NO325114B1 - Fremgangsmate for fremstilling av rette eller forgrenede karbohydratpolymerer - Google Patents
Fremgangsmate for fremstilling av rette eller forgrenede karbohydratpolymerer Download PDFInfo
- Publication number
- NO325114B1 NO325114B1 NO20005545A NO20005545A NO325114B1 NO 325114 B1 NO325114 B1 NO 325114B1 NO 20005545 A NO20005545 A NO 20005545A NO 20005545 A NO20005545 A NO 20005545A NO 325114 B1 NO325114 B1 NO 325114B1
- Authority
- NO
- Norway
- Prior art keywords
- fructooligosaccharides
- sucrose
- enzyme
- glucose
- polymers
- Prior art date
Links
- 229920001282 polysaccharide Polymers 0.000 title claims description 26
- 238000004519 manufacturing process Methods 0.000 title claims description 22
- 108090000790 Enzymes Proteins 0.000 claims description 52
- 102000004190 Enzymes Human genes 0.000 claims description 52
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 claims description 49
- 229930006000 Sucrose Natural products 0.000 claims description 49
- 239000005720 sucrose Substances 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 46
- 229920000642 polymer Polymers 0.000 claims description 45
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 claims description 42
- 239000012528 membrane Substances 0.000 claims description 35
- 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 32
- 150000001720 carbohydrates Chemical class 0.000 claims description 32
- 239000008103 glucose Substances 0.000 claims description 32
- 238000006243 chemical reaction Methods 0.000 claims description 31
- 235000014633 carbohydrates Nutrition 0.000 claims description 29
- 229930091371 Fructose Natural products 0.000 claims description 22
- 239000005715 Fructose Substances 0.000 claims description 22
- 239000000203 mixture Substances 0.000 claims description 20
- 235000000346 sugar Nutrition 0.000 claims description 20
- 239000006227 byproduct Substances 0.000 claims description 19
- 239000011541 reaction mixture Substances 0.000 claims description 19
- 150000002772 monosaccharides Chemical class 0.000 claims description 16
- 108010042889 Inulosucrase Proteins 0.000 claims description 13
- 238000012546 transfer Methods 0.000 claims description 11
- 238000000926 separation method Methods 0.000 claims description 10
- 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 9
- 239000012141 concentrate Substances 0.000 claims description 9
- 150000002482 oligosaccharides Polymers 0.000 claims description 9
- 230000008569 process Effects 0.000 claims description 9
- 238000004064 recycling Methods 0.000 claims description 9
- -1 glycosyl phosphate Chemical compound 0.000 claims description 8
- 150000002016 disaccharides Chemical class 0.000 claims description 7
- 230000000694 effects Effects 0.000 claims description 7
- 229920001542 oligosaccharide Polymers 0.000 claims description 7
- 229920002670 Fructan Polymers 0.000 claims description 6
- BJHIKXHVCXFQLS-UYFOZJQFSA-N fructose group Chemical group OCC(=O)[C@@H](O)[C@H](O)[C@H](O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 claims description 6
- FTSSQIKWUOOEGC-RULYVFMPSA-N fructooligosaccharide Chemical compound OC[C@H]1O[C@@](CO)(OC[C@@]2(OC[C@@]3(OC[C@@]4(OC[C@@]5(OC[C@@]6(OC[C@@]7(OC[C@@]8(OC[C@@]9(OC[C@@]%10(OC[C@@]%11(O[C@H]%12O[C@H](CO)[C@@H](O)[C@H](O)[C@H]%12O)O[C@H](CO)[C@@H](O)[C@@H]%11O)O[C@H](CO)[C@@H](O)[C@@H]%10O)O[C@H](CO)[C@@H](O)[C@@H]9O)O[C@H](CO)[C@@H](O)[C@@H]8O)O[C@H](CO)[C@@H](O)[C@@H]7O)O[C@H](CO)[C@@H](O)[C@@H]6O)O[C@H](CO)[C@@H](O)[C@@H]5O)O[C@H](CO)[C@@H](O)[C@@H]4O)O[C@H](CO)[C@@H](O)[C@@H]3O)O[C@H](CO)[C@@H](O)[C@@H]2O)[C@@H](O)[C@@H]1O FTSSQIKWUOOEGC-RULYVFMPSA-N 0.000 claims description 5
