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NMR Spectroscopy Molecular Dynamics, and Conformation of a Synthetic Octasaccharide Fragment of the O-Specific Polysaccharide of Shigella Dysenteriae Type 1
Published
Author(s)
B Coxon, Fahriye N. Sari, G Batta, V Pozsgay
Abstract
A synthetic octasaccharide fragment of the O-polysaccharide from Shigella dysenteriae type 1 has been studied as its methyl glycoside derivative by one-dimensional and two-dimensional homonuclear and heteronuclear NMR spectroscopy. Complete 1H and 13C NMR assignments have been generated for the octasaccharide derivative, namely methyl O-α-L-rhamnopyranosyl-(1 -> 2)-O-α-D-galactopyranosyl-(1 -> 3)-O-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-(1 -> 3)-O-α-L-rhamnopyranosyl-(1 -> 3)-O-α-L-rhamnopyranosyl-(1 -> 2)-O-α-D-galactopyranosyl-(1 -> 3)-O-(2-acetamido-2-deoxy-α-D-glucopyranosyl)-(1 -> 3)-O-α-L-rhamnopyranoside. 13C spin-lattice relaxation times have also been measured for this derivative. An octasaccharide derivative containing one D-galactose residue with a specific 13C label at C-1 has been synthesized and used to measure interglycosidic 13C-1H coupling by the 2D J-resolved 1H NMR method. From the NMR data, three types of conformational restraints were developed; (a) 29 inter-residue, distance restraints, (b) 48 intra-residue, ring atom dihedral angle restraints, (c) one heteronuclear, inter-residue dihedral angle restraint. The use of these restraints in a restrained molecular dynamics computation with simulated annealing yielded a conformation resembling a short, irregular spiral, with methyl substituents on the exterior.
Coxon, B.
, Sari, F.
, Batta, G.
and Pozsgay, V.
(2000),
NMR Spectroscopy Molecular Dynamics, and Conformation of a Synthetic Octasaccharide Fragment of the O-Specific Polysaccharide of Shigella Dysenteriae Type 1, Carbohydrate Research
(Accessed December 22, 2024)