DE69923356T2 - Gereinigte polysaccharide aus "alteromonas macleodii" und seine verwendungen - Google Patents
Gereinigte polysaccharide aus "alteromonas macleodii" und seine verwendungen Download PDFInfo
- Publication number
- DE69923356T2 DE69923356T2 DE69923356T DE69923356T DE69923356T2 DE 69923356 T2 DE69923356 T2 DE 69923356T2 DE 69923356 T DE69923356 T DE 69923356T DE 69923356 T DE69923356 T DE 69923356T DE 69923356 T2 DE69923356 T2 DE 69923356T2
- Authority
- DE
- Germany
- Prior art keywords
- polysaccharide
- polysaccharide according
- product
- weight
- residues
- 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
Links
- 150000004676 glycans Chemical class 0.000 title claims description 48
- 229920001282 polysaccharide Polymers 0.000 title claims description 48
- 239000005017 polysaccharide Substances 0.000 title claims description 48
- 241001135315 Alteromonas macleodii Species 0.000 title 1
- 229940011158 alteromonas macleodii Drugs 0.000 title 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 claims description 11
- AEMOLEFTQBMNLQ-YMDCURPLSA-N D-galactopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-YMDCURPLSA-N 0.000 claims description 7
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 claims description 7
- 239000008103 glucose Substances 0.000 claims description 7
- 230000008719 thickening Effects 0.000 claims description 7
- AEMOLEFTQBMNLQ-AQKNRBDQSA-N D-glucopyranuronic acid Chemical compound OC1O[C@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-AQKNRBDQSA-N 0.000 claims description 6
- 229930182830 galactose Natural products 0.000 claims description 6
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- 229940097043 glucuronic acid Drugs 0.000 claims description 5
- WQZGKKKJIJFFOK-PHYPRBDBSA-N alpha-D-galactose Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@H]1O WQZGKKKJIJFFOK-PHYPRBDBSA-N 0.000 claims description 4
- 235000019728 animal nutrition Nutrition 0.000 claims description 4
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 230000000087 stabilizing effect Effects 0.000 claims description 4
- 239000004615 ingredient Substances 0.000 claims description 3
- 150000001720 carbohydrates Chemical group 0.000 claims description 2
- 125000000311 mannosyl group Chemical class C1([C@@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims description 2
- 239000002562 thickening agent Substances 0.000 claims description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 10
- 238000004458 analytical method Methods 0.000 description 9
- 239000000203 mixture Substances 0.000 description 8
- -1 methyl glycosides Chemical class 0.000 description 7
- 239000000047 product Substances 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- 229920002444 Exopolysaccharide Polymers 0.000 description 5
- LCTONWCANYUPML-UHFFFAOYSA-N Pyruvic acid Chemical compound CC(=O)C(O)=O LCTONWCANYUPML-UHFFFAOYSA-N 0.000 description 5
- 238000001595 flow curve Methods 0.000 description 5
- 229930182470 glycoside Natural products 0.000 description 5
- 239000011780 sodium chloride Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 241000519604 Alteromonas macleodii subsp. fijiensis Species 0.000 description 4
- WQZGKKKJIJFFOK-QTVWNMPRSA-N D-mannopyranose Chemical compound OC[C@H]1OC(O)[C@@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-QTVWNMPRSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- 238000004817 gas chromatography Methods 0.000 description 4
- 150000002500 ions Chemical class 0.000 description 4
- 150000002704 mannoses Chemical class 0.000 description 4
- 229920001223 polyethylene glycol Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 230000007062 hydrolysis Effects 0.000 description 3
- 238000006460 hydrolysis reaction Methods 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 238000001228 spectrum Methods 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 230000021736 acetylation Effects 0.000 description 2
- 238000006640 acetylation reaction Methods 0.000 description 2
- 238000004737 colorimetric analysis Methods 0.000 description 2
