Method suitable for tissue rapid cultivation of Acer rubrum
A red maple and tissue technology, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problem of not yet established the rapid propagation system of American red maple tissue, and achieve fine lateral roots, strong main roots and good seedling growth. Effect
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[0025] Example 1: Primary culture
[0026] 1. The effect of different sterilization time combinations on the growth of explants
[0027] For the initial explants, select young shoots that were born in the same year, remove the leaves, cut the shoots into a single pair of bud stem segments with a length of 1 to 2 cm, soak them in a saturated washing powder aqueous solution for about 20 minutes, rinse them under running water for about 30 minutes, and transfer them to an ultra-clean workbench on. First use 75% alcohol to sterilize for 35, 50, 65 seconds, then use 0.1% mercury to sterilize for 8, 10, 12 minutes (1 to 2 times), then rinse with sterile water 4 times, 2min / time, and finally use The sterile filter paper absorbs the moisture on the surface of the explant. The specific time and frequency of each treatment are shown in Table 1. Inoculate on the culture medium under aseptic conditions, inoculate 10 explants, 1 explant / bottle for each treatment, repeat 3 times, after 10 days...
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[0042] Example 2: Proliferation culture
[0043] After the axillary buds of the stem segment are elongated and have about 3 pairs of leaves, they are cut from the base, the leaves are removed and cut into 1-2cm long stems, and then transferred to the propagation medium. Using WPM as the basic medium and adding 0.65% agar powder, the sterile stem segments were respectively inoculated on the medium (pH=5.8) added with different concentrations of growth regulators and different concentrations of sugar for light culture. The concentration combinations of growth regulators are shown in Table 3, and the sugar concentration combinations are shown in Table 4. Each treatment is inoculated with 15 stem segments and 3 stem segments / bottle. Repeat 3 times. After 30 days of cultivation, observe the germination and growth of axillary buds. Calculate the proliferation coefficient, average plant height, and determine the optimal growth regulator and sugar addition amount for the proliferation me...
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[0057] Example 3: Rooting culture
[0058] Select the sprouts that have been subcultured for more than 3 generations and the height is more than 2cm, cut off, and transferred to the rooting medium. Take WPM as the basic medium, add 0.65% agar powder and 0.1% activated carbon, and inoculate the sterile sprouts on the medium (pH=5.8) with different salt concentration, different growth regulator concentration, and different sugar concentration. Light cultivation. See Table 5 for each salt concentration combination, Table 6 for each growth regulator concentration combination, and Table 7 for each sugar concentration combination. Inoculate 10 stem segments and 2 stem segments / bottle for each treatment. Repeat 3 times. After 60 days of culture, Observe the root germination and growth, and calculate the rooting rate, average root number, average root length and average plant height to determine the best rooting medium.
[0059] Rooting rate (%)=number of roots / number of inoculation×100 ...
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