Test tube cottage method for huperzia serrata sporophyte
A technology of Huperzia serrata and sporophyte, which is applied in the field of test tube cutting of Huperzia serrata sporophyte, can solve the problems of cutting or transplanting experiment failure, and achieve the effect of accelerating propagation
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Embodiment 1
[0028] (1) Preparation of culture substrate
[0029] Fully soak the dried sphagnum moss in 1 / 2MS culture solution containing 0.5 mg / L 3-indolebutyric acid (IBA), then put it into a wide-mouth culture bottle up to 1 / 3 volume, and seal it with bottle sealing film. Seal the mouth of the bottle, sterilize at 121°C for 25 minutes, and let it cool for later use;
[0030] (2) Surface sterilization of materials
[0031] Fresh materials of Huperzia serrata (Thunb.) Trev. were collected from the wild, rinsed with tap water, cut off 6 cm terminal buds, and immersed in an ethanol solution with a mass fraction of 75% for 30 seconds in an ultra-clean workbench; At a concentration of 0.1% mercury chloride (HgCl 2 ) solution for 8 minutes, then rinsed with sterile water for 3 times, as cutting material;
[0032] (3) Cutting culture of sporophytes
[0033] The terminal bud cuttings were placed in a sterilized culture bottle, and the culture temperature was 22±2°C, and the light time was 16...
Embodiment 2
[0037] (1) Preparation of culture substrate
[0038] Fully soak the dried water moss in 1 / 2MS culture solution containing 0.5mg / L 3-indolebutyric acid, then put it into a wide-mouth culture bottle up to 1 / 3 of its volume, and seal the bottle mouth with a sealing film Live, sterilize at 121°C for 25 minutes, and let it cool for later use;
[0039] (2) Surface sterilization of materials
[0040] Fresh materials of Huperzia serrata (Thunb.) Trev. were collected from the wild, rinsed with tap water, cut off 8 cm terminal buds, and immersed in an ethanol solution with a mass fraction of 75% for 60 seconds in an ultra-clean workbench; Mercury chloride (HgCl) at a concentration of 0.1% 2 ) solution for 5 minutes, then rinsed with sterile water for 3 times, as cutting material;
[0041] (3) Cutting culture of sporophytes
[0042] Cuttings of the terminal buds were placed in a culture bottle, cultured for 12 weeks at a culture temperature of 22 ± 2°C and a light time of 12 h / d. The...
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