Plant regeneration from axillary bud derived callus in white yam (Dioscorea rotundata)

cg.authorship.typesCGIAR single centreen
cg.contributor.affiliationInternational Institute of Tropical Agricultureen
cg.contributor.crpRoots, Tubers and Bananas
cg.coverage.countryNigeria
cg.coverage.iso3166-alpha2NG
cg.coverage.regionAfrica
cg.coverage.regionWestern Africa
cg.howPublishedFormally Publisheden
cg.identifier.doihttps://doi.org/10.1007/s11240-016-1017-2en
cg.isijournalISI Journalen
cg.issn0167-6857en
cg.issue3en
cg.journalPlant Cell, Tissue and Organ Cultureen
cg.reviewStatusPeer Reviewen
cg.subject.iitaYAMen
cg.volume126en
dc.contributor.authorManoharan, R.en
dc.contributor.authorTripathi, J.N.en
dc.contributor.authorTripathi, L.en
dc.date.accessioned2016-08-09T17:29:55Zen
dc.date.available2016-08-09T17:29:55Zen
dc.identifier.urihttps://hdl.handle.net/10568/76366
dc.titlePlant regeneration from axillary bud derived callus in white yam (Dioscorea rotundata)en
dcterms.abstractDioscorea rotundata, commonly known as white yam, is an important staple food crop widely cultivated in West Africa and provides food security to millions of people. Genetic improvements of this crop using the advanced biotechnology tools have been hampered hitherto by the recalcitrant nature of regeneration through somatic embryogenesis. Therefore, we have developed an efficient and reproducible system for plant regeneration via somatic embryogenesis. Explants of different types (immature leaf, node, stem internode, root segment, petiole, and axillary bud) of D. rotundata accession TDr 2436 were tested for their embryogenic potentials on Murashige and Skoog (MS) medium supplemented with various auxins (2,4-D, NAA, and picloram). Among all explants tested, axillary bud explants cultured on MS medium supplemented with picloram (0.5–12 mg/l) favored the production of calli. Maximum proliferation of calli (526 mg fresh weight/explant) was achieved on MS medium supplemented with picloram (0.5 mg/l), casein hydrolysate (600 mg/l), and proline (1 g/l). Histology analysis confirmed that the embryogenic calli produced on this medium were mixed with non-embryogenic calli. Transfer of calli on MS basal medium supplemented with activated charcoal (1 %) changed the color of calli to purple and promoted the production of somatic embryos (87 embryos/callus) as well as adventitious shoot buds. Furthermore, upon transfer to MS medium supplemented with BAP (0.4 mg/l), the embryos continued their differentiation and maturation and germinated into complete plantlets. The adventitious shoot buds produced multiple shoots on MS medium supplemented with BAP (0.4 mg/l). Well-developed germinated plantlets were acclimatized in the screen house with 90 % survivability. Histology studies confirmed that the regeneration of D. rotundata reported here followed dual regeneration pathways. The embryogenic calli regenerated through development of somatic embryos and germinated into complete plantlets, however non-embryogenic calli regenerated through organogenesis and developed multiple shoots. The developed protocol has potential for somatic hybridization, mass clonal propagation, and genetic transformation applications.en
dcterms.accessRightsOpen Access
dcterms.audienceScientistsen
dcterms.available2016-06-14
dcterms.bibliographicCitationManoharan, R., Tripathi, J., & Tripathi, L. (2016). Plant regeneration from axillary bud derived callus in white yam (Dioscorea rotundata). Plant Cell, Tissue and Organ Culture,en
dcterms.extentp. 481-497en
dcterms.issued2016-09
dcterms.languageen
dcterms.licenseCC-BY-4.0
dcterms.publisherSpringeren
dcterms.subjectdioscorea rotundataen
dcterms.subjectsomatic embryogenesisen
dcterms.subjectpicloramen
dcterms.subjectactivated charcoalen
dcterms.subjectwhite yamen
dcterms.typeJournal Article

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