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Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/889
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dc.contributor.authorSAMSUDEEN, K-
dc.contributor.authorNIRMAL BABU, K-
dc.contributor.authorMINOO, D-
dc.contributor.authorRAVINDRAN, P N-
dc.date.accessioned2017-12-05T07:35:36Z-
dc.date.available2017-12-05T07:35:36Z-
dc.date.issued2000-
dc.identifier.citationJournal of Horticultural Science & Biotechnology, 2000, Vol.75, No.4, pp.447-450en_US
dc.identifier.urihttp://hdl.handle.net/123456789/889-
dc.description.abstractGinger anthers collected at the uninucleate microspore stage were subjected to a cold treatment (0°) for 7 d and induced to develop profuse callus on MS medium supplemented with 2-3 mg 1-1 2, 4-D. Plantlets could be regenerated from these calli on MS. medium supplemented with 5-10 mgI-I BAP and 0.2mgI-I 2,4-D. The regenerated plantlets couid be established in soil with 85% success, when they were planted in potting mixture of garden soil, sand and vermiculite in equal proportions and kept in a humid chamber initially for 22-30 d. This is the first report of successful regeneration of plants from ginger anther cultures and the protocol can be used for possible development of androgenic haploids and dihaploids in ginger.en_US
dc.subjectGingeren_US
dc.titlePlant regeneration from anther derived callus cultures of ginger (Zingiber officinale Rose.)en_US
dc.typeArticleen_US
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