Microbial preparation for treating excrement, preparation method thereof and application
A microbial preparation and microbial technology, applied in the field of animal husbandry, can solve the problems of large production volume and difficult treatment, and achieve the effect of solving technical problems and solving heavy pollution control
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Embodiment 1
[0031] Embodiment 1: the enrichment of high-efficiency microbial preparation
[0032] Basic liquid medium (W / V) contains 1.0% rice bran, 1.0% rapeseed meal, 2.0% fish meal, 0.5% rice straw; weigh 0.1g indole and skatole (3-methylindole), dissolve in 1mL anhydrous Add 100 μL (0.1%, V / V) acetic acid, propionic acid, n-butyric acid, isobutyric acid, n-valeric acid, isovaleric acid and 100 μL (0.01% , W / V) indole, skatole (3-methylindole). In order to mix well, indole and skatole can be dissolved in absolute ethanol first, and then added to the medium. Adjust the pH to 6.0, and sterilize with high pressure steam at 121°C for 20 minutes.
[0033] Weigh 0.1g of composted cow dung, inoculate it in the above liquid medium, inoculum size 0.1% (W / V), 30°C, 200r min -1 Shaking table culture; continuous culture for 48 hours, the collected bacterial liquid is used as seed culture liquid for solid enrichment and scale-up cultivation.
Embodiment 2
[0034] Embodiment 2: the expansion cultivation of high-efficiency microbial preparation (1 kilogram)
[0035] The solid culture substrate contains (W / W) 38.0% rice bran, 10.0% rape meal, 10.0% fish meal, 14.0% straw, 3.0% cow dung, and the rest is water. Put the prepared medium in a large glass beaker, cover it with aluminum foil, put it in a sterilizer, and sterilize it by high-pressure steam at 121°C for 20 minutes;
[0036] Get 50g of the seed culture solution enriched in Example 1, insert it into the above-mentioned solid culture medium cooled to room temperature after sterilization, the inoculum size is 5.0% (W / W), and add 0.1% ( V / V) acetic acid, propionic acid, n-butyric acid, isobutyric acid, n-valeric acid, isovaleric acid and 0.02% (W / V) of indole and skatole. In order to mix well, indole and skatole can be dissolved in absolute ethanol first, and then added to the medium. After fully mixing evenly, put the mixture into a 1kg breathing bag, seal it, put it in a con...
Embodiment 3
[0038] Embodiment 3: the expansion cultivation of high-efficiency microbial preparation (10 kilograms)
[0039]First prepare solid culture medium 1kg, the formula of 1kg medium is as follows (W / W): 38.0% rice bran, 10.0% rape meal, 10.0% fishmeal, 14.0% rice straw, 3.0% cow dung, all the other are moisture, culture medium is put in large in a non-woven bag, placed in a steel tray, placed in a sterilizer, and sterilized by high-pressure steam at 121°C for 20 minutes;
[0040] Get 500g of the solid culture after expansion in Example 2, insert it into the above-mentioned solid culture medium, inoculum size 5.0% (W / W), mix evenly, pack into a 10kg breathing bag, and add 0.1 to the above-mentioned mixture respectively % (V / V) of acetic acid, propionic acid, n-butyric acid, isobutyric acid, n-valeric acid, isovaleric acid and 0.01% (W / V) of indole and skatole. In order to mix well, indole and skatole can be dissolved in absolute ethanol first, and then added to the medium. Seal th...
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