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 claims description 4
- 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 4
- SHZGCJCMOBCMKK-UHFFFAOYSA-N D-mannomethylose Natural products CC1OC(O)C(O)C(O)C1O SHZGCJCMOBCMKK-UHFFFAOYSA-N 0.000 claims description 3
- PNNNRSAQSRJVSB-SLPGGIOYSA-N Fucose Natural products C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C=O PNNNRSAQSRJVSB-SLPGGIOYSA-N 0.000 claims description 3
- SHZGCJCMOBCMKK-DHVFOXMCSA-N L-fucopyranose Chemical compound C[C@@H]1OC(O)[C@@H](O)[C@H](O)[C@@H]1O SHZGCJCMOBCMKK-DHVFOXMCSA-N 0.000 claims description 3
- 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 3
- 230000003197 catalytic effect Effects 0.000 claims description 3
- 238000004587 chromatography analysis Methods 0.000 claims description 3
- 229940107187 fructooligosaccharide Drugs 0.000 claims description 3
- 229930182830 galactose Natural products 0.000 claims description 3
- 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 claims description 2
- OVRNDRQMDRJTHS-CBQIKETKSA-N N-Acetyl-D-Galactosamine Chemical compound CC(=O)N[C@H]1[C@@H](O)O[C@H](CO)[C@H](O)[C@@H]1O OVRNDRQMDRJTHS-CBQIKETKSA-N 0.000 claims description 2
- OVRNDRQMDRJTHS-UHFFFAOYSA-N N-acelyl-D-glucosamine Natural products CC(=O)NC1C(O)OC(CO)C(O)C1O OVRNDRQMDRJTHS-UHFFFAOYSA-N 0.000 claims description 2
- MBLBDJOUHNCFQT-UHFFFAOYSA-N N-acetyl-D-galactosamine Natural products CC(=O)NC(C=O)C(O)C(O)C(O)CO MBLBDJOUHNCFQT-UHFFFAOYSA-N 0.000 claims description 2
- OVRNDRQMDRJTHS-FMDGEEDCSA-N N-acetyl-beta-D-glucosamine Chemical compound CC(=O)N[C@H]1[C@H](O)O[C@H](CO)[C@@H](O)[C@@H]1O OVRNDRQMDRJTHS-FMDGEEDCSA-N 0.000 claims description 2
- MBLBDJOUHNCFQT-LXGUWJNJSA-N N-acetylglucosamine Natural products CC(=O)N[C@@H](C=O)[C@@H](O)[C@H](O)[C@H](O)CO MBLBDJOUHNCFQT-LXGUWJNJSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 claims description 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 claims description 2
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims description 2
- 229940097043 glucuronic acid Drugs 0.000 claims description 2
- 238000011065 in-situ storage Methods 0.000 claims description 2
- 229950006780 n-acetylglucosamine Drugs 0.000 claims description 2
- 239000002773 nucleotide Substances 0.000 claims description 2
- 125000003729 nucleotide group Chemical group 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 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 1
- AEMOLEFTQBMNLQ-HNFCZKTMSA-N L-idopyranuronic acid Chemical compound OC1O[C@@H](C(O)=O)[C@@H](O)[C@H](O)[C@H]1O AEMOLEFTQBMNLQ-HNFCZKTMSA-N 0.000 claims 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 claims 1
- 235000012239 silicon dioxide Nutrition 0.000 claims 1
- 239000000047 product Substances 0.000 description 29
- 229920001202 Inulin Polymers 0.000 description 23
- 241000196324 Embryophyta Species 0.000 description 21
- 229940029339 inulin Drugs 0.000 description 21
