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Angew Chem Int Ed Engl ; 60(51): 26555-26560, 2021 12 13.
Artigo em Inglês | MEDLINE | ID: mdl-34661966

RESUMO

Accessing large numbers of structurally diverse glycans and derivatives is essential to functional glycomics. We showed a general tolerance of galactosyltransferases toward uridine-diphosphate-galactosamine (UDP-GalN), which is not a commonly used sugar nucleotide donor. The property was harnessed to develop a two-step chemoenzymatic strategy for facile synthesis of novel and divergent N-acetylgalactosamine (GalNAc)-glycosides and derivatives in preparative scales. The discovery and the application of the new property of existing glycosyltransferases expand their catalytic capabilities in generating novel carbohydrate linkages, thus prompting the synthesis of diverse glycans and glycoconjugates for biological studies.


Assuntos
Galactosiltransferases/metabolismo , Uridina Difosfato N-Acetilgalactosamina/análogos & derivados , Configuração de Carboidratos , Helicobacter pylori/enzimologia , Neisseria meningitidis/enzimologia , Uridina Difosfato N-Acetilgalactosamina/biossíntese , Uridina Difosfato N-Acetilgalactosamina/química
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