A kind of tissue culture rapid propagation method of American red maple
A technology of tissue culture rapid propagation and red maple, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve problems such as low germination rate and survival rate, low reproduction coefficient, long reproduction cycle, etc., to achieve The seedling propagation time is short, the cultivation process is simple, and the formula is simple
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Embodiment 1
[0030] A kind of tissue culture rapid propagation method of American red maple described in the present embodiment, comprises the following steps:
[0031] (1) Selection and sterilization of explants: select young branches of American red maple, remove leaves, soak in washing liquid for 5-15 minutes, and then rinse in running water for 20-35 minutes; treated with alcohol for 25-40s, rinsed with sterile water for 2-4 times, then treated with 0.1% mercuric chloride for 4-8 minutes, rinsed with sterile water for 5-7 times, dried, and cut into 1-2cm in length with buds. The stem section is enough;
[0032] (2) Initiate culture: inoculate the explants treated in step (1) into an initiating medium with a pH value of 6.0 and cultivate them for 2-3 weeks to produce axillary buds. The initiating medium consists of MS basic medium , supplemented with 1.0mg / L PVP, 30g / L sucrose, 6g / L agar;
[0033] (3) Proliferation culture: cut out the axillary buds obtained in step (2), inoculate the...
Embodiment 2
[0039]A kind of tissue culture rapid propagation method of American red maple described in the present embodiment, the difference with embodiment 1 is:
[0040] In step (2), the composition of starting medium is: MS basic medium supplemented with 0.1mg / L PVP, 30g / L sucrose, 6g / L agar;
[0041] In step (3), the composition of the proliferation medium is: WPM basic medium, supplemented with 0.01mg / L 6-BA, 30g / L sucrose, 6g / L agar;
[0042] In step (4), the composition of the rooting medium is: 1 / 2 MS basic medium, supplemented with 0.05 mg / L NAA, 20 g / L sucrose, and 6 g / L agar.
[0043] In this example, during the start-up culture process, the first axillary buds were generated for 8 days, and at the end of the start-up culture, the axillary buds elongated by about 2 cm; Certain callus, the time that the first cluster buds generate is 14 days, and when the proliferation culture ends, the cluster bud plant height is 1-4cm, and the multiplication coefficient is 1.7; , the averag...
Embodiment 3
[0045] A kind of tissue culture rapid propagation method of American red maple described in the present embodiment, the difference with embodiment 1 is:
[0046] In step (2), the composition of starting medium is: MS basic medium supplemented with 2.0mg / L PVP, 30g / L sucrose, 6g / L agar;
[0047] In step (3), the composition of the proliferation medium is: WPM basic medium, supplemented with 0.5mg / L 6-BA, 30g / L sucrose, 6g / L agar;
[0048] In step (4), the composition of the rooting medium is: 1 / 2 MS basic medium, supplemented with 0.5 mg / L NAA, 20 g / L sucrose, and 6 g / L agar.
[0049] In this example, during the start-up culture process, the first axillary buds were formed on 9 days, and at the end of the start-up culture, the axillary buds elongated by 1-2 cm; Callus, the time when the first clustered shoots were generated was 14 days, and when the proliferation culture ended, the plant height of the clustered shoots was 1-4cm, and the proliferation coefficient was 2.33; in t...
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