Abstract
Mass multiplication of Plumbago rosea was achieved by indirect organogenesis in young stem, leaf and root explant cultures of 6 - 9-month-old plants. All the explants responded similarly in a hormonal regime of 2.5 mg/L BA and 1.5 mg/L NAA with the formation of nodular callus in 4 weeks; the callus was divided and subcultured at 4-week intervals in the presence of 3.0 mg/L BA to produce up to 23.5 ± 1.6 shoots in 18 weeks and then at 2.0 mg/L BA to produce up to 79.6 ± 1.5 shoots in 23 weeks. The shoots of 2.0 - 3.5 cm length were rooted easily in half-strength MS agar medium supplemented with 0.1 mg/L IBA and rooted plants established within 4 weeks at a 95 - 98 % rate without hardening. Eight weeks after establishment, the micropropagated plants were transferred to experimental plots and cultivated for 10 months to obtain a significantly higher number (18.0 ± 0.5) of larger tuberous roots (137.4 ± 3.4 g fw/plant) compared to conventional rooted cuttings (14.0 ± 1.7, 47.9 ± 1.6 g fw/plant). During this period, the concentration of the root-specific compound, plumbagin recorded per g dw (1.5 %), was higher than that of conventionally propagated plants (0.9 - 1.0 %). The early formation of plumbagin-rich tuberous roots holds significant potential for the commercial cultivation of the micropropagated plants.
Abbreviations
fw:fresh weight
dw:dry weight
2,4-D:2,4-dichlorophenoxyacetic acid
KN:Kinetin
NAA:α-naphthaleneacetic acid
BA:benzylaminopurine
IBA:indole 3-butyricacid
IAA:indole 3-aceticacid
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K. Satheeshkumar
Plant Biotechnology Division
Tropical Botanic Garden and Research Institute
Palode - Thiruvananthapuram
695 562 Kerala
India
Phone: +91-472-869226/869626
Fax: +91-472-869646
Email: moon012@reddifmail.com