Method for ecologically interplanting sarcandra glabra under phyllostachys edulis forest
A technology for coral and moso bamboo, applied in the fields of botanical equipment and methods, horticulture, application, etc., can solve the problems of low maturity rate and harvest rate of grass coral seeds, seasonal restrictions on materials, difficult seed sources, etc., and achieves simple and easy breeding. , Conducive to management and improve the effect of land utilization
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[0030] Example 1:
[0031] (1) Group breeding seedlings
[0032] Choose healthy and disease-free young leaves of Coral Coral as explants, soak them in 75% alcohol for 20 seconds in a clean bench, then soak them in 0.1% mercury solution for 1 min, rinse with sterile water 3 to 4 times, and cut the area. About 1cm 2 The small squares on the left and right are spare. The sterilized leaves were placed on the adventitious shoot induction medium with the paraxial side up, and 5 days after the inoculation, they were transferred to a fresh medium and cultured for another 30 days. Adventitious bud induction medium is based on MS as the basic medium, plus 2.5 mg / L TDZ, 0.15 mg / L NAA, 120g / L banana puree, and 0.8g / L activated carbon; 15 days after the leaves are inoculated to the fresh medium, the cut is slightly There are swelling and green bud spots, and then the regeneration of adventitious buds begins. When cultured for 30 days, the regeneration frequency of explants and the average nu...
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[0043] Example 2:
[0044] (1) Group breeding seedlings
[0045] Choose healthy and disease-free young leaves of Coral Coral as explants, soak them in 75% alcohol for 20 seconds in a clean bench, then soak them in 0.1% mercury solution for 1 min, rinse with sterile water 3 to 4 times, and cut the area. About 1cm 2 The small squares on the left and right are spare. The sterilized leaves were placed on the adventitious shoot induction medium with the paraxial side up, and 5 days after inoculation, they were transferred to fresh medium and cultured for 35 days. Adventitious bud induction medium is MS as the basic medium, plus 2.0 mg / L TDZ, 0.1 mg / L NAA, 150g / L banana puree and 0.5g / L activated carbon; 17 days after the leaves are inoculated to the fresh medium, the cut is slightly There are swelling and green bud spots, and then the regeneration of adventitious buds begins. When cultured for 30 days, the regeneration frequency of explants and the average number of regenerated adve...
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[0054] Example 3:
[0055] The operation steps and parameters of this example refer to Example 1. The difference is: the leaf adventitious bud induction medium is MS as the basic medium, plus 4.0 mg / L TDZ, 0.2 mg / L NAA, 100g / L banana puree and 1.0g / L activated carbon; 15 days after the leaves were inoculated to fresh medium, the incision was slightly enlarged and green bud spots appeared, and then adventitious buds began to regenerate. When cultured for 30 days, the regeneration frequency of explants and the average number of regenerated adventitious buds were 78.4% and 4.7, respectively. The adventitious buds growing from the edge of the leaves were cut into individual buds and inoculated into a proliferation medium. The proliferation medium was based on MS as the basic medium, plus 2.0 mg / L TDZ and 0.05 mg / L NAA. The same proliferation medium can be used for multiple subcultures, subcultured once every 25 to 30 days, and the average proliferation multiple of cluster buds...
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