Abstract
Embryogenic callus cultures of ginger were induced from young leaf segments taken from in vitro shoot cultures. Among the four auxins tested in Murashige & Skoog medium, dicamba at 2.7 μM was most effective in inducing and maintaining embryogenic cultures. Efficient plant regeneration was achieved when embryogenic cultures were transferred to Murashige & Skoog medium containing 8.9 μM benzyladenine. Histological studies revealed various stages of somatic embryogenesis characteristic of the monocot system. The in vitro-raised plants have been established in soil.
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Abbreviations
- BA:
-
benzyladenine
- 2,4-d :
-
2,4-dichlorophenoxyacetic acid
- IAA:
-
indole-3-acetic acid
- MS:
-
Murashige and Skoog
- NAA:
-
naphthaleneacetic acid
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Kackar, A., Bhat, S.R., Chandel, K.P.S. et al. Plant regeneration via somatic embryogenesis in ginger. Plant Cell Tiss Organ Cult 32, 289–292 (1993). https://doi.org/10.1007/BF00042291
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DOI: https://doi.org/10.1007/BF00042291