Entomopathogenic fungus as well as screening method and application thereof
A technology of pathogenic fungi and screening methods, which is applied in the field of entomopathogenic fungi and their screening, can solve problems such as the impact of control effects and the reduction of spore production, and achieve the effects of good pest control, large spore production, and avoidance of adverse effects
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Embodiment 1
[0030] Example 1. Isolation and identification of entomopathogenic fungi
[0031] (1) Isolation of strain SGSF125
[0032] The strains were isolated from the under-forest litter of Changbai Mountain. First, the collected air-dried litter samples were pulverized to a granular shape, and filtered with a filter screen to obtain particles with a particle size of 100-200 μm in the litter samples. Then use the plate dilution method to mix the granular sample with sterile water in a mass ratio of 1:100 to prepare a granular suspension. Then use a pipette gun to draw 50 μL, 100 μL, 150 μL, 200 μL and 250 μL respectively and spread them on the PDA medium plate, spread them with a coating rod until the particles are evenly dispersed, and place them at room temperature. out, the colonies were picked to PDA plates for purification. After purification and culture, a fungus was obtained, which was numbered SGSF125.
[0033] (2) Isolation of strain SGSF355
[0034] The strains were isol...
Embodiment 2
[0045] Embodiment 2, the biological characteristic of novel metarhizium anisopliae
[0046] 1. Test method
[0047] (1) Determination of strain growth rate and spore production at different temperatures
[0048] Punch holes in the colonies of strain SGSF125 and strain SGSF355 with a hole puncher, then transfer them to PDA medium, and place them in incubators at 20°C, 25°C, and 30°C, respectively. Each treatment was repeated three times, and every day The colony growth diameter was measured regularly 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.
[0049] (2) Determination of strain growth rate and spore production under different pH
[0050] Holes were punched on the colonies of strain SGSF125 and strain...
Embodiment 3
[0068] Embodiment 3, Metarhizium anisopliae insect-resistant activity assay
[0069] (1) Test method
[0070] First prepare the spore suspension, inoculate the strain on the PDA medium and cultivate for 14 days, add 5 mL of sterilized 0.05% Tween 80 aqueous solution on the plate, and scrape the surface spores. After filtering out excess mycelium and agar with sterilized cotton, use a hemocytometer to count and adjust the spore suspension to a final concentration of 1×10 8 spores / mL.
[0071] Soak the two-spotted firefly beetle (adult) in 1×10 8 spores / mL concentration of spore suspension for 5s, and then transferred to a Erlenmeyer flask filled with corn kernels for observation, and each treatment was inoculated with 35 adults. Soak mung bean weevil (adult) in 1×10 8 spores / mL concentration of spore suspension for 5 s, and then transferred to a Erlenmeyer flask containing mung beans with a brush for observation, and 20 adults were inoculated for each treatment. Use a brus...
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