Tissue culture method of Hosta plantiginea Ascherson
A tissue culture and white hosta technology, applied in the field of plant tissue culture, can solve problems such as no report on the white flower hosta tissue culture technology, and achieve the effects of reducing the probability of variation, simple operation and high reproduction coefficient
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Embodiment 1
[0019] 1. In spring, cut the new buds with a length of about 1 cm in the current year, rinse with washing powder water for 5 minutes, rinse with running water for 30 minutes, treat with 70% alcohol on the ultra-clean workbench for 10 seconds, and then use 0.1% mercury chloride Soak and shake for 6 minutes, wash 6 times with sterile water, absorb water with filter paper, and insert into induction medium: MS+BA 0.2mg / L +NAA 0.01mg / L , additional agar powder 0.6%, sucrose 3%. The culture temperature was 20 °C, the light intensity was 2000 Lux, and the light was 14 hours a day. After 35 days, sterile seedlings were basically formed. The pollution rate is 28%, and the seedling rate is 100%.
[0020] 2. Peel off the outer leaves of the test tube seedlings and inoculate them in MS+BA 2mg / L +NAA 0.1mg / L On the medium of 15 days or so, new axillary buds began to sprout from the exposed leaf scars. After 35 days, most of the axillary buds are more than 1 cm long, and they can be d...
Embodiment 2
[0023] The process of Example 1 was repeated, and the induction medium was supplemented with the hormones BA 0.5 mg / L and NAA 0.05 mg / L. The seedling rate is 100%.
[0024] Proliferation medium is MS+BA 3mg / L +NAA 0.3mg / L , bud differentiation number 3.67.
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