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Journal of Lipid Research, Vol 22, 536-541, Copyright © 1981 by Lipid Research, Inc.
NS Radin and GP Evangelatos
Galactose oxidase can be used to oxidize the terminal carbon atom of lipids
containing galactose or N-acetylgalactosamine, and the resultant aldehyde
group can be reduced back to the original carbinol with radioactive
borohydride. The efficiency of the first reaction has been investigated
systematically by using [6-3H]galactosyl ceramide as substrate and
measuring the amount of radioactive water formed. This enabled us to
establish that the addition of catalase and peroxidase greatly speeded the
oxidation, that phosphate and PIPES buffers were the best among those
tested, that the reaction continued for 24 hr without a second addition of
galactose oxidase, and that the optimum concentration of organic solvent
(tetrahydrofuran) was 50%. The suggestion if made that a similar set of
variables be studied for each lipid or nonlipid by the same basic
technique: labeling by the oxidase/borohydride method and use of the
resultant compound as substrate.
ARTICLES
The use of galactose oxidase in lipid labeling
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