Biological enzyme method for extracting fish oil from leftovers of sardine
A bio-enzymatic and scrap technology, which is applied in the production of fat, fat oil/fat, etc., can solve the problems of low extraction rate and poor quality of fish oil, and achieve the effect of clear and transparent quality, low cost and good quality of fish oil.
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Embodiment 1
[0021] (1) After removing debris such as the fish head, fish tail, viscera of the sardines, clean them, grind them with a meat grinder, and form a homogenate of the leftovers;
[0022] (2) The weight ratio of the leftovers homogenate and water is 1:0.5 for deployment, and added to the enzymolysis tank, the temperature rises to 40 ° C, and the weight of the sardine leftovers is used as a standard to add alkaline protease at 300U / g. Adjust the acid-base to keep the pH at 6.0, stir at a constant speed of 100r / min, keep warm for 1 hour, and inactivate the enzyme at 90°C for 15 minutes;
[0023] (3) Centrifuge the enzymolysis solution at 5000r / min for 10 minutes while it is hot. After centrifugation, the enzymolysis solution is divided into three layers, which are the enzymolysis solution in the lower layer, the insoluble matter in the middle layer, and the fish oil in the upper layer. The fish oil is obtained by absorbing the upper layer.
Embodiment 2
[0025] (1) After removing debris such as the fish head, fish tail, viscera of the sardines, clean them, grind them with a meat grinder, and form a homogenate of the leftovers;
[0026] (2) Prepare the leftovers homogenate and water at a weight ratio of 1:1, add it to the enzymolysis tank, raise the temperature to 45°C, add alkaline protease at 450U / g based on the weight of the sardine leftovers, and use Adjust the acid-base to keep the pH at 6.5, stir at a constant speed of 150r / min, keep warm for 2 hours, and inactivate the enzyme at 92°C for 16 minutes;
[0027] (3) Centrifuge the enzymolysis solution at 5500r / min for 12 minutes while it is hot. After centrifugation, the enzymolysis solution is divided into three layers, which are respectively the enzymolysis solution in the lower layer, the insoluble matter in the middle layer, and the fish oil in the upper layer. The fish oil is obtained by absorbing the upper layer.
Embodiment 3
[0029] (1) After removing debris such as the fish head, fish tail, viscera of the sardines, clean them, grind them with a meat grinder, and form a homogenate of the leftovers;
[0030] (2) The weight ratio of the leftovers homogenate and water is 1:1.5 for deployment, and added to the enzymolysis tank, the temperature rises to 50 ° C, and the weight of the sardine leftovers is used as a standard to add alkaline protease at 600U / g. Adjust the acid-base to keep the pH at 7.0, stir at a constant speed of 180r / min, keep warm for 3 hours, and inactivate the enzyme at 93°C for 18 minutes;
[0031] (3) Centrifuge the enzymolysis liquid at 6000r / min for 13 minutes while it is still hot. After centrifugation, the enzymolysis liquid is divided into three layers, which are respectively the enzymatic hydrolysis liquid in the lower layer, the content in the middle layer and the fish oil in the upper layer. The fish oil is obtained by absorbing the upper layer.
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