Method for rapid propagation and cultivation of carnation seedling by tissue culture
A technology of carnation group and cultivation method, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems that do not systematically involve the one-time seedling technology of the outer stem section of carnation bottle, complex cultivation procedures, and rooting coefficient. It can reduce the number of transplanting seedlings, simplify the cultivation procedure, and achieve the effect of good quality.
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Embodiment 1
[0021] A, material collection and sterilization: select a single plant with normal flower type, pure flower color, straight branches, no damage by diseases and insect pests, and full plant shape among the plants that have bloomed, and take the vegetative buds that are strong at the base and have not undergone flower bud differentiation as explants, Peel off the leaves at 2cm from the top buds of the branches, leave 2-3 pairs of new leaves and cut off 1.5cm, wash with washing powder, treat with 0.15% mercuric chloride for 20 minutes, and then treat with 2% sodium hypochlorite for 20 minutes , rinsed twice with sterile water, and cut the explants into sections;
[0022] B. Induction culture: Inoculate the explant sections obtained in step A into the following induction medium, namely: 6-benzylaminopurine + 0.1mg / L naphthaleneacetic acid + 30000mg / L MS+1.0mg / L Sucrose+7000mg / L agar, under the culture conditions of temperature 25±2℃, light time 10 hours / day, and light intensity 15...
Embodiment 2
[0026]A, material collection and sterilization: select a single plant with normal flower type, pure flower color, straight branches, no damage by diseases and insect pests, and full plant shape among the plants that have bloomed, and take the vegetative buds that are strong at the base and have not undergone flower bud differentiation as explants, Peel off the leaves at 2cm from the top buds of the branches, leave 2-3 pairs of new leaves and cut off 1.5cm, wash with washing powder, treat with 0.15% mercuric chloride for 20 minutes, and then treat with 2% sodium hypochlorite for 20 minutes , rinsed twice with sterile water, and cut the explants into sections;
[0027] B. Induction culture: Inoculate the explant sections obtained in step A into the following induction medium, namely: MS+1.5mg / L of 6-benzylaminopurine+0.5mg / L of naphthaleneacetic acid+30000mg / L of Sucrose+7000mg / L agar, under the culture conditions of temperature 25±2℃, light time 12 hours / day, and light intensit...
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