Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as Explant

Costus pictus D. Don is a potent anti-diabetic plant used in folk, ayurvedic and homeopathic system of medicine. Gene and protein expression of key targets in insulin signaling pathway have revealed that methyl tetracosonoate, a bio-active molecule from Costus pictus extract has anti-diabetic activi...

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Main Authors: Kshetrimayum PUNYARANI, Jitendra G. SHARMA
Format: Article
Language:English
Published: Society of Land Measurements and Cadastre from Transylvania (SMTCT) 2012-05-01
Series:Notulae Scientia Biologicae
Online Access:http://notulaebiologicae.ro/index.php/nsb/article/view/7303
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author Kshetrimayum PUNYARANI
Jitendra G. SHARMA
author_facet Kshetrimayum PUNYARANI
Jitendra G. SHARMA
author_sort Kshetrimayum PUNYARANI
collection DOAJ
description Costus pictus D. Don is a potent anti-diabetic plant used in folk, ayurvedic and homeopathic system of medicine. Gene and protein expression of key targets in insulin signaling pathway have revealed that methyl tetracosonoate, a bio-active molecule from Costus pictus extract has anti-diabetic activity. The axillary buds of Costus pictus are dormant. The dormancy of axillary buds were broken when cultured in Murashige and Skoog (MS) medium supplemented with 3-4 ?M 6-benzylaminopurine (BAP) in combination with 0.2-1 ?M naphthalene acetic acid (NAA). The highest bud-break percentage was achieved in those supplemented with 0.6 ?M NAA and 3 ?M BAP. The sprouted axillary buds were transferred onto medium supplemented with 0.6 ?M NAA and 6-10 ?M BAP for shoot multiplication. The maximum average number of shoot was achieved in medium supplemented with 0.6 ?M NAA and 8 ?M BAP. The shoots were successfully rooted when transferred onto media supplemented with 1-12 ?M NAA or indole-3-acetic acid (IAA) and 3 ?M BAP. The maximum number of roots was found in 8 ?M NAA and 3 ?M BAP. The dormancy of in vitro axillary buds were also successfully broken in stems from which shoot apex were decapitated and cultured in MS medium with 0.6 ?M NAA, 7 ?M BAP and 5-13% sucrose. These sprouted in vitro axillary buds could be used as secondary explants for shoot multiplication. The maximum was in medium supplemented with 9% sucrose. Rhizomes were successfully induced when 4-month old plantlets were cultured on � strength MS medium supplemented with 2.4 ?M NAA, 32 ?M BAP and 5-13% sucrose. Microrhizomes formed in 9% sucrose was largest in size with highest average fresh weight.
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spelling doaj.art-eae4f2d9f8074f9088aea78452810c032022-12-22T02:08:02ZengSociety of Land Measurements and Cadastre from Transylvania (SMTCT)Notulae Scientia Biologicae2067-32052067-32642012-05-014272787093Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as ExplantKshetrimayum PUNYARANI0Jitendra G. SHARMA1Manipur University, Department of Life Sciences, Imphal-795003Manipur University, Department of Life Sciences, Imphal-795003Costus pictus D. Don is a potent anti-diabetic plant used in folk, ayurvedic and homeopathic system of medicine. Gene and protein expression of key targets in insulin signaling pathway have revealed that methyl tetracosonoate, a bio-active molecule from Costus pictus extract has anti-diabetic activity. The axillary buds of Costus pictus are dormant. The dormancy of axillary buds were broken when cultured in Murashige and Skoog (MS) medium supplemented with 3-4 ?M 6-benzylaminopurine (BAP) in combination with 0.2-1 ?M naphthalene acetic acid (NAA). The highest bud-break percentage was achieved in those supplemented with 0.6 ?M NAA and 3 ?M BAP. The sprouted axillary buds were transferred onto medium supplemented with 0.6 ?M NAA and 6-10 ?M BAP for shoot multiplication. The maximum average number of shoot was achieved in medium supplemented with 0.6 ?M NAA and 8 ?M BAP. The shoots were successfully rooted when transferred onto media supplemented with 1-12 ?M NAA or indole-3-acetic acid (IAA) and 3 ?M BAP. The maximum number of roots was found in 8 ?M NAA and 3 ?M BAP. The dormancy of in vitro axillary buds were also successfully broken in stems from which shoot apex were decapitated and cultured in MS medium with 0.6 ?M NAA, 7 ?M BAP and 5-13% sucrose. These sprouted in vitro axillary buds could be used as secondary explants for shoot multiplication. The maximum was in medium supplemented with 9% sucrose. Rhizomes were successfully induced when 4-month old plantlets were cultured on � strength MS medium supplemented with 2.4 ?M NAA, 32 ?M BAP and 5-13% sucrose. Microrhizomes formed in 9% sucrose was largest in size with highest average fresh weight.http://notulaebiologicae.ro/index.php/nsb/article/view/7303
spellingShingle Kshetrimayum PUNYARANI
Jitendra G. SHARMA
Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as Explant
Notulae Scientia Biologicae
title Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as Explant
title_full Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as Explant
title_fullStr Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as Explant
title_full_unstemmed Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as Explant
title_short Micropropagation and Microrhizome Induction in Costus pictus D. Don Using In Vitro and Ex Vitro Nodal Segments as Explant
title_sort micropropagation and microrhizome induction in costus pictus d don using in vitro and ex vitro nodal segments as explant
url http://notulaebiologicae.ro/index.php/nsb/article/view/7303
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