Bacillus licheniformis mes816 and its products and applications
A technology of Bacillus licheniformis and MES816, which is applied in the field of microorganisms, can solve the problems that Bacillus licheniformis can be used to prevent and control cotton blight, and achieve the effect of preventing cotton blight, low cost, and promoting production
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Embodiment 1
[0039] The isolation and identification of embodiment 1 bacterial strain
[0040] The soil in Baoding, Hebei Province was serially diluted with sterile water, cultured at 37°C for 12 hours by streaking on the plate, and a single colony was picked to make a slant strain, and refrigerated at 4°C. A single colony was picked, stained with crystal violet, and examined under a microscope. It was identified as Bacillus licheniformis by the strain detection agency of the Ministry of Agriculture.
[0041] After morphological observation, microscopic examination, enzymatic analysis and carbohydrate utilization experiments, combined with 16S rDNA sequencing comparison, it was identified as Bacillus licheniformis and named MES816. Bacillus licheniformis MES816 is a Gram-positive bacterium that can grow under anaerobic conditions. Bacteria are straight rods, arranged singly, in pairs or in short chains. There are spores, the spores are nearly oval, middle-growing, and the sporangia are n...
Embodiment 2
[0046] The preparation of embodiment 2 microbial bacterial agents
[0047] (1) Shake flask culture: the strain activated on the slant was subjected to seed shake flask culture.
[0048] Shake flask medium is: beef extract peptone medium (beef extract 0.5%-3%, peptone 0.5%-3%, yeast extract 0.2%-2%, sodium chloride 0.3-0.5%, medium pH 6.0-7.5 ).
[0049] The culture conditions are: rotation speed 180-230r / min, temperature 32-37°C, culture for 10-12h.
[0050] (2) Primary seed culture: 100mL primary seed culture medium is placed in a 500mL eggplant bottle, sterilized by moist heat at 116°C-121°C for 20-35min, and 1mL live bacteria of Bacillus licheniformis in a freeze-dried tube is used to inoculate the primary seed In culture medium, culture at 30°C-37°C for 10-12h.
[0051] The raw materials and dosage of the medium used for primary seed cultivation are: beef extract 0.5%-3%, peptone 0.5%-3%, yeast extract 0.2%-2%, sodium chloride 0.3-0.5%, nutrient agar 1.5%-2.0 %, the pH...
Embodiment 3
[0059] Example 3 Antagonism test of Bacillus licheniformis MES816 to Rhizoctonia solani
[0060] (1) Source of cotton blight pathogen: The cotton blight was collected from the cotton blight strain in Gaoyang County, Baoding City, Hebei Province. It was isolated and purified by the company's researchers and identified as Rhizoctonia solani Kohn. The determination of pathogenicity showed strong pathogenicity.
[0061] (2) Tablet confrontation experiment:
[0062] First inoculate the cotton blight on the center of the nutrient agar medium plate, then dip a small amount of activated Bacillus licheniformis MES816 and inoculate it at about 2 cm on both sides of the pathogen, and set only the cotton blight inoculated as the blank control. Cultivate at a constant temperature of 30°C. When the blank control is about to cover the entire petri dish, measure the control growth amount (colony radius) and treatment growth amount (inhibition growth radius after inoculation of MES816) of the...
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