiently produced with the highest titer of 18.062 g/L and the productivity yield of 0.301 g/L<middle dot>h.
引用
收藏
页码:10469 / 10476
页数:8
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