Commercial-use tissue culture seedling breeding method of American red maple October Glory
A technology of tissue culture and tissue culture seedlings, applied in horticultural methods, botany equipment and methods, applications, etc., can solve the problems of being out of economic feasibility, unable to apply large-scale commercial production, etc., and achieve stable traits and neat seedlings Effect
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Embodiment 1
[0050] (1) selection of explants: selecting the non-lignified tender shoots of 4-year-old seedlings in the spring of natural germination with the age of greenhouse growth, the tender shoots taking materials length is 15cm, with 4 internodes; remove leaves and overlong petioles, sterilize; The disinfection method is as follows:
[0051]Wipe the dust on the surface of the explant with alcohol cotton, then rinse it in 1:3 bleach (commercial bleach: sterile water, volume ratio) for 15 minutes, shake it gently 4 times during this period, and then rinse in sterile water 3 times, let stand for 2 minutes, then use sterile filter paper to absorb the surface water, cut off the dead part of the petiole and the upper and lower incisions of the stem segment, and retain 1 cm at the upper end and 1.5 cm at the lower end;
[0052] (2) Start-up culture: Inoculate the sterilized explants in the start-up medium, and transfer them to the culture room, cultivate at 25°C for 48 hours in dark light,...
Embodiment 2
[0079] (1) selection of explants: selection of growth years is the non-lignified tender shoots of natural germination in spring of 3-year seedlings, and the length of tender shoots is 10cm, with 3 internodes;
[0080] In addition to leaves and long petioles, disinfection; disinfection methods are as follows:
[0081] Disinfection with hydrogen peroxide, the disinfection conditions are: the concentration of hydrogen peroxide is 10%, the disinfection time is 20 minutes, and then the surface water is blotted dry on sterile filter paper;
[0082] (2) Start-up culture: Inoculate the sterilized explants in the start-up medium, and transfer them to the culture room, cultivate at 25°C for 48 hours in dark light, and then give 1500 LUX of light and a light period of 16 / 8 hours for start-up culture After 3 weeks, the dormant axillary buds germinated, and the initiation culture was completed.
[0083] The described start-up medium, with water as a solvent, comprises the following compon...
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