Lucid ganoderma fermented persimmon leaf tea
A technology of ganoderma lucidum fermentation and persimmon leaf tea, which is applied in the direction of tea substitutes, etc., to achieve the effects of strong fragrance, increased total phenol content, and strong antioxidant activity
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[0022] Example 1
[0023] Cut the persimmon leaves into 0.2-1.0cm thin strips, weigh 55kg persimmon leaves, 30kg cornmeal, 7kg soybean flour, 7kg bran, and 1kg sucrose, mix them well, and add water to make the water content reach 65%. Put the mixed material into a 17×45cm polypropylene plastic bag, 0.8Kg (wet weight) per bag, press it firmly, seal it with a plastic collar and cotton, and sterilize it at 0.15MPa for 90 minutes. When the temperature of the material drops to 30°C, each bag is connected to 40ml 10 days old Ganoderma lucidum liquid strain, and cultivated at 25-30°C in the dark for 26 days. The solid fermentation product is taken out of the bag and dried at 80°C, crushed and pulverized into 1-2mm particles. The product is dark brown in color, has a unique Ganoderma lucidum fragrance, total phenol content 4.6mg / g, DPPH free radical scavenging rate 92.3%.
Example Embodiment
[0024] Example 2
[0025] Cut the persimmon leaves into thin strips of 0.2-1.0cm, weigh 65kg persimmon leaves, 24kg cornmeal, 5kg soybean powder, 5kg bran, 1kg sucrose, mix well, add water to control the moisture content at 55%, and mix them. The material is put into a glass bottle to be slightly pressurized, sealed with plastic paper, and sterilized at 0.15MPa for 90 minutes. Inoculate when the temperature of the material drops to 30°C, insert 10 days old Ganoderma lucidum liquid strain, the inoculation amount is 10%, and the rest is the same as in Example 1. The total phenol content of the obtained product is 4.3 mg / g, and the DPPH radical scavenging rate is 90.2%.
Example Embodiment
[0026] Example 3
[0027] Cut the persimmon leaves into 0.2-1.0cm thin strips, weigh 70kg persimmon leaves, 21kg cornmeal, 4kg soybean flour, 4kg bran, 1 gluten sucrose, and add water to control the water content at 50%. Put the mixed material into a polypropylene plastic bottle, press it slightly and leave a certain gap, and sterilize it at 0.15MPa for 90 minutes. When the temperature of the material is lowered to 30°C, 15% of the liquid strain is inserted, and cultured in the dark at 25-30°C for 30 days, and the rest is the same as in Example 1. The total phenol content of the obtained product is 4.0 mg / g, and the DPPH radical scavenging rate is 89.2%.
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