Tissue culture and fast propagation method of South China Sea azalea
A technology for tissue culture and Rhododendron, applied in the field of plant cultivation, can solve the problems of difficult cutting, small seed quantity of Rhododendron in the South China Sea, and low emergence rate, and achieves the effects of solving protection and development, strong disease resistance and robust growth.
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Embodiment 1
[0039] 1. Sterilization of explants: Collect annual shoots of Rhododendron nanhai, cut into 1 cm long bud stem segments, wash with soapy water, and then disinfect them in alcohol with a volume concentration of 75% in an ultra-clean workbench 20 seconds, sterilized in mercuric chloride solution with a mass concentration of 0.1% for 8 minutes, sterilized in a sodium hypochlorite solution with a volume concentration of 1.5% for 8 minutes, and then rinsed with sterile water for 3 times;
[0040] 2. Adventitious bud induction culture: Inoculate the explants sterilized in the above step 1 into the following induction medium in a sterile working environment: WPM+ZT2mg / L+IAA0.5mg / L+sugar 30g / L+agar 4g / L, PH5.5, cultured for 30 days under the conditions of light intensity of 1200LX, culture temperature of 25°C, and photoperiod of 8h / d, 65% of the explants were free from pollution, and clustered buds were induced. Cut off the bud cluster in a sterile environment, divide it into individu...
Embodiment 2
[0045] 1. Sterilization of explants: collect the annual shoots of Rhododendron chinensis, cut into 2 cm long bud stem segments, wash with soapy water, and then disinfect them in alcohol with a volume concentration of 75% in an ultra-clean workbench 30 seconds, sterilized in mercuric chloride solution with a mass concentration of 0.1% for 10 minutes, sterilized in a sodium hypochlorite solution with a volume concentration of 1.5% for 15 minutes, and then rinsed with sterile water for 3 times;
[0046] 2. Adventitious bud induction culture: inoculate the explants sterilized in the above step 1 into the following induction medium in a sterile working environment: WPM+ZT2.5mg / L+IAA0.8mg / L+sugar 30g / L+agar 5g / L, PH5.2, cultured for 30 days under the conditions of light intensity of 1500LX, culture temperature of 22°C, and photoperiod of 8h / d, 58% of the explants were free from pollution, and clustered buds were induced , cut off the bud cluster in a sterile environment, divide it ...
Embodiment 3
[0051] 1. Sterilization of explants: collect the annual shoots of Rhododendron nanhai, cut into 1 cm long bud stem segments, wash with soapy water, and then disinfect them in 70% alcohol in an ultra-clean workbench 40 seconds, sterilized in 0.15% mercuric chloride solution for 10 minutes, sterilized in 2% sodium hypochlorite solution for 15 minutes, and then rinsed with sterile water for 3 times;
[0052] 2. Adventitious bud induction culture: Inoculate the explants sterilized in the above step 1 into the following induction medium in a sterile working environment: WPM+ZT3mg / L+IAA1mg / L+sugar 30g / L+agar 7g / L L, PH5.5, cultured for 35 days under the conditions of light intensity of 1500LX, culture temperature of 20°C and photoperiod of 10h / d, 76% of the explants were free from pollution, and clustered buds were induced. Cut off the bud cluster in the environment, be divided into individual plants, and the individual plants are cut into stem segments with 2 nodes, and enter the n...
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