Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4578
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dc.contributor.authorGhanti S.K
dc.contributor.authorSujata K.G
dc.contributor.authorRao M.S
dc.contributor.authorKishor P.B.K.
dc.date.accessioned2020-06-12T15:04:14Z-
dc.date.available2020-06-12T15:04:14Z-
dc.date.issued2010
dc.identifier.citationBiologia Plantarum , Vol. 54 , 1 , p. 121 - 125en_US
dc.identifier.uri10.1007/s10535-010-0018-y
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4578-
dc.description.abstractA protocol for plant regeneration via somatic embryogenesis was developed in two chickpea (Cicer arietinum L.) cultivars ICCV-10 and Annigeri. Somatic embryos were induced from immature cotyledons on Murashige and Skoog's (MS) medium supplemented with different concentrations of 2,4-dichlorophenoxyacetic acid (2,4-D), 2,4,5-trichlorophenoxyacetic acid (2,4,5-T), ?-naphthaleneacetic acid (NAA) and picloram alone or in combination with 0.5 - 2.0 mg dm-3 N6-benzylaminopurine (BA) or kinetin (KIN). NAA was better for somatic embryo induction compared to other auxins. The well formed, cotyledonary shaped embryos germinated into plantlets with 36.6% frequency on MS medium supplemented with 2.0 mg dm-3 BA + 0.5 mg dm-3 abscisic acid (ABA). The frequency of embryogenesis and plantlet regeneration was higher in cv. ICCV-10 as compared to cv. Annigeri. Regenerated plants were transferred to soil (40% survival) and grown to maturity. Histological studies of explants at various developmental stages of somatic embryogenesis reveled that somatic embryos developed directly from the cotyledon cells and they were single cell origin. © Springer Science+Business Media B.V 2010.en_US
dc.subjectAbscisic acid
dc.subjectAuxins
dc.subjectCytokinins
dc.subjectGermination
dc.subjectHistology
dc.subjectMature somatic embryos
dc.titleDirect somatic embryogenesis and plant regeneration from immature explants of chickpeaen_US
dc.typeArticle
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