Isolation and structure elucidation of GM4-type gangliosides from the Okinawan starfish Protoreaster nodosus

Mar Drugs. 2012 Nov 5;10(11):2467-80. doi: 10.3390/md10112467.

Abstract

Three new ganglioside molecular species, termed PNG-1, PNG-2A, and PNG-2B were isolated from pyloric caeca of the starfish Protoreaster nodosus. Their structures were elucidated using a combination of spectroscopic and chemical methods, and characterized as 1-O-[8-O-methyl-N-acetyl-α-neuraminosyl-(2→3)-β-galactopyranosyl]-ceramide for PNG-1, 1-O-[β-galactofuranosyl-(1→3)-α-galactopyranosyl-(1→4)-8-O-methyl-N-acetyl-α-neuraminosyl-(2→3)-β-galactopyranosyl]-ceramide for PNG-2A, and 1-O-[β-galacto furanosyl-(1→3)-α-galactopyranosyl-(1→9)-N-acetyl-α-neuraminosyl-(2→3)-β-galactopyr anosyl]-ceramide for PNG-2B. PNG-2A and PNG-2B represent the first GM4 elongation products in nature.

MeSH terms

  • Animals
  • Gangliosides / chemistry*
  • Gangliosides / isolation & purification
  • Japan
  • Spectrum Analysis
  • Starfish / chemistry*

Substances

  • Gangliosides
  • ganglioside, GM4