Quick breeding method for inducing spheroidal embryo directly from tissue of anthurium
An Anzu flower and spherical technology, which is applied in the field of rapid propagation of the Anzu flower tissue directly inducing spherical embryo clusters, and achieves the effects of low price, convenient material selection and convenient operation.
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Embodiment 1
[0034] Embodiment 1: Leaf, blade stalk end tissue culture forms spherical embryo group and seedling
[0035] Take the young leaves of mature plants or young plants (flower seedlings) of Anthurium (taken from the greenhouse of the flower sales office of Guolian Flower Base, Changchun City, Jilin Province), and sterilize as above (wash with tap water first, then rinse with distilled water for 3 times , then put in 75% ethanol for 1 minute, rinse twice with sterile water, soak with mercuric chloride or sodium hypochlorite for 5-10 minutes, take it out, and rinse with sterile water for 3 times, then it can be used as tissue culture material) , cut it into pieces under aseptic conditions as shown in Figure 10, and put it into the above medium: 1 / 2MS (basic medium) + BA (6-benzyl adenine) 0.5mg / L + NAA (α-naphthaleneacetic acid) 0.1mg / L+KT(N 6 -furylmethyladenine) 0 mg / L+2,4-D (2,4-dichlorophenoxyacetic acid) 0 mg / L+3% sucrose. Cultivate under light, light for 7-15 hours a day, li...
Embodiment 2
[0036] Embodiment 2: Stem axis, stem tip, stem node tissue culture form spherical embryo group and seedling
[0037] Take Anthurium anthurium (taken from the greenhouse of the flower sales office of Guolian Flower Base, Changchun City, Jilin Province) as an adult plant or seedling, remove its leaves and get its stem axis, stem tip, and stem nodes, and sterilize as above (wash with tap water first, Rinse with distilled water for 3 times, then put in 75% ethanol for 1 minute, rinse with sterile water for 2 times, soak in mercuric chloride or sodium hypochlorite for 5-10 minutes, take it out, and rinse with sterile water for 3 times. Standby as tissue culture material), chop it up under sterile conditions as shown in Figure 13, and put it into the above medium: 1 / 2MS (basic medium) + BA (6-benzyl adenine) 1mg / L + NAA (α-Naphthylacetic acid) 0.1mg / L+KT(N 6-furyl methyl adenine) 0.1 mg / L+2,4-D (2,4-dichlorophenoxyacetic acid) 0 mg / L+3% sucrose or glucose were put on the above-ment...
Embodiment 3
[0038] Embodiment 3: Petiole, aerial root tip tissue culture form spherical embryo group and seedling
[0039] Take the petiole, aerial root tip or petiole of the seedling of Anthurium anthurium (taken from potted flowers in Changchun Flower, Bird, Fish and Insect Wholesale Market), and sterilize as above (wash with tap water first, then rinse with distilled water for 3 times, then put into 75% ethanol for 1 minute, rinse twice with sterile water, soak in mercuric chloride or sodium hypochlorite for 5-10 minutes, take it out, and rinse with sterile water for 3 times, ready to be used as tissue culture material), in the absence of Under bacterial conditions, it was cut into 3mm long sections as shown in Figure 16, and put into the above-mentioned medium: 1 / 2MS (basic medium)+BA (6-benzyl adenine) 1mg / L+2,4-D (2 , 4-dichlorophenoxyacetic acid) 0.1mg / L+KT(N 6 -furylmethyladenine) 0mg / L+3% sucrose, cultivate under light, light 7-15 hours every day, light intensity is 25000 lux, c...
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