A procedure for plant regeneration from callus culture of potato, Solunum tuberosum L. is described. Calli were induced from l-2 mm long shoot apices of potato cultivars Cara and A25/19 on half-strength Murashige and Skoog's medium (half-MS) supplemented with 3.2 mg IAA (indole-3-acetic acid), 1.0 m
Plant regeneration from embryo-callus culture in barley
β Scribed by B. S. Ahloowalia
- Publisher
- Springer
- Year
- 1987
- Tongue
- English
- Weight
- 473 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0014-2336
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β¦ Synopsis
Plants were regenerated from callus cultures initiated from immature embryos of barley, Hordeum vulgure L. Immature embryos from seven diverse genotypes were cultured on modified Murashige and Skoog (MS) medium supplemented with 1.5 mg 2,4-D and 6.5 mg IAA/l. Of the 249 embryos cultured, 30% initiated callus within 8 days. Subculture of callus for 80 to 100 days on half-MS medium supplemented with 0.5 mg/l 2,4-D and 1.0 mgjl zeatin resulted in organogenesis. Culture of organogenic calli for 30 days on half-MS medium without growth regulators produced plants which originated mostly via multiple shoot formation. Callusing response of the tested genotypes ranged from zero to 44%; however, only 23% of the calli were regenerative. Regenerated plants included variants for chlorophyll deficiency, plant height, stem thickness, spike shape, pollen fertility, seed set and ploidy.
π SIMILAR VOLUMES
Complete plants were regenerated from callus derived embryo culture of Citrus aurantium, Poncirus trifoliata and of Carrizo citrange (C. sinensis Γ Poncirus trifoliata) via somatic embryogenesis and organogenesis. Isolated embryoids were differentiated on medium containing 1000 to 1500mgl -~ malt ex