A biological fermentation product for preventing and treating colitis and its preparation method
A technology of biological fermentation and colitis, applied in the field of bioengineering, can solve problems such as short research time, and achieve the effects of high viable bacteria, improved product performance, and increased polysaccharide content
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Embodiment 1
[0052] The fermentation process of embodiment 1 clostridium butyricum fermented longan
[0053] (1) Extraction method of longan extract
[0054] Take dried longan, mash and homogenate, mix water and longan pulp according to the liquid-to-material ratio of 15ml:1g, and homogenize to obtain longan pulp slurry, the amount of cellulase added is 1.2% w / v, the enzymolysis temperature is 45.0°C, and the enzyme Under the condition that the hydrolysis time was 187.0min, the enzyme hydrolysis extraction experiment was carried out on a shaker with a rotation speed of 120r / min. After the extraction, the enzyme was inactivated in a water bath at 80°C for 10 minutes. Filter through eight layers of gauze, discard the residue, and obtain the supernatant. The supernatant was concentrated under reduced pressure to 40% of the original volume to obtain a longan extract.
[0055] (2) Standard curve creation
[0056]Accurately weigh 100mg of dried glucose, dissolve it with deionized water and s...
Embodiment 2
[0069] The fermentation process of embodiment 2 clostridium butyricum fermentation longan
[0070] (1) Extraction method of longan extract
[0071] Take dried longan, mash and homogenate, mix water and longan pulp according to the liquid-to-material ratio of 20ml:1g, and homogenize to obtain longan pulp slurry, the amount of cellulase added is 2% w / v, the enzymolysis temperature is 60.0°C, and the enzyme Under the condition that the hydrolysis time was 210min, the enzyme hydrolysis extraction experiment was carried out on a shaker with a rotational speed of 120r / min. After the extraction, the enzyme was inactivated in a water bath at 80°C for 10 minutes, filtered through eight layers of gauze, and the residue was discarded to obtain the supernatant. The supernatant was concentrated under reduced pressure to 30% of the original volume to obtain a longan extract.
[0072] (2) Standard curve creation
[0073] Accurately weigh 100mg of dried glucose, dissolve it with deionized ...
Embodiment 3
[0085] The fermentation process of embodiment 3 clostridium butyricum fermented longan
[0086] (1) Extraction method of longan extract
[0087] Take dried longan, mash and homogenate, mix water and longan pulp according to the liquid-to-material ratio of 16ml:1g, and homogenize to obtain longan pulp slurry, the amount of cellulase added is 1.5% w / v, the enzymolysis temperature is 45.0°C, and the enzyme Under the condition of the hydrolysis time of 180min, the enzymolysis extraction experiment was carried out on a shaker with a rotation speed of 120r / min. After the extraction, the enzyme was inactivated in a water bath at 80°C for 10 minutes, filtered through eight layers of gauze, and the residue was discarded to obtain the supernatant. The supernatant was concentrated under reduced pressure to 30% of the original volume to obtain a longan extract.
[0088] (2) Standard curve creation
[0089] Accurately weigh 100mg of dried glucose, dissolve it with deionized water and se...
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