Technical method for decoloring and deproteinizing corn stigma polysaccharide
A corn silk polysaccharide and deproteinization technology is applied in the field of refining and processing plant active ingredients, and can solve the problems of inability to remove apparent pigments, large amount of reagents, solvent residues and the like
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Embodiment 1
[0035] bleaching
[0036] 1. Determination of absorbance of corn silk crude polysaccharide pigment
[0037] The crude polysaccharide solution was scanned at all wavelengths, and the results showed that the solution had no maximum absorption wavelength in the visible range. According to the principle of complementary colors, the color presented by the solution is the complementary color that it absorbs light. Since the polysaccharide solution is orange-yellow after dilution before and after decolorization, the solution mainly absorbs visible light in the blue band. Therefore, the 450nm wavelength at the center of the band is selected as the detection wavelength to measure the absorbance of the solution. Use distilled water as the blank solution, and measure the absorbance of the decolorized sample solution at a wavelength of 450nm. Polysaccharide decolorization rate (%)=(pigment absorbance before decolorization-pigment absorbance after decolorization) / pigment absorbance befor...
Embodiment 2
[0058] Example 2 Enzymatic protein removal
[0059] Table 5 Enzymatic factor level table
[0060]
[0061] Table 6 Enzymatic orthogonal test results
[0062]
[0063] From Table 6, it can be concluded that the best combination of A>D>B>C deproteinization is A>D>B>C. 1 B 3 C 3 D 1 , that is, when the enzyme-to-bottom ratio is 1%, the pH is 5.5, the enzymolysis time is 1.5h, and the temperature is 40 °C, the protein removal effect is the best.
Embodiment 3
[0064] Example 3 Protein removal by sevag method
[0065] Table 7 The factor level table of orthogonal experiment of sevag method
[0066]
[0067] Table 8 L 9 (3 4 ) Orthogonal experimental results
[0068]
[0069] From Table 8, the influence relationship is D>C>A>B, that is, the best deproteinization conditions: 4 times of deproteinization, 11min shaking time, sample solution: sevag reagent (v:v) = 2:1, chloroform : n-butanol (v:v)=5:1; the protein removal rate was 64.2%, and the polysaccharide loss rate was 34.3%.
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