Bacillus amyloliquefaciens and application thereof
A technology for dissolving starch spores and bacilli, applied in the application, bacteria, fungicides and other directions, can solve the problems of residual edible fungus fruiting bodies, pollute the environment, unsatisfactory effects, etc., and achieve good development prospects and remarkable effects.
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Embodiment 1
[0040] Embodiment 1, the acquisition of Bacillus amyloliquefaciens B43-1
[0041]1. Collection of samples: The whole process of sampling is aseptic. In the mixing room, bottling operation room, sterilization room, cooling room, inoculation room (original seed and cultivation bottle), washing room, culture room (original seed and cultivation bottle), scratching room, breeding room, packaging room, Take points in the five orientations of the east, south, west, north, and center of the bottle digging room and cooling room, and repeat each point three times. Pour about 30ml of NA medium (beef extract 3g, peptone 10g, sodium chloride 5g, agar 20g, adjust pH to 7.0-7.2, water 1000ml, sterilize at 121°C for 20min) and place it at these sampling points for 30min, cover Cover the plate, seal it, and place it in an incubator at 28°C for 3 days.
[0042] 2. Isolation of bacteria: Carefully pick out the bacteria with an inoculation needle, streak and purify them, and culture them in a ...
Embodiment 2
[0059] Embodiment two, the preparation of Bacillus amyloliquefaciens B43-1 fermentation metabolic liquid, concrete process is as follows:
[0060] 1. Preparation of Bacillus amyloliquefaciens B43-1 seed solution: After activation, Bacillus amyloliquefaciens B43-1 strains stored in a 4°C refrigerator were inoculated in NB liquid medium (3g of beef extract, 10g of peptone, 5g of sodium chloride , adjusted to pH 7.0-7.2, 1000ml of water, sterilized at 121°C for 20min), cultured with shaking at 150rpm / min for 12h at 28°C, as the seed solution.
[0061] 2. Obtaining the fermentation and metabolism liquid of Bacillus amyloliquefaciens B43-1: inoculate the above seed liquid into NB liquid culture medium at an inoculum amount of 2%, and shake and culture at 28°C and 150 rpm / min for 48 hours to obtain a fermentation liquid. Centrifuge at 10000rpm / min for 10min, take the fermentation supernatant, filter it with a 0.2μm microporous membrane, and store it at -20°C for later use.
Embodiment 3
[0062] Embodiment three, fermented liquid (embodiment two) are to the inhibitory effect of edible fungus pathogenic bacteria:
[0063] The antagonistic activity of the fermentation supernatant was detected by agar diffusion method. Inoculate the above four kinds of edible fungus pathogenic bacteria in the center of the PDA medium plate respectively, culture at 25°C for a period of time, punch 4 holes evenly around the pathogenic bacteria with a hole diameter of 6mm, and number the 4 holes, Well 1: CK without adding any substance, well 3: add 100 μl NB medium, well 2 and well 4, add 100 μl B43-1 filter-sterilized fermentation supernatant to each well, incubate at 25°C for a period of time, and observe the pH value. Bacteria. The result is as image 3 shown.
[0064] It can be seen from the figure that the fermentation supernatant of Bacillus amyloliquefaciens B43-1 can effectively inhibit edible fungus diseases caused by various pathogenic fungi such as Cladophyllum heteromo...
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