Method for culturing autotetraploid paris polyphylla plant
A technology of aesculus and one flower, allotetraploid, applied in the directions of botanical equipment and methods, horticultural methods, plant regeneration, etc., can solve problems such as degradation, and achieve expansion of planting area, high induction success rate, and increase of planting income. Effect
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Embodiment 1
[0025] Embodiment 1 The cultivation method of autotetraploid Aesculus aesculinum plant
[0026] Proceed as follows:
[0027] (1) Breeding tissue cultured seedlings: get the leaf buds of Aesculus aesculinum plant, and breed tissue cultured seedlings by plant tissue culture technology;
[0028] (2) Colchicine treatment: Under aseptic conditions, select tissue-cultured subcultured seedlings with strong growth potential, cause several (2-5) wounds on the stem, then wrap them tightly with absorbent cotton, and then drop them into the absorbent cotton. The mass concentration is 0.05% colchicine solution infiltration, cultured on the differentiation medium for 12 days, washed with sterile water, cut into single buds and then transferred to cluster bud induction medium;
[0029] The components of the differentiation medium consist of: MS+BA 0.6mg / L+GA 3 0.3mg / L+NAA 0.2mg / L+CTK0.4mg / L;
[0030] The culture conditions for culturing in the differentiation medium are: temperature 28°C...
Embodiment 2
[0038] Embodiment 2 The cultivation method of autotetraploid Aesculus aesculinum plant
[0039] The steps are as follows: (1) Breeding tissue cultured seedlings: take the leaf buds of the Aesculus aesculata plant, and breed the tissue cultured seedlings through the plant tissue culture technique;
[0040] (2) Colchicine treatment: transfer the tissue-cultured seedlings to a differentiation medium with a mass concentration of 0.08% colchicine, and after culturing for 25 days, cut into single buds and transfer them to clustered bud induction medium;
[0041] The components of the differentiation medium consist of: MS+BA 0.6mg / L+GA 3 0.3mg / L+NAA 0.2mg / L+CTK0.4mg / L;
[0042] The culture conditions for culturing in the differentiation medium are: temperature 28°C, sunshine 10h per day, light intensity 60μmol·m -2 ·s -1 ;
[0043] The components of the cluster bud induction medium consist of: MS+BA 1.8mg / L+GA 3 0.3mg / L+NAA 0.3mg / L+sucrose 25g / L;
[0044] (3) Inducing plant d...
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