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Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant

Polyalthia bullata is an endangered medicinal plant species. Hence, establishment of P. bullata callus culture is hoped to assist in mass production of secondary metabolites. Leaf and midrib were explants for callus induction. Both of them were cultured on Murashige and Skoog (MS) and Woody Plant Me...

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Autores principales: Kamarul Zaman, Munirah Adibah, Azzeme, Azzreena Mohamad, Ramle, Illy Kamaliah, Normanshah, Nurfazlinyana, Ramli, Siti Nurhafizah, Shaharuddin, Noor Azmi, Ahmad, Syahida, Abdullah, Siti Nor Akmar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765093/
https://www.ncbi.nlm.nih.gov/pubmed/33327608
http://dx.doi.org/10.3390/plants9121772
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author Kamarul Zaman, Munirah Adibah
Azzeme, Azzreena Mohamad
Ramle, Illy Kamaliah
Normanshah, Nurfazlinyana
Ramli, Siti Nurhafizah
Shaharuddin, Noor Azmi
Ahmad, Syahida
Abdullah, Siti Nor Akmar
author_facet Kamarul Zaman, Munirah Adibah
Azzeme, Azzreena Mohamad
Ramle, Illy Kamaliah
Normanshah, Nurfazlinyana
Ramli, Siti Nurhafizah
Shaharuddin, Noor Azmi
Ahmad, Syahida
Abdullah, Siti Nor Akmar
author_sort Kamarul Zaman, Munirah Adibah
collection PubMed
description Polyalthia bullata is an endangered medicinal plant species. Hence, establishment of P. bullata callus culture is hoped to assist in mass production of secondary metabolites. Leaf and midrib were explants for callus induction. Both of them were cultured on Murashige and Skoog (MS) and Woody Plant Medium (WPM) containing different types and concentrations of auxins (2,4-dichlorophenoxyacetic acid (2,4-D), α-naphthaleneacetic acid (NAA), picloram, and dicamba). The callus produced was further multiplied on MS and WPM supplemented with different concentrations of 2,4-D, NAA, picloram, dicamba, indole-3-acetic acid (IAA), and indole-3-butyric acid (IBA) media. The quantification of total phenolic content (TPC), total flavonoid content (TFC) and antioxidant capacity was further carried out on P. bullata callus, and the results were subjected to correlation analysis. Among the media, the WPM + 16.56 µM picloram (53.33 ± 22.06%) was the best for callus induction while MS + 30 µM dicamba was the best for callus multiplication. The TPC, TFC, and EC(50) of DPPH scavenging activity were determined at 0.657 ± 0.07 mg GAE/g FW, 0.491 ± 0.03 mg QE/g, and 85.59 ± 6.09 µg/mL in P. bullata callus, respectively. The positive correlation between DPPH scavenging activity with TPC was determined at r = 0.869, and that of TFC was at r = 0.904. Hence, the P. bullata callus has an ability to accumulate antioxidants. It therefore can be a medium for secondary metabolites production.
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spelling pubmed-77650932020-12-27 Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant Kamarul Zaman, Munirah Adibah Azzeme, Azzreena Mohamad Ramle, Illy Kamaliah Normanshah, Nurfazlinyana Ramli, Siti Nurhafizah Shaharuddin, Noor Azmi Ahmad, Syahida Abdullah, Siti Nor Akmar Plants (Basel) Article Polyalthia bullata is an endangered medicinal plant species. Hence, establishment of P. bullata callus culture is hoped to assist in mass production of secondary metabolites. Leaf and midrib were explants for callus induction. Both of them were cultured on Murashige and Skoog (MS) and Woody Plant Medium (WPM) containing different types and concentrations of auxins (2,4-dichlorophenoxyacetic acid (2,4-D), α-naphthaleneacetic acid (NAA), picloram, and dicamba). The callus produced was further multiplied on MS and WPM supplemented with different concentrations of 2,4-D, NAA, picloram, dicamba, indole-3-acetic acid (IAA), and indole-3-butyric acid (IBA) media. The quantification of total phenolic content (TPC), total flavonoid content (TFC) and antioxidant capacity was further carried out on P. bullata callus, and the results were subjected to correlation analysis. Among the media, the WPM + 16.56 µM picloram (53.33 ± 22.06%) was the best for callus induction while MS + 30 µM dicamba was the best for callus multiplication. The TPC, TFC, and EC(50) of DPPH scavenging activity were determined at 0.657 ± 0.07 mg GAE/g FW, 0.491 ± 0.03 mg QE/g, and 85.59 ± 6.09 µg/mL in P. bullata callus, respectively. The positive correlation between DPPH scavenging activity with TPC was determined at r = 0.869, and that of TFC was at r = 0.904. Hence, the P. bullata callus has an ability to accumulate antioxidants. It therefore can be a medium for secondary metabolites production. MDPI 2020-12-14 /pmc/articles/PMC7765093/ /pubmed/33327608 http://dx.doi.org/10.3390/plants9121772 Text en © 2020 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
Kamarul Zaman, Munirah Adibah
Azzeme, Azzreena Mohamad
Ramle, Illy Kamaliah
Normanshah, Nurfazlinyana
Ramli, Siti Nurhafizah
Shaharuddin, Noor Azmi
Ahmad, Syahida
Abdullah, Siti Nor Akmar
Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant
title Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant
title_full Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant
title_fullStr Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant
title_full_unstemmed Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant
title_short Induction, Multiplication, and Evaluation of Antioxidant Activity of Polyalthia bullata Callus, a Woody Medicinal Plant
title_sort induction, multiplication, and evaluation of antioxidant activity of polyalthia bullata callus, a woody medicinal plant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7765093/
https://www.ncbi.nlm.nih.gov/pubmed/33327608
http://dx.doi.org/10.3390/plants9121772
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