Method for culturing and propagating visible tiller tissues at connecting part of cedar stem
A technology of tissue culture and tissue culture medium, which is applied in horticultural methods, botany equipment and methods, horticulture, etc., can solve the problems of low success rate of cultivation and immature technology, etc., achieve large quantity, low induction cost, and reduce pollution rate effect
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Embodiment 1
[0012] Embodiment 1, a kind of bright tiller tissue culture propagation method of Chinese fir stem junction, comprises the following steps:
[0013] (1) Sterilization of explants: select the 7-8-year-old Chinese fir root-stem junction as explants, immerse the explants in silver iodide aqueous solution with a mass concentration of 4.5%, and treat them under ultrasonic waves with a power of 160W 8 seconds;
[0014] (2) Induce callus formation: inoculate the sterilized explants into callus culture medium, and the composition of callus culture medium is MS medium + Moringa oleifera seed extract 3mg / L;
[0015] (3) Bud tissue induction: Inoculate the explants into the bud tissue culture medium, and the bud tissue culture medium is composed of MS medium + datura seed extract 1mg / L; during the bud tissue induction, the explanted The body was incubated at 18°C for 10 hours, and then at 28°C for 30 hours;
[0016] (4) Root induction: the explants were artificially fixed and inocula...
Embodiment 2
[0018] Embodiment 2, a kind of bright tiller tissue culture propagation method of Chinese fir stem junction, comprises the following steps:
[0019] (1) Sterilization of explants: Select the bright tiller at the junction of the 7-8-year-old Chinese fir rhizome as explants, immerse the explants in silver iodide aqueous solution with a mass concentration of 5%, and use an ultrasonic wave with a power of 160-180W to sterilize the explants. Down processing for 10 seconds;
[0020] (2) Induce callus formation: inoculate the sterilized explants into callus culture medium, and the composition of callus culture medium is MS medium + Moringa oleifera seed extract 3.4mg / L;
[0021] (3) Bud tissue induction: the explants were inoculated into the bud tissue culture medium, and the bud tissue culture medium was composed of MS medium + datura seed extract 1.2 mg / L; during the bud tissue induction, the explants were first The implants were incubated at 20°C for 12 hours, and then at 30°C fo...
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