A strain of Metarhizium anisopliae pathogenic to the Laotian beetle and its application
A technology of Acanthus acanthus and Metarhizium anisopliae, applied in application, fungi, insecticides, etc., can solve the problems of differences in pathogenicity of target pests, and achieve reduced larval populations, strong pathogenicity, and sporulation powerful effect
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Embodiment 1
[0030] Metarhizium anisopliae ( Metarhizium anisopliae ) Morphology of FJMa200902
[0031] Inoculate the isolated and purified Metarhizium anisopliae strains on a flat PPDA medium with a diameter of 90mm and inoculate them by the spot method, and then culture them at 25±1°C. After 4-5 days, pick mycelia to make slices and observe the strains under a microscope. Morphology of hyphae and conidiophores; 10-12 days later, pick mature conidia and make slices to observe the shape and size of conidia. Observe and record the morphological characteristics of the colony for about 15 days. The colony texture of this strain is cotton-wool, and the colony is white at the beginning, and gradually expands, and dark green conidia are produced on it, which are distributed in rings and rays. Mycelia branched, gridded, colorless and smooth, 2.3μm~3.2μm wide, conidiophores solitary or branched, with 2~5 columnar sporulation cells at the top of the branches, on which basal sporozoites are produ...
Embodiment 2
[0034] Metarhizium anisopliae ( Metarhizium anisopliae ) Biological properties of FJMa200902
[0035] Metarhizium anisopliae ( Metarhizium anisopliae ) FJMa200902 was inoculated in the center of the PPDA plate medium, cultured in an incubator at 25±1°C, and the colony diameter was measured once a day by the cross method, and 3 plates (repeated) were set up for each treatment, and observed for 15 days in total. At the same time, record the start time of sporulation. On the 15th day (sporulation is basically over), use a puncher with a diameter of 1.5 cm to punch out a small plate from the center of the colony to the edge 1 / 2, take out the plate and place it in a 30 mL container In a conical flask with 0.3‰ Tween-80 sterile water, shake to fully disperse the spores and dilute them appropriately. Measure the spore concentration with a hemocytometer and convert it into the sporulation per unit area. Three bacterial discs were measured on each plate, and the average value was t...
Embodiment 3
[0040] Metarhizium anisopliae ( Metarhizium anisopliae ) Determination of the pathogenicity of FJMa200902 to the larvae of the Laotian beetle
[0041] A certain amount of 0.03% Tween-80 solution was prepared, then sterilized at high temperature, and cooled for later use. Scrape a certain amount of Metarhizium anisopliae from the PPDA plate ( Metarhizium anisopliae ) FJMa200902 spores were placed in the above solution and prepared into 10 7Spores / mL of spore suspension; immerse healthy Laotian beetle larvae in the spore suspension for 10 seconds, then put them back into the insect culture box and feed them with sterilized sawdust, and inoculate 30 Laotian beetle larvae , repeated 3 times; soaking 0.3‰ Tween-80 sterile aqueous solution as a blank control, and inoculating Metarhizium anisopliae MaZPTR-01 strain (a strain preserved by Fujian Academy of Forestry, a known strain) as a control, the inoculation method was the same as that of Concentrations are the same as above. ...
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