Rooting induction, root promoting and seedling cultivation method of oil palm plantlets
A technology for induction medium and tissue culture seedlings, which is applied in the fields of rooting induction and root promotion of oil palm tissue culture seedlings, can solve the problems of poor population uniformity, difficulty in realizing clonal breeding, and difficulty in preserving the excellent characteristics of parents, etc. To achieve the effect of short hair root time, saving the amount of agar and growth regulator substances, and high hair root synchronization
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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 filled with about 25-30ml of culture medium, and after being covered, the 3 , Sterilize under saturated steam pressure at 121°C for 20 minutes.
[0020] 2. Select 200 rootless seedlings regenerated from robust 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, remove part of the leaves and part of the base tissue of the stem, and transfer to step 1 under sterile conditions ) prepared in the rooting induction medium, culture conditions: temperature 28 ± 1 ℃, light intensity about 1000lx, light 12h per day. Cultured for 8 weeks. Recorded data: the number of rooted plants is 128, and the root length is 0.5-3 cm. The rooting induction rate is 64%.
[0021] 3. Preparation of root-promoting and seedling-promoting medium: WPM+sucrose 75g....
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, and after being covered, the 3 , Sterilize under saturated steam pressure at 121°C for 20 minutes.
[0025] 2. Select 200 rootless seedlings regenerated from robust oil palm leaf-derived somatic embryos with a diameter of 5-6 mm at the base of the stem and a height of 8-10 cm. After cutting off part of the leaves and part of the base tissue of the stem section, they are transferred to step 1 under sterile conditions. 1) Cultivate in the prepared rooting induction medium, culture conditions: temperature 26±1°C, light intensity about 1100lx, light 12h per day. Cultured for 10 weeks. Recorded data: the number of rooted plants is 184, and the root length is 0.5-3 cm. The rooting induction rate is 92%.
[0026] 3. Preparation of root-promoting and seedling-...
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, and after being covered, the 3 , Sterilize under saturated steam pressure at 121°C for 20 minutes.
[0030] 2. Select 200 rootless seedlings regenerated from robust oil palm leaf-derived somatic embryos with a diameter of 5-6 mm at the base of the stem and a height of 8-10 cm. After cutting off part of the leaves and part of the base tissue of the stem section, they are transferred to step 1 under sterile conditions. 1) Cultivate in the prepared rooting induction medium, culture conditions: temperature 27±2°C, light intensity about 900lx, light 12h per day. Cultured for 9 weeks. Recorded data: the number of rooted plants is 173, and the root length is 0.5-3cm. The rooting induction rate is 86.5%.
[0031] 3. Preparation of root-promoting and seedling-p...
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