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Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies

Plants in the Amaryllidaceae family synthesize a diversity of bioactive alkaloids. Some of these plant species are not abundant and have a low natural multiplication rate. The aims of this work were the alkaloids analysis of a Habranthus cardenasianus bulbs extract, the evaluation of its inhibitory...

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Autores principales: Zaragoza-Puchol, Daniel, Ortiz, Javier E., Orden, Alejandro A., Sanchez, Marianela, Palermo, Jorge, Tapia, Alejandro, Bastida, Jaume, Feresin, Gabriela E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795992/
https://www.ncbi.nlm.nih.gov/pubmed/33401696
http://dx.doi.org/10.3390/molecules26010192
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author Zaragoza-Puchol, Daniel
Ortiz, Javier E.
Orden, Alejandro A.
Sanchez, Marianela
Palermo, Jorge
Tapia, Alejandro
Bastida, Jaume
Feresin, Gabriela E.
author_facet Zaragoza-Puchol, Daniel
Ortiz, Javier E.
Orden, Alejandro A.
Sanchez, Marianela
Palermo, Jorge
Tapia, Alejandro
Bastida, Jaume
Feresin, Gabriela E.
author_sort Zaragoza-Puchol, Daniel
collection PubMed
description Plants in the Amaryllidaceae family synthesize a diversity of bioactive alkaloids. Some of these plant species are not abundant and have a low natural multiplication rate. The aims of this work were the alkaloids analysis of a Habranthus cardenasianus bulbs extract, the evaluation of its inhibitory activity against cholinesterases, and to test several propagation strategies for biomass production. Eleven compounds were characterized by GC-MS in the alkaloid extract, which showed a relatively high proportion of tazettine. The known alkaloids tazettine, haemanthamine, and the epimer mixture haemanthidine/6-epi-haemanthidine were isolated and identified by spectroscopic methods. Inhibitory cholinesterases activity was not detected. Three forms of propagation were performed: bulb propagation from seed, cut-induced bulb division, and micropropagated bulbs. Finally, different imbibition and post-collection times were evaluated in seed germination assays. The best propagation method was cut-induced bulb division with longitudinal cuts into quarters (T1) while the best conditions for seed germination were 0-day of post-collection and two days of imbibition. The alkaloids analyses of the H. cardenasianus bulbs showed that they are a source of anti-tumoral alkaloids, especially pretazettine (tazettine) and T1 is a sustainable strategy for its propagation and domestication to produce bioactive alkaloids.
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spelling pubmed-77959922021-01-10 Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies Zaragoza-Puchol, Daniel Ortiz, Javier E. Orden, Alejandro A. Sanchez, Marianela Palermo, Jorge Tapia, Alejandro Bastida, Jaume Feresin, Gabriela E. Molecules Article Plants in the Amaryllidaceae family synthesize a diversity of bioactive alkaloids. Some of these plant species are not abundant and have a low natural multiplication rate. The aims of this work were the alkaloids analysis of a Habranthus cardenasianus bulbs extract, the evaluation of its inhibitory activity against cholinesterases, and to test several propagation strategies for biomass production. Eleven compounds were characterized by GC-MS in the alkaloid extract, which showed a relatively high proportion of tazettine. The known alkaloids tazettine, haemanthamine, and the epimer mixture haemanthidine/6-epi-haemanthidine were isolated and identified by spectroscopic methods. Inhibitory cholinesterases activity was not detected. Three forms of propagation were performed: bulb propagation from seed, cut-induced bulb division, and micropropagated bulbs. Finally, different imbibition and post-collection times were evaluated in seed germination assays. The best propagation method was cut-induced bulb division with longitudinal cuts into quarters (T1) while the best conditions for seed germination were 0-day of post-collection and two days of imbibition. The alkaloids analyses of the H. cardenasianus bulbs showed that they are a source of anti-tumoral alkaloids, especially pretazettine (tazettine) and T1 is a sustainable strategy for its propagation and domestication to produce bioactive alkaloids. MDPI 2021-01-02 /pmc/articles/PMC7795992/ /pubmed/33401696 http://dx.doi.org/10.3390/molecules26010192 Text en © 2021 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
Zaragoza-Puchol, Daniel
Ortiz, Javier E.
Orden, Alejandro A.
Sanchez, Marianela
Palermo, Jorge
Tapia, Alejandro
Bastida, Jaume
Feresin, Gabriela E.
Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies
title Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies
title_full Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies
title_fullStr Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies
title_full_unstemmed Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies
title_short Alkaloids Analysis of Habranthus cardenasianus (Amaryllidaceae), Anti-Cholinesterase Activity and Biomass Production by Propagation Strategies
title_sort alkaloids analysis of habranthus cardenasianus (amaryllidaceae), anti-cholinesterase activity and biomass production by propagation strategies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7795992/
https://www.ncbi.nlm.nih.gov/pubmed/33401696
http://dx.doi.org/10.3390/molecules26010192
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