Abstract:
The glycosylating activities of two enzymatic preparations from potato tubers were compared, using β-sitosterol and β-solanidine as substrate. The 25 000 g fraction synthesized steryl glucoside (SG) and acylsteryl glucoside (ASG) when β-sitosterol as well as β-solanidine was included in the reaction mixture. The AS fraction formed SG but not ASG from β-sitosterol and glycosylated β-solanidine forming six different derivatives. We tentatively related these products to the six components of solanine: α-, β- and γ-solanine and α-, β- and γ-chaconine. © 1977.
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Citas:
---------- APA ----------
Lavintman, N., Tandecarz, J. & Cardini, C.E.
(1977)
. Enzymatic glycosylation of steroid alkaloids in potato tuber. Plant Science Letters, 8(1), 65-70.
http://dx.doi.org/10.1016/0304-4211(77)90173-0---------- CHICAGO ----------
Lavintman, N., Tandecarz, J., Cardini, C.E.
"Enzymatic glycosylation of steroid alkaloids in potato tuber"
. Plant Science Letters 8, no. 1
(1977) : 65-70.
http://dx.doi.org/10.1016/0304-4211(77)90173-0---------- MLA ----------
Lavintman, N., Tandecarz, J., Cardini, C.E.
"Enzymatic glycosylation of steroid alkaloids in potato tuber"
. Plant Science Letters, vol. 8, no. 1, 1977, pp. 65-70.
http://dx.doi.org/10.1016/0304-4211(77)90173-0---------- VANCOUVER ----------
Lavintman, N., Tandecarz, J., Cardini, C.E. Enzymatic glycosylation of steroid alkaloids in potato tuber. 1977;8(1):65-70.
http://dx.doi.org/10.1016/0304-4211(77)90173-0