Catalysis Communications (Jan 2021)

Access to both anomers of rutinosyl azide using wild-type rutinosidase and its catalytic nucleophile mutant

  • Michael Kotik,
  • Katerina Brodsky,
  • Petr Halada,
  • Hana Javůrková,
  • Helena Pelantová,
  • Dorota Konvalinková,
  • Pavla Bojarová,
  • Vladimír Křen

Journal volume & issue
Vol. 149
p. 106193

Abstract

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Rutinosidases hydrolyze β-rutinosylated flavonoids. As retaining glycosidases they also have a transglycosylation activity. Here we show that two newly identified wild-type rutinosidases, which are members of the glycoside hydrolase family 5–23, are capable of glycosylation of an inorganic azide with rutin as a glycosyl donor, yielding rutinosyl β-azide. On the other hand, rutinosyl α-azide was synthesized by the catalytic nucleophile mutant of the rutinosidase from Aspergillus niger, which also belongs to GH5–23. Thus, we were able to synthesize at a preparatory scale both anomers of rutinosyl azide from rutin using either wild-type or mutant rutinosidases of GH5–23.

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