A kind of method for tissue culture rapid propagation of dendrobium nobile
A high-speed technology of Dendrobium nobile, which is applied in the field of tissue culture and rapid propagation of Dendrobium nobile, can solve the problems of long cultivation period, difficult large-scale and standardized production of Dendrobium nobile, and achieve low cost, reduced drug consumption and high output Effect
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Embodiment 1
[0046] (1) Sterilize the self-dehiscated mature seeds of Dendrobium nobile with 3% hydrogen peroxide for 10 minutes, blot the surface liquid, and then inoculate the seeds in the following protocorm induction medium:
[0047] MS medium
[0048] 6-Benzylaminopurine 6-BA0.2mg / L
[0049] Naphthaleneacetic acid NAA0.1mg / L
[0050] Sucrose 30000mg / L
[0051] Agar 4500mg / L
[0052] Banana 50000mg / L
[0053] Potatoes 25000mg / L
[0054] pH5.8,
[0055] Under the condition that the light intensity is 1500lx, the temperature is 27°C, and the light time is 10h / d, cultivate for 20 days to obtain enlarged protocorms, and continue to cultivate for 55 days to differentiate the protocorms into seedlings;
[0056] (2) Transfer the seedlings obtained in step (1) to the following proliferation medium:
[0057] 1 / 2MS medium
[0058] 6-Benzylaminopurine 6-BA0.05mg / L
[0059] Naphthaleneacetic acid NAA0.2mg / L
[0060] Sucrose 30000mg / L
[0061] Agar 4500mg / L
[0062] Banana 50000mg / L
...
Embodiment 2
[0079] (1) Sterilize the self-dehiscated mature seeds of Dendrobium nobile with 3% hydrogen peroxide for 13 minutes, blot the surface liquid, and then inoculate the seeds in the following protocorm induction medium:
[0080] MS medium
[0081] 6-Benzylaminopurine 6-BA0.5mg / L
[0082] Naphthaleneacetic acid NAA0.05~0.5mg / L
[0083] Sucrose 30000mg / L
[0084] Agar 4500mg / L
[0085] Banana 50000mg / L
[0086] Potatoes 25000mg / L
[0087] pH5.9
[0088] Under the condition that the light intensity is 1800lx, the temperature is 25°C, and the light time is 11h / d, cultivate for 25 days to obtain enlarged protocorms, and continue to cultivate for 50 days to differentiate the protocorms into seedlings;
[0089] (2) Transfer the seedlings obtained in step (1) to the following proliferation medium:
[0090] 1 / 2MS medium
[0091] 6-Benzylaminopurine 6-BA0.01mg / L
[0092] Naphthaleneacetic acid NAA0.5mg / L
[0093] Sucrose 30000mg / L
[0094] Agar 4500mg / L
[0095] Banana 50000mg / L...
Embodiment 3
[0112] (1) Sterilize the self-dehiscated mature seeds of Dendrobium nobile with 3% hydrogen peroxide for 15 minutes, blot the surface liquid, and then inoculate the seeds in the following protocorm induction medium:
[0113] MS medium
[0114] 6-Benzylaminopurine 6-BA0.01mg / L
[0115] Naphthaleneacetic acid NAA0.05mg / L
[0116] Sucrose 30000mg / L
[0117] Agar 4500mg / L
[0118] Banana 50000mg / L
[0119] Potatoes 25000mg / L
[0120] pH6.0,
[0121] Under the condition that the light intensity is 2000lx, the temperature is 27°C, and the light time is 12h / d, cultivate for 30 days to obtain enlarged protocorms, and continue to cultivate for 60 days to differentiate the protocorms into seedlings;
[0122] (2) Transfer the seedlings obtained in step (1) to the following proliferation medium:
[0123] 1 / 2MS medium
[0124] 6-Benzylaminopurine 6-BA0.5mg / L
[0125] Naphthaleneacetic acid NAA0.05mg / L
[0126] Sucrose 30000mg / L
[0127] Agar 4500mg / L
[0128] Banana 50000mg / L ...
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