Method for in-vitro rapid propagation of dendrobium officinale
A consistent technology of Dendrobium officinale, which is applied to the field of in vitro flowering of Dendrobium officinale, can solve the problem of low bud induction rate of flowers, and achieve the effects of solving pest and disease infection, shortening breeding years, and solving long flowering cycle.
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Embodiment 1
[0030] Utilize the present invention to carry out in vitro flowering induction culture of dendrobium officinale.
[0031] 1) Proliferation induction culture: select aseptic seedlings of Dendrobium officinale with vigorous growth, emerald green leaves and uniform growth and inoculate them into the proliferation medium for conventional induction culture. The proliferation induction medium of Dendrobium candidum is the culture medium with MS solid medium as the basic medium, and the contained sucrose concentration is 30g / L, the concentration of naphthaleneacetic acid is 0.1mg / L, and the concentration of 6-benzylaminopurine is 3.0mg / L. Base, the pH of the medium was 5.8. (Cultivation conditions are the same as step 2). After culturing for 30 days, each Dendrobium officinale seedling can form about 3 clustered buds with a length of 1.5-2 cm.
[0032] 2) Rooting induction culture: select the clustered shoots of Dendrobium officinale in step 1), inoculate them into the rooting medi...
Embodiment 2
[0036] Utilize the present invention to carry out flowering culture in test tube of dendrobium officinale.
[0037] The proliferation-inducing medium is a medium with MS solid medium as the basic medium, and the contained sucrose concentration is 30g / L, the concentration of naphthaleneacetic acid is 0.1mg / L, and the concentration of 6-benzylaminopurine is 3.0mg / L. The pH of the medium was 5.8. Other conditions are with embodiment 1.
[0038] Described rooting induction culture medium is to take 1 / 2MS solid culture medium as basic culture medium, contained sucrose concentration is 30g / L, naphthalene acetic acid concentration is 0.05mg / L, gac concentration is the culture medium of 1.0mg / L, culture medium The pH value is 5.8, and other conditions are the same as in Example 1.
[0039] The flowering induction medium is a medium with MS solid medium as the basic medium, and the contained sucrose concentration is 30g / L, the concentration of naphthaleneacetic acid is 0.1mg / L, and t...
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