Dendrobium candidum tissue culture plant hormone control method
A technology of Dendrobium officinale and plant hormones, which is applied in the directions of botanical equipment and methods, plant regeneration, horticultural methods, etc., can solve the problems of shortening the tissue culture time of seedlings, slow proliferation, and low differentiation rate of Dendrobium officinale, and shortens the culture period. , improve the efficiency of cultivation, and optimize the quality of seedlings
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Embodiment 1
[0012] A method for controlling phytohormones in tissue culture of Dendrobium officinale, the present invention cultivates 8 hours / day under 1800LX light at humidity of 70%-80%, temperature 23°C, 1800LX at 23°C, 8 hours / day at 23°C, 400LX at 23°C, 400LX for 8 hours / day Under the condition of hour / day; Dendrobium candidum is cultivated through the following three stages sequentially after routine disinfection procedures:
[0013] 1) Callus culture: put Dendrobium officinale into MS basic medium + 6-benzyl adenine (6BA) 0.25 mg / L + naphthaleneacetic acid (NNA) 0.5 mg / L + sucrose 3% + agar 0.8%, pH value Cultivate for 45 days in the medium of 5.0-6.5 to form protocorms;
[0014] 2) Adventitious bud induction culture: put protocorms through 1 / 2MS basic medium + 6-benzyl adenine (6BA) 0.05 mg / L + naphthalene acetic acid (NNA) 2.0 mg / L + sucrose 2% + agar 0.8%+ Banana juice 20%, cultivated in a medium with a pH value of 5.0-6.5 for 45 days to form seedlings;
[0015] 3) Cultivatio...
Embodiment 2
[0018] A method for controlling phytohormones in tissue culture of Dendrobium officinale, the present invention cultivates 8 hours / day at a humidity of 70%-80%, at a temperature of 28°C, at 2200LX; at 29°C, at 1400LX for 8 hours / day; at 25°C, at 800LX for 8 hours / day Under the condition of hour / day; Dendrobium candidum is cultivated through the following three stages sequentially after routine disinfection procedures:
[0019] 1) Callus culture: put Dendrobium officinale into MS basic medium + 6-benzyl adenine (6BA) 0.25 mg / L + naphthaleneacetic acid (NNA) 0.5 mg / L + sucrose 3% + agar 0.8%, pH value Cultivate in the medium of 5.0-6.5 for 35 days to form protocorms;
[0020] 2) Adventitious bud induction culture: put protocorms through 1 / 2MS basic medium + 6-benzyl adenine (6BA) 0.05 mg / L + naphthalene acetic acid (NNA) 2.0 mg / L + sucrose 2% + agar 0.8%+ Banana juice 20%, cultivated in a medium with a pH value of 5.0-6.5 for 35 days to form seedlings;
[0021] 3) Cultivation ...
Embodiment 3
[0024] A method for controlling phytohormones in tissue culture of Dendrobium officinale, the present invention cultivates 8 hours / day under 2000LX illumination at humidity of 70%-80%, temperature 25°C; 26°C, 1200LX for 8 hours / day; 24°C, 600LX for 8 hours / day Under the condition of hour / day; Dendrobium candidum is cultivated through the following three stages sequentially after routine disinfection procedures:
[0025] 1) Callus culture: put Dendrobium officinale into MS basic medium + 6-benzyl adenine (6BA) 0.25 mg / L + naphthaleneacetic acid (NNA) 0.5 mg / L + sucrose 3% + agar 0.8%, pH value Cultivate for 40 days in the medium of 5.0-6.5 to form protocorms;
[0026] 2) Adventitious bud induction culture: put protocorms through 1 / 2MS basic medium + 6-benzyl adenine (6BA) 0.05 mg / L + naphthalene acetic acid (NNA) 2.0 mg / L + sucrose 2% + agar 0.8%+ Banana juice 20%, cultivated in a medium with a pH value of 5.0-6.5 for 40 days to form seedlings;
[0027] 3) Cultivation of root...
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