Method for producing Gypsophila seedling using mini-type cuttage
A technology of miniature cuttings and gypsophila, applied in the field of plant biology, can solve the problems of low survival rate and seedling rate of tall seedlings, long time for seedling supply, difficulty in mass production of seedlings, etc. The effect of improving the quality of seedlings and improving the survival rate of transplanting
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Embodiment 1
[0019] 1. Selection of explants and establishment of a sterile system: When selecting explants, select newly germinated and strong vegetative buds from plants with obvious variety characteristics and good flowering performance, remove the leaves, and cut off the 0.5cm terminal buds. Peel off the outer leaves, wash in water with a small amount of detergent, sterilize in 0.14% mercuric solution for 15 minutes, then sterilize in 0.2% sodium hypochlorite solution for 10 minutes, rinse twice with sterile water and inoculate Proliferation medium: MS+BA1.0mg / L+NAA0.1mg / L+agar 6.5g / L+sugar 30g / L culture medium, at a temperature of 24°C, light intensity of 2000Lx, light time of 12 hours / Under the condition of 1 day, proliferate and cultivate for 20 days, and then get clump-like seedlings;
[0020] 2. Subculture proliferation culture: cut the tufted seedlings obtained in step A into 1.5cm-long sections with 1-3 buds, and transfer them to MS+BA1.0mg / L+NAA0.1mg / L+agar 6.5 g / L+sugar 30g / ...
Embodiment 2
[0026] 1. Selection of explants and establishment of a sterile system: When selecting explants, select newly germinated and strong vegetative buds from plants with obvious variety characteristics and good flowering performance, remove the leaves, and cut off the 1.0cm terminal buds. Peel off the outer leaves, wash in water with a small amount of detergent, sterilize in 0.14% mercuric solution for 15 minutes, then sterilize in 0.2% sodium hypochlorite solution for 10 minutes, rinse twice with sterile water and inoculate Proliferation medium: MS+BA1.5mg / L+NAA0.1mg / L+agar 7.0g / L+sugar 40g / L culture medium, at a temperature of 26°C, light intensity of 2500Lx, light time of 10 hours / Under the condition of 1 day, cultured for 10 days;
[0027] 2. Subculture proliferation culture: cut the clump-like seedlings obtained in step A into 1.5cm-long sections with 1-3 buds, and transfer them to MS+BA1.5mg / L+NAA0.1mg / L+agar 7.0 g / L+white sugar 40g / L on the subculture medium, under the cond...
Embodiment 3
[0035] The selection of explants and the establishment of the sterile system were the same as in Example 1.
[0036] Induction of root primordia: Cut the subcultured seedlings into 1cm seedlings with shoot tips, inoculate them on the medium of MS+IBA0.3mg / L+agar 7.0g / L+sugar 30g / L, pH value 6.0, and culture The temperature is 26°C, the light intensity is 2500Lx, and the light time is 8 hours / day, and cultured for 6-7 days. After the root primordia are formed, micro-cuttings are carried out.
[0037] Miniature cuttage: above-mentioned rooted seedling is taken out from the bottle and soaked in 0.15% thiophanate-methyl solution for 1 minute, after taking out, the base of the seedling is stained with the root sun solution of 100ppm and cuttage is used as the seedling tray of the matrix with perlite, The substrate thickness is 2.5-3.0cm, and the cutting density is 1.0cm×1.5cm.
[0038] Management of cutting seedlings: with embodiment 1.
[0039] The transplanting of cutting seedl...
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