Tissue culture and rapid propagation method for ilex purpurea superior plant
A technology for tissue culture and rapid propagation of holly, which is applied in horticultural methods, botany equipment and methods, horticulture, etc., and can solve the problems that cannot meet the production requirements of fine varieties, unfavorable cultivation of holly tissue culture seedlings, unfavorable rapid propagation of holly, etc. problem, achieve the effect of reducing the possibility of seedling pollution, increasing the rooting rate and transplanting survival rate, and facilitating the transplanting speed
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Embodiment 1
[0034] Embodiment 1: tissue culture rapid propagation method one:
[0035] A. Obtaining explants: Select 200 young shoots of the high-quality female plants of Ilex chinensis that year, cut off the excess leaves, and leave the bud tips, wash them with clean water, then wash them with detergent, and then rinse them with running water for 4 minutes. Wash with detergent, then disinfect with 75wt% alcohol for 23s, clean the alcohol with sterile water and filter dry, then sterilize with 0.1wt% mercuric acid solution for 8 minutes, wash and filter the mercuric solution with sterile water to obtain sterile explants;
[0036] B. Induction culture: transfer the sterile explants to the induction medium for budding, the induction medium is made of MS medium+NAA0.2mg / L+6BA 1.5mg / L+agar 6.5g / L+sucrose 30g / L , pH=5.8, cultivated for 40 days under the conditions of a culture temperature of 25°C, a light intensity of 1800lx, and a light time of 12h / d to obtain induced sprouts;
[0037] C. Pr...
Embodiment 2
[0041] Embodiment 2: tissue culture rapid propagation method two:
[0042] A. Obtain explants: choose 200 young shoots of the high-quality female plants of Ilex red fruit identical to those in Example 1, cut off the excess leaves, leave the bud tips, wash them with clean water, and then clean them with detergent. Rinse with running water for 3 minutes to clean the detergent, then disinfect with 75wt% alcohol for 20 seconds, wash the alcohol with sterile water and filter dry, then sterilize with 0.1wt% mercury chloride solution for 8 minutes, and use sterile water to dissolve the mercury The solution was washed and filtered dry to obtain sterile explants;
[0043] B. Induction culture: transfer the sterile explants to the induction medium for budding, the induction medium is made of MS medium+NAA0.2mg / L+6BA 1.5mg / L+agar 6.5g / L+sucrose 30g / L , pH=5.8, cultivated for 30 days under the conditions of a culture temperature of 25°C, a light intensity of 1800lx, and a light time of 1...
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