Method for preparing local brewer's yeast dry powder
A technology for extracting peptone from Saccharomyces cerevisiae and yeast is applied in the field of preparation of Saccharomyces cerevisiae dry powder, which can solve the problems of complex yeast bran preparation process, imbalanced microbial ratio, low yeast quantity, etc. The effect of rate increase in milk reduction and chemical stability
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Embodiment 1
[0026] 1) Preparation of self-produced medium temperature Daqu:
[0027] The self-produced medium-temperature Daqu is produced locally in the brewing enterprise, using the traditional medium-temperature Daqu production process to produce medium-temperature Daqu. That is to say, the grains are full and fresh, no sand, no insects, no mildew and deterioration, and the moisture content is less than 13%. The wheat moistened material, crushed material, and mixed material are pressed into a rectangular bent embryo, and the prepared bent embryo is placed on the koji. In the room, the koji is regularly turned over to carry out the natural enrichment and cultivation of environmental microorganisms. By controlling the temperature, humidity and ventilation conditions in the koji room, after 20-30 days of cultivation, the koji pieces are matured and stored in the warehouse for 3-6 months for later use.
[0028] 2) Screening of native yeast: Weigh 10g of crushed self-produced medium-tempera...
Embodiment 2
[0035] 1) According to the above method, carry out the screening, cultivation, and concentration of native yeast to collect the bacterial sediment.
[0036] 2) Lyoprotectant: mix trehalose, Vc-Na (vitamin C-sodium), maltodextrin, and deionized water in a ratio of 1:1:2:20.
[0037] 3) Add 5.4mL of lyoprotectant to every 300mL of native yeast concentrated mother solution, and mix well to fully emulsify and protect the yeast.
[0038] 4) The above mixture was frozen at -80°C for 12 hours to convert the moisture into solid ice crystals, pre-frozen in the freeze dryer to below -40°C, transferred the frozen yeast liquid to the sample rack, and put it in the freeze dryer Inside, cover with a plexiglass cover, turn on the vacuum pump to evacuate, the internal vacuum degree should not be greater than 30pa, when the actual temperature of the sample rises above 10°C, the freeze-drying can be stopped.
Embodiment 3
[0040]1) According to the method of Example 1, the local yeast was screened, cultivated, concentrated and collected the bacterial sediment.
[0041] 2) Lyoprotectant: mix trehalose, Vc-Na, maltodextrin, and deionized water in a ratio of 1:1:1:10.
[0042] 3) Add 6.0mL of lyoprotectant to every 300mL of native yeast concentrated mother solution, and mix well to fully emulsify and protect the yeast.
[0043] 4) The above mixture was frozen at -70°C for 18 hours to convert the moisture into solid ice crystals, pre-frozen in the freeze dryer to below -40°C, transferred the frozen yeast liquid to the sample rack, and put it in the freeze dryer Inside, cover with a plexiglass cover, turn on the vacuum pump to evacuate, the internal vacuum degree shall not be greater than 30pa, and the freeze-drying can only be stopped when the actual temperature of the sample rises to 10°C.
[0044] Examples 1, 2, and 3 are only different in the protective agent solution used, and the rest of the p...
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