A kind of artificial pathogenic method of in vitro inoculation of tobacco blight
A technology for blight and tobacco, applied in the field of agricultural technology and biology, to achieve the effect of good reproducibility, less space occupation and simple equipment
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Embodiment 1
[0033] An artificial pathogenic method of in vitro inoculation of tobacco blight, inoculating tobacco blight bacterial strain Rs-1 on the in vitro leaves of tobacco seedling variety Yunyan 87, operates according to the following steps:
[0034] 1. Preparation of main equipment: Use a common petri dish with a diameter of 15cm as the equipment for inoculation, clean and disinfect it for later use.
[0035] 2. Cultivation of tobacco seedlings: Cultivate the tobacco seedling variety Yunyan 87 according to the conventional method, and manage the conventional water and fertilizer until the length of the leaves of the tobacco seedlings is consistent with the diameter of the petri dish in step 1 (the length of the leaves is about 14cm), and then it can be used.
[0036] 3. Preparation of inoculated mycelium: transplant the strain Rs-1 to the center of the PSA medium plate. The components of the PSA medium are: 200 grams of potatoes, 20 grams of sucrose, 18 grams of agar, and 1000 mL of...
Embodiment 2
[0043] An artificial pathogenesis method for in vitro inoculation of tobacco blight, inoculating tobacco solanum blight strain Rs-1 on the in vitro leaves of tobacco seedling variety Yunyan 87, the operation steps are carried out according to step 1 to step 7 of embodiment 1, wherein The operation in step 7 is different from the operation in step 7 of Example 1. In step 7 of Example 1, the culture temperature after inoculation is maintained at 25-27 ° C, and in step 7 of this embodiment) the culture temperature after inoculation is maintained at 19 ~ 21°C. The results also showed as Figure 3 ~ Figure 5 The same clear leaf necrosis symptoms, but the lesion enlargement rate is slower than the speed of embodiment 1, and the necrotic lesion diameter is 1.7cm in 72 hours after inoculation.
Embodiment 3
[0045] Adopt a kind of artificial pathogenesis method of in vitro inoculation of tobacco blight of the present invention, inoculate tobacco blight bacilli strain Rs-1 on the in vitro leaves of tobacco seedling variety Yunyan 87, the operation steps are according to step 1) to step 7 of embodiment 1 ) operation implementation, wherein the operation in step 3) is different from the operation in step 3) of Example 1, the cultivation time of the inoculum hyphae in step 3) of Example 1 is 48 hours, and the step 3) inoculation of this example The culture time of somatic mycelium is 96 hours. The results also showed as Figure 3 ~ Figure 5 The same clear leaf necrosis symptoms, but the lesion enlargement rate is slower than the speed of embodiment 1, and the necrotic lesion diameter is 1.9cm in 72 hours after inoculation.
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