Method for rapidly obtaining virus-free garlic
A garlic, fast technology, applied in the field of rapid acquisition of virus-free garlic, can solve the problems of restricting large-scale production and sustainable and healthy development of garlic, no virus-free research on garlic shoot tip plants, and degeneration of varieties, so as to improve the budding shoot tip. number and bud induction rate, providing economic value, and high survival rate
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Embodiment 1
[0026] Embodiment 1 shoot tip induction culture
[0027] Taking Yundingzao, Ershuizao, Pengxianzao and Wenjiang Hongqixing (referred to as Wenjiang Garlic) as the research objects, the garlic heads were heat-treated at 30°C for 30 days, then the stem tips were peeled off, and the stem tips of 0.1-0.2mm were respectively selected and placed on the stems. In the pointed induction medium, the culture temperature is 25° C., the light intensity is 2000 lx, and the light is 10-12 hours per day for 30-35 days.
[0028] The screening process of Yundingzao shoot tip induction medium:
[0029] (1) The shoot tip induction medium of Yundingzao is based on B5+BA 2-3.5mg / L+KT 0.3-0.6mg / L+NAA0.05-0.15mg / L as the screening basis, in which the BA content is 0.25mg / L The concentration gradient of L was changed, KT was changed according to the concentration gradient of 0.1mg / L, and NAA was changed according to the concentration gradient of 0.025mg / L. Orthogonal experiments were carried out, and...
Embodiment 2
[0041] Embodiment 2 Subculture
[0042] 1. Shoot tip subculture
[0043] The shoot tip culture obtained in Example 1 is subcultured to obtain test-tube plantlets. If the culture medium components and contents are different during the culture process, the shoot tip culture subculture can produce shoots, roots, and callus in an irregular manner, and some only Turn green, or even die, so the composition and content of the subculture medium are very important. The medium is based on MS or B5 medium, and also includes the following components: BA, KT and NAA. Change the content of BA, KT and NAA , screened out the following medium, and calculated its multiplication factor, see Table 2 for details.
[0044]G2(B5+BA 3.5mg / L+KT 0.5mg / L+NAA 0.1mg / L) and G21(MS+KT1mg / L+NAA 0.5mg / L) are suitable for the subculture of Yundingzao; G8(B5+BA 3mg / L+KT0.1mg / L+NAA 0.1mg / L) and G3 (B5+BA 4mg / L+KT0.5mg / L+NAA 0.1mg / L) are suitable for the subculture of Dishuizao; G18 (MS +BA 2mg / L+NAA 0.01mg / L)...
Embodiment 3
[0051] Embodiment 3 induces test tube bulb
[0052] The tissue culture seedling propagation lines obtained by subculture were placed in the bulb induction medium, and the culture temperature was 25°C, the light intensity was 2000lx, and the light was 12h per day and cultivated for 65 days; wherein, the bulb induction medium was MS medium The basal medium also includes the following components: BA 0.5-1.5mg / L, KT0-0.5mg / L and NAA 0.1-1.5mg / L; among them, the content of BA is changed according to the concentration gradient of 0.1mg / L, and the content of KT is changed according to the concentration gradient of 0.05 The concentration gradient of mg / L changes, NAA changes according to the concentration gradient of 0.1mg / L, carries out the orthogonal experiment, draws the bulb induction medium that is beneficial to 4 varieties to be MS+BA 1mg / L+NAA 1.5mg / L and The induction rates of MS+NAA 0.1mg / L+KT 0.5mg / L were 76.5% and 73.9% respectively.
[0053] The bulbs of Ershuizao, Yundin...
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