Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/43334
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dc.contributor.authorRaja, H David-
dc.contributor.authorArockiasamy, D I-
dc.date.accessioned2018-01-04T06:17:17Z-
dc.date.available2018-01-04T06:17:17Z-
dc.date.issued2017-07-
dc.identifier.issn0975-0967 (Online); 0972-5849 (Print)-
dc.identifier.urihttp://nopr.niscair.res.in/handle/123456789/43334-
dc.description366-369en_US
dc.description.abstractMass propagation of tree species has always been a challenging task. An efficient protocol for rapid in vitro mass propagation of Nyctanthes arbor-tristis L. has been developed from shoot tip and internodal explants. Explants were cultured on Murashige and Skoog (MS) medium supplemented with 6-benzylamino purine (BAP) and thidiazuron (TDZ) in various concentrations. 2. 0 mg/l BAP was proved to be best for high frequency multiple shoot induction from shoot-tip explants and 2. 5 mg/l BAP was produced maximum shoots proliferation from internodal explants. The well elongated healthy shoots were transferred for rooting on MS medium supplemented with indole-3-butyric acid (IBA) in different concentration. Maximum numbers of roots were achieved in 2.0 mg/l of IBA medium. The rooted plantlets were hardened and transferred to field conditions. All the regenerated plants with 80-85% survival rate were normal with respect to morphology and growth characteristics.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJBT Vol.16(3) [July 2017]en_US
dc.subjectIn vitro propagationen_US
dc.subjectNyctanthes arbor-tristisen_US
dc.subjectPlant regenerationen_US
dc.subjectCulture conditionen_US
dc.titleIn vitro propagation of Nyctanthes arbor-tristis L.en_US
dc.typeArticleen_US
Appears in Collections:IJBT Vol.16(3) [July 2017]

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