Method for rapid breeding by pinellia ternate stems
A pinellia, rapid technology, applied in the field of traditional Chinese medicine, can solve the problems of unfavorable large-scale production, etc., and achieve the effects of favorable air circulation, fast breeding speed and simple operation
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Embodiment 1
[0047] Example 1 Breeding by the method of the present invention
[0048] Sterilization and sterilization of the culture container: use an autoclaveable plant tissue culture box (the material is polypropylene, the culture box is a 25 × 25cm square box, and the lid has 1 to 3 openable and closable ventilation holes). The body and the box cover form a box with an overall height of 4.5cm, which can be sterilized by autoclaving.
[0049] Preparation of medium: The medium used in the present invention is a liquid MS induction medium without any auxin, which is shown in Table 1.
[0050] Inoculation: Select strong virus-free seedlings that have been cultured for 30 days. In a sterile workbench, cut off the petioles and pearl buds of the virus-free seedlings, cut the petioles and pearl buds into 3-5 segments, and inoculate them evenly into in the above induction medium. After 2 weeks of culture, the segments were cut into about 5 to 10 small segments. The cut sections were planted...
Embodiment 2
[0053]Embodiment 2 adopts the method of the present invention to carry out breeding
[0054] Sterilization and sterilization of the culture container: A plant tissue culture box that can be sterilized by autoclaving is used. The box is composed of a box body and a box cover.
[0055] Media Preparation: The media was liquid MS induction medium without any auxin, which is shown in Table 1.
[0056] Inoculation: Select strong virus-free seedlings that have been cultured for 40 days. In a sterile workbench, cut off the petioles and pearl buds of the virus-free seedlings, cut the petioles and pearl buds into 3 to 5 segments, and inoculate them evenly. in the above induction medium. After 1.5 weeks of culture, the segments were cut into 5-10 small segments. Small segments were inoculated at a density of 1.0 × 1.0 cm, and 240 segments were placed in each culture box, for a total of 10 boxes.
[0057] Induction culture: The culture box inoculated with avirulent cut seedlings of Pin...
Embodiment 3
[0059] Example 3 Breeding by the method of the present invention
[0060] Sterilization and sterilization of the culture container: A plant tissue culture box that can be sterilized by autoclaving is used. The box is composed of a box body and a box cover.
[0061] Media Preparation: The media was liquid MS induction medium without any auxin, which is shown in Table 1.
[0062] Inoculation: Select strong tissue culture detoxified seedlings with a seedling age of 35 days. In a sterile workbench, cut off the petioles and buds of the detoxified seedlings. Inoculated into the above induction medium. After 1 week of culture, the segments were cut into 5-10 small segments. The cut sections were planted at a density of 1.3 × 1.3 cm, and 230 sections were placed in each culture box, for a total of 10 boxes.
[0063] Induction culture: The culture box inoculated with avirulent cut seedlings of Pinellia sinensis was treated for 5 weeks under a total dark photoperiod of 24 hours a day...
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