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Preparation method and application of oat beta-dextran with small and medium molecular weight

A low-molecular-weight, glucan technology, which is applied in medical preparations containing active ingredients, skin care preparations, pharmaceutical formulations, etc., can solve the problems of low yield of oat β-glucan, increase production, avoid The effect of wasting resources

Active Publication Date: 2019-03-29
SHANGHAI SHENG WEI BIOTECHNOLOGY CO LTD +2
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the hydrolysis of oat β-glucan by this method has the problem of low yield of oat β-glucan with medium and small molecular weight

Method used

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  • Preparation method and application of oat beta-dextran with small and medium molecular weight
  • Preparation method and application of oat beta-dextran with small and medium molecular weight
  • Preparation method and application of oat beta-dextran with small and medium molecular weight

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Effect test

Embodiment 1

[0066] The enzymatic hydrolysis method is as follows: use water as the carrier, use commercially available oat β-glucan powder with a content of 70% as the substrate raw material, adjust the concentration of the substrate (namely oat β-glucan) to 5%, and use enzyme 1 as the Hydrolase; adjust the enzyme-to-substrate ratio (enzyme:substrate mass ratio) to 1:1000; adjust the pH to 4.5; enzymolysis temperature to 45°C; enzymolysis time to 0.5h. After enzymolysis, carry out molecular weight classification. The molecular weight classification method is: use ultrafiltration membrane to divide the molecular weight into parts with a molecular weight greater than 30000 Daltons and parts with a molecular weight less than 30000 Daltons. Step 3 times, combine oat β-glucan solutions less than 30,000 Daltons, heat to 95°C to inactivate enzymes for 30 minutes, remove protein by isoelectric point method (conventional technology in this field), and concentrate to β-glucan content The 2.5% solut...

Embodiment 2

[0068] The enzymatic hydrolysis method is as follows: use water as the carrier, use oat bran as the substrate raw material, adjust the concentration of the substrate (ie oat β-glucan) to 1%, use enzyme 2 as the hydrolytic enzyme; adjust the enzyme-to-substrate ratio to 1: 5000; adjust the pH to 5.0; enzymatic hydrolysis temperature is 50°C; each enzymatic hydrolysis time is 1h. After enzymatic hydrolysis, carry out molecular weight classification. The molecular weight classification method is: use ultrafiltration membrane to divide the molecular weight into parts with a molecular weight greater than 10,000 Daltons and those with a molecular weight less than 10,000 Daltons. Twice, combine oat β-glucan solutions less than 10,000 Daltons, heat to 95°C to inactivate enzymes for 30 minutes, remove protein by flocculation, concentrate to a solution with β-glucan content greater than 2.5%, add deionized Water and butanediol are prepared into a solution containing 8% butylene glycol a...

Embodiment 3

[0070]The enzymatic hydrolysis method is as follows: use water as the carrier, use commercially available oat β-glucan powder with a content of 70% as the substrate raw material, adjust the concentration of the substrate (namely oat β-glucan) to 10%, and use enzyme 2 as the Hydrolase; adjust the enzyme-to-substrate ratio to 1:100; adjust the pH to 9.0, enzymatic hydrolysis temperature to 80°C, and each enzymatic hydrolysis time to 0.1h. After enzymatic hydrolysis, carry out molecular weight classification. The molecular weight classification method is: use molecular sieve method to divide the molecular weight into parts with a molecular weight greater than 1000 Daltons and those with a molecular weight less than 1000 Daltons. 1 time, combine oat β-glucan solutions less than 1000 Daltons, heat to 95°C to inactivate enzymes for 30 minutes, remove protein by flocculation, concentrate to a solution with β-glucan content greater than or equal to 0.5%, and freeze-dry , to obtain oat...

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Abstract

The invention discloses a preparation method and application of oat beta-dextran with small and medium molecular weight. The preparation method of the oat beta-dextran with small and medium molecularweight comprises a step of performing enzymatic hydrolysis on a substrate by using enzymes, wherein the enzymes include beta-endoglucanase and / or beta exoglucanase, and the substrate includes oat beta-dextran to be subjected to enzymatic hydrolysis at a concentration of 0.5-10% in percentage by mass; the mass ratio of the enzymes to the substrate is 1 to (100-100000); and the molecular weight of the oat beta-dextran with small and medium molecular weight is 60000 dalton or below. Promotion effects of the oat beta-dextran on expression of caspase-14 gene in HaCaT cells are discovered for the first time by the invention; moreover, the smaller the molecular weight of the oat beta-dextran is, the better the promotion effects on the expression of the caspase-14 gene in the HaCaT cells will be.

Description

technical field [0001] The invention belongs to the field of medicinal chemistry, and in particular relates to a preparation method and application of oat β-glucan with medium and small molecular weight. Background technique [0002] Oat (Latin scientific name: Avena sativa L.) is a grass plant, which is called brome and wild wheat in "Compendium of Materia Medica". Oats are cold-resistant, drought-resistant, highly adaptable to soil, and can reproduce by themselves. At present, the grains of oats are used for flour grinding, and the bran is mainly used as feed. Part of the bran has been used to extract oat β-glucan, which is used for new resource foods, but the proportion is not high. The present invention makes new discoveries And technology, made in-depth development and utilization of oat β-glucan, further broadened the application range of oat by-products, and increased its social and economic value. [0003] North latitude 41°~43° is the world-recognized golden oat g...

Claims

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Application Information

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IPC IPC(8): C12P19/08C12P19/14A61K31/716A61P17/00A61P17/06A61P17/04A61K8/73A61Q19/00
CPCA61K8/73A61K31/716A61Q19/00A61P17/00A61P17/04A61P17/06C12P19/08C12P19/14
Inventor 翟春涛卢向艳金敏蓉王风楼
Owner SHANGHAI SHENG WEI BIOTECHNOLOGY CO LTD