Tissue culture and rapid propagation method for campanumoea
A technology of tissue culture rapid propagation and soil Codonopsis pilosula, applied in horticultural methods, soilless cultivation, botanical equipment and methods, etc., can solve the problems of uneven quality of seedlings, difficulty in meeting high-quality seedlings, and lack of natural resources. To achieve the effect of strong pertinence, feasible operation, and expansion of sources
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Embodiment 1
[0030] 1), the selection and pretreatment of explants: cut the newly germinated shoots with a length of 5-10 cm, cut off the leaves, rinse with tap water with 1% (volume ratio) detergent for 10-30 minutes , Rinse with tap water for 20-40 minutes;
[0031] 2), explant sterilization: cut the pretreated twigs into 1-2.cm long stem sections with terminal buds or stem sections with axillary buds as explants, and use them for later use after surface sterilization;
[0032] 3), induction culture: under aseptic conditions, after the surface-sterilized stem section with apical bud or the stem section with axillary bud explant, one end or two ends of the incision browning are removed, and the apical bud and the stem section with axillary bud are removed. The buds are inoculated upwards in the induction medium, and after 30-45 days of cultivation under culture conditions, the terminal buds and axillary buds are induced to germinate, and then clustered buds are induced to grow into rattan...
Embodiment 2
[0054] In this example, basic medium: select MS medium, sucrose or white sugar 20-30g / L, agar 7-9g / L, pH5.6-5.8; induction medium: MS+BA 0.1-5.0mg / L+NAA 0.0~0.5mg / L+sucrose or white sugar 30g / L; proliferation medium: MS+BA 0.1~3.0mg / L+NAA 0.0~0.5mg / L+sucrose or white sugar 30g / L; rooting medium: 1 / 2MS+NAA0 .1~1.0mg / L+sucrose or white sugar 20g / L.
[0055] All the other steps and conditions are the same as in Example 1.
Embodiment 3
[0057] In this example, basic medium: select MS medium, sucrose or white sugar 20-30g / L, agar 7-9g / L, pH5.6-5.8; induction medium: MS+KT 0.1-5.0mg / L+IAA 0.0~0.5mg / L+sucrose or white sugar 30g / L; proliferation medium: MS+KT 0.1~3.0mg / L+IAA 0.0~0.5mg / L+sucrose or white sugar 30g / L; rooting medium: 1 / 2MS+IAA 0.1~1.0mg / L+sucrose or white sugar 20g / L.
[0058] All the other steps and conditions are the same as in Example 1.
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