Preparation method of seaweed ferment having function of reducing blood sugar
A seaweed enzyme, hypoglycemic technology, applied in the functions of food ingredients, bacteria used in food preparation, yeast-containing food ingredients, etc., can solve the problems of long time, single metabolite, easy to produce miscellaneous bacteria, etc. , Good hypoglycemic effect, great effect of toxic and side effects
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Embodiment 1
[0030] Take fresh seaweed, ginseng, kudzu root, medlar, ganoderma lucidum, Atractylodes macrocephala, Ophiopogon japonicus, Tianqi, Coptis chinensis, Astragalus membranaceus, and corn silk, washed and cleaned to remove impurities, and then pasteurized.
[0031] Add 60g of seaweed, and add a total of 40g of other raw materials in a ratio of 1:1.
[0032] Chop the above raw materials and add an equal volume of pure water to grind them into a slurry for later use; the weight ratio of raw materials to water is 1:8.
[0033] Heat the slurry raw material to 30°C to maintain a constant temperature, and add 2.5g of chromium-enriched yeast and selenium-enriched yeast for primary fermentation;
[0034] After 10 hours, add 2g of Lactobacillus plantarum, 1g of Lactobacillus rhamnosus and 3g of Streptococcus thermophilus, heat to 37°C and keep a constant temperature for secondary fermentation. After 10 days, the measured pH value of the enzyme is stable at 3.0, and the compound seaweed enz...
Embodiment 2
[0047] Take fresh seaweed, ginseng, kudzu root, medlar, ganoderma lucidum, Atractylodes macrocephala, Ophiopogon japonicus, Tianqi, Coptis chinensis, Radix Astragali, and corn silk, washed and removed, and then pasteurized. Add 70g of seaweed, and add a total of 30g of other raw materials in a ratio of 1:1. Chop the above raw materials and add an equal volume of purified water to grind them into a slurry for later use.
[0048] Heat the slurry raw material to 30°C to keep a constant temperature, add 4g of chromium-enriched yeast and selenium-enriched yeast for primary fermentation
[0049] After 10 hours, 2g of Lactobacillus plantarum, 1g of Lactobacillus rhamnosus and 3g of Streptococcus thermophilus were added, heated to 37°C and kept at a constant temperature for secondary fermentation. After 8 days, the pH value of the enzyme was found to be stable at 3.0, and a compound seaweed enzyme solution was obtained. The fermentation is over.
[0050] Reduce the pressure of seawe...
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