Method for extracting hemin and globin from animal blood
A technology for hemin and globin peptides, which is applied in the field of extracting hemin and globin peptides with leech protease, can solve the problems of high price and great impact on industrial production costs, achieve high quality, reduce production costs, Operational Security Effects
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Embodiment 1
[0036] Take 100g of leech, wash it and dry it in the sun; chop it up; put it into 0.08% sodium citrate buffer solution, the ratio of solid to liquid is 1:5, the pH value is 5.5, the temperature is 40°C, soak for 15 minutes; centrifuge Separating and collecting the supernatant; adding ammonium sulfate to the supernatant to reach a saturation of 30%, performing fractional precipitation, and obtaining the supernatant leech protease solution for later use. Take 200ml of fresh pig blood, add anticoagulant trisodium citrate at a ratio of 0.8%, mix evenly for 10 minutes, centrifuge, remove the supernatant, and collect the lower layer of hemoglobin cells, about 100ml; then add at a ratio of 1:1 Pure water, ultrasonic treatment for 15 minutes to crush the cells; filter the crushed liquid through a 100-mesh sieve, leave the filtrate, and slowly adjust the pH value of the filtrate to 2.5 with dilute hydrochloric acid; quickly raise the temperature to 85°C, and keep it warm for 10 minutes ...
Embodiment 2
[0038]Take 2kg of leeches, wash them and dry them in the sun; chop them; put them into 0.10% sodium citrate buffer solution, the ratio of solid to liquid is 1:5, the pH value is 6.0, the temperature is 45°C, soak for 20 minutes; centrifuge Separating and collecting the supernatant; adding ammonium sulfate to the supernatant to reach a saturation of 50%, performing fractional precipitation, and obtaining the supernatant leech protease solution for later use. Take 100kg of fresh chicken blood, add anticoagulant trisodium citrate at a ratio of 1.0%, mix evenly for 10 minutes, centrifuge, remove the supernatant, and collect the lower layer of hemoglobin cells, about 50kg; then add at a ratio of 1:1 Pure water, ultrasonic treatment for 20 minutes to crush the cells; filter the crushed liquid through a 100-mesh sieve, leave the filtrate, slowly adjust the pH value of the filtrate to 3.0 with dilute hydrochloric acid; quickly raise the temperature to 95°C, and keep it warm for 15 minu...
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