Tissue culture method of Hemerocallis dumortieri
A technology of Hemerocallis Hemerocallis and tissue culture, which is applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of few introductions, slow ramets, limited supply of seedlings, etc., and improves the uniformity of seedlings. , The effect of maintaining maternal traits and increasing reproduction speed
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Embodiment 1
[0025] (1) Obtaining sterile materials
[0026] Pick the buds of "Jinhuang" Evergreen Daylilies when they are blooming, rinse them with tap water for 1 hour, and then soak them on the ultra-clean workbench for 10 seconds in ethanol with a mass concentration of 60% and mercury with a volume concentration of 0.5‰ After 10 minutes, rinse with sterile water for 4 times, use sterile filter paper to absorb the water on the surface of the flower bud, cut the base of the flower bud into 0.5 cm long segments, and inoculate it with MS+KT0.1mg / L+NAA1.0mg / L flower bud induction medium;
[0027] (2) Differentiation and proliferation of buds
[0028] The flower buds were inoculated on the flower bud induction medium. After 1 week, they began to swell, and yellow-green protrusions appeared. After 3 weeks, the callus was visible. After another month of cultivation, the callus was divided, cut and connected to MS+6 -BA0.5mg / L+NAA0.1mg / L adventitious bud proliferation medium for proliferation and c...
Embodiment 2
[0037] (1) Obtaining sterile materials
[0038] Pick the buds of "Jinhuang" Evergreen Daylily when it blooms, rinse with tap water for 2 hours, and then soak it on the ultra-clean workbench for 30s in ethanol with a mass concentration of 75% and mercury with a volume concentration of 1‰ After 15 minutes, rinse with sterile water for 5 times, use sterile filter paper to absorb the water on the surface of the flower buds, cut the base of the flower buds into 1 cm long segments, and inoculate them with MS+KT0.5mg / L+NAA3.0mg / L On the bud induction medium;
[0039] (2) Differentiation and proliferation of buds
[0040] The flower buds were inoculated on the flower bud induction medium. After 2 weeks, they began to expand and appeared yellow-green protrusions. After 3 weeks, the callus could be seen. After another month of cultivation, the callus was divided and cut and connected to MS+6. -BA2.0mg / L+NAA0.2mg / L adventitious bud proliferation medium for proliferation and culture. Although ...
Embodiment 3
[0049] (1) Obtaining sterile materials
[0050] Pick the buds of "Jinhuang" Evergreen Hemerocallis when it is blooming, rinse with tap water for 3 hours, and then soak it on the ultra-clean workbench for 50s in ethanol with a mass concentration of 75% and mercury with a volume concentration of 2‰ After 30 minutes, rinse with sterile water for 6 times, use sterile filter paper to absorb the water on the surface of the flower buds, cut the base of the flower buds into 2cm-long segments, and inoculate them with MS+KT1.0mg / L+NAA5.0mg / L On the bud induction medium;
[0051] (2) Differentiation and proliferation of buds
[0052] The flower buds were inoculated on the flower bud induction medium. After 3 weeks, they began to swell and appeared yellow-green protrusions. After 5 weeks, the callus could be seen. After another 2 months, the callus was divided and cut and connected to MS+6. -BA4.0mg / L+NAA0.2mg / L adventitious bud proliferation medium for proliferation and culture. Although ther...
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