Method for fast breeding allium ampeloprasun var.ampeloprasun
An elephant and garlic technology, applied in the field of rapid reproduction of elephant garlic, can solve the problems such as being unsuitable for the rapid reproduction of elephant garlic, different biological learning, and achieve the advantages of low cost of ingredients, improved reproduction coefficient, and high transplant survival rate. Effect
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Embodiment 1
[0033] Materials: Elephant garlic (Allium ampeloprasun var.ampeloprasun), provided by Science and Technology Bureau of Cangshan City, Shandong Province, purchased from the United States.
[0034] A method for rapidly propagating elephant garlic, the steps comprising explant disinfection, induction of sterile seedlings, induction of adventitious buds and subculture proliferation, rooting of tissue cultured seedlings, transplanting of tissue cultured seedlings, is characterized in that it includes the following steps:
[0035] A. Disinfection of explants
[0036] Select the bulbs of elephant garlic as explants, soak them in a solution with 10% by weight of tap water for 5 to 10 minutes, rinse them under tap water, and carry out surface disinfection on an ultra-clean workbench;
[0037] On the ultra-clean workbench, use 75% alcohol to disinfect the surface for 1 minute, then rinse with sterile water for 1 to 2 times, then disinfect with 15% sodium hypochlorite solution for 10 to ...
Embodiment 2
[0064] Present embodiment material is with embodiment 1.
[0065] The operating method, sterile seedling induction medium, rooting medium, and tissue culture room culture conditions of this embodiment are the same as those in Example 1.
[0066] The adventitious bud induction and proliferation medium described in this embodiment is based on MS basic medium, adding 1.0 mg / L of 6-benzyl adenine 6-BA, 1.0 mg / L of kinetin KT, and indole butyric acid IBA1.0mg / L (abbreviated as: MS+6-BA 1.0mg / L+KT1.0mg / L+IBA1.0mg / L);
[0067] No vitrification phenomenon was observed in the apical meristem described in step B during the induction of the sterile vaccine.
[0068] No vitrification phenomenon was observed in the base of the sterile seedlings and the base of adventitious buds described in step C during the induction of adventitious buds and subculture.
[0069] In this embodiment, the multiplying rate is 3.5, the rooting rate is 100%, and the survival rate is 100%.
[0070] In the pre...
Embodiment 3
[0072] Present embodiment material is with embodiment 1.
[0073] The operating method, sterile seedling induction medium, rooting medium, and tissue culture room culture conditions of this embodiment are the same as those in Example 1.
[0074] The adventitious bud induction and proliferation medium described in this example is based on the 1 / 2 MS medium obtained by reducing the macroelements in the MS basic medium components to 1 / 2 of the original and keeping other components unchanged, and adding α - Naphthaleneacetic acid NAA 0.1mg / L, indole butyric acid IBA 1.5mg / L (abbreviated as: 1 / 2MS+NAA0.1mg / L+IBA 1.5mg / L);
[0075] No vitrification phenomenon was observed in the apical meristem described in step B during the induction of the sterile vaccine.
[0076] No vitrification phenomenon was observed in the base of the sterile seedlings and the base of adventitious buds described in step C during the induction of adventitious buds and subculture.
[0077] In this embodiment...
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