Formula of botanical antioxidant and preparation method
A technology of antioxidants and plants, which is applied in the direction of food ingredients as antioxidants, food science, and the function of food ingredients. It can solve the problems of unsatisfactory antioxidant effects of natural vitamin E, and achieve easy large-scale production and large-scale production. The effect of chemical production and enhancement of physiological function
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Embodiment 1
[0046] A plant antioxidant formulation such as figure 1 As shown, it includes the following components by weight: 150 parts of nicotinamide mononucleotide, 60 parts of nicotinamide adenine dinucleotide, 25 parts of grape seed extract, 25 parts of ginsenoside, 40 parts of magnesium stearate, 5 parts of silicon, 150 parts of hydroxypropyl methylcellulose.
[0047] The preparation method of the nicotinamide mononucleotide comprises the following steps:
[0048] S1: Add substrate solution to the reaction kettle: 30ml of ATP, 30ml of xylose, 20ml of MgCl2, 10ml of KC1 and 100ml of Tris-HCl buffer, adjust the pH of the substrate solution to 7.5-8.0;
[0049]S2: then add following catalytic enzyme: ribose phosphate pyrophosphate kinase 6g / L substrate solution, ribose-5-phosphate isomerase 10g / L substrate solution, ribulose-3-phosphate isomerase 11g / L bottom substance solution, xylulokinase 10g / L substrate solution, xylose isomerase 10g / L substrate solution, react after stirring;
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Embodiment 2
[0077] A plant antioxidant formulation such as figure 1 As shown, it includes the following ingredients by weight: 130 parts of nicotinamide mononucleotide, 50 parts of nicotinamide adenine dinucleotide, 45 parts of grape seed extract, 35 parts of ginsenoside, 50 parts of magnesium stearate, 5 parts of silicon, 130 parts of hydroxypropyl methylcellulose.
[0078] The preparation method of the nicotinamide mononucleotide comprises the following steps:
[0079] S1: Add substrate solution to the reaction kettle: 30ml of ATP, 30ml of xylose, 20ml of MgCl2, 10ml of KC1 and 100ml of Tris-HCl buffer, adjust the pH of the substrate solution to 7.5-8.0;
[0080] S2: then add following catalytic enzyme: ribose phosphate pyrophosphate kinase 6g / L substrate solution, ribose-5-phosphate isomerase 10g / L substrate solution, ribulose-3-phosphate isomerase 11g / L bottom substance solution, xylulokinase 10g / L substrate solution, xylose isomerase 10g / L substrate solution, react after stirring; ...
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