Sorbus alnifolia tissue culture and rapid propagation method
A technique for rapid propagation by tissue culture of Aronia serrata, applied in the field of plant tissue culture, can solve the problems of resource exhaustion, low seed reproduction rate, insufficient seed collection resources, etc. effect of value
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Embodiment 1
[0018] (1) Seed disinfection and sowing: Select the Sorbus elm seeds of the year, and treat them at 2°C for 45 days. Select plump seeds and wash them under running water for 1.5 hours, soak them in 75% ethanol solution for 35 seconds in an ultra-clean workbench, rinse them with sterile water for 3 times, then disinfect them with 0.1% mercuric solution for 10 minutes, rinse them with sterile water for 3 times before using them. The moisture on the surface was blotted with sterile filter paper, the complete seed embryo was taken out, and the radicle was vertically inserted into the seed germination medium for cultivation. After inoculation, the seed germination rate reached 93.6% after being cultured for 30 days under the conditions of 13 hours of light per day, light intensity of 2500lx, culture temperature of 26°C, and relative air humidity of 75%. The germination medium is: MS+3.0mg / LGA 3 +1.5g / L AC+18g / L sucrose+4.5g / L agar, the pH is 5.7.
[0019] (2) Induction culture: C...
Embodiment 2
[0024] (1) Seed disinfection and sowing: Select the Sorbus elm seeds of that year, and treat them at a low temperature of 3°C for 50 days. Pick plump seeds and wash them under running water for 2 hours, soak them in 75% ethanol solution for 40 seconds in an ultra-clean workbench, rinse them with sterile water for 4 times, then disinfect them with 0.1% mercuric chloride solution for 15 minutes, rinse them with sterile water for 3 times, and then rinse them with sterile water. Bacteria filter paper blots the water on the surface, takes out the complete seed embryo, and inserts the radicle vertically into the seed germination medium for cultivation. After inoculation, the seed germination rate reached 95.3% after being cultivated for 30 days under the conditions of 14 hours of light per day, 2500lx of light intensity, 27°C of culture temperature and 75% relative air humidity. The germination medium is: MS+4.0mg / LGA 3 +2.0g / L AC+20g / L sucrose+4.5g / L agar, the pH is 5.7.
[0025]...
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