IN VITRO REGENERATION OF ARUNDINA GRAMINIFOLIA (D. DON) HOCHR

dc.contributor.authorSharone gladies E
dc.contributor.authorChithra Devi B.S
dc.date.accessioned2023-09-23T08:29:00Z
dc.date.available2023-09-23T08:29:00Z
dc.date.issued2021-04
dc.description.abstractWe can see Orchids come in a wide variety of shapes, sizes, colours, and textures far beyond the human mind’s imagination. They emerge from seeds in nature, but in the absence of suitable hosts, they do not germinate in sufficient numbers. This problem was solved by using the tissue culture technique for its germination. One of the successful method used for mass propogation of orchid plantlets is in vitro techniques. Therefore, an initial analysis was conducted in order establish an appropriate procedure for mass multiplication of Arundina graminifolia. MS (Murashige and Skoog) medium was found to be suitable for the asymbiotic seed germination of Arundina graminifolia. Direct protocorm like bodies were induced by using combinations and individual supplement of MS medium with IAA (Indole-3-acetic acid), IBA (Indole-3- butyric acid), BAP (6-Benzylaminopurine) and KIN (Kinetin). Hormone-free MS basal medium was found suitable for the conversion of PLBs (protocorm-like bodies) into complete plantletsen_US
dc.identifier.issn0972-5210
dc.identifier.urihttp://www.plantarchives.org/article/in-vitro-regeneration-of-arundina-graminifolia-d-don-hochr.pdf
dc.language.isoen_USen_US
dc.publisherPlant Archivesen_US
dc.subjectContaminateen_US
dc.subjectspoilageen_US
dc.subjectfungien_US
dc.subjectbacteriaen_US
dc.subjectsurface sterilizeden_US
dc.titleIN VITRO REGENERATION OF ARUNDINA GRAMINIFOLIA (D. DON) HOCHRen_US
dc.typeArticleen_US

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