A method for vegetative propagation of dormant buds of Acer japonica
A technology of dormant buds and white maple, applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems of no regeneration plant formation, lack of research, low induction rate, etc., to improve breeding efficiency and popularize Good performance and high efficiency
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example 1
[0019] Example 1 The germination and multiplication of dormant buds of Acer japonica
[0020] In the early spring, in the Heilongjiang Forest Botanical Garden, the budded branches of the maple in the dormant period were selected, and the branches were cut into about 3.0cm budded stems, rinsed with running water for 10 minutes, and then disinfected in the ultra-clean workbench as follows: Soak in 75% alcohol for 5 minutes, soak in 5% sodium hypochlorite for 12 minutes, rinse with sterilized water for 5 times, and finally dry the surface moisture on sterile filter paper. The sterilized buds were peeled off the bud scales in the ultra-clean bench, and the cut buds were inoculated under the following culture conditions: containing 20g / L sucrose and 7.47g / L agar plant gel, and different plant growth regulators (BA, NAA 、GA 3 , KT, TDZ, IBA, ZT) cultured in DKW medium, and cultured under light. It was found that dormant buds began to germinate within 1 week, adventitious buds bega...
example 2
[0024] Example 2 Proliferation of Adventitious Buds of Acer japonica
[0025] The adventitious buds that example 1 obtains are cut into 2.0cm length, inoculate under following conditions: contain 20g / L sugar and 7.47g / L agar plant gel, and plant growth regulator (NAA, GA 3 , ZT, BA, TDZ) in the DKW medium for proliferation culture, and cultured under light. The proliferation of adventitious buds after 4 weeks of cultivation, the statistical results are shown in Table 2. The results showed: in the culture condition DKW+0.03mg / L TDZ+0.01 mg / L NAA+0.5mg / L GA 3 Under the above conditions, the induction rate of adventitious buds was the highest and the number of induced adventitious buds was more, 88.9% and 7.5, respectively, and the growth state of the seedlings was the best. Finally, this condition was determined to be the most suitable culture condition for adventitious bud proliferation.
[0026] The effect of table 2 plant growth regulators on the proliferation of adventitio...
example 3
[0028] Example 3 Adventitious shoots take root
[0029] Cut the tender adventitious buds obtained in Example 2, the length is 2.0cm, inoculate into the 1 / 2DKW medium containing IAA, IBA, NAA, 20g / L sucrose, 0.1% gac, 7.47g / L agar to induce rooting, form regeneration whole plant. After 3 weeks of cultivation, the statistical test results showed that as shown in Table 3, the rooting rate of 1 / 2DKW+0.1% activated carbon+0.5mg / L IBA+1.0mg / L IAA was higher, 50%, and the average rooting number was 4.
[0030] The influence of table 3 auxin plant growth regulator on rooting
[0031]
[0032] Note: "-" means no root build
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