Application of gliocladium roseum NF-06 and conidia in inhibiting fusarium graminearum perithecium
A technology of Glioma pink and NF-06, applied in the field of microorganisms, can solve problems such as unsatisfactory chemical control and toxin reduction effects, affecting wheat quality and agricultural ecological environment safety, resistance to Fusarium graminearum, etc., to achieve green Effects of Controlling Wheat Scab
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[0023] The invention provides a method for preparing conidia of Glioplasma pink NF-06, comprising the steps of:
[0024] (1) Insert Glioma pink NF-06 into the spore-forming medium, and cultivate to obtain a culture solution containing conidia;
[0025] (2) Filtrate the culture solution containing conidia, centrifuge the filtrate, and take the precipitate to obtain NF-06 conidia.
[0026] In the present invention, the classification of the NF-06 is named Glioma pink, and the Latin name is Clonostachysrosea. The depository unit is the General Microbiology Center (CGMCC) of the China Microbiological Culture Collection Management Committee, and the address is Beichen West, Chaoyang District, Beijing. No. 3, Courtyard No. 1, the preservation date is August 07, 2018, and the preservation number is CGMCCNo.16262.
[0027] In the present invention, the sporulation medium is CMC liquid medium.
[0028] In the present invention, the CMC liquid medium includes the following components ...
Embodiment 1
[0038] In an incubator at 25°C, after Fusarium graminearum overgrows on the carrot culture medium with a diameter of 6cm plastic plate, add sterile 0.1% Tween-20 (Tween-20), and use a sterilized spoon to strain the aerial The hyphae are overwhelmed to make them attach to the surface of the medium, and the results are shown in figure 1 .
[0039] Insert the isolated Gliocladium rosea NF-06 into the CMC sporulation medium, cultivate it for 2 days, filter the filtrate with a sterilized filter cloth, and centrifuge the filtrate at 3000rpm for 4min, and the precipitate is Glioma rosea NF-06. -06 conidia. Prepare the conidia of Glioplasma pink NF-06 with sterile water at a concentration of 1×10 5 cfu / mL of the suspension.
[0040] 10 μL of the obtained NF-06 conidia suspension was sprayed on the culture medium of Fusarium graminearum plate as a treatment group, and those without spraying the NF-06 conidia suspension were used as a control group, with 3 replicates in each group. ...
Embodiment 2
[0047] According to the method of Example 1, the Gliocladium pinkica NF-06 that is isolated is formulated into a concentration of conidia that is 1×10 6 cfu / mL of the suspension.
[0048] Referring to CN110741889A, a method for predicting the richness of the initial infection source of wheat scab in Example 1, preparing corn stalks and selecting the pathogen Fusarium graminearum as the inoculum , prepare a spore suspension of the inoculum strain, and inoculate corn stover. The straw inoculated with Fusarium graminearum was grown in a 25°C incubator for 24 hours, and the NF-06 conidia suspension was mixed with 1×10 6 cfu / mL was sprayed on the corn stalks inoculated with Fusarium graminearum as the treatment group, and the stalks not sprayed with NF-06 conidia suspension were used as the control group, with 3 replicates in each group. The stalks of the treatment group and the control group were placed in the incubator at 25°C for 6-7 days. After the cultivation, the straw was...
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