Please use this identifier to cite or link to this item: http://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4840
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dc.contributor.authorDevendra N.K
dc.contributor.authorRajanna L
dc.contributor.authorSheetal C
dc.contributor.authorSeetharam Y.N.
dc.date.accessioned2020-06-12T15:05:24Z-
dc.date.available2020-06-12T15:05:24Z-
dc.date.issued2008
dc.identifier.citationPlant Tissue Culture and Biotechnology , Vol. 18 , 2 , p. 103 - 111en_US
dc.identifier.urihttp://gukir.inflibnet.ac.in:8080/jspui/handle/123456789/4840-
dc.description.abstractAn efficient protocol was established for in vitro shoot multiplication from shoot tip explant of Trichosanthes cucumerina L. var. cucumerina on semisolid MS basal medium supplemented with BA. NAA in the culture medium along with BA promoted higher number of shoot multiplication than BA alone. The rate of shoot multiplication was maximum 12.00 ± 0.70 after four weeks of culture on MS basal medium supplemented with BA 1.0 mg/l + NAA 0.1 mg/l. The elongated shoots rooted within seven - eight days in half strength of MS basal salts supplemented 1.0 mg/l IBA and 3% (w/v) sucrose. About 90% of the rooted plantlets were acclimatized and transferred to the greenhouse and successfully transferred to the field with 80% survival rate. The histological study shows that the organogenesis occurs directly, without callus formation on epidermal and sub epidermal layer of the explants. Adventitious shoots were characterized by the development of shoots apical meristem and leaf primordial.en_US
dc.subjectClonal propagation
dc.subjectCucumerina
dc.subjectOntogeny
dc.subjectShoot multiplication
dc.subjectTrichosanthes cucumerina var
dc.titleIn vitro clonal propagtion of Trichosanthes cucumerina L. var. cucumerinaen_US
dc.typeArticle
Appears in Collections:1. Journal Articles

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