Culture medium for agriophyllum squarrosum tissue culture, adventitious bud induction method and adventitious root induction method
A technology of tissue culture and culture medium, applied in the field of culture medium of Sapona tissue culture, to achieve the effects of high rooting efficiency, improved induction efficiency and high induction rate
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Embodiment 1
[0036] The method that the induced saponica callus that the present embodiment provides forms adventitious buds is as follows:
[0037] (1) Callus induction culture:
[0038] In each embodiment of the present invention, hypocotyls or cotyledons are used as explants, and the reference application number 201611144975.7, the method of the Chinese invention patent named Shami callus tissue and its induction and proliferation method, is used to obtain the Sapona callus organization (see figure 1 In A and B), the callus medium used includes: MS+0.5mg / L 6-BA+3.0mg / L 2,4-D+0.70% agar+2.0% sucrose, pH 5.8-6.0.
[0039] (2) Adventitious bud induction culture
[0040] Inoculate the saponin callus piece that step (1) obtains in the adventitious bud induction medium and carry out bud induction culture;
[0041] The adventitious bud induction medium used included: MS+2 mg / L 6-BA+1 mg / L NAA+0.70% agar+2.0% sucrose.
[0042] Conditions for adventitious bud induction culture: humidity: 40%...
Embodiment 2
[0045] The method that the induced saponica callus that present embodiment provides forms adventitious root is as follows:
[0046] The callus of Example 1 was inoculated in the adventitious root induction medium for root induction culture; the adventitious root induction culture used included: 1 / 2MS+3mg / L IBA+0.70% agar+2.0% sucrose, pH 5.8-6.0;
[0047] Conditions for adventitious root induction culture: temperature: 22-28°C, humidity: 40%, time: 2-6 weeks, photoperiod: 16h light / 8h dark.
[0048] adventitious roots figure 2 Middle D, the arrow points to the adventitious root formed after 6 weeks of induction.
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