Enzymatic glycosylation of steroid alkaloids in potato tuber

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...

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Autores principales: Lavintman, N., Tandecarz, J., Cardini, C.E.
Formato: JOUR
Acceso en línea:http://hdl.handle.net/20.500.12110/paper_03044211_v8_n1_p65_Lavintman
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spelling todo:paper_03044211_v8_n1_p65_Lavintman2023-10-03T15:20:53Z Enzymatic glycosylation of steroid alkaloids in potato tuber Lavintman, N. Tandecarz, J. Cardini, C.E. 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. Fil:Lavintman, N. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Tandecarz, J. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_03044211_v8_n1_p65_Lavintman
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
description 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.
format JOUR
author Lavintman, N.
Tandecarz, J.
Cardini, C.E.
spellingShingle Lavintman, N.
Tandecarz, J.
Cardini, C.E.
Enzymatic glycosylation of steroid alkaloids in potato tuber
author_facet Lavintman, N.
Tandecarz, J.
Cardini, C.E.
author_sort Lavintman, N.
title Enzymatic glycosylation of steroid alkaloids in potato tuber
title_short Enzymatic glycosylation of steroid alkaloids in potato tuber
title_full Enzymatic glycosylation of steroid alkaloids in potato tuber
title_fullStr Enzymatic glycosylation of steroid alkaloids in potato tuber
title_full_unstemmed Enzymatic glycosylation of steroid alkaloids in potato tuber
title_sort enzymatic glycosylation of steroid alkaloids in potato tuber
url http://hdl.handle.net/20.500.12110/paper_03044211_v8_n1_p65_Lavintman
work_keys_str_mv AT lavintmann enzymaticglycosylationofsteroidalkaloidsinpotatotuber
AT tandecarzj enzymaticglycosylationofsteroidalkaloidsinpotatotuber
AT cardinice enzymaticglycosylationofsteroidalkaloidsinpotatotuber
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