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Preparation method of oat beta-glucan

A technology of dextran and oats, which is applied in the direction of anti-toxins, digestive system, metabolic diseases, etc., can solve the problems of unfavorable industrial production, instability, cumbersome process, etc., and achieve large-scale production, stable properties, and good solubility Effect

Active Publication Date: 2011-08-31
INNOBIO CORP LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the removal rate of protein by isoelectric point method is low and unstable, and the purification time of ammonium sulfate precipitation is long and the process is cumbersome, which is not conducive to industrial production.

Method used

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  • Preparation method of oat beta-glucan
  • Preparation method of oat beta-glucan

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0014] The concrete preparation method of embodiment 1 is as follows:

[0015] (1) Low-temperature extraction: add oat bran to 0.01 mol / L NaOH solution at a mass ratio of 1:10, shake in a constant temperature water bath at 30°C for 2 hours. Water was added according to the mass ratio of oat bran to water at 1:15, passed through a 180-mesh sieve, centrifuged at 4000 rpm for 20 min, and the supernatant was poured into the oat bran.

[0016] (2) High-temperature leaching: adjust the pH value of the mixture to 10.0, shake in a constant temperature water bath at 80°C for 3 hours. Cool to room temperature, centrifuge at 4000rpm for 20min, and discard the precipitate.

[0017] (3) Pectinase and amylase treatment: adjust the pH value of the extract to 5.5, add pectinase 0.06mg / 5g oat bran, stir at 60°C for 5min, then inactivate the enzyme at 100°C for 5min, cool to room temperature, and centrifuge at 4000rpm for 20min , discard the precipitate. Adjust the pH of the extract to 6.5, ...

Embodiment 2

[0027] The concrete preparation method of embodiment 2 is as follows:

[0028] (1) Low-temperature extraction: add 0.01mol / L NaOH solution to oat bran at a mass ratio of 1:8, shake in a constant temperature water bath at 30°C for 3 hours; add water at a mass ratio of oat bran to water of 1:10, and pass through a 100-mesh sieve Net, centrifuged at 4000rpm for 30min, poured out the supernatant in oat bran;

[0029] (2) High-temperature leaching: adjust the pH value of the mixture to 10.0, shake in a constant temperature water bath at 80°C for 3 hours, cool to room temperature, centrifuge at 4000rpm for 20 minutes, and discard the precipitate;

[0030] (3) Pectinase and amylase treatment: adjust the pH value of the extract to 5, add pectinase 0.01mg / 5g oat bran, stir at 65°C for 30min, then inactivate the enzyme at 100°C for 5min, cool to room temperature, and centrifuge at 5000rpm for 25min , discard the precipitate; adjust the pH value of the extract to 5.5, add high temperatu...

Embodiment 3

[0035] The concrete preparation method of embodiment 3 is as follows:

[0036] (1) Low-temperature extraction: Add 0.05mol / L NaOH solution to oat bran at a mass ratio of 1:12, shake in a constant temperature water bath at 25°C for 1 hour; add water at a mass ratio of oat bran to water of 1:15, and pass through a 200-mesh sieve Net, centrifuged at 5000rpm for 15min, poured out the supernatant in oat bran;

[0037] (2) High-temperature leaching: adjust the pH value of the mixture to 10.0, shake in a constant temperature water bath at 80°C for 3 hours, cool to room temperature, centrifuge at 4000rpm for 20 minutes, and discard the precipitate;

[0038] (3) Pectinase and amylase treatment: adjust the pH value of the extract to 6, add pectinase 0.1mg / 5g oat bran, stir at 65°C for 5min, then inactivate the enzyme at 100°C for 5min, cool to room temperature, and centrifuge at 4000rpm for 15 ~30min, discard the precipitate; adjust the pH value of the extract to 6.5, add high temperat...

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Abstract

The invention relates to a preparation method of oat beta-glucan. Oat bran is adopted as a raw material, and the oat beta-glucan is obtained by low-temperature extraction, high-temperature extraction, treatment by pectase and amylase, primary alcohol precipitation, vacuum drying, secondary alcohol precipitation and vacuum drying. The purity of a prepared product can achieve 67.1%, the yield is 4.2%, the protein content is 1.7%, the main advantage of the preparation method is that the extraction and the purification processes are simple, and the characteristics of the preparation method are mainly represented as the unique low-temperature extraction step and the pectase treatment process in the technology. The low-temperature extraction can remove most of starch in the raw material so as to enable the follow-up process to be performed better. By using the pectase, the traditional protein removal step is abandoned in the technology, and impurities, such as proteins and the like, are ingeniously removed by centrifugation while removing pectine. In the technology, the secondary alcohol precipitation is finally adopted for further purification, thereby obtaining the product with good dissolubility and stable characters, and having important significant for large-scale production, development and utilization.

Description

technical field [0001] The invention relates to a research on extracting water-soluble β-glucan from oat bran. Background technique [0002] Oat β-glucan is a high molecular polymer formed by the monomer β-D-glucopyranose linked by β-(1-3) and β-(1-4) glycosidic bonds. With modern processing techniques, most of the beta-glucan is concentrated in the by-product bran after milling. Oat β-glucan can anti-aging, regulate human immune function, prevent and treat cardiovascular and cerebrovascular diseases caused by hyperlipidemia, and at the same time control non-insulin-dependent diabetes, prevent rectal cancer, gallstones, dental caries, etc. [0003] At present, the preparation of oat β-glucan is generally obtained by removing protein by the isoelectric point method, followed by repeated purification by ammonium sulfate precipitation. However, the removal rate of protein removal by isoelectric point method is low and unstable, and the ammonium sulfate precipitation purificat...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C08B37/02A61P1/02A61P1/16A61P3/06A61P3/10A61P9/00A61P35/00A61P37/04A61P39/06
Inventor 田晶徐龙权翟滨伏萃翠邹丽萍
Owner INNOBIO CORP LTD