Method for detoxification tissue culture and rapid propagation of dianthus caryophyllus
A technology of tissue culture rapid propagation and carnation, applied in the field of plant tissue culture, can solve the problems affecting germplasm quality and breeding, regenerated plants infected with viruses or fungi, etc., and achieve the effect of avoiding the influence of uncertain factors and simple operation and process
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Embodiment 1
[0016] A method for detoxification tissue culture and rapid propagation of carnation, comprising the steps of:
[0017] (1) Heat treatment: Carnation plants were heat-treated at 36-38°C for one week, the light intensity was 3000-4000Lx, and the photoperiod was 12h;
[0018] (2) Disinfection of the surface of the explants: use the lateral buds grown between the leaf axils of Carnation plants as the explants, wash them with tap water for 30 minutes, then disinfect them with 75% ethanol for 30 seconds, and then treat them with 4% sodium hypochlorite for 7 minutes. Finally, wash 5 times with sterile distilled water, and absorb excess water with sterile absorbent paper for later use;
[0019] (3) Shoot apex stripping: cut off the leaves to expose the bud body, and peel off the young leaves with a sterilized dissecting needle until only the 2 youngest leaf primordia are left;
[0020] (4) Shoot tip culture: Inoculate the leaf primordia with the last 2 young leaves on the induction ...
Embodiment 2
[0022] The method is the same as in Example 1, except that the formulation of the induction medium is that 30 g of sucrose, 7 g of agar, 3 mg of IAA, 1.5 mg of NAA, and 2 mg of ZT are added to 1 L of MS medium; a total of 100 leaf primordia are inoculated, of which 55 are directly Differentiated into regenerated plants, the regeneration rate was 55%, and 10 differentiated into clustered buds.
Embodiment 3
[0024] The method is the same as in Example 1, except that the formulation of the induction medium is that 30 g of sucrose, 7 g of agar, 1.5 mg of IAA, 0.5 mg of NAA, and 1 mg of ZT are added to 1 L of MS medium; a total of 100 leaf primordia are inoculated, of which 67 1 directly differentiated into regenerated plants with a regeneration rate of 67%, and 15 differentiated into clustered buds.
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