Method for producing A by using huperzia serrata prothallium
A technology of huperzine A and Huperzia serrata, which is applied in the field of plant biology, can solve the problems of small reserves and low content of Huperzia serrata, and limit the regeneration of wild resources of Huperzia serrata, and achieve large-scale production and content differences. small effect
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Embodiment 1
[0022] (1) Induction of prothallus
[0023] Soak the sporangia of Hupermus serrata in a clean bench first in 70% ethanol solution for 30s; then place them in 0.1% HgCl 2 Soak in the solution for 8 minutes, then rinse with sterile water for 3 times, and use the sporangia or the spores released from the sporangia after the sporangia rupture as explants induced by prothallus; inoculate the obtained explants in conventional MS medium , cultured for 12 weeks under conditions of a culture temperature of 22±2°C, a light time of 12h / d, and a light intensity of 1000Lx, and green prothallus tissues grew from the explants;
[0024] (2) Culture of prothallus
[0025] Cut the obtained prothallus tissue into 0.3 cm 2 Then transferred to the production medium containing 2mg / L iron trichloride huperzine A to continue culturing, the culture conditions were the same as in step (1), that is, the culture temperature was 22±2°C, the light time was 12h / d, and the light The strength is 1000Lx, an...
Embodiment 2
[0029] (1) Induction of prothallus
[0030] Soak the sporangia of Hupermus serrata in a clean bench first in 70% ethanol solution for 30s; then place them in 0.1% HgCl 2 Soak in the solution for 8 minutes, then rinse with sterile water for 3 times, and use the sporangia or the spores released from the sporangia after the sporangia rupture as explants induced by prothallus; inoculate the obtained explants in conventional MS medium , cultured for 12 weeks under conditions of a culture temperature of 22±2°C, a light time of 12 / d, and a light intensity of 1000Lx, and green prothallus tissues grew from the explants;
[0031] (2) Culture of prothallus
[0032] Cut the obtained prothallus tissue into 0.3 cm 2 Then transfer to the production medium containing 10mg / L iron trichloride huperzine A to continue culturing. The culture conditions are the same as in step (1), that is, the culture temperature is 22±2°C, the light time is 12h / d, and the light time is 12h / d. The strength is 1...
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