Tissue culture rapid propagation method of ploygonatum cirrhifolium royle
A technology of tissue culture, rapid propagation, and Polygonatum chinensis is applied in the field of plant tissue culture, which can solve problems such as rare, and achieve the effects of improving seedling rate, improving reproduction coefficient and seedling quality, and cooperating closely.
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[0031] Example 1
[0032] A method for tissue culture and rapid propagation of Polygonatum leaf roll, including the following steps:
[0033] (1) Selection and disinfection of explants: take the side buds of Polygonatum sylvestris as explants, soak in 2% detergent aqueous solution for 5 minutes, rinse with linear tap water for 15 minutes, and add 2 drops of Tween-20 100mL0.1 Disinfect with% mercury for 8 minutes, rinse with sterile water for 3 times, and finally remove the surface moisture with sterile filter paper to obtain explants, where the sterile water is autoclaved distilled water;
[0034] (2) Induction of the first generation of explants to obtain sterile test tube seedlings: Place the explants obtained in step (1) in MS medium at a culture temperature of 23℃, light intensity of 1500lux, and light time of 8 hours / day Cultivate for 30 days under the conditions to obtain a sterile test tube plantlet, in which 1.0 mg / L 6-benzyl adenine 6-BA, 0.2 mg / L indole acetate IAA, 30 g / L...
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[0039] Example 2
[0040] A method for tissue culture and rapid propagation of Polygonatum leaf roll, including the following steps:
[0041] (1) Selection and disinfection of explants: Take the side buds of Polygonatum serrata as explants, soak them in 2% detergent solution for 5 minutes, rinse with linear tap water for 30 minutes, and add 3 drops of Tween-20 to 100mL0.1 Disinfect with% mercury for 10 minutes, rinse with sterile water for 5 times, and finally remove the surface moisture with sterile filter paper to obtain explants with distilled water;
[0042] (2) Induction of the first generation of explants to obtain sterile test tube plantlets: Place the explants obtained in step (1) in MS medium at a culture temperature of 27°C, light intensity of 1500 lux, and light time of 10 hours / day. Cultivate for 30 days under the conditions to obtain a sterile test tube seedling, in which 1.5 mg / L 6-benzyl adenine 6-BA, 0.2 mg / L indole acetate IAA, 30 g / L sucrose and 5 g / L were added t...
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[0047] Example 3
[0048] A method for tissue culture and rapid propagation of Polygonatum leaf roll, including the following steps:
[0049] (1) Selection and disinfection of explants: take the side buds of Polygonatum vulgaris as explants, soak them in a 2% detergent solution for 5 minutes, rinse with linear tap water for 20 minutes, and add 3 drops of Tween-20 to 100mL0.1 Disinfect with% mercury for 9 minutes, rinse with sterile water 4 times, and finally remove the surface moisture with sterile filter paper to obtain explants, where the sterile water is autoclaved distilled water;
[0050] (2) Induction of the first generation of explants to obtain sterile test tube seedlings: Place the explants obtained in step (1) in MS medium at a culture temperature of 25°C, light intensity of 1500 lux, and light time of 9 hours / day Cultivate for 30 days under the conditions to obtain a sterile test tube plantlet, in which 1.5 mg / L 6-benzyl adenine 6-BA, 0.5 mg / L indole acetate IAA, 30 g / L ...
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