Method for extracting peanut meal polysaccharide
An extraction method and peanut meal technology, applied in the field of biochemistry, can solve the problems of polysaccharide food safety impact, strong reaction conditions, environmental pollution, etc., to avoid the destruction of polysaccharide activity and safety, and improve reaction efficiency and conversion rate , the effect of improving the extraction efficiency
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Embodiment 1
[0026] A method for extracting peanut meal polysaccharides, comprising the steps of:
[0027] (1) Pretreatment: take the raw material of hot-pressed peanut meal, grind it to 500-1000 mesh, add a 70% ethanol solution according to the ratio of solid to liquid (kg / L), and then heat it at a temperature of 30°C and a stirring speed of Under the condition of 150~260r / min, fully stir for 30min, filter with suction, and take the filter residue;
[0028] (2) Enzymatic hydrolysis of protein: take the filter residue after pretreatment, add 8 times the weight of culture medium, and prepare a suspension to facilitate the full combination of enzymes, then add neutral protease (Novozymes), the amount of enzyme added Add according to 0.3g / ml suspension, enzymolysis temperature is 25°C, pH value is 6, and enzymolysis time is 2 hours;
[0029] The culture medium is (per liter): (NH 4 ) 2 SO 4 0.3g, FeSO 4 ·7H 2 O 0.02g, MnSO 4 ·H 2 O 0.03g, MgSO 4 0.02g, KH 2 PO 4 0.1g, pH 6.0;
[...
Embodiment 2
[0035] A method for extracting peanut meal polysaccharides, comprising the steps of:
[0036] (1) Pretreatment: take the raw material of hot-pressed peanut meal, grind it to 500-1000 mesh, add a 70% ethanol solution according to the ratio of solid to liquid of 1:10, and then heat it at 40°C with a stirring speed of 150-260r / min. Under the same conditions, fully stir for 30 minutes, filter with suction, and take the filter residue;
[0037] (2) Enzymatic hydrolysis of protein: take the filter residue after pretreatment, add 10 times the weight of culture medium, and prepare a suspension to facilitate the full combination of enzymes, then add neutral protease (Novozymes), the amount of enzyme added Add according to 0.3g / ml suspension, enzymolysis temperature is 30°C, pH value is 7, and enzymolysis time is 2 hours;
[0038] The culture medium is (per liter): (NH 4 ) 2 SO 4 0.3g, FeSO 4 ·7H 2 O 0.02g, MnSO 4 ·H 2 O 0.03g, MgSO 4 0.02g, KH 2 PO 4 0.1g, pH 6.0;
[003...
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