CN1219786C - Guluronicacid oligosaccharides production method utilizing Fenton-type reaction - Google Patents
Guluronicacid oligosaccharides production method utilizing Fenton-type reaction Download PDFInfo
- Publication number
- CN1219786C CN1219786C CN 200310105694 CN200310105694A CN1219786C CN 1219786 C CN1219786 C CN 1219786C CN 200310105694 CN200310105694 CN 200310105694 CN 200310105694 A CN200310105694 A CN 200310105694A CN 1219786 C CN1219786 C CN 1219786C
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- CN
- China
- Prior art keywords
- guluronic acid
- reaction
- concentration
- acid oligosaccharide
- water solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
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- 238000006243 chemical reaction Methods 0.000 title claims abstract description 19
- AEMOLEFTQBMNLQ-UHFFFAOYSA-N beta-D-galactopyranuronic acid Natural products OC1OC(C(O)=O)C(O)C(O)C1O AEMOLEFTQBMNLQ-UHFFFAOYSA-N 0.000 title claims abstract description 18
- -1 Guluronicacid oligosaccharides Chemical class 0.000 title claims abstract description 17
- 229920001542 oligosaccharide Polymers 0.000 title claims abstract description 17
- 238000004519 manufacturing process Methods 0.000 title abstract description 3
- 229910021645 metal ion Inorganic materials 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 7
- AEMOLEFTQBMNLQ-BZINKQHNSA-N D-Guluronic Acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@@H](O)[C@H]1O AEMOLEFTQBMNLQ-BZINKQHNSA-N 0.000 claims abstract description 6
- 238000000746 purification Methods 0.000 claims abstract description 5
- 238000000926 separation method Methods 0.000 claims abstract description 5
- 239000012564 Q sepharose fast flow resin Substances 0.000 claims abstract description 4
- 238000004587 chromatography analysis Methods 0.000 claims abstract description 4
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical group OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 8
- 239000007864 aqueous solution Substances 0.000 claims description 6
- 239000000243 solution Substances 0.000 claims description 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 claims description 2
- 229910001448 ferrous ion Inorganic materials 0.000 claims description 2
- 230000000694 effects Effects 0.000 abstract description 2
- 239000007800 oxidant agent Substances 0.000 abstract description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 4
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 abstract 1
- 230000036632 reaction speed Effects 0.000 abstract 1
- 229920000615 alginic acid Polymers 0.000 description 4
- 235000010443 alginic acid Nutrition 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 2
- AEMOLEFTQBMNLQ-AZLKCVHYSA-N (2r,3s,4s,5s,6r)-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid Chemical compound O[C@@H]1O[C@@H](C(O)=O)[C@@H](O)[C@H](O)[C@@H]1O AEMOLEFTQBMNLQ-AZLKCVHYSA-N 0.000 description 1
- AEMOLEFTQBMNLQ-SYJWYVCOSA-N (2s,3s,4s,5s,6r)-3,4,5,6-tetrahydroxyoxane-2-carboxylic acid Chemical compound O[C@@H]1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@@H]1O AEMOLEFTQBMNLQ-SYJWYVCOSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- 229920001586 anionic polysaccharide Polymers 0.000 description 1
- 150000004836 anionic polysaccharides Chemical class 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000000845 anti-microbial effect Effects 0.000 description 1
- 230000000259 anti-tumor effect Effects 0.000 description 1
- 230000000840 anti-viral effect Effects 0.000 description 1
- 239000003146 anticoagulant agent Substances 0.000 description 1
- 229940127219 anticoagulant drug Drugs 0.000 description 1
- 235000003891 ferrous sulphate Nutrition 0.000 description 1
- 239000011790 ferrous sulphate Substances 0.000 description 1
- 239000012634 fragment Substances 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 230000003053 immunization Effects 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 1
- 150000002482 oligosaccharides Chemical class 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
The present invention relates to a method for preparing guluronic acid oligosaccharide by Fenton reaction, which comprises the steps that poly guluronic acid is prepared into 0.1 to 5 wt % of water solution; the present invention is characterized in that an oxidizing agent is added in the water solution until the concentration is from 0.05 to 0.5%, metal ions are added until the concentration of the water solution is from 0.05 to 0.5%, and the water solution is reacted at the temperature of 20 to 40 DEG C; then, reaction solution is separated and purified by Bio-gelP10 and a Q-Sepharose Fast Flow chromatography column after the stopping of reaction. The present invention for preparing the guluronic acid oligosaccharide has the advantages of high reaction speed, high product purity, easy separation and purification, mass production of the guluronic acid oligosaccharide, full utilization of the guluronic acid oligosaccharide, and wide development of function and activity of the mannuronic acid oligosaccharide.
Description
Technical field
The present invention relates to a kind of method of utilizing Fenton (Fenton) prepared in reaction guluronic acid oligosaccharides.
Background technology
Algin is the linear anionic polysaccharide that is connected to form by 1,4 glycosidic link by beta-D-mannuronic acid and α-L-guluronic acid.Above-mentioned two kinds of uronic acid homogeneous or alternately arrangement, the algin fragment that homogeneous is arranged comprises polymannuronic acid (PM) and poly-guluronic acid (PG).The algin source is abundant, and has been widely used in food, chemical industry and pharmaceutical sector etc.Algin oligosaccharide comprised that the physiological action of guluronic acid oligosaccharides constantly was found in recent years, and it has the function of stronger promotion plant-growth, and anticoagulant active, antiviral activity, anti-microbial activity are arranged; Can improve immunizing power, anti-tumor activity and anti-inflammatory activity.Therefore the demand of guluronic acid oligosaccharides grows with each passing day, and has caused the concern that people are bigger.
