A breeding method of root cancer resist cherry rootstock sprout as well as group culturation rapid propagating technology
A technology for root cancer and rootstock seedlings, applied in the direction of recombinant DNA technology, other methods of inserting foreign genetic materials, gardening methods, etc., can solve the problems of fruit farmers' economic losses, poor fruit quality, and easy death of large trees, and achieve good growth , to meet the effect of mass production
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Embodiment 1
[0088] 1, explant is the selection of anti-root cancer cherry rootstock test-tube seedling:
[0089] Take early spring hydroponic new shoots or new shoots of greenhouse seedlings. When the new shoots grow to about 10 cm, cut the new shoots for explant materials for tissue culture and rapid propagation;
[0090] The obtained aseptic test-tube plantlets were screened for root cancer resistance, and the root-cancer-resistant cherry rootstock test-tube plantlets were selected. The steps were as follows: After inoculating the middle and lower part of the stems of the sterile cherry rootstock test-tube plantlets with Agrobacterium, place them in a hormone-free MS culture. Carry out cultivation in the base, choose the anti-root cancer cherry rootstock test-tube plantlet of 0 grade according to the weight classification of gall tumor after 40 days as the material of follow-up operation;
[0091] 2. Propagation and cultivation:
[0092] After the selection of explants in step 1, after...
Embodiment 2
[0100] Using the same steps as in Example 1, in step 2, the conditions for the propagation of test-tube plantlets were changed to medium MS+6BA 1.0mg / L, the temperature was controlled at about 22°C, the light intensity was 1800Lx, and the light was 12 hours. In 3, change the strong seedling culture condition into strong seedling medium MS+GA 7mg / L, strong seedling 30 days, the rooting culture condition in the step 4 becomes in the rooting medium of MS+NAA 0.5mg / L.
Embodiment 3
[0102] Using the same steps as in Example 1, in step 2, the conditions for the propagation of test-tube plantlets were changed to medium MS+6BA 1.1mg / L, the temperature was controlled at about 24°C, the light intensity was 2000Lx, and the light was illuminated for 12 hours. In 3, change the strong seedling culture condition into strong seedling medium MS+GA 8mg / L, strong seedling 31 days, the rooting culture condition in the step 4 becomes in the rooting medium of MS+NAA 0.5mg / L.
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