Glucosylceramide having a novel tri-unsaturated long-chain base from the spermatozoa of the starfish, Asterias amurensis

J Biochem. 1990 Apr;107(4):578-86. doi: 10.1093/oxfordjournals.jbchem.a123089.

Abstract

Glucosylceramide (Glc beta 1-1Cer) was isolated from the spermatozoa of the starfish, Asterias amurensis. The long-chain bases of the glycolipid consisted of dihydroxy (d18:2, d18:3, d19:3, and d22:2), and trihydroxy (t22:1) types. Long-chain aldehydes derived from them were analyzed mainly by proton nuclear-magnetic resonance to determine the detailed structures. Two of the tri-unsaturated bases were identified as (4E,8E,10E)-2-amino-4,8,10-octadecatriene-1,3-di ol (d18:3) and (4E,8E,10E)-2-amino-9-methyl-4,8,10-octadecatriene+ ++-1,3-diol (d19:3), which is a novel base. Both d22:2 and t22:1 had a cis double bond at the C9 or C13 position. All fatty acids were 2-hydroxylated (C14-C25): Most of them were saturated and unbranched. About 10% was mono-unsaturated and unbranched (C22-C25), while saturated but branched (iso- and anteiso-types) C15-C18 acids were found as minor components. The main fatty acids, which summed up to more than 93% of the fatty acids in the glucosylceramide, were n-14h:0, n-15h:0, n-16h:0, n-17h:0, n-18h:0, and n-24h:1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / analysis
  • Animals
  • Carbohydrate Sequence
  • Cerebrosides / analysis*
  • Chromatography, High Pressure Liquid
  • Fatty Acids, Unsaturated / analysis*
  • Glucosylceramides / analysis*
  • Isomerism
  • Magnetic Resonance Spectroscopy
  • Male
  • Mass Spectrometry
  • Molecular Sequence Data
  • Osmium Tetroxide / pharmacology
  • Spermatozoa / analysis*
  • Starfish / analysis*

Substances

  • Aldehydes
  • Cerebrosides
  • Fatty Acids, Unsaturated
  • Glucosylceramides
  • Osmium Tetroxide