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Journal of Lipid Research, Vol. 13, 169-176, March 1972
Copyright © 1972 by Lipid Research, Inc.
Department of Medical Biochemistry, University of Göteborg, Fack, 400 33 Göteborg 33, Sweden
A pentose-containing cerebroside has been identified in the salt gland of the herring gull, using mass spectrometry of acetyl and trimethylsilyl derivatives. A detailed interpretation of the spectra allowed a conclusion concerning the major long-chain base (the C20 homolog of sphingosine) and the major fatty acids (C22-C25 2-hydroxy fatty acids), using reference spectra of synthetic galactosylceramides. A six-membered glycose ring (aldopyranose) was demonstrated by mass spectrometry of the acetyl derivative of periodic acid-oxidized and sodium borodeuteride-reduced pentosylceramide. By gas-liquid chromatography and mass spectrometry of methanolysis products, the pentose was shown to be identical with xylose. The procedures were applied to 25-50 µg of glycolipid.
Supplementary key words sphingosine 2-hydroxy fatty acids pentosylceramide periodic acid oxidation sodium borodeuteride reduction mass spectrometry
Submitted on June 21, 1971
Accepted on October 18, 1971
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