Establishing method for tissue culture and rapid propagation system for amorphophallus konjac
A technology of tissue culture and establishment method, which is applied in the field of plant tissue culture, can solve the problems of konjac industry development constraints, low natural reproduction rate, degradation of seed taro, etc., and achieve the effect of solving the shortage of seedlings and promoting development
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Embodiment 1
[0018] (1) Callus induction: Select the vigorously growing flower konjac taro, wash it with water first, brush the vicinity of the main bud with a brush, dry it, and then cut the top core block with buds (2cm×2cm×2cm) , and scrape and wash its epidermis, put it in clean ceramic red, and cover a layer of gauze on the porcelain red, rinse it under tap water for 1 hour, first soak it in 75% ethanol for 5 seconds, and rinse it with sterile water for 3 times , 3 minutes each time, then disinfected with 0.1% mercuric chloride solution for 5 minutes, and then rinsed with sterilizing water 3 times, 3 minutes each time. Blot the water droplets on the surface of the taro with sterile filter paper, cut off the surface layer of 1mm, cut into small pieces of 0.5cm×0.5cm×0.5cm, soak them in 70mg / L citric acid for 2s, and inoculate them into the induction medium for healing. Injury tissue induction. After inoculation, culture in total darkness at 28°C for 7 days, then place in light for 12...
Embodiment 2
[0024](1) Callus induction: Select the vigorously growing flower konjac taro, wash it with water first, brush the vicinity of the main bud with a brush, dry it, and then cut the top core block with buds (2cm×2cm×2cm) , and scrape and wash its epidermis, put it in clean ceramic red, and cover a layer of gauze on the porcelain red, rinse it under tap water for 2 hours, first soak it in 75% ethanol for 7 seconds, and rinse it with sterile water for 5 times , 5 minutes each time, then disinfected with 0.1% mercuric chloride solution for 6 minutes, and then rinsed with sterilizing water 4 times, 3 minutes each time. Blot the water drops on the surface of taro with sterile filter paper, cut off the surface layer 2mm, cut into small pieces of 0.5cm×0.5cm×0.5cm, soak them in 100mg / L citric acid for 3s, and inoculate them into the induction medium for healing. Injury tissue induction. After inoculation, culture in total darkness at 26°C for 9 days, then place in light for 14 hours a d...
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