NL139559B - Werkwijze ter bereiding van polysacchariden. - Google Patents
Werkwijze ter bereiding van polysacchariden.Info
- Publication number
- NL139559B NL139559B NL63299907A NL299907A NL139559B NL 139559 B NL139559 B NL 139559B NL 63299907 A NL63299907 A NL 63299907A NL 299907 A NL299907 A NL 299907A NL 139559 B NL139559 B NL 139559B
- Authority
- NL
- Netherlands
- Prior art keywords
- beta
- linked
- scleroglucan
- polysaccharide
- glucose
- Prior art date
Links
- 150000004676 glycans Chemical class 0.000 title abstract 7
- 229920001282 polysaccharide Polymers 0.000 title abstract 7
- 239000005017 polysaccharide Substances 0.000 title abstract 7
- 238000004519 manufacturing process Methods 0.000 title 1
- FEBUJFMRSBAMES-UHFFFAOYSA-N 2-[(2-{[3,5-dihydroxy-2-(hydroxymethyl)-6-phosphanyloxan-4-yl]oxy}-3,5-dihydroxy-6-({[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}methyl)oxan-4-yl)oxy]-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl phosphinite Chemical compound OC1C(O)C(O)C(CO)OC1OCC1C(O)C(OC2C(C(OP)C(O)C(CO)O2)O)C(O)C(OC2C(C(CO)OC(P)C2O)O)O1 FEBUJFMRSBAMES-UHFFFAOYSA-N 0.000 abstract 6
- 229920002305 Schizophyllan Polymers 0.000 abstract 6
- 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 abstract 5
- 239000007864 aqueous solution Substances 0.000 abstract 3
- 238000009472 formulation Methods 0.000 abstract 3
- 239000008103 glucose Substances 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 241001558929 Sclerotium <basidiomycota> Species 0.000 abstract 2
- 244000005700 microbiome Species 0.000 abstract 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 abstract 1
- 241001529717 Corticium <basidiomycota> Species 0.000 abstract 1
- 125000002353 D-glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 abstract 1
- AYRXSINWFIIFAE-UHFFFAOYSA-N O6-alpha-D-Galactopyranosyl-D-galactose Natural products OCC1OC(OCC(O)C(O)C(O)C(O)C=O)C(O)C(O)C1O AYRXSINWFIIFAE-UHFFFAOYSA-N 0.000 abstract 1
- 229910004679 ONO2 Inorganic materials 0.000 abstract 1
- 241000221662 Sclerotinia Species 0.000 abstract 1
- 241000932081 Stromatinia Species 0.000 abstract 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract 1
- 238000005903 acid hydrolysis reaction Methods 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 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 abstract 1
- 229940041514 candida albicans extract Drugs 0.000 abstract 1
- 150000001720 carbohydrates Chemical class 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 abstract 1
- 150000001768 cations Chemical group 0.000 abstract 1
- 239000011248 coating agent Substances 0.000 abstract 1
- 238000000576 coating method Methods 0.000 abstract 1
- MHDVGSVTJDSBDK-UHFFFAOYSA-N dibenzyl ether Chemical class C=1C=CC=CC=1COCC1=CC=CC=C1 MHDVGSVTJDSBDK-UHFFFAOYSA-N 0.000 abstract 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 abstract 1
- 239000000499 gel Substances 0.000 abstract 1
- DLRVVLDZNNYCBX-CQUJWQHSSA-N gentiobiose Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)C(O)O1 DLRVVLDZNNYCBX-CQUJWQHSSA-N 0.000 abstract 1
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 125000001893 nitrooxy group Chemical group [O-][N+](=O)O* 0.000 abstract 1
- 239000003960 organic solvent Substances 0.000 abstract 1
- 229920000642 polymer Polymers 0.000 abstract 1
- 238000001556 precipitation Methods 0.000 abstract 1
- 238000002360 preparation method Methods 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 241000894007 species Species 0.000 abstract 1
- 229910021653 sulphate ion Inorganic materials 0.000 abstract 1
- 239000012991 xanthate Substances 0.000 abstract 1
- 239000012138 yeast extract Substances 0.000 abstract 1
Classifications
-
- 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
-
- 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
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0024—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/04—Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/14—Preparation of compounds containing saccharide radicals produced by the action of a carbohydrase (EC 3.2.x), e.g. by alpha-amylase, e.g. by cellulase, hemicellulase
-
- C—CHEMISTRY; METALLURGY
- C13—SUGAR INDUSTRY
- C13K—SACCHARIDES OBTAINED FROM NATURAL SOURCES OR BY HYDROLYSIS OF NATURALLY OCCURRING DISACCHARIDES, OLIGOSACCHARIDES OR POLYSACCHARIDES
- C13K13/00—Sugars not otherwise provided for in this class
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Materials Engineering (AREA)
- Polymers & Plastics (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Paper (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US23590462A | 1962-10-30 | 1962-10-30 | |
DEP0037135 | 1963-10-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
NL139559B true NL139559B (nl) | 1973-08-15 |
