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Shoot proliferation and rooting treatments influence secondary metabolite production and antioxidant activity in tissue culture-derived Aloe arborescens grown ex vitro
Aloe species are valuable plants with great ornamental and medicinal value. Although micropropagation protocols have been developed to meet the increasing global demand, the effects of the series of events during micropropagation on the phytochemical and pharmacological efficacy of ex-vitro plants r...
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Published in: | Plant growth regulation 2013-06, Vol.70 (2), p.115-122 |
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creator | Amoo, S. O. Aremu, A. O. Van Staden, J. |
description | Aloe
species are valuable plants with great ornamental and medicinal value. Although micropropagation protocols have been developed to meet the increasing global demand, the effects of the series of events during micropropagation on the phytochemical and pharmacological efficacy of ex-vitro plants remains poorly understood. Thus, we evaluated the effects of cytokinin and rooting compounds used during the shoot regeneration and rooting phases respectively, on secondary metabolite production in greenhouse-grown in vitro-derived
Aloe arborescens
. Shoots derived from
meta
-methoxytopolin (Me
m
T)-containing medium and rooted with either smoke–water (SW) or indole butyric acid (IBA) had higher levels of total phenolics and flavonoids than those rooted on plant growth regulator (PGR)-free medium. Iridoid content was significantly reduced in cytokinin-regenerated shoots rooted with IBA in comparison to PGR-free regenerated shoots rooted with IBA. Conversely, the use of SW for rooting in cytokinin-regenerated shoots significantly increased iridoid content when compared to PGR-free regenerated shoots rooted with SW. These findings suggest an antagonistic interaction between cytokinins used in this study and IBA as well as a possible synergistic or additive interaction of the cytokinins with SW on iridoid production. Significantly higher antioxidant activity was recorded in shoots regenerated from
meta
-topolin riboside (
m
TR) and Me
m
T and rooted with IBA or SW when compared to those rooted without PGR. Overall, the type of cytokinin and rooting treatments individually and interactively had a significant carry-over effect on secondary metabolite production and antioxidant potential of tissue culture-derived
A
.
arborescens
. Therefore, when micropropagating plants for medicinal uses, it is prudent to select the right cytokinin and rooting compound for optimal production of secondary metabolites and ultimately the pharmacological efficacy of acclimatized plants. |
doi_str_mv | 10.1007/s10725-013-9783-x |
format | article |
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species are valuable plants with great ornamental and medicinal value. Although micropropagation protocols have been developed to meet the increasing global demand, the effects of the series of events during micropropagation on the phytochemical and pharmacological efficacy of ex-vitro plants remains poorly understood. Thus, we evaluated the effects of cytokinin and rooting compounds used during the shoot regeneration and rooting phases respectively, on secondary metabolite production in greenhouse-grown in vitro-derived
Aloe arborescens
. Shoots derived from
meta
-methoxytopolin (Me
m
T)-containing medium and rooted with either smoke–water (SW) or indole butyric acid (IBA) had higher levels of total phenolics and flavonoids than those rooted on plant growth regulator (PGR)-free medium. Iridoid content was significantly reduced in cytokinin-regenerated shoots rooted with IBA in comparison to PGR-free regenerated shoots rooted with IBA. Conversely, the use of SW for rooting in cytokinin-regenerated shoots significantly increased iridoid content when compared to PGR-free regenerated shoots rooted with SW. These findings suggest an antagonistic interaction between cytokinins used in this study and IBA as well as a possible synergistic or additive interaction of the cytokinins with SW on iridoid production. Significantly higher antioxidant activity was recorded in shoots regenerated from
meta
-topolin riboside (
m
TR) and Me
m
T and rooted with IBA or SW when compared to those rooted without PGR. Overall, the type of cytokinin and rooting treatments individually and interactively had a significant carry-over effect on secondary metabolite production and antioxidant potential of tissue culture-derived
A
.
