Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/23813
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dc.contributor.authorGururaj, H B-
dc.contributor.authorGiridhar, P-
dc.contributor.authorSharma, Ashwani-
dc.contributor.authorPrasad, B C N-
dc.contributor.authorRavishankar, G A-
dc.date.accessioned2013-11-19T09:51:27Z-
dc.date.available2013-11-19T09:51:27Z-
dc.date.issued2004-11-
dc.identifier.issn0975-1009 (Online); 0019-5189 (Print)-
dc.identifier.urihttp://hdl.handle.net/123456789/23813-
dc.description1136-1140en_US
dc.description.abstractAn efficient and highly reproducible protocol for micropropagation of bird eye chilli Capsicum frutescens was attempted. Murashige and Skoog (MS) medium containing 0.5-3.0 mgl-1 of 6-benzyladenine (BA), 2-isopentenyl adenine (2 iP), kinetin and 0.5-2.0 mg l-1 of indole-3-acetic acid (IAA), indole-3-butyric acid (IBA) along with 1 gl-1 activated charcoal (AC) were used for shoot regeneration from both shoot tip and nodal explants. Shoot tip explants (100%) grew well on medium containing 1 mg l-1 of kinetin and l mgl-1 of IBA. Shoot proliferation (1-3) from nodal explants was effective on this medium. The regenerated shoots with 4-7 nodes had further growth upon sub-culturing on to kinetin (1 mg l-1) and IBA(1 mgl-1) and rooted simultaneously. The rooted plants were transferred to pots after hardening under controlled conditions. The survival percentage in pots was 80-90%.en_US
dc.language.isoen_USen_US
dc.publisherNISCAIR-CSIR, Indiaen_US
dc.relation.ispartofseriesInt Cl7. A01H/00en_US
dc.rights CC Attribution-Noncommercial-No Derivative Works 2.5 Indiaen_US
dc.sourceIJEB Vol.42(11) [November 2004]en_US
dc.subjectBird eye chillien_US
dc.subjectCapsicum frutescensen_US
dc.subjectNodal explanten_US
dc.subjectPlantleten_US
dc.subjectRegenerationen_US
dc.subjectRootingen_US
dc.subjectShoot tipen_US
dc.titleIn vitro clonal propagation of bird eye chilli (Capsicum frutescens Mill.)en_US
dc.typeArticleen_US
Appears in Collections:IJEB Vol.42(11) [November 2004]

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