Family
ID=25990418
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL299907D NL299907A (enrdf_load_stackoverflow) | 1962-10-30 | ||
NL63299907A NL139559B (nl) | 1962-10-30 | 1963-10-30 | Werkwijze ter bereiding van polysacchariden. |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL299907D NL299907A (enrdf_load_stackoverflow) | 1962-10-30 |
Country Status (8)
Country | Link |
---|---|
BE (1) | BE639361A (enrdf_load_stackoverflow) |
CH (1) | CH470476A (enrdf_load_stackoverflow) |
DE (2) | DE1442286A1 (enrdf_load_stackoverflow) |
DK (1) | DK116501B (enrdf_load_stackoverflow) |
GB (1) | GB1061043A (enrdf_load_stackoverflow) |
NL (2) | NL139559B (enrdf_load_stackoverflow) |
NO (1) | NO135096C (enrdf_load_stackoverflow) |
SE (1) | SE333125B (enrdf_load_stackoverflow) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3415929A (en) * | 1965-07-14 | 1968-12-10 | Ciba Geigy Corp | Ophthalmic solution containing poly-1,3-beta-glucoside |
DE3214953A1 (de) * | 1982-04-22 | 1983-10-27 | Hoechst Ag, 6230 Frankfurt | Mikrobielle polysaccharide, verfahren zu ihrer herstellung, dafuer geeignete mikroorganismen und verwendung der polysaccharide |
CN116370389A (zh) * | 2023-03-02 | 2023-07-04 | 海孵(海南自贸区)医疗科技有限责任公司 | 一种重组ⅲ型人源化胶原蛋白敷料贴及其制备方法和应用 |
-
0
- NL NL299907D patent/NL299907A/xx unknown
- BE BE639361D patent/BE639361A/xx unknown
-
1963
- 1963-10-22 NO NO150541A patent/NO135096C/no unknown
- 1963-10-23 GB GB41789/63A patent/GB1061043A/en not_active Expired
- 1963-10-29 DK DK509663AA patent/DK116501B/da unknown
- 1963-10-30 CH CH1333263A patent/CH470476A/de not_active IP Right Cessation
- 1963-10-30 DE DE19631442286 patent/DE1442286A1/de active Pending
- 1963-10-30 SE SE11933/63A patent/SE333125B/xx unknown
- 1963-10-30 DE DE19631442141 patent/DE1442141A1/de active Pending
- 1963-10-30 NL NL63299907A patent/NL139559B/xx not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
NO135096C (enrdf_load_stackoverflow) | 1977-02-09 |
DK116501B (da) | 1970-01-19 |
GB1061043A (en) | 1967-03-08 |
BE639361A (enrdf_load_stackoverflow) | |
NL299907A (enrdf_load_stackoverflow) | |
DE1442286A1 (de) | 1968-11-21 |
SE333125B (sv) | 1971-03-08 |
NO135096B (enrdf_load_stackoverflow) | 1976-11-01 |
CH470476A (de) | 1969-03-31 |
DE1442141A1 (de) | 1969-12-11 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Sasaki et al. | Antitumor activity of carboxymethylglucans obtained by carboxymethylation of (1→ 3)-β-D-glucan from Alcaligenes faecalis var. myxogenes IFO 13140 | |
US3301848A (en) | Polysaccharides and methods for production thereof | |
US3453257A (en) | Cyclodextrin with cationic properties | |
US3096293A (en) | Method of increasing the viscosity of an aqueous solution of a deacetylated polysaccharide | |
Orentas et al. | Pyruvic acid content and constituent sugars of exocellular polysaccharides from different species of the genus Xanthomonas | |
KR830001375A (ko) | 박테리아 발효에 의한 다당류 s-60의 제조방법 | |
US3349077A (en) | Etherified xanthomonas hydrophilic colloids and process of preparation | |
ES8101645A1 (es) | Un procedimiento para la produccion de heteropolisacarido s-60 | |
NL139559B (nl) | Werkwijze ter bereiding van polysacchariden. | |
O'Neill et al. | Structure of the extracellular gelling polysaccharide produced by Enterobacter (NCIB 11870) species | |
Love et al. | 633. The polysaccharides of the green seaweed codium fragile. Part III. A β-1, 4-linked mannan | |
Sidebotham et al. | Studies on dextrans and dextranases: Part IX. Dextrans elaborated by cariogenic organisms | |
DE3670309D1 (de) | Heteropolysaccharid, seine herstellung und verwendung. | |
DE69116601T2 (de) | Verfahren zur Herstellung von Antitumordextran | |
GB1187614A (en) | Food Products | |
Seno et al. | Substrate specificity of chondrosulfatases from Proteus vulgaris for sulfated tetrasaccharides | |
US2203703A (en) | Ethers of dextran | |
US3244695A (en) | Cationic ethers of xanthomonas hydrophilic colloids | |
Kishida et al. | Preparation of Water-soluble Methyl Konjac Gluco-mannan | |
US3256271A (en) | Method of improving viscosity characteristics of xanthomonas hydrophilic colloids and esters produced thereby | |
Waksman et al. | Micromonosporin, an antibiotic substance from a little-known group of microorganisms | |
Nunn et al. | Sulphated polysaccharides of the grateloupiaceae family: Part III. A polysaccharide from Phyllymenia cornea | |
US3236831A (en) | Xanthomonas hydrophilic colloid ethers | |
JPH05271306A (ja) | 抗ウイルス性硫酸化多糖類 | |
Murphy et al. | A mannan produced by Bacillus polymyxa |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
NL80 | Abbreviated name of patent owner mentioned of already nullified patent |
Owner name: CECA |
|
V4 | Lapsed because of reaching the maximum lifetime of a patent |