arborescens
. Therefore, when micropropagating plants for medicinal uses, it is prudent to select the right cytokinin and rooting compound for optimal production of secondary metabolites and ultimately the pharmacological efficacy of acclimatized plants.</description><identifier>ISSN: 0167-6903</identifier><identifier>EISSN: 1573-5087</identifier><identifier>DOI: 10.1007/s10725-013-9783-x</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Agriculture ; Antioxidants ; Biomedical and Life Sciences ; Flavonoids ; Growth regulators ; Life Sciences ; Metabolites ; Original Paper ; Phenols ; Plant Anatomy/Development ; Plant growth ; Plant Physiology ; Plant Sciences ; Secondary metabolites ; Shoots</subject><ispartof>Plant growth regulation, 2013-06, Vol.70 (2), p.115-122</ispartof><rights>Springer Science+Business Media Dordrecht 2013</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-b5e963670b5f9a5afbea42464d08506089d51feb82b2885366d499bda138e3ee3</citedby><cites>FETCH-LOGICAL-c316t-b5e963670b5f9a5afbea42464d08506089d51feb82b2885366d499bda138e3ee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Amoo, S. O.</creatorcontrib><creatorcontrib>Aremu, A. O.</creatorcontrib><creatorcontrib>Van Staden, J.</creatorcontrib><title>Shoot proliferation and rooting treatments influence secondary metabolite production and antioxidant activity in tissue culture-derived Aloe arborescens grown ex vitro</title><title>Plant growth regulation</title><addtitle>Plant Growth Regul</addtitle><description>Aloe
species are valuable plants with great ornamental and medicinal value. Although micropropagation protocols have been developed to meet the increasing global demand, the effects of the series of events during micropropagation on the phytochemical and pharmacological efficacy of ex-vitro plants remains poorly understood. Thus, we evaluated the effects of cytokinin and rooting compounds used during the shoot regeneration and rooting phases respectively, on secondary metabolite production in greenhouse-grown in vitro-derived
Aloe arborescens
. Shoots derived from
meta
-methoxytopolin (Me
m
T)-containing medium and rooted with either smoke–water (SW) or indole butyric acid (IBA) had higher levels of total phenolics and flavonoids than those rooted on plant growth regulator (PGR)-free medium. Iridoid content was significantly reduced in cytokinin-regenerated shoots rooted with IBA in comparison to PGR-free regenerated shoots rooted with IBA. Conversely, the use of SW for rooting in cytokinin-regenerated shoots significantly increased iridoid content when compared to PGR-free regenerated shoots rooted with SW. These findings suggest an antagonistic interaction between cytokinins used in this study and IBA as well as a possible synergistic or additive interaction of the cytokinins with SW on iridoid production. Significantly higher antioxidant activity was recorded in shoots regenerated from
meta
-topolin riboside (
m
TR) and Me
m
T and rooted with IBA or SW when compared to those rooted without PGR. Overall, the type of cytokinin and rooting treatments individually and interactively had a significant carry-over effect on secondary metabolite production and antioxidant potential of tissue culture-derived
A
.
arborescens
. Therefore, when micropropagating plants for medicinal uses, it is prudent to select the right cytokinin and rooting compound for optimal production of secondary metabolites and ultimately the pharmacological efficacy of acclimatized plants.</description><subject>Agriculture</subject><subject>Antioxidants</subject><subject>Biomedical and Life Sciences</subject><subject>Flavonoids</subject><subject>Growth regulators</subject><subject>Life Sciences</subject><subject>Metabolites</subject><subject>Original Paper</subject><subject>Phenols</subject><subject>Plant Anatomy/Development</subject><subject>Plant growth</subject><subject>Plant Physiology</subject><subject>Plant Sciences</subject><subject>Secondary metabolites</subject><subject>Shoots</subject><issn>0167-6903</issn><issn>1573-5087</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kctKBDEQRYMoOD4-wF3AdTTpdJLupQy-YMCFug7pTvWYoSfRJK3jF_mbZhgRN66qKO65RdVF6IzRC0apukyMqkoQyjhpVcPJZg_NmFCcCNqofTSjTCoiW8oP0VFKK0pp0wg2Q1-PLyFk_BrD6AaIJrvgsfEWxzJ2folzBJPX4HPCzg_jBL4HnKAP3pr4ideQTVfYDFsPO_W_BsaXduNsqdiU8bvLn8UCZ5fSBLifxjxFIBaieweLr8YA2MQuREg9-ISXMXx4DBtcwBhO0MFgxgSnP_UYPd9cP83vyOLh9n5-tSA9ZzKTTkAruVS0E0NrhBk6MHVVy9rSRlBJm9YKNkDXVF1VHsCltHXbdtYw3gAH4MfofOdbrnmbIGW9ClP0ZaVmvFayrivVFhXbqfoYUoow6Nfo1uUfmlG9zUPv8tAlD73NQ28KU-2YVLR-CfGP87_QN9-Kk_M</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>Amoo, S. 