Metarhizium anisopliae IPPMHBC-009 and application thereof
A technology of scarab metarhizium anisopliae and locust, applied in the direction of application, fungi, biocides, etc., can solve the problems of fungal knockdown and slow action of killing pests, and achieve the effect of good application prospects
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Embodiment 1
[0031] Example 1 Screening of Metarhizium anisopliae IPPMHBC-009
[0032] Metarhizium anisopliae strains were lured from the collected soil by the method of trapping Mellonella mellonella. Put the sterilized waste film boxes into the soil samples to be tested, and bury one wax moth in each box, and repeat 3 times. The soil sample box is placed at 24-27°C, after moisturizing and trapping for 1 week, the dead insects are sorted out, cultured at a constant temperature of 25-26°C and relative humidity of 100 for 7-10 days, and the target strain is isolated from the dead insects, which is used for strain isolation The culture medium is PDAY.
[0033] Inoculate the isolated Metarhizium anisopliae on the PDAY solid medium, cultivate until spore production, suspend the spore powder with 0.1% Tween water, oscillate evenly with a vortex oscillator, and adjust the spore concentration to 1×10 8 individual / mL. Take 1 mL of the spore suspension and inoculate 100 mL of mycelia-producing m...
Embodiment 2
[0034] Example 2. Bioassay of the pathogenicity of Metarhizium anisopliae Cang 09 to the nymph Crypterus pubescens
[0035] The virulence effects of the above nine Metarhizium anisopliae strains on locusts were determined by stomach poisoning method.
[0036] First weigh 0.2g of Metarhizium anisopliae spore powder and add it to 2.0g of wheat bran, then add 0.1ml of edible oil, and stir well. Then weigh 0.2g of the prepared Metarhizium anisopliae wheat bran bait and put it into a petri dish, put it into a glass-covered insect rearing basket together with the petri dish, number them, and then put 20 of the same size into the insect rearing basket. 3rd instar hairy-legged locust gnat. No Metarhizium anisopliae spore powder was added to the wheat bran bait of the blank control group. In this experiment, there were 9 kinds of spore powders of Metarhizium anisopliae and one control CK. Each spore powder was set up for 3 repetitions and raised in the insect culture room. The bait ...
Embodiment 3
[0044] Embodiment 3. Metarhizium anisopliae is to the bioassay of the pathogenicity of Asian locust
[0045] Determination of 9 bacterial strains is to the curative power of Asian carcus, and assay method is the same as the method for embodiment 2.
[0046] The bioassay results of the pathogenicity of 9 strains of Metarhizium anisopliae to P. figure 2 ,Table 2.
[0047] Table 2 Comparison of the pathogenicity of 9 strains of Metarhizium anisopliae to P.
[0048]
[0049] From the analysis in Table 2, it can be seen that the tested strains are all pathogenic to locust gnats, the half-lethal time is between 3.55d and 10.67d, and the cadaveric rate is between 38.33% and 93.33%. The lethal time was 3.55 days, and the zombie rate was 93.33%. Therefore, there are significant differences between the Metarhizium anisopliae strain IPPMHBC-009 and the Metarhizium anisopliae strains IPPM803 and IPPM200614, indicating that the strain IPPMHBC-009 has higher pathogenicity to P.
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