Unnatural cyclodextrins can be accessed from enzyme-mediated dynamic combinatorial libraries

Chem Commun (Camb). 2022 Feb 15;58(14):2287-2290. doi: 10.1039/d1cc06452e.

Abstract

Dynamic systems of cyclodextrins (CDs) enabled by a native cyclodextrin glucanotransferase (CGTase) can incorporate unnatural glucopyranose-derived building blocks, expanding the applicability of enzyme-mediated dynamic combinatorial chemistry by using synthetically modified substrates. Starting dynamic combinatorial libraries from CDs with a single 6-modified glucopyranose results in a dynamic mixture of CDs containing several modified glucopyranoses. The relative concentrations of modified α, β or γ-CDs can be controlled by the addition of templates, providing a novel way to access modified CDs.

MeSH terms

  • Cyclodextrins / chemistry
  • Cyclodextrins / metabolism*
  • Glucosyltransferases / metabolism*
  • Molecular Structure

Substances

  • Cyclodextrins
  • Glucosyltransferases
  • cyclomaltodextrin glucanotransferase