Application of pathogenic fungi, method for preventing and controlling pests and insecticide
A technology of pathogenic fungi and insecticides, applied in the direction of insecticides, applications, biocides, etc., can solve the problems of aphids rampant again, affecting human health, and aphids developing drug resistance
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Embodiment 1
[0031] Embodiment 1, isolation and identification of pathogenic fungi
[0032] (1) Isolation of bacterial strain SGSF001 and bacterial strain SGSF221
[0033]The strains were isolated from the understory litter in Daxing'an Mountains as the source of isolation. Firstly, the collected air-dried litter samples were pulverized into particles, and filtered with a filter screen to obtain particles of litter samples with a particle size of 100-200 μm. Then, using the plate dilution method, the granular sample was mixed with sterile water at a mass ratio of 1:100 to prepare a particle suspension. Then use a pipette gun to draw 50 μL, 100 μL, 150 μL, 200 μL and 250 μL and apply them on the PDA medium plate respectively, spread it with a coating rod until the particles are evenly dispersed, place it at room temperature and observe it every 12 hours. Colonies were picked to PDA plates for purification. Two strains of fungi were obtained after purification and culture, which were numb...
Embodiment 2
[0046] Embodiment 2, the biological characteristics of two strains of pathogenic fungi
[0047] 1. Experimental method
[0048] (1) Determination of strain growth rate and spore production at different temperatures
[0049] Use a hole puncher to punch holes in the colonies of strain SGSF001 and strain SGSF221, and then transfer them to PDA medium, and place them in incubators at 20°C, 25°C, 30°C, and 35°C, respectively, and repeat for each treatment. Three times, the colony growth diameter was regularly measured every day for a total of 14 days. At the end of the measurement experiment, 5 mL of sterilized 1% Tween 80 aqueous solution was added to the plate, the surface spores were scraped off, and after the excess mycelium and agar were filtered out with sterile cotton, the amount of spore production was determined using a hemocytometer.
[0050] (2) Determination of strain growth rate and spore production under different pH
[0051] The colonies of strain SGSF001 and strai...
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