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O. ; Van Staden, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-b5e963670b5f9a5afbea42464d08506089d51feb82b2885366d499bda138e3ee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Agriculture</topic><topic>Antioxidants</topic><topic>Biomedical and Life Sciences</topic><topic>Flavonoids</topic><topic>Growth regulators</topic><topic>Life Sciences</topic><topic>Metabolites</topic><topic>Original Paper</topic><topic>Phenols</topic><topic>Plant Anatomy/Development</topic><topic>Plant growth</topic><topic>Plant Physiology</topic><topic>Plant Sciences</topic><topic>Secondary metabolites</topic><topic>Shoots</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amoo, S. O.</creatorcontrib><creatorcontrib>Aremu, A. O.</creatorcontrib><creatorcontrib>Van Staden, J.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central</collection><collection>ProQuest Agricultural & Environmental Science</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Biological Sciences</collection><collection>Agricultural Science Database</collection><collection>ProQuest research library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central Basic</collection><jtitle>Plant growth regulation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amoo, S. O.</au><au>Aremu, A. O.</au><au>Van Staden, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Shoot proliferation and rooting treatments influence secondary metabolite production and antioxidant activity in tissue culture-derived Aloe arborescens grown ex vitro</atitle><jtitle>Plant growth regulation</jtitle><stitle>Plant Growth Regul</stitle><date>2013-06-01</date><risdate>2013</risdate><volume>70</volume><issue>2</issue><spage>115</spage><epage>122</epage><pages>115-122</pages><issn>0167-6903</issn><eissn>1573-5087</eissn><abstract>Aloe
species are valuable plants with great ornamental and medicinal value. Although micropropagation protocols have been developed to meet the increasing global demand, the effects of the series of events during micropropagation on the phytochemical and pharmacological efficacy of ex-vitro plants remains poorly understood. Thus, we evaluated the effects of cytokinin and rooting compounds used during the shoot regeneration and rooting phases respectively, on secondary metabolite production in greenhouse-grown in vitro-derived
Aloe arborescens
. Shoots derived from
meta
-methoxytopolin (Me
m
T)-containing medium and rooted with either smoke–water (SW) or indole butyric acid (IBA) had higher levels of total phenolics and flavonoids than those rooted on plant growth regulator (PGR)-free medium. Iridoid content was significantly reduced in cytokinin-regenerated shoots rooted with IBA in comparison to PGR-free regenerated shoots rooted with IBA. Conversely, the use of SW for rooting in cytokinin-regenerated shoots significantly increased iridoid content when compared to PGR-free regenerated shoots rooted with SW. These findings suggest an antagonistic interaction between cytokinins used in this study and IBA as well as a possible synergistic or additive interaction of the cytokinins with SW on iridoid production. Significantly higher antioxidant activity was recorded in shoots regenerated from
meta
-topolin riboside (
m
TR) and Me
m
T and rooted with IBA or SW when compared to those rooted without PGR. Overall, the type of cytokinin and rooting treatments individually and interactively had a significant carry-over effect on secondary metabolite production and antioxidant potential of tissue culture-derived
A
.
arborescens
. Therefore, when micropropagating plants for medicinal uses, it is prudent to select the right cytokinin and rooting compound for optimal production of secondary metabolites and ultimately the pharmacological efficacy of acclimatized plants.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10725-013-9783-x</doi><tpages>8</tpages></addata></record> |
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source | Springer Nature |
subjects | Agriculture Antioxidants Biomedical and Life Sciences Flavonoids Growth regulators Life Sciences Metabolites Original Paper Phenols Plant Anatomy/Development Plant growth Plant Physiology Plant Sciences Secondary metabolites Shoots |
title | Shoot proliferation and rooting treatments influence secondary metabolite production and antioxidant activity in tissue culture-derived Aloe arborescens grown ex vitro |
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