Tissue culture method for rapid propagation of Dendrobium candidum
A technology of Dendrobium officinale and a culture medium, applied in the biological field, can solve the problems of low natural reproduction ability, high production cost, single provenance of Dendrobium officinale, etc., and achieves the development and robustness of the root system of the cultured plant, the more root system of the cultured plant, the higher the The effect of transplanting survival rate
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Embodiment 1
[0025] Embodiment 1: as figure 1 As shown, first, wild Dendrobium candidum or field-cultivated Dendrobium candidum were selected to collect stem buds, and after routine disinfection procedures, they were put into N6 basic medium + indole butyric acid 1.5mg / L+6-benzyl adenine 0.5mg / L+ Carrageenan 7g / L + soft white sugar 40g / L + 50g / L potato juice induction medium, placed in an environment with a temperature of 22-25°C, a light of 2000-3000lx, and a daily light of 10-12h for protocorm After induction culture, the formation of protocorms can be observed after 2 months.
[0026] Put the formed protocorm into the differentiation medium prepared by N6 basic medium + 6-benzyl adenine 2.0mg / L + carrageenan 7g / L + soft white sugar 20g / L + 50g / L potato juice, place The temperature is 22-25°C, the light is 2000-3000lx, and the daily light is 10-12h for differentiation culture. After 2 months of culture, it can be observed that the protocorms in the bottle have undergone redifferentiatio...
Embodiment 2
[0028] Embodiment 2: as figure 1 As shown, first select the artificially cultivated Dendrobium candidum to collect stem buds, and after routine disinfection procedures, put them into N6 basic medium + indole butyric acid 1.5mg / L + 6-benzyl adenine 0.5mg / L + carrageenan 8g / L+soft white sugar 30g / L+100g / L potato juice preparation medium, placed in the temperature of 22-25 ℃, light 2000-3000lx, daily light 10-12h environment for protocorm induction culture. Protocorm formation was observed after 2 months.
[0029] Put the formed protocorm into the differentiation medium prepared by N6 basic medium + 6-benzyl adenine 2.0mg / L + carrageenan 8g / L + soft white sugar 30g / L + 100g / L potato juice, and place it at temperature The temperature is 22-25°C, the light is 2000-3000lx, and the daily light is 10-12h for differentiation culture. After 2 months of cultivation, it can be observed that the protocorms in the bottle have undergone redifferentiation to form seedlings, and the height o...
Embodiment 3
[0031] Embodiment 3: as figure 1 As shown, first, wild Dendrobium candidum or field-cultivated Dendrobium candidum were selected to collect stem buds, and after routine disinfection procedures, they were put into N6 basic medium + indole butyric acid 1.5mg / L+6-benzyl adenine 0.5mg / L+ Carrageenan 8.5g / L + soft white sugar 30g / L + 150g / L potato juice prepared induction medium, placed in the environment of temperature 22-25 ℃, light 2000-3000lx, daily light 10-12h After corm induction culture, the formation of protocorms can be observed after 2 months.
[0032] Put the formed protocorm into the differentiation medium configured by N6 basic medium+6-benzyl adenine 2.0mg / L+carrageenan 8.5g / L+soft white sugar 40g / L+150g / L potato juice, place Carry out differentiation culture at a temperature of 22-25°C, light of 2000-3000 lx, and light of 10-12 hours per day. After 2 months of cultivation, it can be observed that the protocorms in the bottle have undergone re-differentiation to for...
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