Tissue culture method of dwarf radix ophiopogonis
A dwarf Ophiopogon japonicus and tissue culture technology, applied in the field of plant tissue culture, can solve the problems of low survival or germination rate, achieve easy reproduction, shorten the reproduction cycle, and solve the effects of slow sowing and reproduction
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Embodiment 1
[0020] A method for tissue culture of dwarf Ophiopogon japonicus, comprising the following steps:
[0021] Step 1, disinfection and sterilization:
[0022] Select young leaves that have just germinated that year, rinse them with tap water, soak them in 70% alcohol for 15 seconds on an ultra-clean workbench, then sterilize them in 0.1% mercuric solution for 1 minute, pour off the sterilizing solution, and use the pre- Rinse the prepared sterile water 4 times, drain the water, and inoculate the sterilized leaves on the germination medium;
[0023] Step 2, primary culture:
[0024] Inoculate the sterilized leaves on MS+BA 0.5mg / L+NAA0.5mg / L+KT1.0mg / L+sucrose 30g / L+agar 5g / L medium, the pH value of the medium is 5.6, and the MS medium passes through 1.1kg / cm 2 Autoclave for 20 minutes, and cultivate in the dark at a temperature of 25±2°C for about 20 days. The leaves begin to callus. By the 30th day, most of the leaves have formed callus. Cut off the callus and enter the next st...
Embodiment 2
[0034] A method for tissue culture of dwarf Ophiopogon japonicus, comprising the following steps:
[0035] Step 1, disinfection and sterilization:
[0036] Select young leaves that have just germinated that year, rinse them with tap water, soak them in 70% alcohol for 15 seconds on an ultra-clean workbench, then sterilize them in 0.1% mercuric solution for 3 minutes, pour off the sterilizing solution, and use Rinse the prepared sterile water 5 times, drain the water, and inoculate the sterilized leaves on the germination medium;
[0037] Step 2, primary culture:
[0038] Inoculate the sterilized leaves on MS+BA 0.5mg / L+NAA0.5mg / L+KT1.0mg / L+sucrose 30g / L+agar 7g / L medium, the pH value of the medium is 5.8, and the MS medium is passed through 1.1kg / cm 2 Autoclave for 20 minutes, and cultivate in the dark at a temperature of 25±2°C for about 20 days. The leaves begin to callus. By the 33rd day, most of the leaves have formed callus. Cut off the callus and enter the next stage o...
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