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1. (Article ID: 829)
 
Isshiki Y, Kawahara K, Zähringer U
Isolation and characterisation of disodium (4-amino-4-deoxy-β-L-arabonofuranosyl)-(1->8)-(D-glycero-α-D-talo-oct-2-ulopyranosylon ate)-(2->4)-(methyl 3-deoxy-D-manno-oct-2-ulopyranosid)onate from the lipopolysaccharide of Burkholderia cepacia
Carbohydrate Research 313 (1998) 21-27
 

A trisaccharide was isolated from the core oligosaccharide in the lipopolysaccharide (LPS) of Burkholderia cepacia GIFU 645 (ATCC 25416, type strain) by methanolysis followed by HPLC and saponification. It was identified by MS, methylation analysis and 1 H and 13 C NMR spectroscopy as disodium (4-amino-4-deoxy-b-L-arabinopyranosyl)-(1→8)-(d-glycero-a-D-talo-oct-2-ulopyranosylonate)-(2→4)-(methyl 3-deoxy-d-manno-oct-2-ulopyranosid)onate. In addition to the trisaccharide derivative, methanolysis gave dimethyl (d-glycero-a-D-talo-oct-2-ulopyranosylonate)-(2→4)-(methyl 3-deoxy-d-manno-oct-2-ulopyranosid)onate in a relative proportion to the trisaccharide of 3:1, indicating a non-stoichiometric (~25%) substitution of the octulosonic acid by 4-amino-4-deoxyarabinose in the LPS.

Lipopolysaccharide, structure, Burkholderia cepacia, 3-deoxy-D-manno-oct-2-ulosonic acid (Kdo), 4-amino-4-deoxy-L-arabinose (L-Ara4N), D-glycero-D-talo-oct-2-ulosonic acid (Ko)

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