Fucose-containingoligosaccharides play a central role in physio-pathological events, and fucosylated oligosaccharides have interesting potential applications in biomedicine. No methods for the large-scale production of oligosaccharides are currently available, but thechemo-enzymatic approach is very promising. Glycosynthases, mutated glycosidases that synthesize oligosaccharides in high yields, have been demonstrated to be an interesting alternative. However, examples of glycosynthases available so far are restricted to a limited number of glycosidases families and to only one retaining a-glycosynthase. We show here that newmutants of two a-L-fucosidases are efficient a-L-fucosynthases. The approach shown utilized b-L-fucopyranosyl azide as donor substrate leading to transglycosylation yields up to 91%. This is the first method exploiting a b-glycosyl azide donor for a-glycosynthases; its applicability to the glycosynthetic methodology in a wider perspective is presented.

Beta-glycosyl azides as substrates for a-glycosynthases: preparation of efficient alpha-L-fucosynthases

CobucciPonzano B;Rossi M;Moracci M
2009

Abstract

Fucose-containingoligosaccharides play a central role in physio-pathological events, and fucosylated oligosaccharides have interesting potential applications in biomedicine. No methods for the large-scale production of oligosaccharides are currently available, but thechemo-enzymatic approach is very promising. Glycosynthases, mutated glycosidases that synthesize oligosaccharides in high yields, have been demonstrated to be an interesting alternative. However, examples of glycosynthases available so far are restricted to a limited number of glycosidases families and to only one retaining a-glycosynthase. We show here that newmutants of two a-L-fucosidases are efficient a-L-fucosynthases. The approach shown utilized b-L-fucopyranosyl azide as donor substrate leading to transglycosylation yields up to 91%. This is the first method exploiting a b-glycosyl azide donor for a-glycosynthases; its applicability to the glycosynthetic methodology in a wider perspective is presented.
2009
Istituto di Biochimica delle Proteine - IBP - Sede Napoli
glycobiology
carbohydrate synthesis
carbohydrate active enzymes
fucosyl-azide
thermophilic enzymes
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/125785
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