Method of preparing fermented coffee by using intestinal bacteria of cats
A technology of intestinal bacteria and intestinal flora, which is applied in the treatment of roasted coffee, biochemical equipment and methods, microorganisms, etc., can solve the problems of high price, low caffeine concentration, and difficulty in the production of cat feces coffee. Low, pleasant mood, weak bitterness effect
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specific Embodiment 1
[0044] Specific Example 1: (1) Isolation and purification of the intestinal flora of civet cats: 10 g of feces and 100 mL of sterile water were put into a homogenization bag, beat for 5 minutes with a homogenizer, centrifuged in a high-speed refrigerated centrifuge, and removed the supernatant , to make a homogenate; identification: first prepare the identification medium of enteropathogenic bacteria (peptone 17.2g, tryptophan 0.9g, Hepes buffer 0.4g, mixed color source 6.87g, agar 18g, purified water 1L, pH 7.3 ) to identify whether there are pathogenic bacteria in the intestinal flora, if there are no pathogenic bacteria, the following experiments are carried out; preparation medium: prepare beef extract peptone medium, Sabouraud dextrose peptone agar, yeast enrichment medium , Eosin methylene blue lactose medium, and Hektoen medium, about 500mL each, aliquoted, sterilized at 121°C for 15 minutes; pour plate: beef extract peptone medium, Sabouraud dextrose peptone agar, yeast...
specific Embodiment 2
[0045] Specific Example 2: (1) Isolation and purification of the intestinal flora of civet cats: 10 g of feces and 100 mL of sterile water were put into a homogenate bag, beat for 5 minutes with a homogenizer, centrifuged in a high-speed refrigerated centrifuge, and removed the supernatant , to make a homogenate; identification: first prepare the identification medium of enteropathogenic bacteria (peptone 17.2g, tryptophan 0.9g, Hepes buffer 0.4g, mixed color source 6.87g, agar 18g, purified water 1L, pH 7.3 ) to identify whether there are pathogenic bacteria in the intestinal flora, if there are no pathogenic bacteria, the following experiments are carried out; preparation medium: prepare beef extract peptone medium, Sabouraud dextrose peptone agar, yeast enrichment medium , Eosin methylene blue lactose medium, and Hektoen medium, about 500mL each, aliquoted, sterilized at 121°C for 15 minutes; pour plate: beef extract peptone medium, Sabouraud dextrose peptone agar, yeast enr...
specific Embodiment 3
[0046]Specific Example 3: (1) Isolation and purification of the intestinal flora of civet cats: 10 g of feces and 100 mL of sterile water were put into a homogenization bag, beat for 5 minutes with a homogenizer, centrifuged in a high-speed refrigerated centrifuge, and removed the supernatant , to make a homogenate; identification: first prepare the identification medium of enteropathogenic bacteria (peptone 17.2g, tryptophan 0.9g, Hepes buffer 0.4g, mixed color source 6.87g, agar 18g, purified water 1L, pH 7.3 ) to identify whether there are pathogenic bacteria in the intestinal flora, if there are no pathogenic bacteria, the following experiments are carried out; preparation medium: prepare beef extract peptone medium, Sabouraud dextrose peptone agar, yeast enrichment medium , Eosin methylene blue lactose medium, and Hektoen medium, about 500mL each, aliquoted, sterilized at 121°C for 15 minutes; pour plate: beef extract peptone medium, Sabouraud dextrose peptone agar, yeast ...
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