- JYJIGFIDKWBXDU-MNNPPOADSA-N inulin Chemical group O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@]1(OC[C@]2(OC[C@]3(OC[C@]4(OC[C@]5(OC[C@]6(OC[C@]7(OC[C@]8(OC[C@]9(OC[C@]%10(OC[C@]%11(OC[C@]%12(OC[C@]%13(OC[C@]%14(OC[C@]%15(OC[C@]%16(OC[C@]%17(OC[C@]%18(OC[C@]%19(OC[C@]%20(OC[C@]%21(OC[C@]%22(OC[C@]%23(OC[C@]%24(OC[C@]%25(OC[C@]%26(OC[C@]%27(OC[C@]%28(OC[C@]%29(OC[C@]%30(OC[C@]%31(OC[C@]%32(OC[C@]%33(OC[C@]%34(OC[C@]%35(OC[C@]%36(O[C@@H]%37[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O%37)O)[C@H]([C@H](O)[C@@H](CO)O%36)O)[C@H]([C@H](O)[C@@H](CO)O%35)O)[C@H]([C@H](O)[C@@H](CO)O%34)O)[C@H]([C@H](O)[C@@H](CO)O%33)O)[C@H]([C@H](O)[C@@H](CO)O%32)O)[C@H]([C@H](O)[C@@H](CO)O%31)O)[C@H]([C@H](O)[C@@H](CO)O%30)O)[C@H]([C@H](O)[C@@H](CO)O%29)O)[C@H]([C@H](O)[C@@H](CO)O%28)O)[C@H]([C@H](O)[C@@H](CO)O%27)O)[C@H]([C@H](O)[C@@H](CO)O%26)O)[C@H]([C@H](O)[C@@H](CO)O%25)O)[C@H]([C@H](O)[C@@H](CO)O%24)O)[C@H]([C@H](O)[C@@H](CO)O%23)O)[C@H]([C@H](O)[C@@H](CO)O%22)O)[C@H]([C@H](O)[C@@H](CO)O%21)O)[C@H]([C@H](O)[C@@H](CO)O%20)O)[C@H]([C@H](O)[C@@H](CO)O%19)O)[C@H]([C@H](O)[C@@H](CO)O%18)O)[C@H]([C@H](O)[C@@H](CO)O%17)O)[C@H]([C@H](O)[C@@H](CO)O%16)O)[C@H]([C@H](O)[C@@H](CO)O%15)O)[C@H]([C@H](O)[C@@H](CO)O%14)O)[C@H]([C@H](O)[C@@H](CO)O%13)O)[C@H]([C@H](O)[C@@H](CO)O%12)O)[C@H]([C@H](O)[C@@H](CO)O%11)O)[C@H]([C@H](O)[C@@H](CO)O%10)O)[C@H]([C@H](O)[C@@H](CO)O9)O)[C@H]([C@H](O)[C@@H](CO)O8)O)[C@H]([C@H](O)[C@@H](CO)O7)O)[C@H]([C@H](O)[C@@H](CO)O6)O)[C@H]([C@H](O)[C@@H](CO)O5)O)[C@H]([C@H](O)[C@@H](CO)O4)O)[C@H]([C@H](O)[C@@H](CO)O3)O)[C@H]([C@H](O)[C@@H](CO)O2)O)[C@@H](O)[C@H](O)[C@@H](CO)O1 JYJIGFIDKWBXDU-MNNPPOADSA-N 0.000 description 20
- 238000003786 synthesis reaction Methods 0.000 description 16
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- ZFTFOHBYVDOAMH-XNOIKFDKSA-N (2r,3s,4s,5r)-5-[[(2r,3s,4s,5r)-5-[[(2r,3s,4s,5r)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4-dihydroxy-2-(hydroxymethyl)oxolan-2-yl]oxymethyl]-2-(hydroxymethyl)oxolane-2,3,4-triol Chemical class O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)OC[C@@H]1[C@@H](O)[C@H](O)[C@](CO)(OC[C@@H]2[C@H]([C@H](O)[C@@](O)(CO)O2)O)O1 ZFTFOHBYVDOAMH-XNOIKFDKSA-N 0.000 description 4
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- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 3
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- SQVRNKJHWKZAKO-UHFFFAOYSA-N beta-N-Acetyl-D-neuraminic acid Natural products CC(=O)NC1C(O)CC(O)(C(O)=O)OC1C(O)C(O)CO SQVRNKJHWKZAKO-UHFFFAOYSA-N 0.000 description 2
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- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
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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
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0051—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Fructofuranans, e.g. beta-2,6-D-fructofuranan, i.e. levan; Derivatives thereof
- C08B37/0054—Inulin, i.e. beta-2,1-D-fructofuranan; Derivatives thereof
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/18—Stationary reactors having moving elements inside
- B01J19/1868—Stationary reactors having moving elements inside resulting in a loop-type movement
- B01J19/1881—Stationary reactors having moving elements inside resulting in a loop-type movement externally, i.e. the mixture leaving the vessel and subsequently re-entering it
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/18—Stationary reactors having moving elements inside
- B01J19/1893—Membrane reactors
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M29/00—Means for introduction, extraction or recirculation of materials, e.g. pumps
- C12M29/18—External loop; Means for reintroduction of fermented biomass or liquid percolate
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M47/00—Means for after-treatment of the produced biomass or of the fermentation or metabolic products, e.g. storage of biomass
- C12M47/10—Separation or concentration of fermentation products
