Isaria fumosorosea oil suspending agent and preparation method as well as application thereof
A technology of I. fumigatus and oil suspending agent, which is applied in the direction of botanical equipment and methods, applications, insecticides, etc., can solve the problems of poor quick-acting performance and unstable effect, and achieve the effect of no residue in the environment
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Embodiment 1
[0030] The strain of I. fumigatus used in this example is derived from the house termite Coptotermes formosanus PFCF-O strain PFCF-O isolated from Shiraki-infected worms (see "Biological Characteristics of I. rosea and Its Correlation with Pathogenicity to Plutella xylostella", Acta Plant Protection Volume 37, Issue 3, June 2010, Lei Yanyuan et al.), the Insect Ecology Room of South China Agricultural University stored the strain on a PDA slant in a -80°C refrigerator. The strain grows rapidly on the PDA medium. At 25°C, the colony is long and villous, and after forming spores, it is flesh red, powdery, colorless on the back, and the pink spore bundles are solitary or aggregated into spore bundles. , the wall is smooth, transparent, mostly composed of whorled branches with 4 to 6 phialides forming whorls. The base of the bottle stem is spherical, or nearly elliptical, and the upper part is slender. The conidia are cylindrical to fusiform, smooth, transparent to light red, wi...
Embodiment 2
[0033]Transfer the commercially purchased I. fumigatus (for example, Shanghai Fuzhong Biotechnology Development Co., Ltd. or Guangzhou Institute of Microbiology) to the PDA plate, and then place it in an incubator (25 ℃, 12L:12D) for 7 days, after spore production, add rapeseed oil or plant blended oil containing 0.03% Tween 80 by mass percentage on the plate, gently scrape the spores on the plate with an inoculation needle, and the prepared Pour the bacterial solution into a beaker and stir with a magnetic stirrer for 30 minutes. After the spores are completely dispersed, drop the spore suspension onto a hemocytometer and observe with a microscope to ensure that the spore content is 1 to 10 billion / mL. If it is lower than this content, continue to add spore powder, if it is higher than this content, dilute it with the same kind of vegetable oil, observe the hemocytometer through a microscope, and make the spore content 1 to 10 billion / mL.
Embodiment 3
[0035] 1. Weigh 10.0g of 1 billion pieces / g of I. fumigatus spore suspension, peanut oil 5.0g, castor oil polyoxyethylene ether 3.0g, fatty alcohol polyoxyethylene ether 2.0, alkylphenol formaldehyde resin polyoxyethylene Vinyl ether sulfate 1.0g, epoxy linseed oil 2.0, dispersant NNO and ethylene glycol 4.0g, white mineral oil to make up to 100%, put into the grinder together, cool with water during the grinding process, the temperature should not exceed 40 ℃, 3000 revs / min and grind for 30 minutes to prepare a 10% mass percent concentration of I. fumigatus oil suspension concentrate.
[0036] 2. Indoor activity determination experiment of 10% I. fumigatus oil suspension concentrate
[0037] Test object: Pieris rapae, a sensitive strain raised indoors;
[0038] Reagent for testing: 10% Ifusaria rosea oil suspension, 10% Ifusia rosea suspension;
[0039] Conditions: Temperature: 25°C, Humidity: RH70%, Light: L:D=12:12
[0040] Test method: Accurately weigh the test agent ...
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