Summary of the invention
The purpose of this invention is to provide a kind of method of the Fenton of utilization prepared in reaction guluronic acid oligosaccharides, it can satisfy the demand of prior art.
A kind of method of utilizing Fenton's reaction to prepare the guluronic acid oligosaccharides, comprise and to gather guluronic acid to be made into concentration expressed in percentage by weight be 0.1～5% the aqueous solution, it is characterized in that adding oxygenant to concentration to this aqueous solution is 0.05-0.5%, add metal ion to concentration 0.05-0.5%, 20～40 ℃ of reactions down, after the stopping of reaction, reaction solution is concentrated, use Bio-gel P10 then, the separation and purification of Q-Sepharose Fast Flow chromatography column; Described oxygenant is a hydrogen peroxide; Described metal ion is a ferrous ion.
The method for preparing the guluronic acid oligosaccharides of the present invention, speed of response is fast, and the product purity height is easy to separation and purification, and energy mass production guluronic acid oligosaccharides is fully used it, and its function and activity also can be developed widely.
Embodiment
To gather guluronic acid and be made into 2% (concentration expressed in percentage by weight, as follows) the aqueous solution, adding oxidants hydrogen peroxide to concentration is 0.1%, and adding ferrous sulfate to concentration is 0.4%, 25 ℃ of reactions down, after the stopping of reaction, reaction solution is concentrated, use Bio-gel P10 then, the separation and purification of Q-Sepharose FastFlow chromatography column, obtain guluronic acid series oligosaccharides, its structural formula is:
N is 1-19 in the formula.
Oxygenant described in the present invention is hydrogen peroxide, hypochlorous acid, hypochlorite or sulfuric acid.Described metal ion is bivalent cupric ion, iron ion.The concentration expressed in percentage by weight of described poly-guluronic acid in the aqueous solution is 0.1-1.5%, and the concentration of oxygenant and metal ion is 0.05-0.5%, and temperature of reaction is 20-40 ℃.
Claims (1)
1, a kind of method of utilizing Fenton's reaction to prepare the guluronic acid oligosaccharides, comprise and to gather guluronic acid to be made into concentration expressed in percentage by weight be 0.1～5% the aqueous solution, it is characterized in that adding oxygenant to concentration to this aqueous solution is 0.05-0.5%, add metal ion to concentration 0.05-0.5%, 20～40 ℃ of reactions down, after the stopping of reaction, reaction solution is concentrated, use Bio-gelP10 then, the separation and purification of Q-Sepharose Fast Flow chromatography column; Described oxygenant is a hydrogen peroxide; Described metal ion is a ferrous ion.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200310105694 CN1219786C (en) | 2003-11-22 | 2003-11-22 | Guluronicacid oligosaccharides production method utilizing Fenton-type reaction |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN 200310105694 CN1219786C (en) | 2003-11-22 | 2003-11-22 | Guluronicacid oligosaccharides production method utilizing Fenton-type reaction |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1544446A CN1544446A (en) | 2004-11-10 |
| CN1219786C true CN1219786C (en) | 2005-09-21 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN 200310105694 Expired - Fee Related CN1219786C (en) | 2003-11-22 | 2003-11-22 | Guluronicacid oligosaccharides production method utilizing Fenton-type reaction |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1219786C (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN103446165B (en) * | 2013-09-12 | 2016-04-13 | 中国海洋大学 | Oligoguluronic acid is preparing the application in the medicine of prevention and therapy alcoholic liver injury, health product or dietary supplement |
| CA3067582A1 (en) * | 2017-06-20 | 2018-12-27 | The Regents Of The University Of California | Production of bioactive oligosaccharides |
| CN111214441B (en) * | 2020-03-16 | 2021-06-08 | 深圳大学 | Guluronic acid oligosaccharide liposome and preparation method thereof |
-
2003
- 2003-11-22 CN CN 200310105694 patent/CN1219786C/en not_active Expired - Fee Related
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| Publication number | Publication date |
|---|---|
| CN1544446A (en) | 2004-11-10 |
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| C06 | Publication | ||
| PB01 | Publication | ||
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| C14 | Grant of patent or utility model | ||
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| C41 | Transfer of patent application or patent right or utility model | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20151030 Address after: 266071 Hongkong East Road, Laoshan District, Shandong, China, No. 23, No. Patentee after: Qingdao Ocean University of China Holdings Ltd. Address before: 266003 No. 5 fish Hill Road, Shandong, Qingdao Patentee before: Ocean University of China |
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| C41 | Transfer of patent application or patent right or utility model | ||
| TR01 | Transfer of patent right |
Effective date of registration: 20160525 Address after: 266071 Hongkong East Road, Laoshan District, Shandong, China, No. 23, No. Patentee after: MARINE BIOMEDICAL RESEARCH INSTITUTE OF QINGDAO Co.,Ltd. Address before: 266071 Hongkong East Road, Laoshan District, Shandong, China, No. 23, No. Patentee before: Qingdao Ocean University of China Holdings Ltd. |
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| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20050921 |