Asexual Rapid Propagation Method of Maca Hybrid
A technology for hybrids and maca, applied in the biological field, can solve the problems of character separation, loss of heterosis and excellent characters of maca hybrids, etc., and achieve the effects of improving the quality of seedlings, being easy to standardize, and improving economic benefits.
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Embodiment 1
[0037] 1. Acquisition of maca hybrid explants
[0038] Select healthy maca hybrid plants with good growth potential, no pests and diseases, and no deformities. Take the young inflorescences in the afternoon on a sunny day. At this time, the surface of the plants is clean and dry, and the content of bacteria and fungi is low; wash the young inflorescences with tap water first The unclean matter and dust on the surface were rinsed under running water for 2 h, placed on the ultra-clean workbench, and the young lazy inflorescences were taken out of the beaker one by one with scorched tweezers, and put into the beaker with a volume ratio of 75%. Disinfect in alcohol for 15 s, then use 0.1% HgCl 2 (mercuric chloride) (mass ratio) sterilized for 5 min, and finally rinsed with sterile water for 8 times to remove residual mercury chloride on the inflorescences of young larks, and then placed on sterile filter paper to absorb the surface moisture; shake the vessel;
[0039] 2. Callus ...
Embodiment 2
[0076] 1. Acquisition of maca hybrid explants The acquisition and treatment of maca hybrid explants described in this example are the same as in Example 1.
[0077] 2. Callus induction The composition of the callus induction medium A is: B 5 Basic culture medium, zeatin ZT 1.0 mg / L, naphthalene acetic acid NAA 0.1 mg / L, sucrose 20000 mg / L, agar powder 4800 mg / L, pH 5.4; culture method and other requirements are the same as in Example 1.
[0078] 3. The composition of the clump seedling generation and proliferation medium B is: B 5 Basic culture medium, 6-benzylaminopurine 6-BA 1.0mg / L, naphthaleneacetic acid NAA 1.5 mg / L, zeatin ZT 0.1mg / L, sucrose 20000 mg / L, agar 4800 mg / L, pH 5.4; Method and other requirements are the same as embodiment one.
[0079]4. The composition of the proliferation medium C is: MS basic culture medium, 6-benzylaminopurine 6-BA 1.0 mg / L, naphthalene acetic acid NAA 1.5 mg / L, zeatin ZT 1.0 mg / L, sucrose 30000 mg / L, agar powder 4800 mg / L, pH 5.8; Al...
Embodiment 3
[0083] Embodiment 3: The acquisition, culture method, steps and culture conditions of the maca hybrid explants in this embodiment are all the same as in Embodiment 2, and the components of each medium are different, as follows:
[0084] (1) Callus induction medium A: B 5 Basic culture medium, rice protein ZT 2.0mg / L, naphthaleneacetic acid NAA 0.01mg / L, sucrose 20000 mg / L agar 4800 mg / L, pH 5.8;
[0085] (2) Germination and Proliferation Medium B: B 5 Basic culture medium, 6-benzylaminopurine 6-BA 1.5mg / L, naphthaleneacetic acid NAA 1.8 mg / L, zeatin ZT 1.0mg / L, sucrose 20000 mg / L, agar powder 4800 mg / L, pH 5.8;
[0086] (3) Medium C: MS basic culture medium, 6-benzylaminopurine 6-BA 1.5 mg / L, naphthaleneacetic acid NAA 1.8 mg / L, zeatin ZT 0.1 mg / L, sucrose 30000 mg / L, agar powder 4800 mg / L, pH 5.8;
[0087] (4) Rooting medium D: 1 / 2 MS basic culture medium, naphthalene acetic acid NAA 0.3 mg / L, indole butyric acid IBA 0.1 mg / L, activated carbon AC 1.5 mg / L, sucrose 15000 m...
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