- 238000010828 elution Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 238000012869 ethanol precipitation Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 125000003563 glycoside group Chemical group 0.000 description 2
- 238000005570 heteronuclear single quantum coherence Methods 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000004949 mass spectrometry Methods 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 230000011987 methylation Effects 0.000 description 2
- 238000007069 methylation reaction Methods 0.000 description 2
- 150000003214 pyranose derivatives Chemical class 0.000 description 2
- 229940107700 pyruvic acid Drugs 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 239000012265 solid product Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 238000001551 total correlation spectroscopy Methods 0.000 description 2
- 102000003886 Glycoproteins Human genes 0.000 description 1
- 108090000288 Glycoproteins Proteins 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 238000005481 NMR spectroscopy Methods 0.000 description 1
- LCTONWCANYUPML-UHFFFAOYSA-M Pyruvate Chemical group CC(=O)C([O-])=O LCTONWCANYUPML-UHFFFAOYSA-M 0.000 description 1
- 229920002684 Sepharose Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000005349 anion exchange Methods 0.000 description 1
- 238000005571 anion exchange chromatography Methods 0.000 description 1
- 239000003125 aqueous solvent Substances 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 238000007068 beta-elimination reaction Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- RTVIDYFRRZCJNH-UHFFFAOYSA-N butan-2-ol;2,2,2-trifluoroacetic acid Chemical compound CCC(C)O.OC(=O)C(F)(F)F RTVIDYFRRZCJNH-UHFFFAOYSA-N 0.000 description 1
- 238000012511 carbohydrate analysis Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000005352 clarification Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 238000005100 correlation spectroscopy Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 150000002243 furanoses Chemical class 0.000 description 1
- 239000006481 glucose medium Substances 0.000 description 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 description 1
- 238000000990 heteronuclear single quantum coherence spectrum Methods 0.000 description 1
- 150000002402 hexoses Chemical class 0.000 description 1
- 239000003906 humectant Substances 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 235000021056 liquid food Nutrition 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 230000004807 localization Effects 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000006140 methanolysis reaction Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 238000005016 nuclear Overhauser enhanced spectroscopy Methods 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910001414 potassium ion Inorganic materials 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229940076788 pyruvate Drugs 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- 241000556533 uncultured marine bacterium Species 0.000 description 1
- 239000000052 vinegar Substances 0.000 description 1
- 235000021419 vinegar Nutrition 0.000 description 1
- 235000014101 wine Nutrition 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12H—PASTEURISATION, STERILISATION, PRESERVATION, PURIFICATION, CLARIFICATION OR AGEING OF ALCOHOLIC BEVERAGES; METHODS FOR ALTERING THE ALCOHOL CONTENT OF FERMENTED SOLUTIONS OR ALCOHOLIC BEVERAGES
- C12H1/00—Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages
- C12H1/02—Pasteurisation, sterilisation, preservation, purification, clarification, or ageing of alcoholic beverages combined with removal of precipitate or added materials, e.g. adsorption material
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23L—FOODS, FOODSTUFFS OR NON-ALCOHOLIC BEVERAGES, NOT OTHERWISE PROVIDED FOR; PREPARATION OR TREATMENT THEREOF
- A23L29/00—Foods or foodstuffs containing additives; Preparation or treatment thereof
- A23L29/20—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents
- A23L29/269—Foods or foodstuffs containing additives; Preparation or treatment thereof containing gelling or thickening agents of microbial origin, e.g. xanthan or dextran
