Antioxidant active peptide and preparation method thereof
An anti-oxidative active peptide and alkaline technology, applied in the field of anti-oxidative active peptide of marine low-value fish blue round trevally protein and its preparation, to achieve the effect of simple preparation method, cheap source and strong applicability
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Embodiment 1
[0026] Mix the protein powder of blue trevally with water to make a reaction raw material solution with a protein content of 1wt%, then add 0.03wt% alkaline protease, hydrolyze at 50°C and pH 8.0 for 3 hours, and finally heat to 100°C to stop enzymatic reaction. Centrifuge the obtained mixture at 4°C and 8000r / min for 10-15min, take the supernatant of enzymatic hydrolysis and use an ultrafiltration membrane with a molecular weight of 5000Da to separate and collect the permeate, and use deionized water as the mobile phase to coagulate with Sephedex G-15. Gel chromatography separates the ultrafiltration permeate, and detects and measures the antioxidant activity of the eluent corresponding to each peak at 280nm with a protein and nucleic acid detector, and collects the No. 2 absorption peak with high activity (see figure 1 ) was further separated by reverse-phase HPLC, using an ODS column (Hedera ODS-C2, 10 × 250mm), adopting water and acetonitrile (5-60% acetonitrile in 55min) ...
Embodiment 2
[0028] Mix the protein powder of blue scorpion fish meat with water to make a reaction raw material solution with a protein content of 3wt%; then add 0.005wt% alkaline protease, hydrolyze at 55°C and pH 10 for 6 hours, and finally heat to 100°C to stop enzymatic reaction. Centrifuge the obtained mixture at 4°C and 8000r / min for 10-15min, take the supernatant of enzymatic hydrolysis and use an ultrafiltration membrane with a molecular weight of 5000Da to separate and collect the permeate, and use deionized water as the mobile phase to coagulate with Sephedex G-15. Gel chromatography separates the ultrafiltration permeate, and detects and measures the antioxidant activity of the eluent corresponding to each peak at 280nm with a protein and nucleic acid detector, and collects the No. 2 absorption peak with high activity (see figure 1 ) was further separated by reverse phase HPLC, using ODS column (Hedera ODS-C2, 10 × 250mm), adopting water and acetonitrile (0-60% acetonitrile wit...
Embodiment 3
[0030] Mix the protein powder of blue scorpion fish meat with water to make a reaction material solution with a protein content of 5wt%; then add 0.05wt% alkaline protease, hydrolyze at 45°C and pH 8.0 for 4.5 hours, and finally heat to 100°C to stop enzymatic reaction. Centrifuge the obtained mixture at 4°C and 8000r / min for 10-15min, take the supernatant of enzymatic hydrolysis and use an ultrafiltration membrane with a molecular weight of 5000Da to separate and collect the permeate, and use deionized water as the mobile phase to coagulate with Sephedex G-15. Gel chromatography separates the ultrafiltration permeate, and detects and measures the antioxidant activity of the eluent corresponding to each peak at 280nm with a protein and nucleic acid detector, and collects the No. 2 absorption peak with high activity (see figure 1 ) was further separated by reverse-phase HPLC, using an ODS column (Hedera ODS-C2, 10 × 250mm), adopting water and acetonitrile (5-55% acetonitrile wi...
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