Method for culture and plant regeneration of ormosia microphylla in-vitro embryo
A technology for culturing small-leafed red beans and embryos, which is applied in plant regeneration, botanical equipment and methods, horticultural methods, etc., can solve the problems of hard seeds, low survival rate, poor water permeability of seed coats, etc. The effect of high, short germination time
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Embodiment 1
[0036] 1) Method of obtaining materials: select the pods with full grains that were strong in the year as the material, and wrap the picked pods with a damp cloth, and bring them back to the laboratory to store in a refrigerator at 4°C for later use;
[0037] 2) Preparation of medium
[0038] Prepare embryo induction medium, primary bud induction medium, bud proliferation medium, strong seedling medium, rooting medium, and add Su: 20 g·L to the medium -1, Ag: 6.0g·L -1 , PH value: 5.8, the addendum is activated carbon Ac; the thickness of the medium is 1.4 cm; the use of a good air-permeable bottle material can reduce the water supply of the culture, thereby preventing the vitrification of the woody plant growth process and ensuring Improve the quality of cultivated seedlings.
[0039] Among them, embryo induction medium: 1 / 2MS (major elements halved) + 1.0mg·L -1 BA + 0.5mg·L -1 IAA + 0.2mg·L -1 NAA +6.0g·L -1 Ag +20g·L -1 Su +1.0 g·L -1 Ac;
[0040] Primary bud induction medium: W...
Embodiment 2
[0052] 1) Method of obtaining materials: select the pods with full grains that were strong in the year as the material, and wrap the picked pods with a damp cloth, and bring them back to the laboratory to store in a refrigerator at 4°C for later use;
[0053] 2) Configuration of medium
[0054] Prepare embryo induction medium, primary bud induction medium, bud proliferation medium, strong seedling medium, and rooting medium. Su and Ag are added to the medium separately, pH value: 5.7, and the addition is activated carbon Ac ; The thickness of the culture medium is 1.6 cm; (and the use of a good air-permeable bottle material can reduce the water supply of the culture, thereby preventing the vitrification of the woody plant growth process and ensuring the quality of the cultivated seedlings).
[0055] Among them, embryo induction medium: 1 / 2MS (major elements halved) + 1.5mg·L -1 BA + 1.0mg·L -1 IAA + 0.3mg·L -1 NAA + 6.0g·L -1 Ag +20g·L -1 Su +1.5 g·L -1 Ac.
[0056] Primary bud indu...
Embodiment 3
[0068] 1) Material collection method: select the pods with full grains that were firm in the year as materials, wrap the picked pods with a damp cloth, and bring them back to the laboratory to store in a refrigerator at 4°C for later use;
[0069] 2) Preparation of medium
[0070] Prepare embryo induction medium, primary bud induction medium, bud proliferation medium, strong seedling medium, and rooting medium respectively. Su and Ag are added to the medium separately, pH value: 5.9, and the addition is activated carbon Ac ; The thickness of the medium is 1.5 cm;
[0071] Among them, embryo induction medium: 1 / 2MS+ 0.5mg·L -1 BA + 0.4mg·L -1 IAA + 0.1mg·L -1 NAA + 6.0g·L -1 Ag +20g·L -1 Su +1.2 g·L -1 Ac;
[0072] Primary bud induction medium: WPM+1.0mg·L -1 BA + 0.4mg·L -1 KT + 0.4mg·L -1 IAA+0.4mg·L -1 NAA+ 6.0g·L -1 Ag +20g·L -1 Su +1.2 g·L -1 Ac;
[0073] Bud propagation medium: WPM+1.0mg·L -1 BA + 0.5mg·L -1 KT + 0.1mg·L -1 TDZ + 0.4mg·L -1 NAA + 6.0g·L -1 Ag +20g·L -1 Su +1.2...
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