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Updated: Apr 17, 2026

Homogeneous Glycoconjugate Produced by Combined Unnatural Amino Acid Incorporation and Click-Chemistry for Vaccine Purposes
Published on: December 19, 2020
Efficient synthesis of O-antigen fragments expressed by Burkholderia anthina by modular synthesis approach
Inga Nilsson1, Dirk Michalik2, Alba Silipo3
1University of Rostock, Institute of Chemistry, Albert-Einstein-Strasse 3a, D-18059 Rostock, Germany.
Abstract:
To facilitate mapping of the interaction region of the O-chain of the lipopolysaccharide from Burkholderia anthina and of a lipopolysaccharide-specific monoclonal antibody, trisaccharide propyl α-L-rhamnopyranosyl-(1 → 2)-α-D-galactopyranosyl-(1 → 3)-α-L-rhamnopyranoside (27) and hexasaccharide propyl α-L-rhamnopyranosyl-(1 → 2)-α-D-galactopyranosyl-(1 → 3)-α-L-rhamnopyranosyl-(1 → 2)-α-L-rhamnopyranosyl-(1 → 2)-α-D-galactopyranosyl-(1 → 3)-α-L-rhamnopyranoside (33) were synthesized. These oligosaccharides represent the repeating monomer and dimer of the O-antigen, respectively.

