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Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging
Biosynthetic investigation of quinonemethide triterpenoid 22β-hydroxy-maytenin (2) from in vitro root cultures of Peritassa laevigata (Celastraceae) was conducted using (13)C-precursor. The mevalonate pathway in P. laevigata is responsible for the synthesis of the quinonemethide triterpenoid scaffol...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778575/ https://www.ncbi.nlm.nih.gov/pubmed/26943243 http://dx.doi.org/10.1038/srep22627 |
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author | Pina, Edieidia S. Silva, Denise B. Teixeira, Simone P. Coppede, Juliana S. Furlan, Maysa França, Suzelei C. Lopes, Norberto P. Pereira, Ana Maria S. Lopes, Adriana A. |
author_facet | Pina, Edieidia S. Silva, Denise B. Teixeira, Simone P. Coppede, Juliana S. Furlan, Maysa França, Suzelei C. Lopes, Norberto P. Pereira, Ana Maria S. Lopes, Adriana A. |
author_sort | Pina, Edieidia S. |
collection | PubMed |
description | Biosynthetic investigation of quinonemethide triterpenoid 22β-hydroxy-maytenin (2) from in vitro root cultures of Peritassa laevigata (Celastraceae) was conducted using (13)C-precursor. The mevalonate pathway in P. laevigata is responsible for the synthesis of the quinonemethide triterpenoid scaffold. Moreover, anatomical analysis of P. laevigata roots cultured in vitro and in situ showed the presence of 22β-hydroxy-maytenin (2) and maytenin (1) in the tissues from transverse or longitudinal sections with an intense orange color. MALDI-MS imaging confirmed the distribution of (2) and (1) in the more distal portions of the root cap, the outer cell layers, and near the vascular cylinder of P. laevigata in vitro roots suggesting a role in plant defense against infection by microorganisms as well as in the root exudation processes. |
format | Online Article Text |
id | pubmed-4778575 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47785752016-03-09 Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging Pina, Edieidia S. Silva, Denise B. Teixeira, Simone P. Coppede, Juliana S. Furlan, Maysa França, Suzelei C. Lopes, Norberto P. Pereira, Ana Maria S. Lopes, Adriana A. Sci Rep Article Biosynthetic investigation of quinonemethide triterpenoid 22β-hydroxy-maytenin (2) from in vitro root cultures of Peritassa laevigata (Celastraceae) was conducted using (13)C-precursor. The mevalonate pathway in P. laevigata is responsible for the synthesis of the quinonemethide triterpenoid scaffold. Moreover, anatomical analysis of P. laevigata roots cultured in vitro and in situ showed the presence of 22β-hydroxy-maytenin (2) and maytenin (1) in the tissues from transverse or longitudinal sections with an intense orange color. MALDI-MS imaging confirmed the distribution of (2) and (1) in the more distal portions of the root cap, the outer cell layers, and near the vascular cylinder of P. laevigata in vitro roots suggesting a role in plant defense against infection by microorganisms as well as in the root exudation processes. Nature Publishing Group 2016-03-04 /pmc/articles/PMC4778575/ /pubmed/26943243 http://dx.doi.org/10.1038/srep22627 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Pina, Edieidia S. Silva, Denise B. Teixeira, Simone P. Coppede, Juliana S. Furlan, Maysa França, Suzelei C. Lopes, Norberto P. Pereira, Ana Maria S. Lopes, Adriana A. Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging |
title | Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging |
title_full | Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging |
title_fullStr | Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging |
title_full_unstemmed | Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging |
title_short | Mevalonate-derived quinonemethide triterpenoid from in vitro roots of Peritassa laevigata and their localization in root tissue by MALDI imaging |
title_sort | mevalonate-derived quinonemethide triterpenoid from in vitro roots of peritassa laevigata and their localization in root tissue by maldi imaging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778575/ https://www.ncbi.nlm.nih.gov/pubmed/26943243 http://dx.doi.org/10.1038/srep22627 |
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