A Atractylodes Rhizoma Atractylodes Regeneration System Using Hypocotyls and Radicles to Directly Differentiate Adventitious Buds
An Atractylodes macrocephala and radicle technology, applied in the field of Atractylodes macrocephala regeneration system, can solve the problems of low frequency, poor quality stability of regenerated plants, long artificial reproduction time, etc., and achieve the effects of increasing the proliferation frequency, improving the quality of Atractylodes macrocephala, and shortening the reproduction time.
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Embodiment 1
[0024] (1) Obtaining sterile vaccines. Select large and plump Atractylodes macrocephala seeds, rinse them with running water, soak them in alcohol with a concentration of 75% by mass for 1 min, and then disinfect them. A two-step method was used for disinfection: before removing the seed coat, soak the seeds with mercuric chloride with a concentration of 0.1% by mass for 10 minutes, rinse with sterile water for 3-5 times, soak in sterile water for 6 hours, and then peel off the seed coat; Disinfect with 1.5% NaClO for 10 min and rinse with sterile water 3-5 times. The sterilized seeds were inoculated in MS medium without adding any growth regulator, cultivated in a dark place at 25±2°C until the seeds germinated, and then transferred to the light to continue culturing, culture temperature: 25±2°C, light time: 14h / d, light intensity: 3500 lx.
[0025] (2) Continue culturing for 1 week after Atractylodes macrocephala seeds germinate, take out when the plant height reaches 2-3c...
Embodiment 2
[0029] The method is the same as in Example 1, except that the bud induction medium in step (2) is changed: 1.0 mg of TDZ, 30 g of sucrose and 8 g of agar are added to 1 L of MS medium, and the pH value is adjusted to 5.8 at 121 ° C. Autoclave for 15 min to prepare the medium.
Embodiment 3
[0031] The method is the same as in Example 1, except that the bud induction medium in step (2) is changed: 0.5 mg of TDZ, 0.2 mg of NAA, 30 g of sucrose and 8 g of agar are added to 1 L of MS medium, and the pH value is adjusted to 5.8 , 121 ° C autoclave for 15 minutes to prepare the culture medium.
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