Abstract

With 14CO 2, d-glucose-[U- 14C] and dl-mevalonate-[4 R-4- 3H 1] used as precursors, a study was made of the labelling dynamics of the steryl glucosides (SG) and steryl acylglucosides (ASG) in Sinapis alba seedlings. The radioactivity of the sterol and sugar moieties, as well as of the fatty acid moieties in the case of ASG, was analysed separately. The course of incorporation of 14C from 14 CO 2 and glucose-[U- 14C] into the sugar part of SG and ASG indicated that about 2 3 of the whole pool of the newly synthesized sterol glycosides of both types underwent rapid deglucosylation. Likewise, fatty acids in the ASG pool were rapidly exchanged. The present results point to a high metabolic activity of the sterol glycoside derivatives in plant cells.

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