Method for efficiently inducing generation of adventitious roots of Pinus densiflora tissue culture plantlets
A technology of tissue culture seedlings and red pine, applied in the biological field, can solve the problems affecting the quality of adventitious roots, callus, etc., achieve the effect of tight vascular connection, less callus, and increase rooting rate
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Embodiment 1
[0021] The test material is the pine wood nematode-resistant Chi pine 1#-A clone
[0022] Select the clustered shoots that grow young, have a small needle angle, and are 1.0-1.5cm high, and cut them out individually, and inoculate them in 1 / 4WPM+NAA 0.1mg / L+IBA1.0mg / L+sucrose 0.5% medium to induce adventitious root primordia After 30 days, the explants were transferred to 1 / 2WPM+AC0.5g / L+sucrose 2.0% medium to promote the expression and elongation of adventitious roots. After 30 days, the incidence of adventitious roots was counted, and the average root number was recorded and observed between rhizomes. The occurrence of callus: wash the agar at the root of the regenerated plant, transplant it in the culture soil, spray water to keep it moist, and count the survival rate of transplanting after 3 months. See Table 1 for specific data.
[0023] The culture conditions of the above process: temperature 24-26° C., light 2000 Lux, 16 hours of light per day.
Embodiment 2
[0025] The test material is Chi pine 3#-5 clone resistant to pine wood nematode
[0026] Except that the medium for inducing adventitious root primordia was changed to 1 / 2WPM+NAA 0.2 mg / L+IBA 1.0 mg / L+sucrose 1.0%, the rest were the same as in Example 1.
Embodiment 3
[0028] The test material is Chi pine 5#-3 clone resistant to pine wood nematode
[0029] Except that the medium for inducing adventitious root primordia was changed to 1 / 2WPM+NAA0.1mg / L+IBA2.0mg / L+sucrose0.5%, the rest were the same as in Example 1.
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