White cherry blossom tissue culture and rapid propagation method
A tissue culture and cherry blossom technology, applied in horticultural methods, botanical equipment and methods, horticulture, etc., can solve the problems of long production cycle and high production cost of tissue culture seedlings, and achieve the advantages of promoting industrial production, increasing the number of inoculations, The effect of reducing the production cost per plant
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Embodiment 1
[0036] White cherry tissue culture and rapid propagation method, it carries out according to the following step order:
[0037] (1) Obtaining of aseptic seedlings of white cherry blossoms:
[0038] Cut off the annual healthy young branches of white cherry blossoms, cut off the petiole and leaves at a distance of 2-3mm from the base of the petiole, and trim the branches into 3-5cm long branches, soak in 2% washing powder for 3-5min, and rinse with running water for 30- 60min, then disinfect with 75% alcohol for 20-30s on the ultra-clean workbench, rinse with sterile water for 1-2 times, then disinfect with 0.05% mercury liter for 8-16min, rinse with sterile water for 6-8 times, and blot dry with filter paper After watering, cut the stem tip or stem section with one or two axillary buds and inoculate them into the culture medium, cultivate them in the dark for 5-7 days, and then transfer them to normal light for cultivation. After 10-12 days, the axillary buds begin to germinate...
Embodiment 2
[0046] Optimization of basic medium for induction and subculture. In order to improve the induction rate and proliferation coefficient of white cherry blossoms, the basic medium for induction culture and subculture was improved and optimized. The specific components of the improved MS mother solution were as follows:
[0047] CaCl 2 2H 2 O 441mg / L; MgSO 4 ·7H 2 O 370mg / L; KNO 3 2022mg / L; NH 4 NO 3 1600mg / L; NaH 2 PO 4 312 mg / L; Na 2 EDTA 37.25mg / L; FeSO 4 ·7H 2 O 27.8mg / L; KI 0.83mg / L; H 3 BO 3 6.2mg / L; MnSO 4 4H 2 O 16.9mg / L; ZnSO 4 ·7H 2 O 11.5mg / L; Na 2 MoO 4 2H 2 O 0.25mg / L; CuSO 4 ·5H 2 O0.03mg / L; CoCl 2 ·6H 2 O 0.03mg / L; inositol 100mg / L; niacin 0.5mg / L; pyridoxic acid hydrochloride 0.5mg / L; thiamine hydrochloride 0.1mg / L; glycine 2mg / L.
[0048] Except that the basic medium for induction and subculture was replaced by the improved MS mother solution, other steps and methods were the same as in Example 1. Using the improved MS as the basic medi...
Embodiment 3
[0050] The screening of the starting medium was based on the improved MS as the basic medium, and L8 (2 7 ) orthogonal design (as shown in Table 1), to screen the effects of different types and concentrations of hormones on the induction rate of white cherry blossoms. Each treatment was inoculated with 20 bottles, and each bottle was inoculated with 3 plants, repeated 3 times. All the other method steps are the same as in Example 1.
[0051] Table 1 Effects of different types and concentrations of hormones on the induction rate of white cherry blossoms
[0052]
[0053] The test results are shown in Table 2:
[0054] Table 2 Effects of different types and concentrations of hormones on the induction rate of white cherry blossoms
[0055]
[0056] It can be seen from the above table that different types and concentrations of hormones are used to induce culture of white cherry blossoms, and the induction rate is different. Among them, GA3 had the most significant inducti...
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