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12M—APPARATUS FOR ENZYMOLOGY OR MICROBIOLOGY; APPARATUS FOR CULTURING MICROORGANISMS FOR PRODUCING BIOMASS, FOR GROWING CELLS OR FOR OBTAINING FERMENTATION OR METABOLIC PRODUCTS, i.e. BIOREACTORS OR FERMENTERS
- C12M47/00—Means for after-treatment of the produced biomass or of the fermentation or metabolic products, e.g. storage of biomass
- C12M47/12—Purification
-
- 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
- C12P19/18—Preparation of compounds containing saccharide radicals produced by the action of a glycosyl transferase, e.g. alpha-, beta- or gamma-cyclodextrins
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Genetics & Genomics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Sustainable Development (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Polysaccharides And Polysaccharide Derivatives (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US8428198P | 1998-05-05 | 1998-05-05 | |
| PCT/US1999/009752 WO1999057300A1 (fr) | 1998-05-05 | 1999-05-04 | Polymeres sacchariques fonctionnels de sources sacchariques peu onereuses et leur appareil de preparation |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO20005545D0 NO20005545D0 (no) | 2000-11-03 |
| NO20005545L NO20005545L (no) | 2000-11-03 |
| NO325114B1 true NO325114B1 (no) | 2008-02-04 |
Family
ID=22183956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO20005545A NO325114B1 (no) | 1998-05-05 | 2000-11-03 | Fremgangsmate for fremstilling av rette eller forgrenede karbohydratpolymerer |
Country Status (6)
| Country | Link |
|---|---|
| US (2) | US6423833B1 (fr) |
| EP (1) | EP1076716A1 (fr) |
| AU (1) | AU759465B2 (fr) |
| BR (1) | BR9911012A (fr) |
| NO (1) | NO325114B1 (fr) |
| WO (1) | WO1999057300A1 (fr) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6423833B1 (en) * | 1998-05-05 | 2002-07-23 | Steven J. Catani | Functional sugar polymers from inexpensive sugar sources and apparatus for preparing same |
| US7029702B2 (en) * | 1998-07-07 | 2006-04-18 | Ritter Natural Sciences Llc | Method for increasing lactose tolerance in mammals exhibiting lactose intolerance |
| KR20070069221A (ko) | 2000-06-28 | 2007-07-02 | 후지 니혼 세이토 코퍼레이션 | 신규한 이눌린 합성효소 및 이를 이용하는 이눌린의제조방법 |
| CN100385008C (zh) | 2001-09-26 | 2008-04-30 | 富士日本精糖株式会社 | 制备菊粉的方法 |
| US20040052915A1 (en) | 2002-09-13 | 2004-03-18 | Carlson Ting L. | Use of low glycemic index sweeteners in food and beverage compositions |
| JP4006385B2 (ja) * | 2002-11-20 | 2007-11-14 | 株式会社日立ハイテクノロジーズ | 糖鎖合成装置 |
| EP1608236B1 (fr) * | 2003-04-02 | 2014-11-05 | Cargill, Incorporated | Fibre dietetique amelioree contenant des matieres comprenant du glucane de faible poids moleculaire |
| BRPI0507583A (pt) * | 2004-03-17 | 2007-07-03 | Cargill Inc | adoçantes com baixo ìndice glicêmico e produtos feitos usando os mesmos |
| JP4252922B2 (ja) * | 2004-03-31 | 2009-04-08 | 株式会社日立ハイテクノロジーズ | 糖鎖合成装置 |
| WO2006012536A2 (fr) * | 2004-07-22 | 2006-02-02 | Ritter Andrew J | Procedes et compositions pour le traitement de l'intolerance au lactose |
| ES2444847T3 (es) * | 2005-02-15 | 2014-02-27 | Cargill, Incorporated | Procedimientos de preparación de jarabes |
| JP2009526528A (ja) * | 2006-02-13 | 2009-07-23 | マクニール ニュートリショナルズ，エル エル シー | 低ラクトース乳組成物及び関連方法 |
| FI20065363A0 (fi) * | 2006-05-30 | 2006-05-30 | Danisco Sweeteners Oy | Erotusmenetelmä |
| US20080044324A1 (en) * | 2006-08-16 | 2008-02-21 | Agency For Science, Technology And Research | Recirculating reactor |
| US20110223248A1 (en) * | 2007-12-12 | 2011-09-15 | Ritter Pharmaceuticals, Inc. | Methods and compositions for treating lactose intolerance |
