Production method of fritillaria hupehensis seed ball
A production method and technology of Fritillaria, applied in the production field of Hubei Fritillary bulbs, can solve the problems of high cost, low output, slow output, etc., to improve yield and quality, high transplant survival rate, and improve economic benefits Effect
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Embodiment 1
[0025] A method for inducing test-tube bulbs of Fritillaria, comprising the following steps:
[0026] a. Preparation of culture medium
[0027] Callus induction medium: MS+ 6-BA 3mg / L+NAA 0.2mg / L+sucrose 30g / L+agar 6-6.5g / L, pH 5.9-6.0;
[0028] Callus proliferation medium: MS+ 6-BA 2mg / L+NAA 0.2mg / L+sucrose 30g / L+agar 6-6.5g / L, pH value 5.9-6.0;
[0029] Callus differentiation medium: MS+ 6-BA 2mg / L+NAA 0.2mg / L+sucrose 30g / L+agar 6-6.5g / L, pH value 5.9-6.0;
[0030] Tube bulb induction medium: 1 / 2MS+NAA 1.0mg / L+sucrose 30g / L+agar 6-6.5g / L, pH 5.9-6.0;
[0031] b. Induction of Hubei Fritillaria in vitro bulbs
[0032] Selection of explants and surface disinfection: In spring, at the peak of the emergence of Fritillaria, select 4 full bulbs without pests and diseases, store them at 4°C for about a week, take out and wash the surface soil, remove the old bulbs on the outer layer, and remove the old bulbs from the outer layer. The tender bulbs were used as explants, soaked in...
Embodiment 2
[0040] A method for inducing test-tube bulbs of Fritillaria, comprising the following steps:
[0041] a. Preparation of culture medium
[0042] Callus induction medium: MS+ 6-BA 2mg / L+ NAA 0.2mg / L+ sucrose 20g / L+ agar 6-6.5g / L, pH value 5.9-6.0;
[0043] Callus proliferation medium: MS+ 6-BA 2mg / L+ NAA 0.5mg / L+ sucrose 30g / L+ agar 6-6.5g / L, pH value 5.9-6.0;
[0044] Callus differentiation medium: MS+ 6-BA 3mg / L+ NAA 0.2mg / L+ sucrose 30g / L+ agar 6-6.5g / L, pH value 5.9-6.0;
[0045] Tube bulb induction medium: 1 / 2MS+NAA 0.5mg / L+sucrose 30g / L+agar 6-6.5g / L, pH 5.9-6.0;
[0046] b. Induction of Hubei Fritillaria in vitro bulbs
[0047] Selection of explants and surface disinfection: In spring, at the peak of the emergence of Fritillaria, select 4 full bulbs without pests and diseases, store them at 4°C for about a week, take out and wash the surface soil, remove the old bulbs on the outer layer, and remove the old bulbs from the outer layer. The tender bulbs were used as expl...
Embodiment 3
[0055] a. Preparation of culture medium
[0056] Callus induction medium: MS+ 6-BA 3mg / L+ NAA 1mg / L+ sucrose 20g / L agar 6-6.5g / L, pH 5.9-6.0;
[0057] Callus proliferation medium: MS+ 6-BA 3mg / L+ NAA 1mg / L+ sucrose 20g / L+ agar 6-6.5g / L, pH 5.9-6.0;
[0058] Callus differentiation medium: MS+ 6-BA 2mg / L+NAA 0.2mg / L+sucrose 30g / L+agar 6-6.5g / L, pH value 5.9-6.0;
[0059] Tube bulb induction medium: 1 / 2MS+NAA 1.0mg / L+sucrose 30g / L+agar 6-6.5g / L, pH 5.9-6.0;
[0060] b. Induction of Hubei Fritillaria in vitro bulbs
[0061] Selection of explants and surface disinfection: In spring, at the peak of the emergence of Fritillaria, select 4 full bulbs without pests and diseases, store them at 4°C for about a week, take out and wash the surface soil, remove the old bulbs on the outer layer, and remove the old bulbs from the outer layer. The tender bulbs were used as explants, soaked in 75% alcohol for 30-60s, soaked in 0.1% mercury chloride aqueous solution for 8min, and then rinsed w...
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