Method for manufacturing probiotic living bacterium kvass by alcohol treatment-composite inhibitor method
A compound inhibitor and manufacturing method technology, which is applied in the fields of alcohol treatment-compound inhibitor method probiotic living kvass production and bread kvass production, which can solve the loss of kvass aroma components and taste substances, bread aroma and fermentation Insufficient fullness of the flavor and other problems, to achieve the effect of ensuring biological stability, smooth and pleasant taste, and strong bread flavor
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Embodiment 1
[0017] A kind of alcohol treatment-compound inhibitor method probiotic living bacteria kvass production method involved in this embodiment, the steps are as follows, the preparation of plant extract: take by weighing 100g of fragrant leaves and 250g of fresh ginger respectively, put the fragrant leaves Add 5000ml of distilled water to the container of leaves and fresh ginger, heat and extract at 80°C for 4 hours, filter with four layers of gauze after natural cooling, and collect the plant extract for later use.
[0018] Slice the kvass bread, bake until golden brown, and then coarsely crush it into 20-40 mesh bread meal, set aside.
[0019] Add 16 times the quality of water to the bread flour and extract at room temperature for 4 hours, then extract the supernatant of 2 / 3 of the total volume by siphon method, and transfer it to a fermenter for later use. The rest of the total volume of 1 / 3 of the turbid liquid, the natural pH value, add high temperature resistant α-amylase ac...
Embodiment 2
[0029] Weigh 100g of fragrant leaves and 250g of fresh ginger, add 5000ml of distilled water into the container with fragrant leaves and fresh ginger, keep leaching at 80°C for 4 hours, filter with four layers of gauze after natural cooling, and collect the plant extract; weigh 100kg of baked bread slices were coarsely crushed and put into a bread extraction tank. After adding 1600kg of water and soaking at room temperature for 4 hours, 1000kg of the supernatant liquid extracted from the bread was extracted by the siphon method and pumped into a fermentation tank for subsequent use. Then add 1,000,000 U of high-temperature-resistant α-amylase to the bread extraction tank, with a natural pH value, and heat and liquefy at 92°C for 0.5 hours. Then lower the temperature to 55°C, add citric acid to adjust the pH value to 4.5, add 1,000,000 U of glucoamylase, 1,000,000 U of xylanase and 500,000 U of papain for enzymatic hydrolysis at constant temperature for 4 hours. Pass the coolin...
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