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. 2011;23(129):33-52.
doi: 10.4052/tigg.23.33.

The Amazing Transglycosylation Activity of Endo-β-N-acetylglucosaminidases

Affiliations

The Amazing Transglycosylation Activity of Endo-β-N-acetylglucosaminidases

Lai-Xi Wang. Trends Glycosci Glycotechnol. 2011.

Abstract

Major advances have been made in exploring the transglycosylation activity of endo-β-N-acetylglucosaminidases (ENGases) for synthetic purpose. The exploration of synthetic sugar oxazolines as donor substrates for the ENGase-catalyzed transglycosylation has expanded the substrate availability and significantly enhanced the overall transglycosylation efficiency. On the other hand, site-directed mutagenesis in combination with activity screening has led to the discovery of the first generation ENGase-based glycosynthases that can use highly active sugar oxazolines as substrates for transglycosylation but lack hydrolytic activity on the ground-state products. ENGases have shown amazing flexibility in transglycosylation and possess much broader substrate specificity than previously thought. Now the ENGase-based chemoenzymatic method has been extended to the synthesis of a range of complex carbohydrates, including homogeneous glycopeptides, glycoproteins carrying well-defined glycans, novel oligosaccharide clusters, unusually glycosylated natural products, and even polysaccharides. This article highlights recent advances related to ENGase-catalyzed transglycosylation with a focus on their synthetic potential.

Keywords: chemoenzymatic synthesis; endoglycosidase; glycoprotein; sugar oxazoline; transglycosylation.

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Figures

Figure 1
Figure 1
ENGase-catalyzed hydrolysis and transglycosylation
Figure 2
Figure 2
Glyco-engineering of human IgG1-Fc
Figure 3
Figure 3
Transglycosylation by glycosynthase mutant EndoM-N175A
Scheme 1
Scheme 1
Synthesis of Man6GlcNAc-oxazoline and its reaction with Endo-A
Scheme 2
Scheme 2
Transglycosylation with the tetrasacharide oxazoline by Endo-A
Scheme 3
Scheme 3
Endo-M catalyzed transglycosylation with modified sugar oxazolines
Scheme 4
Scheme 4
ENGase-catalyzed transglycosylation for N-glycoprotein synthesis
Scheme 5
Scheme 5
Catalytic 1,3-dipolar cycloaddition to introduce αGal epitope into RNase
Scheme 6
Scheme 6
A combined method for producing homogeneous glycoprotein
Scheme 7
Scheme 7
Enzymatic introduction of N-glycans into natural products by Endo A
Scheme 8
Scheme 8
Endo-A catalyzed tandem transglycosylation
Scheme 9
Scheme 9
Chemoenzymatic synthesis of novel N-glycan clusters
Scheme 10
Scheme 10
Endo-A catalyzed transglycosylation with complex type N-glycan oxazoline

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