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/006—Heteroglycans, i.e. polysaccharides having more than one sugar residue in the main chain in either alternating or less regular sequence; Gellans; Succinoglycans; Arabinogalactans; Tragacanth or gum tragacanth or traganth from Astragalus; Gum Karaya from Sterculia urens; Gum Ghatti from Anogeissus latifolia; Derivatives thereof
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Biochemistry (AREA)
- Food Science & Technology (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Nutrition Science (AREA)
- Molecular Biology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Dispersion Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Jellies, Jams, And Syrups (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9807839A FR2780063B1 (fr) | 1998-06-22 | 1998-06-22 | Polysaccharide purifie d'alteromonas macleodii et ses utilisations |
| FR9807839 | 1998-06-22 | ||
| PCT/FR1999/001490 WO1999067411A1 (fr) | 1998-06-22 | 1999-06-22 | Polysaccharide purifie d'alteromonas macleodii et ses utilisations |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69923356D1 DE69923356D1 (de) | 2005-02-24 |
| DE69923356T2 true DE69923356T2 (de) | 2006-03-30 |
Family
ID=9527668
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69923356T Expired - Fee Related DE69923356T2 (de) | 1998-06-22 | 1999-06-22 | Gereinigte polysaccharide aus "alteromonas macleodii" und seine verwendungen |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6545145B1 (enExample) |
| EP (1) | EP1171625B1 (enExample) |
| JP (1) | JP2002518586A (enExample) |
| AU (1) | AU4270499A (enExample) |
| DE (1) | DE69923356T2 (enExample) |
| FR (1) | FR2780063B1 (enExample) |
| WO (1) | WO1999067411A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2871476B1 (fr) * | 2004-06-14 | 2011-04-01 | Ifremer | Derives depolymerises sulfates d'exopolysaccharides (eps) provenant de bacteries marines mesophiles, leur procede de preparation et leurs utilisations en regeneration tissulaire |
| FR2871379B1 (fr) * | 2004-06-14 | 2006-09-29 | Ifremer | Utilisation de derives polysaccharidiques hautement sulfates et de faible masse molaire pour moduler l'angiogenese |
| EP1739094A1 (fr) * | 2005-06-30 | 2007-01-03 | Faculté Universitaire des Sciences Agronomiques de Gembloux | Procédé de purification de polysaccharides chargés électriquement |
| JP4649569B2 (ja) * | 2007-12-12 | 2011-03-09 | 三重県 | 増粘安定剤 |
| CN102040667B (zh) * | 2010-10-30 | 2012-08-22 | 中国海洋大学 | 海参多糖中蛋白的生物脱除方法 |
| US9670395B2 (en) * | 2013-04-22 | 2017-06-06 | Halliburton Energy Services, Inc. | Treatment of a subterranean formation with composition including a microorganism or compound generated by the same |
| CN105087450B (zh) * | 2015-09-29 | 2018-07-31 | 厦门大学 | 一株海洋细菌及其产生的胞外多糖 |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS59156253A (ja) * | 1983-02-28 | 1984-09-05 | Nakano Vinegar Co Ltd | 食品用増粘剤 |
| JPS61183301A (ja) * | 1985-02-08 | 1986-08-16 | Nakano Vinegar Co Ltd | 酸性ヘテロ多糖類の改良製造法 |
| DE3685955D1 (en) * | 1986-02-06 | 1992-08-13 | Celgene Corp | Biosynthese von heteropolysacchariden. |
| FR2701488B1 (fr) * | 1993-02-15 | 1995-05-05 | Ifremer | Bactéries du type Alteromonas, polysaccharides produits par ces bactéries, ose contenu dans ces polysaccharides et applications. |
-
1998
- 1998-06-22 FR FR9807839A patent/FR2780063B1/fr not_active Expired - Fee Related
-
1999
- 1999-06-22 AU AU42704/99A patent/AU4270499A/en not_active Abandoned
- 1999-06-22 US US09/720,238 patent/US6545145B1/en not_active Expired - Fee Related
- 1999-06-22 DE DE69923356T patent/DE69923356T2/de not_active Expired - Fee Related
- 1999-06-22 WO PCT/FR1999/001490 patent/WO1999067411A1/fr not_active Ceased
- 1999-06-22 JP JP2000556051A patent/JP2002518586A/ja not_active Ceased
- 1999-06-22 EP EP99957183A patent/EP1171625B1/fr not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| US6545145B1 (en) | 2003-04-08 |
| EP1171625A1 (fr) | 2002-01-16 |
| WO1999067411A1 (fr) | 1999-12-29 |
| FR2780063A1 (fr) | 1999-12-24 |
| JP2002518586A (ja) | 2002-06-25 |
| DE69923356D1 (de) | 2005-02-24 |
| FR2780063B1 (fr) | 2001-07-13 |
| EP1171625B1 (fr) | 2005-01-19 |
| AU4270499A (en) | 2000-01-10 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |