Method for establishing in-tube leaf-cuttage rapid-propagation system of petrocosmea qinlingensis
An establishment method, a technology in test tube, applied in the field of plant tissue culture, can solve the problems of slow propagation mode, rapid propagation of Qinling stone butterfly without establishment, no successful examples, etc., achieve technology easy to master, overcome the slow natural propagation mode, The effect of high seedling rate
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Embodiment 1
[0023] (1) Preparation of culture medium: first prepare the culture medium used in the Qinling stone butterfly cultivation process, including the basic medium and the specific medium with additional MS nutrient solution and hormones. The preparation process of the basic medium is as follows: 2:1 Measure perlite, vermiculite and peat at a volume ratio of 1 and add water to mix them evenly. After absorbing water and saturate, put them into 240mL culture bottles respectively. The filling volume is 1 / 3 of the culture bottle volume. Sterilize the culture bottle at 121.3°C for 60 minutes; the proliferation culture medium is MS nutrient solution + IBA, and the concentration of IBA is 100 mg / L; the rooting and strong seedling culture medium is MS nutrient solution + IBA, and the concentration of IBA is 200 mg / L; The MS nutrient solution used in the culture solution and the rooting and strong seedling culture solution does not add sucrose, and its pH value is 5.8.
[0024] (2) Disinfec...
Embodiment 2
[0028] The basic steps are the same as in Example 1, except that the proliferation culture medium used in step (3) is composed of 1 mL of MS nutrient solution and 1 mL of IBA with a concentration of 200 mg / L, and the pH is 5.8.
[0029] After adding this proliferation culture solution and cultivating under the same conditions as in Example 1, adventitious buds began to form in the 4th week, and adventitious buds could be formed on the front and back of the blade, most of which occurred at the base of the blade near the petiole, and a few occurred at the edge of the leaf. The multiplication coefficient of each leaf was 11.67 in the fifth week, and the maximum multiplication coefficient of a single leaf was 16. The average multiplication coefficient of each leaf was 51 until the eighth week, and the largest multiplication coefficient of a single leaf reached 68.
Embodiment 3
[0031] The basic steps are the same as in Example 1, except that the proliferation culture medium used in step (3) is composed of 1 mL of MS nutrient solution and 1 mL of IBA with a concentration of 400 mg / L, and the pH is 5.8.
[0032] After adding the proliferation culture solution and culturing under the same conditions as in Example 1, adventitious buds began to form at the base of the petiole of the blade in the 4th week, and a small amount of white hair-like roots were formed at the base of the petiole. The maximum multiplication coefficient of a single leaf was 9.33, and the maximum multiplication coefficient of a single leaf was 12. The average multiplication coefficient of each leaf was 33.67 until the eighth week of cultivation, and the maximum multiplication coefficient of a single leaf was 37.
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