Tissue culture reproduction method of common nepenthes
A tissue culture and Nepenthes technology, applied in the field of culture medium, can solve problems such as no reports of patent applications, and achieve strong resistance, high stability, and good growth effects
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Embodiment 1
[0015] 1. Materials: The terminal buds or segmented stem segments of hybrid Nepenthes (Nepenthes x Dyeriana) are used as explants.
[0016] 2. The method of explant induction material disinfection: in the growing season, select the 3-4 cm long terminal buds or stem segments with lateral buds of vigorously growing Nepenthes as explants, rinse them under tap water, and then put them on the Soak in 70% alcohol for 30 seconds, then disinfect with 0.1% mercuric acid solution for 15 minutes, rinse with sterile water 4 to 5 times, cut off the brown part of the wound at the base, and inoculate it into the medium 1 / 2MS+6-benzylpurine 1.0 mg / L + NAA 0.05 mg / L + 0.05% activated carbon. After 5 days, transfer to a new medium of the same kind to prevent browning, and adventitious buds can be formed in about 40 days.
[0017] 3. Induction and subculture of adventitious buds: the induced adventitious buds were cut and then subcultured in the same medium for proliferation. Generally, 40 day...
Embodiment 2
[0021] The terminal buds or segmented stems of Nepenthes misabilis were used as explants. The basic operation method is consistent with embodiment 1. But its adventitious bud induction and cluster bud proliferation medium is 1 / 2MS + 6-benzyl purine 2.0 mg / L + naphthalene acetic acid 0.1 mg / L + 0.05% activated carbon, and the multiplication rate is 2-3. The survival rate of transplanted test tube seedlings under the same conditions was 85%.
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