Rapid propagation method for hybrid cymbidium seedlings of cymbidium sinense and cymbidium hookerianum
A technology for hybrid orchid and seedlings, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of long cycle, low reproduction coefficient, and no protocorm obtained, and achieves convenient material collection, simplified cultivation process, shortened The effect of incubation time
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Embodiment 1
[0038] A rapid propagation method for the hybrid orchid of Molan and Sagittarius, comprising the following steps:
[0039] 1) Induction culture
[0040]Take the aseptic seedling of "Red Beauty", the hybrid offspring of Molan and Hutoulan, cut off the roots and top leaves, take 0.6 cm of basal tissue, peel off the outer 1-2 layers of leaf sheaths, and inoculate it in the induction medium; carry out light culture, Cultured for 50d to obtain hybrid orchid protocorm (see figure 1 ), the induction rate of protocorm reached 83.3%;
[0041] Among them, the induction medium is: MS+6-BA 5.0mg / L+KT 1.0mg / L+NAA1.0mg / L+PIC 0.3mg / L+hydrolyzed casein 1.0mg / L+activated carbon 0.1g / L+sucrose 30g / L+ Agar powder 6.0g / L, pH=5.6;
[0042] 2) Proliferation culture and differentiation
[0043] Take the hybrid blue protocorm obtained in step 1), cut it, and inoculate it in the protocorm proliferation and differentiation medium. The formed protocorm gradually differentiates into numerous adventi...
Embodiment 2
[0051] A rapid propagation method for the hybrid orchid of Molan and Sagittarius, comprising the following steps:
[0052] 1) Induction culture
[0053] Take the aseptic seedlings of "Red Beauty", the hybrid offspring of Molan and Hutoulan, cut off the roots and top leaves, take 0.8 cm of the basal tissue, peel off 1-2 layers of leaf sheaths, and inoculate them in the induction medium; carry out light culture, After culturing for 53 days, the hybrid orchid protocorm was obtained, and the induction rate of protocorm reached 75.0%;
[0054] Among them, the induction medium is: MS+6-BA 4.0mg / L+KT 1.5mg / L+NAA1.0mg / L+PIC 0.2mg / L+hydrolyzed casein 1.0mg / L+activated carbon 0.4g / L+sucrose 30g / L+ Agar powder 6.0g / L, pH=5.6;
[0055] 2) Proliferation culture and differentiation
[0056] Take the hybrid blue protocorm obtained in step 1), cut it, and inoculate it in the protocorm proliferation and differentiation medium. The formed protocorm gradually differentiates into a large numb...
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