Technology for simultaneously preparing catalase and liver peptide by using raw material of animal liver
A catalase and animal liver technology, applied in the field of separation and extraction of biologically active substances, can solve problems such as environmental pollution, insufficient utilization of raw materials, a large amount of waste residue and waste water, etc., achieve broad application prospects and eradicate environmental pollution problems , to achieve the effect of zero emissions
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example 1
[0013] Take 10kg of pig liver, chop it up, add 40L of water to homogenate it, and keep it warm at 30°C for 12 hours to make it autolyze. After reaching the specified time, adjust the pH value to 6.5, and then vacuum filter to obtain 40 L of filtrate with peroxidase activity of 20,000 U / ml and 9.5 kg of filter residue. The filtrate was concentrated by ultrafiltration with a hollow fiber ultrafiltration membrane with a cut-off molecular weight of 40 kDa to obtain 15 L of ultrafiltration concentrate with a peroxidase activity of 50,000 U / ml and 25 L of ultrafiltration permeate. The ultrafiltration permeate was concentrated with a roll-type reverse osmosis membrane to obtain 1.2 L of reverse osmosis concentrate and 23.7 L of reverse osmosis permeate. Combine the reverse osmosis concentrate with the filter residue, adjust the pH value to the optimum pH of pepsin, hydrolyze at the optimum temperature of pepsin for 12 hours, then adjust the pH value to 6.8, centrifuge (4°C, 8000rpm, ...
example 2
[0015] Take 5 kg of duck liver, mince it, add 20 L of water to homogenate it, and keep it at 35°C for 8 hours to make it autolyze. After reaching the specified time, adjust the pH value to 6.5, and then use a refrigerated centrifuge to centrifuge at 10°C and 9000 rpm to obtain 20 L of supernatant with a peroxidase activity of 28,000 U / ml and 5 kg of residue. The supernatant was concentrated by ultrafiltration with a hollow fiber ultrafiltration membrane with a cut-off molecular weight of 20 kDa to obtain 11 L of ultrafiltration concentrate with a peroxidase activity of 50,000 U / ml and 9 L of ultrafiltration permeate. The ultrafiltration permeate was concentrated with a roll-type nanofiltration membrane (molecular weight cut-off: 150) to obtain 0.4 L of nanofiltration concentrate and 8.5 L of nanofiltration permeate. Combine the nanofiltration concentrate with the residue, adjust the pH value to the optimum pH of trypsin, hydrolyze it at the optimum temperature of trypsin for 1...
example 3
[0017] Take 50kg of grass carp liver, chop it up, add 200L of water to homogenate it, and keep it warm at 33°C for 10 hours to make it autolyze. After reaching the specified time, adjust the pH value to 6.5, then use a butterfly refrigerated centrifuge to centrifuge at 4°C and 9000rpm, and then filter the obtained supernatant with a microporous membrane with a pore size of 5 μm to obtain the peroxidase activity. 155L of 32,000U / ml filtrate and 45kg of residue. The filtrate was concentrated by ultrafiltration with a roll-type ultrafiltration membrane with a cut-off molecular weight of 35 kDa to obtain 98 L of ultrafiltration concentrate with a peroxidase activity of 50,000 U / ml and 56 L of ultrafiltration permeate. The ultrafiltration permeate was concentrated with a roll-type nanofiltration membrane with a cut-off molecular weight of 150 Da to obtain 2.5 L of nanofiltration concentrate and 53.7 L of nanofiltration permeate. Combine the nanofiltration concentrate with the filt...
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