Method for preventing and controlling watermelon wilt and special microbial strains thereof
A watermelon fusarium wilt, prevention and control technology, applied in the field of crop disease prevention and control, can solve the problems of large amount of cotton ron and plastic film, difficult to completely eliminate pathogenic bacteria, unfavorable promotion and application, etc., achieves easy operation, continuous inhibition of pathogenic bacteria increase, The effect of reducing pollution
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Embodiment 1
[0032] Example 1 Inhibitory test of melon on mycelia growth of Fusarium wilt of watermelon
[0033] Watermelon Fusarium wilt was inoculated into a PDA plate, cultured at 28-30° C. for 5 days, and punched with a hole punch to obtain mycelial blocks with a diameter of 5 mm for use.
[0034] Inoculate a mycelium block with a diameter of 5 mm in the middle of the PDA plate medium, add 0, 0.2, 0.4, 0.6, 1, 2, 6, and 10 mg / L of cotton wool to the center of the petri dish cover, and mix with sterile water The mass ratio was 1:1 and mixed quickly, and each treatment was repeated 3 times. At the same time, a control group (without adding cotton wool) was set up; then the half of the culture dish inoculated with the mycelium block was buckled upside down on the lid of the culture dish, and sealed with a parafilm. Incubate at a constant temperature of 28°C, and the results after 72 hours are as follows: figure 1 As shown, the colony diameter of the pathogenic bacteria was measured, and...
Embodiment 2
[0037] Embodiment 2 Trichoderma viridans Tv41 is to the growth inhibition test of watermelon Fusarium wilt
[0038] Test method: Inoculate the spores of Trichoderma viride Tv41 and Fusarium wilt of watermelon separately on a PDA plate, culture at a constant temperature at 30°C for 3 days, and obtain fresh mycelium pieces (5 mm in diameter) of each strain, and then inoculate Trichoderma viride and watermelon Fusarium wilt mycelium blocks were inoculated into the same PDA plate (each plate was inoculated with 1 Trichoderma viride mycelium block and 1 watermelon Fusarium wilt mycelium block), with a distance of 5 cm between the two mycelial blocks, placed at 30 °C Cultivate and observe in an incubator, such as figure 2 Shown, wherein, A is the watermelon wilt fungus inoculated separately; B is the growth of watermelon wilt fungus when Trichoderma viride Tv41 and watermelon wilt fungus are inoculated at the same time, the upper part of the B petri dish is the watermelon wilt fung...
Embodiment 3
[0039] Example 3 Preparation of Trichoderma viride Tv41 solid bacterial agent
[0040] a) Activation of strains
[0041] The activation method of bacterial classification preserved on a test tube slope:
[0042] PDA slant medium: put 5ml of PDA medium into the test tube, autoclave at 121°C for 15 minutes, and then set the slope, the height of the slope should not exceed 1 / 3 of the height of the test tube;
[0043] Trichoderma viride Tv41 spores were inoculated into the above-mentioned PDA slant medium for activation, cultured in an environment of 28±2°C for 3-5 days to form a mycelial block, and a 5mm mycelial block was punched with a hole punch for future use.
[0044] b) liquid culture
[0045] Take a Erlenmeyer flask with a capacity of 1L, add 250ml of PDB medium, and then add three pieces of bacteria with a diameter of 5mm, place the Erlenmeyer flask on a shaker at a speed of 160r / min, and cultivate in an environment of 28±2°C for 3 - Reserved after 4 days;
[0046] c)...
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