A kind of fast propagation method of bellflower tissue culture
A technique for cultivating bellflower and tissue culture, which is applied in horticultural methods, botanical equipment and methods, plant regeneration, etc., can solve the problems that seedling propagation is limited by seasonality and is not ideal, and can improve the quality of seedlings and the reproduction coefficient. Effect
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Embodiment 1
[0025] (1) Selection and disinfection of explants: take the seeds of P. chinensis as explants, sterilize in 100 ml of 30% 84 disinfectant with 2-3 drops of Tween Tween20 added for 5-8min, rinse with sterile water 3-5 times, finally remove the surface moisture with sterilized filter paper to obtain explants, wherein the sterile water is distilled water sterilized by high pressure;
[0026] (2) Germination of explants to obtain sterile test-tube plantlets: Inoculate the explants obtained in step (1) into the basic medium, at a culture temperature of 23-27°C, with a light intensity of 1500 lux, and a light time of 8-10h / d Cultivate under the conditions of 30d to obtain aseptic test-tube plantlets, wherein basic medium is the agar that added 0.5mg / L gibberellin GA3, 2.0g / L activated carbon AC, 30g / L sucrose and 5g / L in MS medium , the pH value of the culture medium is 5.8;
[0027] (3) Test-tube plantlet clustering bud rapid propagation culture: the aseptic test-tube plantlet obt...
Embodiment 2
[0032] Different from Example 1, when the test-tube plantlets in the step (3) are rapidly propagated and cultivated in clusters, the propagation medium used is that 6-benzyl adenine 6-BA, 0.5 mg / L has been added in the WPM medium. 0.2mg / L kinetin KT, 0.5mg / L indole butyric acid IBA, 30g / L sucrose and 5g / L agar, the pH value of the medium is 5.8. Other steps are the same as in Example 1.
Embodiment 3
[0034] Different from Example 1, when the test-tube plantlets in the step (3) were rapidly propagated and cultivated in clusters of shoots, the propagation medium used was that 2.0mg / L of 6-benzyl adenine 6-BA, 0.5mg / L kinetin KT, 0.2mg / L indole butyric acid IBA, 30g / L sucrose and 5g / L agar, the pH value of the medium is 5.8. Other steps are the same as in Example 1.
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