Making method of high-organic selenium cardamine violifolia selenium polypeptide

A high-organic technology of crushed cinnabar leaves, which is applied in the field of preparation of selenium polypeptides of cinnabar leaves, can solve the problems of hair and nail shedding, toxicity, and reduction, and achieve the effect of improving protein extraction rate

Active Publication Date: 2018-06-15
恩施德源硒材料工程科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

At present, most of the selenium supplements on the market are based on inorganic selenium. Exceeding a certain dose of inorganic selenium will cause obvious toxicity to the body, resulting in hair and nail loss and liver and kidney toxicity.
The second-generation selenium supplementation preparation, organic selenium mainly composed of yeast selenium, has significantly lower toxicity than inorganic selenium, but because its main component is selenomethionine, which contains high purine, long-term use has a potential risk of gout
As a new generation of selenium supplement products, plant selenoprotein has obvious safety advantages and functional effects. However, as a biological macromolecule, it needs to be digested in the body to be absorbed, so its bioavailability is limited.

Method used

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  • Making method of high-organic selenium cardamine violifolia selenium polypeptide
  • Making method of high-organic selenium cardamine violifolia selenium polypeptide
  • Making method of high-organic selenium cardamine violifolia selenium polypeptide

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0037] S1. Raw material pretreatment: Select the dry powder of broken rice chestnut with a protein content of more than 15% and a selenium content of 2000ug / g as the production raw material, soak it in ethanol for 20-30min, filter and remove impurities, and then pass cellulase and pectin Obtain the enzymatic hydrolysis product after the pretreatment of the enzyme mixture, and set aside;

[0038] S11. Weigh cellulase and pectinase in equal proportions and mix them, and then put the mixture into the raw material for removing impurities at 50°C (for the raw material after removing impurities, first mix the dry powder of rice chestnut and water at a ratio of 1:20~ 1:40g / mL ratio mixes, then puts cellulase and pectinase mixture), obtains mixed solution A, makes the total mass of cellulase and pectinase account for 1% of mixed solution A quality; Enzymolyze for 1 hour under the condition of 6.0, then adjust the pH to 7.0, add water, and mix the enzymolyzed product obtained at this t...

Embodiment 2

[0044] Adopt embodiment one scheme to do three groups of tests respectively,

[0045] The difference from Example 1 is that:

[0046] Group A, adopt the method of Example 1 (that is, in step S2, use alkaline protease alone for enzymatic hydrolysis, without subsequent neutral protease enzymatic hydrolysis process)

[0047] Group B, using the method of Example 1 (that is, in step S2, neutral protease is used alone for enzymatic hydrolysis, and there is no pre-ordered alkaline protease enzymatic hydrolysis process)

[0048] Group C, using the method of Example 1 (that is, in step S2, acidic protease is used alone for enzymolysis, and alkaline protease and alkaline protease are not used for enzymolysis)

[0049] Subsequently, adopt routine method to detect respectively the amount of broken rice sheath protein in three groups of obtained materials, after group A, group B, group C extract, extraction rate is respectively 51.8%, 47.0%, 34.6% (as figure 1 Shown), it can be seen that...

Embodiment 3

[0051] The difference from Example 1 is:

[0052] In step S2: the enzymatic hydrolysis time of alkaline protease is divided into four groups of 1, 2, 3, and 4 hours in turn for experiments to determine the influence of different enzymatic hydrolysis times on the protein extraction rate in step S2

[0053] Extract results such as figure 2 As shown, within 1-2 hours of adding alkaline protease, the extraction rate increased rapidly with the increase of time, and the extraction rate gradually decreased after 2 hours. The extraction rate decreased due to the excessive hydrolysis of alkaline protease, and the extraction rate remained unchanged after 3 hours. , due to the gradual inactivation of alkaline protease, so the optimal extraction time is preferably 2 hours for the enzymatic hydrolysis reaction.

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Abstract

The invention relates to a making method of a high-organic selenium cardamine violifolia selenium polypeptide. The making method comprises the following steps of: S1, performing pretreatment on a rawmaterial: selecting dried cardamine violifolia powder as a raw material for production, performing soaking with ethano for decolorization, performing filtering for removing impurities, and then performing pretreatment with a mixture of cellulolytic enzymes and pectinase to obtain an enzymatic hydrolysate for standby application; S2, performing double-enzyme composite enzymolysis: firstly adding alkaline protease in a supernatant after pretreatment in step S1 for enzymolysis, performing enzyme deactivation, performing cooling to 50 DEG C, adjusting the pH with hydrochloric acid to 6.0-8.0, adding neutral protease, and performing enzymolysis to obtain an enzymatic hydrolysate; and S3, performing enzyme deactivation and peptide solution separation: boiling over the enzymatic hydrolysate to achieve enzyme deactivation, and performing standing to obtain a clear transparent peptide solution in the lower layer. The making method disclosed by the invention has the advantages that the cardamineviolifolia is used a core raw material, and the cellulolytic enzymes and the pectinase are used for pretreatment before enzymolysis, so that the impurities in the cardamine violifolia are effectivelyremoved and the protein extraction rate of the cardamine violifolia is increased; and then a multi-step double-enzyme enzymolysis method is used for enzymolysis, the content of the selenium polypeptide is higher, and the molecular weight of the selenium polypeptide is smaller.

Description

technical field [0001] The invention relates to the field of biological technology, in particular to a method for preparing a high-organic selenium-leaved selenopolypeptide. Background technique [0002] Selenium is an essential trace element for the human body. It has various functions such as anti-oxidation, delaying aging, improving immunity, preventing cancer and fighting cancer. At present, it has been confirmed that selenium deficiency is closely related to the occurrence of Keshan disease and Kaschin-Beck disease. In addition, a large number of epidemiological studies at home and abroad have found that selenium deficiency is potentially related to cardiovascular disease, tumor development and liver disease. The form of selenium is often divided into organic selenium and inorganic selenium. Inorganic selenium includes selenite, selenate, selenide, and elemental selenium, and organic selenium includes selenomethionine, selenocystine, and selenocysteine, yeast selenium...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): A23J1/00A23J3/34
CPCA23J1/006A23J3/346
Inventor 于添丛欣朱松刘淑君刘雯雯
Owner 恩施德源硒材料工程科技有限公司
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