Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysis

Plant regeneration was achieved from axillary bud, callus and somatic embryos of Dianthus caryophyllus cv.Yellow Dot Com from node and leaf explants cultured on Murashige and Skoog (MS) medium supplemented with plant growth regulators. The explant nodal cutting responded well for direct regeneratio...

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Main Authors: SURINDER KUMAR, RAJNI KUMARI, TRIPTI BAHETI, MANISHA THAKUR, MINERVA GHANI
Format: Article
Language:English
Published: Indian Council of Agricultural Research 2016-11-01
Series:The Indian Journal of Agricultural Sciences
Subjects:
Online Access:https://epubs.icar.org.in/index.php/IJAgS/article/view/62936
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author SURINDER KUMAR
RAJNI KUMARI
TRIPTI BAHETI
MANISHA THAKUR
MINERVA GHANI
author_facet SURINDER KUMAR
RAJNI KUMARI
TRIPTI BAHETI
MANISHA THAKUR
MINERVA GHANI
author_sort SURINDER KUMAR
collection DOAJ
description Plant regeneration was achieved from axillary bud, callus and somatic embryos of Dianthus caryophyllus cv.Yellow Dot Com from node and leaf explants cultured on Murashige and Skoog (MS) medium supplemented with plant growth regulators. The explant nodal cutting responded well for direct regeneration while leaf explant was selected for callus induction. The highest number of direct adventitious shoots were achieved with 9.08 μM TDZ and 5.37 μM NAA. The maximum callus induction was achieved with 2.06 μM 2, 4-D and 2.68 μM NAA. The calli derived from MS medium supplemented with 5.37 μM NAA and 2.27 μM TDZ were found to have maximum shoot regeneration potential. The highest number of calli producing shoots and average number of shoots per callus was recorded on MS medium supplemented with 9.12 μM zeatin and 5.07 μM IAA. The calli derived from leaf explants cultured on medium containing 2.06 μM 2, 4-D and 2.68 μM NAA were highly friable, had poor regeneration potential and were selected for cell suspension studies. The cultures were allowed to grow into micro-colonies in liquid medium and subsequently into embryogenic calli on semi-solid and solid MS medium which later differentiated into somatic embryos without growth regulators. Plantlets were obtained from in vitro derived shoots/somatic embryos with 60-80% survival after 30 day of transfer to pots. The plants regenerated from axillary buds, callus and somatic embryos were compared with mother plant to assess genetic fidelity using RAPD and 2.94%, 26.47% and 20.58% variation was observed, respectively.
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spelling doaj.art-68744026ef004bb194dbf1df5f98f0322023-07-21T08:26:42ZengIndian Council of Agricultural ResearchThe Indian Journal of Agricultural Sciences0019-50222394-33192016-11-01861110.56093/ijas.v86i11.62936Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysisSURINDER KUMAR0RAJNI KUMARI1TRIPTI BAHETI2MANISHA THAKUR3MINERVA GHANI4Dr Y S Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh 173 230Dr Y S Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh 173 230Dr Y S Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh 173 230Dr Y S Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh 173 230Dr Y S Parmar University of Horticulture and Forestry, Solan, Himachal Pradesh 173 230 Plant regeneration was achieved from axillary bud, callus and somatic embryos of Dianthus caryophyllus cv.Yellow Dot Com from node and leaf explants cultured on Murashige and Skoog (MS) medium supplemented with plant growth regulators. The explant nodal cutting responded well for direct regeneration while leaf explant was selected for callus induction. The highest number of direct adventitious shoots were achieved with 9.08 μM TDZ and 5.37 μM NAA. The maximum callus induction was achieved with 2.06 μM 2, 4-D and 2.68 μM NAA. The calli derived from MS medium supplemented with 5.37 μM NAA and 2.27 μM TDZ were found to have maximum shoot regeneration potential. The highest number of calli producing shoots and average number of shoots per callus was recorded on MS medium supplemented with 9.12 μM zeatin and 5.07 μM IAA. The calli derived from leaf explants cultured on medium containing 2.06 μM 2, 4-D and 2.68 μM NAA were highly friable, had poor regeneration potential and were selected for cell suspension studies. The cultures were allowed to grow into micro-colonies in liquid medium and subsequently into embryogenic calli on semi-solid and solid MS medium which later differentiated into somatic embryos without growth regulators. Plantlets were obtained from in vitro derived shoots/somatic embryos with 60-80% survival after 30 day of transfer to pots. The plants regenerated from axillary buds, callus and somatic embryos were compared with mother plant to assess genetic fidelity using RAPD and 2.94%, 26.47% and 20.58% variation was observed, respectively. https://epubs.icar.org.in/index.php/IJAgS/article/view/62936CallusCarnationDianthus caryophyllusGrowth regulatorsPlantletsPolymerase chain reaction
spellingShingle SURINDER KUMAR
RAJNI KUMARI
TRIPTI BAHETI
MANISHA THAKUR
MINERVA GHANI
Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysis
The Indian Journal of Agricultural Sciences
Callus
Carnation
Dianthus caryophyllus
Growth regulators
Plantlets
Polymerase chain reaction
title Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysis
title_full Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysis
title_fullStr Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysis
title_full_unstemmed Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysis
title_short Plant regeneration from axillary bud, callus and somatic embryo in carnation (Dianthus caryophyllus) and assessment of genetic fidelity using RAPD-PCR analysis
title_sort plant regeneration from axillary bud callus and somatic embryo in carnation dianthus caryophyllus and assessment of genetic fidelity using rapd pcr analysis
topic Callus
Carnation
Dianthus caryophyllus
Growth regulators
Plantlets
Polymerase chain reaction
url https://epubs.icar.org.in/index.php/IJAgS/article/view/62936
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