Preparation method of composite beer syrup
A syrup and beer technology, which is applied in the field of compound beer syrup preparation, can solve the problems of low polymer protein content, low fermentable syrup, and low syrup quality, and achieve the effects of reasonable components, simple preparation steps, and increased fermentation degree
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example 1
[0018] First, in parts by weight, 25 parts of peptone, 26 parts of yeast extract, 16 parts of sodium carboxymethylcellulose, 3 parts of ammonium sulfate solution with a mass fraction of 5%, 0.4 part of potassium dihydrogen phosphate and 0.8 part of hydrogen phosphate Dipotassium, stirred evenly, and placed in ultraviolet sterilization to obtain screening medium; according to the volume ratio of 1:2, take biogas slurry and distilled water, stir evenly, and filter, collect the filtrate, and then put the filtrate into a centrifuge , centrifuge at 5000r / min for 8min, collect the supernatant, inoculate the supernatant into the above-mentioned screening medium according to the inoculum size of 25%, and move the medium to a constant temperature incubator, set the temperature at 36°C, Cultivate for 23 hours; after the above-mentioned cultivation ends, use sterile water to rinse the surface of the culture medium until there is no hyphae on the surface, collect the eluate, and use a syri...
example 2
[0021]First, in parts by weight, 23 parts of peptone, 22 parts of yeast extract, 12 parts of sodium carboxymethylcellulose, 3 parts of ammonium sulfate solution with a mass fraction of 5%, 0.4 part of potassium dihydrogen phosphate and 0.8 part of hydrogen phosphate Dipotassium, stirred evenly, and placed in ultraviolet sterilization to obtain screening medium; according to the volume ratio of 1:2, take biogas slurry and distilled water, stir evenly, and filter, collect the filtrate, and then put the filtrate into a centrifuge , centrifuge at 5000r / min for 5min, collect the supernatant, inoculate the supernatant into the above-mentioned screening medium according to the inoculum size of 20%, and move the medium to a constant temperature incubator, set the temperature at 28°C, Cultivate for 22 hours; after the above-mentioned cultivation ends, use sterile water to rinse the surface of the culture medium until there is no hyphae on the surface, collect the eluent, and use a syrin...
example 3
[0024] First, in parts by weight, 24 parts of peptone, 25 parts of yeast extract, 13 parts of sodium carboxymethylcellulose, 2 parts of ammonium sulfate solution with a mass fraction of 5%, 0.3 part of potassium dihydrogen phosphate and 0.7 part of hydrogen phosphate Dipotassium, stirred evenly, and placed in ultraviolet sterilization to obtain screening medium; according to the volume ratio of 1:2, take biogas slurry and distilled water, stir evenly, and filter, collect the filtrate, and then put the filtrate into a centrifuge , centrifuge at 5000r / min for 6min, collect the supernatant, inoculate the supernatant into the above-mentioned screening medium according to the inoculum size of 21%, and move the medium to a constant temperature incubator, set the temperature to 30°C, Cultivate for 23 hours; after the above-mentioned cultivation ends, use sterile water to rinse the surface of the culture medium until there is no hyphae on the surface, collect the eluate, and use a syri...
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