A strain of Penicillium citricaria with the function of preventing disease and promoting growth and its bacterial agent and application
A technology for Penicillium tangerineum and Penicillium tangerineum is applied in the field of microorganisms to achieve the effects of strong growth-promoting ability, growth promotion and reduction of morbidity rates
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Embodiment 1
[0053] Embodiment 1, the separation method of bacterial strain 44M-3
[0054] Penicillium 44M-3 was isolated from soil samples in Yutong Village, Mianchi County, Sanmenxia City, Henan Province.
[0055] Separation method: dry the soil samples at room temperature, grind and sieve them, weigh 10 g of the ground and sieved soil samples, add 90 mL of sterile water and fully shake to obtain a soil suspension, which is 10 of the soil samples. -1 , and then the soil suspension was shaken, and then the gradient was diluted to 10 -2 , 10 -3 , 10 -4 and 10 -5 , take 100 μL of dilutions of different gradients and spread them on red Bengal medium, invert in a constant temperature incubator at 28°C for 48h, until the colonies grow, pick a single colony and cultivate it on PDA medium for 5d, pick the edge of the colony. The mycelial block was transferred to a new PDA plate, and the transfer was repeated 3 times to obtain a pure culture of the isolate.
Embodiment 2
[0056] Example 2. Inhibitory effect of strain 44M-3 on 14 pathogenic fungi on 5 plants
[0057] Plate co-cultivation method: inoculate the strain 44M-3 on the PDA medium plate for 8-10 days, when 44M-3 produces a large number of conidia, elute the spores with 0.05% (v / v) Tween 80 solution, and prepare the spores Suspension (2×10 7 CFU / mL);
[0058] Coat the PDA plate with 44M-3 spore suspension. After culturing at 28°C for 12h, punch the bacterial cake with a 6mm diameter hole punch and transfer it to a new PDA plate at a symmetrical position of 0.5mm from the edge, in the center of the plate. Inoculated with pathogenic bacteria, the pathogenic bacteria are 6 pathogenic bacteria on sesame seeds, Fusarium oxysporum, Fusarium solani, Helminthosporium soxhlet, Coccidioides bean, Rhizoctonia solani, Corynebacterium multimaster and Coccidioides spp. 4 strains of pathogenic bacteria on tobacco, Conchlea, Phytophthora, Fusarium oxysporum and Alternaria, Rhizoctonia graminearum mol...
Embodiment 3
[0064] Embodiment 3, the preparation of strain 44M-3 high sporopollen
[0065] Inoculate Penicillium citricaria on PDA medium, incubate alternately between light and dark for 5-7 days in a constant temperature incubator at 25°C, 8h light / 16h dark, and wash with 0.05% (v / v) Tween 80 sterile water. Desporulate to form spore suspension; divide PDB into 300mL conical flasks, each bottle is 200mL, and each bottle is connected to 5mL spore suspension, 180r / min, 28 ℃ shaker culture for 4d, as the seed liquid of solid fermentation culture.
[0066] Weigh 1500 g of wheat, soak it in distilled water for 8 hours, remove the water to control it, and divide it into fungal culture bags, 100 g per bag, sterilize at 121°C for 30 minutes. Each bag was inoculated with 10 mL of seed solution, and the seed solution was evenly infiltrated by the wheat, placed in a 30°C dark constant temperature incubator for 7-10 days. When the solid fermentation medium is fully sporulated, the solid fermented pr...
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