Cargando…

Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni

Stevia rebaudiana and its diterpene glycosides are one of the main focuses of food companies interested in developing novel zero calorie sugar substitutes since the recognition of steviol glycosides as Generally Recognized as Safe (GRAS) by the United States Food and Drug Administration. Rebaudiosid...

Descripción completa

Detalles Bibliográficos
Autores principales: Perera, Wilmer H., Ghiviriga, Ion, Rodenburg, Douglas L., Alves, Kamilla, Wiggers, Frank T., Hufford, Charles D., Fronczek, Frank R., Ibrahim, Mohamed A., Muhammad, Ilias, Avula, Bharathi, Khan, Ikhlas A., McChesney, James D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321316/
https://www.ncbi.nlm.nih.gov/pubmed/30558268
http://dx.doi.org/10.3390/molecules23123328
_version_ 1783385413152407552
author Perera, Wilmer H.
Ghiviriga, Ion
Rodenburg, Douglas L.
Alves, Kamilla
Wiggers, Frank T.
Hufford, Charles D.
Fronczek, Frank R.
Ibrahim, Mohamed A.
Muhammad, Ilias
Avula, Bharathi
Khan, Ikhlas A.
McChesney, James D.
author_facet Perera, Wilmer H.
Ghiviriga, Ion
Rodenburg, Douglas L.
Alves, Kamilla
Wiggers, Frank T.
Hufford, Charles D.
Fronczek, Frank R.
Ibrahim, Mohamed A.
Muhammad, Ilias
Avula, Bharathi
Khan, Ikhlas A.
McChesney, James D.
author_sort Perera, Wilmer H.
collection PubMed
description Stevia rebaudiana and its diterpene glycosides are one of the main focuses of food companies interested in developing novel zero calorie sugar substitutes since the recognition of steviol glycosides as Generally Recognized as Safe (GRAS) by the United States Food and Drug Administration. Rebaudioside A, one of the major steviol glycosides of the leaves is more than 200 times sweeter than sucrose. However, its lingering aftertaste makes it less attractive as a table-top sweetener, despite its human health benefits. Herein, we report the purification of two novel tetra-glucopyranosyl diterpene glycosides 1 and 3 (rebaudioside A isomers) from a commercial Stevia rebaudiana leaf extract compounds, their saponification products compounds 2 and 4, together with three known compounds isolated in gram quantities. Compound 1 was determined to be 13-[(2-O-β-d-glucopyranosyl-6-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-kaur-16-en-19-oic acid-β-d-glucopyranosy ester (rebaudioside Z), whereas compound 3 was found to be 13-[(2-O-β-d-glucopyranosyl-3-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-hydroxyatis-16-en-19-oic acid -β-d-glucopyranosy ester. Two new tetracyclic derivatives with no sugar at position C-19 were prepared from rebaudiosides 1 and 3 under mild alkaline hydrolysis to afford compounds 2 13-[(2-O-β-d-glucopyranosyl-6-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-kaur-16-en-19-oic acid (rebaudioside Z(1)) and 4 13-[(2-O-β-d-glucopyranosyl-3-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-hydroxyatis-16-en-19-oic acid. Three known compounds were purified in gram quantities and identified as rebaudiosides A (5), H (6) and J (7). Chemical structures were unambiguously elucidated using different approaches, namely HRESIMS, HRESI-MS/MS, and 1D-and 2D-NMR spectroscopic data. Additionally, a high-quality crystal of iso-stevioside was grown in methanol and its structure confirmed by X-ray diffraction.
format Online
Article
Text
id pubmed-6321316
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-63213162019-01-14 Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni Perera, Wilmer H. Ghiviriga, Ion Rodenburg, Douglas L. Alves, Kamilla Wiggers, Frank T. Hufford, Charles D. Fronczek, Frank R. Ibrahim, Mohamed A. Muhammad, Ilias Avula, Bharathi Khan, Ikhlas A. McChesney, James D. Molecules Article Stevia rebaudiana and its diterpene glycosides are one of the main focuses of food companies interested in developing novel zero calorie sugar substitutes since the recognition of steviol glycosides as Generally Recognized as Safe (GRAS) by the United States Food and Drug Administration. Rebaudioside A, one of the major steviol glycosides of the leaves is more than 200 times sweeter than sucrose. However, its lingering aftertaste makes it less attractive as a table-top sweetener, despite its human health benefits. Herein, we report the purification of two novel tetra-glucopyranosyl diterpene glycosides 1 and 3 (rebaudioside A isomers) from a commercial Stevia rebaudiana leaf extract compounds, their saponification products compounds 2 and 4, together with three known compounds isolated in gram quantities. Compound 1 was determined to be 13-[(2-O-β-d-glucopyranosyl-6-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-kaur-16-en-19-oic acid-β-d-glucopyranosy ester (rebaudioside Z), whereas compound 3 was found to be 13-[(2-O-β-d-glucopyranosyl-3-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-hydroxyatis-16-en-19-oic acid -β-d-glucopyranosy ester. Two new tetracyclic derivatives with no sugar at position C-19 were prepared from rebaudiosides 1 and 3 under mild alkaline hydrolysis to afford compounds 2 13-[(2-O-β-d-glucopyranosyl-6-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-kaur-16-en-19-oic acid (rebaudioside Z(1)) and 4 13-[(2-O-β-d-glucopyranosyl-3-O-β-d-glucopyranosyl-β-d-glucopyranosyl) oxy]ent-hydroxyatis-16-en-19-oic acid. Three known compounds were purified in gram quantities and identified as rebaudiosides A (5), H (6) and J (7). Chemical structures were unambiguously elucidated using different approaches, namely HRESIMS, HRESI-MS/MS, and 1D-and 2D-NMR spectroscopic data. Additionally, a high-quality crystal of iso-stevioside was grown in methanol and its structure confirmed by X-ray diffraction. MDPI 2018-12-15 /pmc/articles/PMC6321316/ /pubmed/30558268 http://dx.doi.org/10.3390/molecules23123328 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Perera, Wilmer H.
Ghiviriga, Ion
Rodenburg, Douglas L.
Alves, Kamilla
Wiggers, Frank T.
Hufford, Charles D.
Fronczek, Frank R.
Ibrahim, Mohamed A.
Muhammad, Ilias
Avula, Bharathi
Khan, Ikhlas A.
McChesney, James D.
Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni
title Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni
title_full Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni
title_fullStr Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni
title_full_unstemmed Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni
title_short Tetra-glucopyranosyl Diterpene ent-Kaur-16-en-19-oic Acid and ent-13(S)-Hydroxyatisenoic Acid Derivatives from a Commercial Extract of Stevia rebaudiana (Bertoni) Bertoni
title_sort tetra-glucopyranosyl diterpene ent-kaur-16-en-19-oic acid and ent-13(s)-hydroxyatisenoic acid derivatives from a commercial extract of stevia rebaudiana (bertoni) bertoni
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6321316/
https://www.ncbi.nlm.nih.gov/pubmed/30558268
http://dx.doi.org/10.3390/molecules23123328
work_keys_str_mv AT pererawilmerh tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT ghivirigaion tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT rodenburgdouglasl tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT alveskamilla tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT wiggersfrankt tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT huffordcharlesd tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT fronczekfrankr tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT ibrahimmohameda tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT muhammadilias tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT avulabharathi tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT khanikhlasa tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni
AT mcchesneyjamesd tetraglucopyranosylditerpeneentkaur16en19oicacidandent13shydroxyatisenoicacidderivativesfromacommercialextractofsteviarebaudianabertonibertoni