Blood powder enzymolysis and decolorization method
An enzymatic hydrolysis and blood meal technology, applied in the field of enzymatic hydrolysis and decolorization of blood meal, can solve the problems of difficult animal digestion and absorption, no protein degradation, environmental pollution, etc., and achieve the effects of improving palatability, less ring damage, and easy digestion and absorption.
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Embodiment 1
[0015] Add 100kg of sprayed blood powder to the reaction tank, add 1000L of water, stir for 12 hours, analyze the pH of the blood powder liquid, adjust the pH to 7.0 with 0.5mol / L NaOH; add 6kg of keratinase (enzyme activity is 30000U / g), and react at 55°C React at high temperature for 4 hours; then add 9kg of neutral protease (enzyme activity is 50000U / g), and react for 5 hours at a reaction temperature of 50°C; measure the pH of the reaction solution, adjust the pH to 4.0 with 0.5mol / L HCl, and inhibit the enzyme Live, terminate the reaction, centrifuge at 5000r / min for 10min, discard the residue; add activated carbon at 0.2 g / 100ml to the supernatant, react at 55°C, pH 4.0, decolorize for 50min, discard the residue by centrifugation, and obtain the decolorization reaction solution . Experiments have proved that in this embodiment, the degradation rate of hemoglobin is as high as 92%.
Embodiment 2
[0017] Add 100kg of sprayed blood powder to the reaction tank, add 1000L of water, stir for 12 hours, analyze the pH of the blood powder liquid, adjust the pH to 7.0 with 0.5mol / L NaOH; add 7kg of keratinase (enzyme activity is 30000U / g), and react at 55°C React at high temperature for 4 hours; then add 8kg of neutral protease (enzyme activity is 50000U / g), and react for 5 hours at a reaction temperature of 50°C; measure the pH of the reaction solution, adjust the pH to 4.0 with 0.5mol / L HCl, and inhibit the enzyme Live, terminate the reaction, centrifuge at 5000r / min for 10min, discard the residue; add 0.2 g / 100ml of activated carbon to the supernatant, react at 55°C, pH 4.0, decolorize for 50min, and discard the residue by centrifugation to obtain the decolorization reaction solution . Experiments have shown that in this embodiment, the degradation rate of hemoglobin is as high as 93%.
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