In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated Microrhizome

ABSTRACT In vitro rhizome production, encapsulation and cold storage of Acorus calamus were attempted for its propagation and ‘true-to-type’ conservation. Shoot cultures were initiated using underground rhizome buds, on 6-benzyladenine (BA) containing Murashige and Skoog (MS) medium. Maximum microrh...

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Main Authors: Afaque Quraishi, Snigdha Mehar, Durga Sahu, Shailesh Kumar Jadhav
Format: Article
Language:English
Published: Instituto de Tecnologia do Paraná (Tecpar) 2017-06-01
Series:Brazilian Archives of Biology and Technology
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132017000100412&lng=en&tlng=en
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spelling doaj-ae8fd571c9c14f0c8fda6247479cea642020-11-24T23:34:29ZengInstituto de Tecnologia do Paraná (Tecpar)Brazilian Archives of Biology and Technology1678-43242017-06-0160010.1590/1678-4324-2017160378S1516-89132017000100412In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated MicrorhizomeAfaque QuraishiSnigdha MeharDurga SahuShailesh Kumar JadhavABSTRACT In vitro rhizome production, encapsulation and cold storage of Acorus calamus were attempted for its propagation and ‘true-to-type’ conservation. Shoot cultures were initiated using underground rhizome buds, on 6-benzyladenine (BA) containing Murashige and Skoog (MS) medium. Maximum microrhizome production was observed in presence of 33.3 µM BA, on modified MS medium containing 6% sucrose, 100 mg/L citric acid and 1 g/L polyvinyl pyrrolidone-40. Synthetic seeds were produced from regenerated microtubers by encapsulation in calcium alginate beads. These synthetic seeds were stored in complete darkness at 100C temperature for different durations for mid-term conservation. After cold storage, synthetic seeds were re-cultured in vitro, 100% survival was recorded after the storage of 1, 3 or 6 months; and 80% survival was observed after the storage of 12 months. The microrhizomes were produced roots in 4.9 µM indole-3-butyric acid containing half strength MS medium. All the regenerated plantlets were successfully transferred to field after acclimatization. It is the first report on successful one year in vitro cold storage of A. calamus.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132017000100412&lng=en&tlng=enAromatic plantEncapsulationSweet FlagSynthetic seedsPlant tissue culture
collection DOAJ
language English
format Article
sources DOAJ
author Afaque Quraishi
Snigdha Mehar
Durga Sahu
Shailesh Kumar Jadhav
spellingShingle Afaque Quraishi
Snigdha Mehar
Durga Sahu
Shailesh Kumar Jadhav
In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated Microrhizome
Brazilian Archives of Biology and Technology
Aromatic plant
Encapsulation
Sweet Flag
Synthetic seeds
Plant tissue culture
author_facet Afaque Quraishi
Snigdha Mehar
Durga Sahu
Shailesh Kumar Jadhav
author_sort Afaque Quraishi
title In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated Microrhizome
title_short In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated Microrhizome
title_full In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated Microrhizome
title_fullStr In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated Microrhizome
title_full_unstemmed In Vitro Mid-Term Conservation of Acorus calamus L. via Cold Storage of Encapsulated Microrhizome
title_sort in vitro mid-term conservation of acorus calamus l. via cold storage of encapsulated microrhizome
publisher Instituto de Tecnologia do Paraná (Tecpar)
series Brazilian Archives of Biology and Technology
issn 1678-4324
publishDate 2017-06-01
description ABSTRACT In vitro rhizome production, encapsulation and cold storage of Acorus calamus were attempted for its propagation and ‘true-to-type’ conservation. Shoot cultures were initiated using underground rhizome buds, on 6-benzyladenine (BA) containing Murashige and Skoog (MS) medium. Maximum microrhizome production was observed in presence of 33.3 µM BA, on modified MS medium containing 6% sucrose, 100 mg/L citric acid and 1 g/L polyvinyl pyrrolidone-40. Synthetic seeds were produced from regenerated microtubers by encapsulation in calcium alginate beads. These synthetic seeds were stored in complete darkness at 100C temperature for different durations for mid-term conservation. After cold storage, synthetic seeds were re-cultured in vitro, 100% survival was recorded after the storage of 1, 3 or 6 months; and 80% survival was observed after the storage of 12 months. The microrhizomes were produced roots in 4.9 µM indole-3-butyric acid containing half strength MS medium. All the regenerated plantlets were successfully transferred to field after acclimatization. It is the first report on successful one year in vitro cold storage of A. calamus.
topic Aromatic plant
Encapsulation
Sweet Flag
Synthetic seeds
Plant tissue culture
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1516-89132017000100412&lng=en&tlng=en
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