Botryosphaeria botryoides HN17496 strain, biocontrol inoculant and preparation method and application of biocontrol inoculant
A technology of HN17496, a bio-control agent, applied in the field of bio-control, can solve the problems such as being unsuitable for the bio-control of Helminthium umbilicalus, environmental hazards, etc., and achieve significant bio-control effects, good bio-control effects, and no bio-control effects. The effect of security risks
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[0035] The present invention also provides the preparation method of the above-mentioned biocontrol agent, comprising the following steps:
[0036] The above-mentioned HN17496 strain is inoculated into a PDA medium, and cultured for 5-7 days to obtain the biocontrol agent.
[0037] In the present invention, the temperature of the culture is preferably 25 to 28°C.
[0038] In the present invention, when the biocontrol agent does not contain HN17496 strain, after culturing for 5-7 days, sterilization treatment is preferably included; the sterilization treatment method preferably includes: sterilization at 121° C. for 30 minutes.
[0039] The present invention also provides the application of the above HN17496 strain or the above biocontrol fungicide or the biocontrol fungicide prepared by the above preparation method in preventing and treating plant diseases, wherein the pathogenic bacteria of the plant diseases include Helminthosporium rhizogenes. In the present invention, the...
Embodiment 1
[0042] From the soil under the weeds in Thrushi Valley, Lushan County, Pingdingshan, the HN17496 strain of Staphylococcus aureus was obtained by the dilution plate method. The specific method is as follows:
[0043] Weigh 10 g of soil, add it to a conical flask containing 90 mL of sterilized water, place the conical flask on a shaker at 120 rpm, and shake for 25 min to make soil particles evenly dispersed in distilled water to obtain a soil suspension with a dilution factor of 10; Draw 1 mL of the suspension and put it into a test tube containing 9 mL of sterilized water to obtain a suspension with a dilution factor of 100;
[0044] The WA medium was sterilized at high temperature and cooled to 45°C, added streptomycin 30 μg / mL, 4 drops of chloramphenicol, poured into a petri dish to solidify and cooled down, and the obtained soil suspension with a dilution factor of 100 was fully shaken. Aspirate 1 mL, drop 5 drops into each petri dish, spread it evenly with a sterilized curv...
Embodiment 2
[0054] Identification of rescreened strains
[0055] The HN17496 bacterial strain of the rescreening of Example 1 was inoculated on the PDA medium, cultivated for 7d at 25°C, to obtain a bacterium colony with a diameter of 2.2cm, and the morphological characteristics of the bacterium colony were as follows:
[0056] Colonies are black, sporogenous stems growing on medium, viscous, covered with gray to black sporozoites, dark brown on the back of the petri dish. No ascus. The hyphae will produce dark brown secretions, like impurities, often in bundles, forming hyphal bridges. Conidia giant linear, solitary or aggregated growth, thin-walled, branched or unbranched, erect or slightly curved, 1 to 2 septa, smooth, conidiophores 18.2 to 64.0 μm long, meristematic The width of sporophore is 2.8~4.9μm, and 1~6 sporogenous cells are attached to the top. The sporogenous cells are phialoid, cudgel-like or cudgel-like, transparent, translucent or dark black, with a smooth surface, 6.6...
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