4.7 Article

Transglycosylation Activity of Engineered Bifidobacterium Lacto-N-Biosidase Mutants at Donor Subsites for Lacto-N-Tetraose Synthesis

Journal

Publisher

MDPI
DOI: 10.3390/ijms22063230

Keywords

Bifidobacterium; biocatalysis; human milk oligosaccharides; lacto-N-biosidase; protein engineering; transglycosylation

Funding

  1. MICINN, Spain [BFU2016-77427-C2-1-R, PID2019-104350RB-I00]
  2. AGAUR [2017SGR-727]
  3. Generalitat de Catalunya

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This study focused on mutational strategies in the donor subsites of lacto-N-biosidase to reduce hydrolytic activity and enable transglycosylation for the synthesis of LNT. Mutants with residual hydrolase activity between 0.05% to 1.6% of the wild-type enzyme showed transglycosylating enzymes with LNT yields ranging from 10-30%. Mutations in Trp394 had a significant impact on the transglycosylation/hydrolysis ratio, with the W394F mutant demonstrating the highest biocatalytic efficiency in producing LNT at a yield of 32%.
The health benefits of human milk oligosaccharides (HMOs) make them attractive targets as supplements for infant formula milks. However, HMO synthesis is still challenging and only two HMOs have been marketed. Engineering glycoside hydrolases into transglycosylases may provide biocatalytic routes to the synthesis of complex oligosaccharides. Lacto-N-biosidase from Bifidobacterium bifidum (LnbB) is a GH20 enzyme present in the gut microbiota of breast-fed infants that hydrolyzes lacto-N-tetraose (LNT), the core structure of the most abundant type I HMOs. Here we report a mutational study in the donor subsites of the substrate binding cleft with the aim of reducing hydrolytic activity and conferring transglycosylation activity for the synthesis of LNT from p-nitrophenyl beta-lacto-N-bioside and lactose. As compared with the wt enzyme with negligible transglycosylation activity, mutants with residual hydrolase activity within 0.05% to 1.6% of the wild-type enzyme result in transglycosylating enzymes with LNT yields in the range of 10-30%. Mutations of Trp394, located in subsite -1 next to the catalytic residues, have a large impact on the transglycosylation/hydrolysis ratio, with W394F being the best mutant as a biocatalyst producing LNT at 32% yield. It is the first reported transglycosylating LnbB enzyme variant, amenable to further engineering for practical enzymatic synthesis of LNT.

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