Biocatalyzed synthesis of difuranosides and their ability to trigger production of TNF-α

Bioorg Med Chem Lett. 2016 Mar 15;26(6):1550-1553. doi: 10.1016/j.bmcl.2016.02.018. Epub 2016 Feb 8.

Abstract

Transglycosylation reactions biocatalyzed by the native arabinofuranosidase Araf51 and using d-galactosyl, d-fucosyl and 6-deoxy-6-fluoro-D-galactosyl derivatives as donors and acceptors provided di-to pentahexofuranosides. The immunostimulatory potency of these compounds, and more especially their ability to induce production of TNF-α, was evaluated on the murine macrophage cell line, Raw 264.7. The results obtained showed concentration-dependent and most importantly, structure-dependent responses. Interestingly, oligoarabinofuranosides belonging to the oligopentafuranoside family displayed concentration-, chain length and aglycon-dependent bioactivities irrespective of their fine chemical variations. Thus, neo-oligofuranosides in D-Galf series, as well as their D-Fucf and 6-fluorinated counterparts are indeed potential sources of immunostimulating agents.

Keywords: Carbohydrates; Furanosides; Immunostimulation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biocatalysis*
  • Carbohydrate Conformation
  • Cell Line
  • Disaccharides / biosynthesis*
  • Disaccharides / chemistry
  • Disaccharides / immunology
  • Disaccharides / pharmacology*
  • Mice
  • Tumor Necrosis Factor-alpha / biosynthesis*

Substances

  • Disaccharides
  • Tumor Necrosis Factor-alpha