Method for preparing Kvas bread concentrate
A concentrate and kvass technology, which is applied in the field of kvass bread concentrate preparation, can solve the problems of kvass product quality differences, large differences in the quality of extracts, and differences in the quality of extracts, so as to improve the quality of flavor and clarify The effect of improving the speed and improving the reaction efficiency
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Embodiment 1
[0012] A kind of method for preparing kvass bread concentrate involved in the present embodiment, its steps are:
[0013] Bake the slices of bread until golden yellow, add 4 to 10 times the amount of water according to the weight of the slices of bread, absorb water at room temperature for 1 hour, break the slices of bread into small pieces by mechanical stirring, and continue soaking for 1 hour. It is then pumped into a filter press and the filtrate is collected. After the filter residue is transferred to the saccharification tank, add water 1 to 4 times the mass of bread slices, and add high-temperature-resistant α-amylase at a rate of 5,000-20,000 U per kg of bread slices at a natural pH value, heat up to 85-92°C and then heat-preserve and liquefy 0.5 to 3 hours; then lower the temperature to 50 to 65°C, add citric acid to adjust the pH to 4.5 to 5.5, add 10,000 to 50,000 U of immobilized glucoamylase and 5,000 to 50,000 U of immobilized papain per kilogram of bread slices ...
Embodiment 2
[0021] Weigh 100kg of bread slices, add them to the extraction tank with 600kg of process water in advance, absorb water at room temperature for 1 hour, then turn on the stirring paddle and stir for 20 minutes, stop stirring, continue to soak for 1 hour, then pump into the filter press to collect the filtrate 420kg to obtain 230kg of wet filter residue. Transfer the filter residue into the saccharification tank, add 300kg of water, the natural pH value, add 40g of 20,000U / g high-temperature-resistant α-amylase, heat up to 90°C and keep warm for 30min to liquefy; then pass cooling water to cool down to 55°C, add citric acid Adjust the pH value to 5.0, add 10 g of immobilized glucoamylase at 250,000 U / g and 10 g of immobilized papain at 500,000 U / g, and perform constant temperature enzymatic hydrolysis for 6 hours. After cooling down to room temperature with a plate heat exchanger, it is then pumped into a filter press to collect 280 kg of saccharification liquid filtrate. Comb...
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