Culture medium composition suitable for germ-free germination of orchid seeds and method thereof
A kind of germination medium, the technology of culture medium, is applied in the field of aseptic germination medium composition suitable for Cymbidium cymbidium seeds, can solve long germination period (half a year to more than one year, can't realize large-scale factory production, does not disclose improved MS Formula and other issues, to achieve the effect of improving breeding efficiency, saving rare and endangered plants, and shortening the breeding cycle
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Embodiment 1
[0023] Embodiment 1 (being suitable for Cymbidium seed aseptic sowing optimization medium and rapid germination method 1)
[0024] 1) The preparation of the medium, including the content of basic medium and seed germination medium additives:
[0025] (1) Basic medium: self-improved MS, in which sucrose is 20-30g / L, agar is 6g / L, and pH is 5.2;
[0026] (2) Germination medium: basic medium+6-BA1.0mg / L+NAA 1.0mg / L+activated carbon 1g / L+coconut juice 50ml / L;
[0027] 2) Selection of treatment objects: take the uncracked capsules that have grown for 6 months after pollination as treatment objects;
[0028] 3) Pretreatment of the treatment object: the treatment object was stored in the micro-freezing layer of the refrigerator for 10 days at 1-3°C.
[0029] 4) Aseptic seeding of the treated object: take it out from the refrigerator, rinse it with detergent and tap water, soak it in 75% alcohol for 3.0 minutes under sterile conditions, then sterilize it with 0.1% mercury liter solu...
Embodiment 2
[0032] Embodiment 2 (suitable for Cymbidium seed aseptic sowing optimization medium and rapid germination method 2)
[0033] 1) The preparation of the medium, including the content of basic medium and seed germination medium additives:
[0034] (1) Basic medium: improved MS, in which sucrose is 30g / L, agar is 5g / L, and pH is 5.6;
[0035] (2) Germination medium: basic medium + 6-BA0.5mg / L + NAA 0.5mg / L + activated carbon 1g / L + coconut milk 100ml / L;
[0036] 2) Selection of treatment objects: take the uncracked capsules that have grown for 7 months after pollination as treatment objects;
[0037] 3) Pretreatment of the treatment object: the treatment object was stored in the micro-freezing layer of the refrigerator for 10 days at 1-3°C.
[0038] 4) Aseptic seeding of the treated object: take it out from the refrigerator, rinse it with detergent and tap water, soak it in 75% alcohol for 3.0 minutes under sterile conditions, then sterilize it with 0.1% mercury liter solution f...
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