Penicillium xfsf-8 strain for preventing and treating tobacco bacterial wilt and application
A technology of xfsf-8, tobacco bacterial wilt bacteria, applied in the directions of application, fungi, microorganism-based methods, etc., can solve the problems of economic loss, great influence on tobacco yield and quality, high morbidity and lethality, and achieve the effect. Good, good control effect, highly targeted effect
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Embodiment 1
[0032] Example 1 Detection of the resistance of Penicillium xfsf-8 to R. solanacearum
[0033] Pick Penicillium xfsf-8 isolated and purified from the rhizosphere soil of healthy tobacco plants and inoculate it in PDA liquid medium, and culture it on a shaker at 28°C and 180rpm / min for 5 days. Sterilize by filtration through a 0.22 μm filter.
[0034] Pick a single colony of Ralstia solanacearum from the LB plate and inoculate it in LB liquid medium, culture it on a shaker at 37°C and 180 rpm / min for 24 hours, take an appropriate amount of bacterial solution and dilute it to about OD value 0.2, and spread it on the LB plate . Put the sterilized filter paper on the plate, use a pipette to take 10 μl of sterile Penicillium xfsf-8 fermentation liquid and soak it on the filter paper, and observe the inhibition zone after constant temperature cultivation at 28°C for 24 hours.
[0035] The result shows: if figure 1 , there is an obvious inhibition zone around the filter paper, and...
Embodiment 2
[0036] The optimization of embodiment 2 Penicillium xfsf-8 solid fermentation conditions
[0037] (1) Optimum carbon source and culture medium optimization
[0038] Use corn flour, wheat flour, bran, and rice bran as the carbon source, and nutrient soil and vermiculite soil as the culture substrate. Weigh 7.5g of the carbon source and the culture substrate at a ratio of 1:1 and mix them evenly before placing them in a petri dish. , sterilized at 121°C for 20 minutes for later use, and a total of 8 culture media were prepared. Three replicates were set up for each carbon source.
[0039] Take the cultured Penicillium xfsf-8 solid PDA plate, wash the spores with sterile water under the sterile operating table to make a spore suspension, measure the spore content with a hemocytometer, and adjust the concentration to 1.2×10 7 spores / ml of spore suspension.
[0040] Under sterile conditions, add 6ml of the above-mentioned spore suspension to the petri dish, mix well and place it...
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