High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger Microrhizome

An efficient and reproducible procedure is outlined for rapid in vitro multiplication of <i>Zingiber officinale</i> var. ‘Nadia’ through high frequency shoot proliferation from transverse thin cell layer (tTCL) sections of in vitro derived microrhizome. <i>In vitro</i> derive...

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Main Authors: Dikash Singh THINGBAIJAM, Devi Sunitibala HUIDROM
Format: Article
Language:English
Published: University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca 2014-03-01
Series:Notulae Scientia Biologicae
Online Access:http://notulaebiologicae.ro/index.php/nsb/article/view/9225
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spelling doaj-36d5212159ae43ce921efe5533ba613b2020-11-25T00:49:02ZengUniversity of Agricultural Sciences and Veterinary Medicine, Cluj-NapocaNotulae Scientia Biologicae2067-32052067-32642014-03-0161859110.15835/nsb.6.1.92258012High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger MicrorhizomeDikash Singh THINGBAIJAM0Devi Sunitibala HUIDROM1Medicinal Plants & Horticultural Resources Division, Institute of Bioresources and Sustainable Development, Takyelpat Institutional Area, Imphal-795 001, ManipurMedicinal Plants & Horticultural Resources Division, Institute of Bioresources and Sustainable Development, Takyelpat Institutional Area, Imphal-795 001, ManipurAn efficient and reproducible procedure is outlined for rapid in vitro multiplication of <i>Zingiber officinale</i> var. ‘Nadia’ through high frequency shoot proliferation from transverse thin cell layer (tTCL) sections of in vitro derived microrhizome. <i>In vitro</i> derived microrhizome of size 500 μm in thickness was used as initial explants for induction of somatic embryos. Among the different phytohormones tested, tTCL explants shows maximum calli proliferation in medium containing 2 mg/L 2,4-Dichlorophenoxyacetic acid (88.30±0.11%). Reduced concentration of 2,4 Dichlorophenoxyacetic acid was supplemented with different cytokinins for regeneration of callus. Among the different medium tested, optimum redifferentiation of somatic embryos were observed in medium containing 0.2 mg/L 2,4 Dichlorophenoxyacetic acid and 6.0 mg/L BAP (141.08±0.25). Clump of regenerated plantlets were further subculture and transfer into microrhizome inducing medium containing high sucrose concentration (8%). Plantlets with well developed microrhizome were successfully acclimatized and eventually transferred to the field. The application of studying embryo section for regeneration of plants might be useful alternative to ginger improvement programme. Histological analysis showed formation of somatic embryos and regenerated adventitious shoot.http://notulaebiologicae.ro/index.php/nsb/article/view/9225
collection DOAJ
language English
format Article
sources DOAJ
author Dikash Singh THINGBAIJAM
Devi Sunitibala HUIDROM
spellingShingle Dikash Singh THINGBAIJAM
Devi Sunitibala HUIDROM
High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger Microrhizome
Notulae Scientia Biologicae
author_facet Dikash Singh THINGBAIJAM
Devi Sunitibala HUIDROM
author_sort Dikash Singh THINGBAIJAM
title High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger Microrhizome
title_short High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger Microrhizome
title_full High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger Microrhizome
title_fullStr High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger Microrhizome
title_full_unstemmed High Frequency Plant Regeneration System from Transverse Thin Cell Layer Section of <i>In vitro</i> Derived ‘Nadia’ Ginger Microrhizome
title_sort high frequency plant regeneration system from transverse thin cell layer section of <i>in vitro</i> derived ‘nadia’ ginger microrhizome
publisher University of Agricultural Sciences and Veterinary Medicine, Cluj-Napoca
series Notulae Scientia Biologicae
issn 2067-3205
2067-3264
publishDate 2014-03-01
description An efficient and reproducible procedure is outlined for rapid in vitro multiplication of <i>Zingiber officinale</i> var. ‘Nadia’ through high frequency shoot proliferation from transverse thin cell layer (tTCL) sections of in vitro derived microrhizome. <i>In vitro</i> derived microrhizome of size 500 μm in thickness was used as initial explants for induction of somatic embryos. Among the different phytohormones tested, tTCL explants shows maximum calli proliferation in medium containing 2 mg/L 2,4-Dichlorophenoxyacetic acid (88.30±0.11%). Reduced concentration of 2,4 Dichlorophenoxyacetic acid was supplemented with different cytokinins for regeneration of callus. Among the different medium tested, optimum redifferentiation of somatic embryos were observed in medium containing 0.2 mg/L 2,4 Dichlorophenoxyacetic acid and 6.0 mg/L BAP (141.08±0.25). Clump of regenerated plantlets were further subculture and transfer into microrhizome inducing medium containing high sucrose concentration (8%). Plantlets with well developed microrhizome were successfully acclimatized and eventually transferred to the field. The application of studying embryo section for regeneration of plants might be useful alternative to ginger improvement programme. Histological analysis showed formation of somatic embryos and regenerated adventitious shoot.
url http://notulaebiologicae.ro/index.php/nsb/article/view/9225
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