A kind of rooting induction of oil palm tissue culture seedlings and cultivation method for promoting roots and strong seedlings
A technology for inducing culture medium and tissue culture seedlings, which is applied in the field of oil palm tissue culture seedling rooting induction and root-promoting and strong seedling cultivation, can solve the problems of difficulty in preserving the excellent characteristics of parents, difficulty in realizing clonal breeding, poor population uniformity, and the like, To achieve the effect of saving the amount of agar and growth regulating substances, high synchronization of hair roots, and short hair root time
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Embodiment 1
[0019] 1. Preparation of rooting induction medium: WPM+NAA0.1mg.L -1 + Paclobutrazol 1mg.L -1 +Sucrose 3g.L -1 +Agar 7g.L -1 +Activated carbon 1g.L -1 , PH5.6. Each test tube is packed with about 25~30ml culture medium, after capping, at 1.2Kg / cm 3 , Sterilize at 121℃ under saturated steam pressure for 20min.
[0020] 2. Select strong oil palm leaf-derived somatic embryos with a stem base diameter of 2 to 3 mm and a seedling height of 5 to 6 cm to regenerate rootless seedlings. Part of the leaves and part of the base tissue of the stem are removed, and go to step 1 under aseptic conditions. ) Cultivation in the prepared rooting induction medium, culture conditions: temperature 28±1℃, light intensity about 1000lx, light for 12h per day. Cultivate for 8 weeks. Record data: 128 rooting plants, with root length of 0.5-3cm. The rooting induction rate is 64%.
[0021] 3. Preparation of medium for promoting roots and strong seedlings: WPM+sucrose 75g.L -1 , PH5.6. Each test tube is fi...
Embodiment 2
[0024] 1. Preparation of rooting induction medium: WPM+NAA1mg.L -1 + Paclobutrazol 1mg.L -1 +Sucrose 60g.L -1 +Agar 7g.L -1 +Activated carbon 1g.L -1 , PH5.6. Each test tube is filled with about 25ml of culture medium, after capping, at 1.2Kg / cm 3 , Sterilize at 121℃ under saturated steam pressure for 20min.
[0025] 2. Select strong oil palm leaf-derived somatic embryos with a stem base diameter of 5-6mm and a seedling height of 8-10cm to regenerate rootless seedlings. After cutting off part of the leaves and part of the stem base tissue, proceed to the steps respectively under aseptic conditions 1) Cultivate in the prepared rooting induction medium, the culture conditions: temperature 26±1℃, light intensity about 1100lx, light for 12h per day. Cultivate for 10 weeks. Record data: The number of rooting plants is 184, and the root length is 0.5-3cm. The rooting induction rate was 92%.
[0026] 3. Preparation of medium for promoting roots and strong seedlings: WPM+sucrose 75g.L -...
Embodiment 3
[0029] 1. Preparation of rooting induction medium: WPM+NAA5mg.L -1 + Paclobutrazol 1mg.L -1 +Sucrose 60g.L -1 +Agar 7g.L -1 +Activated carbon 1g.L -1 , PH6.0. Each test tube is filled with about 25ml of culture medium, after capping, at 1.2Kg / cm 3 , Sterilize at 121℃ under saturated steam pressure for 20min.
[0030] 2. Select strong oil palm leaf-derived somatic embryos with a stem base diameter of 5-6mm and a seedling height of 8-10cm to regenerate rootless seedlings. After cutting off part of the leaves and part of the stem base tissue, proceed to the steps respectively under aseptic conditions 1) Cultivate in the prepared rooting induction medium, the culture conditions: temperature 27±2℃, light intensity about 900lx, light for 12h per day. Cultivate for 9 weeks. Recorded data: The number of rooting plants was 173, and the root length was 0.5-3cm. The rooting induction rate was 86.5%.
[0031] 3. Preparation of medium for promoting roots and strong seedlings: WPM+sucrose 75g...
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