Application of Isaria javanica in control of coccoiol
A technology of Isyria clavus and scale insects, applied in the fields of application, insecticide, animal repellent, etc., to achieve the effects of no pollution to the environment, easy preparation, and good market application prospects
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Embodiment 1
[0036] Example 1 Isolation of Corynespora javanicus strain IJID003
[0037] A highly pathogenic fungus was obtained from the naturally susceptible Pygmycidae from Bailan in Yuexiu Park, Guangzhou City, Guangdong Province. The method is as follows:
[0038] (1) Separation of fungi
[0039] The hyphae were picked from the susceptible Pseudococcidae, inoculated on the PDA medium and cultured at 27±1℃ for 7 days. The hyphae were picked from the center of the colony, purified and cultured on the PDA medium, and the purification culture was repeated 3 times, and placed in a refrigerator at 4°C for later use.
[0040] (2) Fungus tieback experiment
[0041] Cultivate the isolated fungi on a PDA plate for 7-15 days. After the bacteria are formed, add 0.02% Tween-80 sterile water to wash the spores, stir for 15 minutes on a magnetic stirrer, and adjust the spore concentration to 1 with a hemocytometer. ×10 7 The spore suspension was prepared with a small hand sprayer, and sprayed evenly on the ...
Embodiment 2
[0044] Example 2 Screening of Corynespora javanicus strain IJID003
[0045] Entomopathogenic fungi have diversity in genetics, ecology, and biology. Among them, different strains of fungi show significant differences in their pathogenicity to target pests. The selection and acquisition of high-yield and high-quality strains is the primary prerequisite for achieving better control effects. The selection of excellent strains mainly considers three indicators, namely, spore production, colony growth rate, and pathogenicity. The present invention uses these three indicators as the main basis to screen excellent highly pathogenic strains.
[0046] (1) Material preparation
[0047] Purified IJID001, IJID002, IJID003, IJID004, IJID005, IJID006, IJID007, IJID008, 8 isolates, were cultured on a PDA plate in a constant temperature incubator at 27±1°C.
[0048] (2) Test insects and host plants
[0049] The Egyptian Pseudococcidae comes from the successive breeding population on the greenhouse w...
Embodiment 3
[0064] Example 3 Identification of strain IJID003
[0065] (1) Morphological characteristics of strain IJID003
[0066] Inoculate the strain IJID003 into the center of the PDA medium plate, place it at 27±1℃ for constant temperature culture, observe the growth of the colony every day and record the colony color and shape. Inoculate the strain IJID003 into the center of another PDA medium plate, and at the same time insert the sterilized cover glass (1cm×1cm) obliquely into the medium about 1cm away from the inoculation point, and place it at 27±1℃ for 5 days. Allow the hyphae to extend to the cover glass, take out the cover glass and place it under an optical microscope to observe the hypha and spore morphology.
[0067] Morphological characteristics of strain IJID003 ( figure 1 with figure 2 ): On the PDA plate, the colonies are round, with a diameter between 49mm and 55mm, with concentric ring patterns, and a ravine is formed on the medium, and the texture is thick and fluffy. T...
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