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Process for preparing red alga oligose

A technology of red algae oligosaccharide and red algae polysaccharide, applied in oligosaccharide and other directions, can solve the problems of serious oxidation degree of products, unsuitable for industrial production, difficult separation and purification, etc., and achieves inhibition of Bacillus subtilis growth, low price, and optimized process. effect of steps

Inactive Publication Date: 2007-01-24
NINGBO UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Red algal polysaccharides have a long history of application in food and medicine, and red algal oligosaccharides are low-molecular-weight compounds obtained after polysaccharide degradation. In recent years, many physiological activities of this type of oligosaccharides and their derivatives have been gradually recognized. Oligosaccharides have been reported in anti-oxidation, anti-inflammation, hypoglycemic and anti-tumor aspects; and carrageenan oligosaccharides are a kind of natural polyanionic sulfate oligosaccharides, so they have anti-tumor, antibacterial, anticoagulant and other aspects. Its unique activity, in addition, as an antiviral active substance, carrageenan oligosaccharide has a good inhibitory effect on HIV virus, HSV virus, herpes and hepatitis virus, etc., so its application prospect is good; The degradation methods mainly include enzymatic degradation, liquid acid degradation and oxidative degradation. In the Chinese patent (Patent No. CN1467226), the Fenton oxidative degradation method is adopted. This method causes the oxidation degree of the product to be serious, and there are many by-products, which cause great harm to the subsequent separation and purification. Big difficulty; Japanese patent (patent No. JP2000116376) uses carrageenase to prepare κ-carrageenan oligosaccharide, and Chinese patent (patent No. CN1513989) also uses agarase to degrade agar, but enzymatic hydrolysis first needs to separate Extract the required enzyme, and then degrade it to obtain the oligosaccharide mixture. Because the source of the enzyme is generally marine microorganisms or snails, it is expensive and not suitable for industrial production; Chinese patents (patent No. CN1394879A, CN1513860) use Oxalic acid, hydrochloric acid, sulfuric acid, etc. degrade agar, and in the Chinese patent (CN1513880A), a dilute sulfuric acid solution is used as a hydrolysis medium to produce carrageenan oligosaccharides. If these methods of using liquid acids are used for industrial production, it will cause Equipment corrosion and discharged waste water can easily lead to environmental pollution, and the neutralization step in the method will produce a large amount of salt. Therefore, a desalination process is also required in production, resulting in complex processes, increased production costs, and low production efficiency.

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0023] Weigh 40g of κ-carrageenan and add it to 2 liters of water, boil it to make it into a sol, treat the 732-type cation exchange resin with hydrochloric acid, and wash it until neutral, take 420g and add it to the carrageenan sol, and stir in a water bath at 90°C for reaction After reacting for 6 hours, the solid cation exchange resin was removed by suction filtration; neutral activated carbon with a particle size of 50 mesh was installed in a 6×60 cm chromatographic column, and the solution after suction filtration was directly adsorbed on the chromatographic column, and the solution could be repeatedly adsorbed twice. The second time, the adsorption speed is 5ml / min and 10ml / min respectively, after all the adsorption, wash with water, first remove the small molecular impurities and monosaccharide part, and then elute with 8% ethanol solution to obtain The eluate of oligosaccharides (2 sugars) was eluted with a concentration of 15% ethanol solution to obtain an eluate of o...

Embodiment 2

[0025] Weigh 40g of λ-carrageenan and add it to 2 liters of water, boil it to make it into a sol; treat the 732-type cation exchange resin with sulfuric acid, and wash it until neutral, take 420g and add it to the carrageenan sol; stir and react in a water bath at 90°C, After reacting for 6 hours, remove the solid cation exchange resin by suction filtration; put the neutral activated carbon with a particle size of 50 mesh in a 6×60cm chromatographic column, and the solution after suction filtration is directly adsorbed on the chromatographic column, and the solution can be repeatedly adsorbed twice , the adsorption speed is 5ml / min and 10ml / min respectively, after all the adsorption, wash with water, firstly remove the small molecular impurities and monosaccharide part, then elute with the concentration of 8% ethanol solution to obtain the polysaccharide with a degree of polymerization of 2 The eluate of oligosaccharides (2 sugars) was eluted with a concentration of 15% ethanol...

Embodiment 3

[0027] Weigh 40g of agar gel and add it to 2 liters of water, boil it to make it into a sol, treat the 732-type cation exchange resin with hydrochloric acid, and wash it until neutral, take 420g and add it to the agar sol; stir and react in a water bath at 90°C for 6 hours Finally, the solid cation exchange resin was removed by suction filtration; the neutral activated carbon with a particle size of 50 mesh was installed in a 6×60cm chromatographic column, and the solution after suction filtration was directly adsorbed on the chromatographic column, and the solution could be repeatedly adsorbed twice. The speeds are 5ml / min and 10ml / min respectively. After all the adsorption, wash with water to remove small molecular impurities and monosaccharides, and then elute with 8% ethanol solution to obtain oligosaccharides with a degree of polymerization of 2. The eluate of sugar (2 sugars) was eluted with a concentration of 15% ethanol solution to obtain an eluate of oligosaccharides (...

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Abstract

The present invention discloses process of preparing red algae oligose with acid treated solid cationic exchange resin as medium. The preparation process has the advantages of the repeated use of acid treated solid cationic exchange resin, low cost, no acid liquid exhaust, no corrosion to the production apparatus and less technological steps. The product has carrgeenin oligose with obvious effect of antagonizing pneumonia virus and herpes virus, relatively high effect of inhibiting tumor cell, effect of inhibiting the growth of Bacillus subtilis, etc; and agaragar oligose with high antioxidant and liver protecting effect.

Description

technical field [0001] The invention relates to a method for preparing oligosaccharides, in particular to a method for preparing red algae oligosaccharides. Background technique [0002] Red algae polysaccharides extracted from red algae mainly include agar gum and carrageenan. Red algal polysaccharides have a long history of application in food and medicine, and red algal oligosaccharides are low-molecular-weight compounds obtained after polysaccharide degradation. In recent years, many physiological activities of this type of oligosaccharides and their derivatives have been gradually recognized. Oligosaccharides have been reported in anti-oxidation, anti-inflammation, hypoglycemic and anti-tumor aspects; and carrageenan oligosaccharides are a kind of natural polyanionic sulfate oligosaccharides, so they have anti-tumor, antibacterial, anticoagulant and other aspects. Its unique activity, in addition, as an antiviral active substance, carrageenan oligosaccharide has a good...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C07H3/06
Inventor 陈海敏严小军徐继林
Owner NINGBO UNIV
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