Method for quickly reproducing bletilla striata seedlings
A Bletilla striata seedling and rapid technology are applied in the field of rapid propagation of Bletilla striata seedlings, which can solve the problems of extreme shortage of supply in the market, quality degradation, low effective yield and the like, and achieve the effect of alleviating the contradiction between supply and demand in the market and increasing the output.
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Embodiment 1
[0020] 1) Disinfection of explants: first rinse the capsules with running water, rinse with washing powder solution, wash with distilled water, soak in 75% alcohol for 28 seconds, then soak in 0.15% mercury liter solution for 12 minutes, finally rinse with sterile water 3 times, and set aside.
[0021] 2) Protocorm formation and proliferation: evenly shake off the sterilized seeds into sterile water or germination medium, which is 1 / 2 MS solid medium with 1.05 mg / Kg 6-benzylaminopurine added. After about 7 days, the seed embryo starts to expand, and the protocorm is formed in about 14 days. After the protocorm is cut, it is transferred to the protocorm proliferation medium to obtain a large number of protocorms. Wherein the protocorm proliferation medium is 1 / 2MS solid medium supplemented with 1.08mg / Kg 6-benzylaminopurine, 0.95mg / Kg naphthaleneacetic acid, 28g / Kg sucrose and 4.6g / Kg agar. The culture conditions are: temperature 24°C, relative humidity 70%, light time 12 hours...
Embodiment 2
[0026] 1) Disinfection of explants: first rinse the capsules with running water, rinse with washing powder solution, wash with distilled water, soak in 75% alcohol for 25 seconds, then soak in 0.1% mercury liter solution for 10 minutes, and finally rinse with sterile water twice, and set aside.
[0027] 2) Protocorm formation and proliferation: Shake the sterilized seeds evenly into sterile water or germination medium. After about 7 days, the embryos start to expand, and form a protocorm after about 14 days. Cut the protocorm and transfer it to the protocorm for proliferation culture medium to obtain a large number of protocorms. Wherein the protocorm proliferation medium is 1 / 2MS solid medium with 0.9mg / Kg 6-benzylaminopurine, 0.08mg / Kg naphthaleneacetic acid, 25g / Kg sucrose and 4g / Kg agar; the culture conditions are: temperature 23°C, The relative humidity is 65%, the light time is 11 hours / day, and the light intensity is 2000Lx.
[0028] 3) Cluster bud induction and prolif...
Embodiment 3
[0032] 1) Disinfection of explants: first rinse the capsules with running water, rinse with washing powder solution, wash with distilled water, soak in 75% alcohol for 35 seconds, then soak in 0.2% mercuric solution for 15 minutes, finally rinse with sterile water 5 times, and set aside.
[0033] 2) Protocorm formation and proliferation: Shake the sterilized seeds evenly into sterile water or germination medium. After about 7 days, the embryos start to expand, and form a protocorm after about 14 days. Cut the protocorm and transfer it to the protocorm for proliferation culture medium to obtain a large number of protocorms. Among them, the protocorm proliferation medium is 1 / 2MS solid medium with 1.2mg / Kg 6-benzylaminopurine, 0.12mg / Kg naphthaleneacetic acid, 35g / Kg sucrose and 6g / Kg agar; the culture conditions are: temperature 26°C, The relative humidity is 80%, the light time is 14 hours / day, and the light intensity is 5000Lx.
[0034]3) Cluster bud induction and proliferat...
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