Cultivation method of tissue cultured seedlings of clematis
A cultivation method and tissue culture seedling technology are applied in the field of cultivating clematis clematis tissue culture seedlings, which can solve the problems of low germination rate of clematis seeds, low rooting rate of seedlings, etc., and meet the requirements of large-scale planting clematis Need, promote growth and reproduction, improve the effect of germination rate
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Embodiment 1
[0020] A method for cultivating clematis tissue culture seedlings, the specific steps are as follows:
[0021] A. After the wild clematis capsules are disinfected, the seeds in the clematis capsules are used; the disinfection treatment is to place the clematis capsules in 75% alcohol for 30 seconds on the ultra-clean workbench, Then soak in 0.1% HgCl2 aqueous solution for 8 minutes, and then wash 5 times with sterile water; the seeds are evenly sprinkled on the surface of the induction medium for cultivation. After 25 days, the seeds germinated and formed white protocorms; the formulation of the induction medium was: on the basis of MS medium, 1.5 mg / L of 6-benzylaminopurine (6-BA), 0.1 mg / L of a- Naphthaleneacetic acid (NAA), 200mg / L hydrolyzed casein (CH), 30g / L sucrose, 4.5g / L agar, adjust pH5.4;
[0022] B. Transfer the protocorm to the proliferation medium for cultivation. After 2 months, it develops into seedlings. The seedlings are transferred to the proliferation medi...
Embodiment 2
[0037] A method for cultivating clematis tissue culture seedlings, the specific steps are as follows:
[0038] A. After the wild clematis capsules are disinfected, the seeds in the clematis capsules are used; the disinfection treatment is to place the clematis capsules in 75% alcohol for 30 seconds on the ultra-clean workbench, Then soak in 0.1% HgCl2 aqueous solution for 10 minutes, and then rinse with sterile water for 6 times; the seeds are evenly sprinkled on the surface of the induction medium for cultivation, the cultivation temperature is 25°C, the light intensity is 2000 lux, and the light time is 12 hours / day. On day 35, the seeds germinated and formed white protocorms; the formulation of the induction medium was: on the basis of MS medium, 1.5 mg / L of 6-benzylaminopurine (6-BA), 0.1 mg / L of a- Naphthaleneacetic acid (NAA), 200mg / L hydrolyzed casein (CH), 30g / L sucrose, 4.5g / L agar, adjustment 5.6;
[0039]B. Transfer the protocorm to the proliferation medium for cul...
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