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Biology of Reproduction, Vol 11, 534-542, Copyright © 1974 by Society for the Study of Reproduction
1 Department of Biochemistry and Biophysics, University of California,
Davis, California 95616 [35S]-sulfate injected into ovulating Xenopus laevis was incorporated into eggs and egg
jelly coats. The extent of [35S] incorporation was dependent on the dose administered and
time the eggs were ovulated after injection. The radioactivity was incorporated predominately into the innermost jelly coat layer J1; J1 contained the majority if not all of the
sulfate in the jelly coat as determined by chemical analysis for sulfate. The [35S] incorporated
was chemically in the form of sulfate esters as determined by chromatography of acid
hydrolysates. Hydrolysis rates the [35S]-sulfate from the jelly coat macromolecules and
the infrared absorption spectra of jelly suggested that sulfate was present as sugar ester
of a secondary axial hydroxyl group, most likely on the C4 position of Ga1, Ga1NAc, or
Fuc residues. The sulfated jelly coat macromolecules were not incorporated into the egg
during its passage through the oviduct nor into the embryo during development up to the
hatching stage.
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