Nori small peptide chelate manganese compound and preparation method as well as application thereof
A small peptide chelation and complex technology, applied in the application, animal feed, animal feed and other directions, can solve the problems of unfavorable industrial production and use, long preparation time, etc., and achieve improved utilization value, rapid dissolution, and good stability. Effect
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Embodiment 1
[0028] Take 500g of seaweed as protein raw material, mash it with water, add deionized water according to the ratio of material to liquid 1:50, heat up to 40°C, natural pH, add manganese ion amount 0.1mg / mL, add cellulase and fruit Glue enzyme, the amount of enzyme added is 0.1g / 100mL, the compound ratio is 1:1, enzymolysis is 1h, and the enzyme is inactivated (temperature 100°C, time 20min); after the above enzymolysis solution is cooled to 50°C, add neutral protease and papain, The amount of enzyme added is 0.1g / 100mL, the compound ratio is 1:5, the enzymolysis is 0.5h, the enzyme is inactivated (temperature 100°C, time 30min), centrifuged (speed 6000rpm, time 15min), the chelation rate is measured, and the quantitative enzymolysis solution is taken Freeze-dry to obtain a grade I laver chelated manganese salt with a chelation rate of 20% (±5%), which is recorded as Experiment No. 1.
Embodiment 2
[0030] Take the enzymolysis solution in (1), control the temperature at 40°C, stir and shake for 0.5h, measure the chelation rate (Yang Shen, 2008), centrifuge, freeze-dry, and obtain II with a chelation rate of 40% (± 5%) Grade laver small peptide chelated manganese salt, recorded as Experiment No. 2.
Embodiment 3
[0032] Take 500g of seaweed as the protein material, mash it with water, add deionized water according to the material-to-liquid ratio of 1:30, heat up to 50°C, and add manganese ions of 0.08mg / mL at the natural pH, and add cellulase and fruit at the same time Glue enzyme, add enzyme amount 0.5g / 100mL, compound ratio 1:2, enzymolysis for 1h, inactivate enzyme (temperature 100°C, time 20min); after the above enzymolysis solution is cooled to 60°C, add neutral protease and papain, The amount of enzyme added is 0.3g / 100mL, the compound ratio is 1:3, the enzymolysis is 1h, the enzyme is inactivated (temperature 100°C, time 30min), centrifuged (speed 6000rpm, time 15min), the chelation rate is measured, and the quantitative enzymolysis solution is frozen Dried to obtain a grade I laver chelated manganese salt with a chelation rate of 30% (±5%), which was recorded as Experiment No. 3.
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