| BRPI0912847A2 (pt) * | 2008-05-19 | 2015-10-13 | Otsuka America Pharmaceutical Inc | método e aparelho para preparar uma solução de um material sensível de cisalhamento. |
| US20110189148A1 (en) * | 2008-06-25 | 2011-08-04 | Ritter Pharmaceuticals, Inc. | Lactose compositions with decreased lactose content |
| WO2010098822A1 (fr) | 2009-02-24 | 2010-09-02 | Ritter Pharmaceuticals, Inc. | Formulations prébiotiques et méthodes d'utilisation |
| WO2011137249A1 (fr) | 2010-04-28 | 2011-11-03 | Ritter Pharmaceuticals, Inc. | Formulations prébiotiques et méthodes d'utilisation |
| CA2906984A1 (fr) | 2013-03-15 | 2014-09-18 | Cargill, Incorporated | Compositions d'hydrate de carbone |
| EP3166981A4 (fr) | 2014-07-09 | 2018-03-07 | Cadena Bio, Inc. | Compositions d'oligosaccharides et leurs procédés de production |
| PT3250048T (pt) | 2015-01-26 | 2019-11-18 | Cadena Bio Inc | Composições de oligossacáridos para utilização como ração para animais e métodos para a sua produção |
| CA2983236A1 (fr) | 2015-04-23 | 2016-10-27 | Kaleido Biosciences, Inc. | Agents therapeutiques de glycanes et procedes de traitement |
Family Cites Families (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4423150A (en) | 1977-06-16 | 1983-12-27 | Cpc International Inc. | Preparation of high fructose syrups from sucrose |
| GB2072679B (en) | 1980-03-31 | 1983-11-09 | Meiji Seika Kaisha | Sweetener |
| US4309505A (en) | 1980-05-19 | 1982-01-05 | Cpc International Inc. | Process for the production of fructose transferase enzyme |
| US4335207A (en) | 1980-06-03 | 1982-06-15 | Cpc International Inc. | Process for the production of high fructose syrups and ethanol |
| US4356262A (en) | 1980-06-03 | 1982-10-26 | Cpc International Inc. | Process for the production of high fructose syrups and ethanol |
| US4317880A (en) | 1980-06-03 | 1982-03-02 | Cpc International Inc. | Process for the production of fructose polymers and high fructose syrups |
| GB8316790D0 (en) * | 1983-06-21 | 1983-07-27 | Tate & Lyle Plc | Chemical process |
| JPS6027395A (ja) * | 1983-07-21 | 1985-02-12 | Satoshi Shinohara | フラクトオリゴ糖の製造方法 |
| DE3580350D1 (de) * | 1985-01-18 | 1990-12-06 | Satoru Shinohara | Verfahren zur herstellung einer frukto-oligosaccharose. |
| JPS6214792A (ja) * | 1985-07-10 | 1987-01-23 | Meiji Seika Kaisha Ltd | フラクトオリゴ糖高含有物の製造法 |
| NZ222902A (en) * | 1986-12-15 | 1990-08-28 | Yakult Honsha Kk | Method for producing galactooligosaccharide |
| NL8701616A (nl) | 1987-07-09 | 1989-02-01 | Stamicarbon | Fructosyltransferase en bereiding van fructose-oligomeren daarmee. |
| JP2693528B2 (ja) * | 1988-12-01 | 1997-12-24 | 農林水産省食品総合研究所長 | 高純度フラクトオリゴ糖の製造方法 |
| JPH03180189A (ja) * | 1989-08-31 | 1991-08-06 | Toto Ltd | 高純度フラクトオリゴ糖の製造方法 |
| DE4003140A1 (de) | 1990-02-02 | 1991-08-08 | Suedzucker Ag | Verfahren zur herstellung eines glucose-, fructose- und saccharosearmen inulooligosaccharid-produktes |
| CA2038485A1 (fr) * | 1990-03-23 | 1991-09-24 | Donald K. Hadden | Procede de nanofiltration pour la fabrication du dextrose |
| WO1991016449A1 (fr) | 1990-04-16 | 1991-10-31 | The Trustees Of The University Of Pennsylvania | Compositions saccharides et procedes et appareil servant a les synthetiser |
| JPH04237496A (ja) * | 1991-01-17 | 1992-08-25 | Mitsubishi Kasei Corp | 環状イヌロオリゴ糖の製造方法 |
| MX9304638A (es) | 1992-07-31 | 1994-05-31 | Neose Pharm Inc | Composicion para tratar e inhibir las ulceras gastricas y duodenales. |
| US5968365A (en) | 1996-02-05 | 1999-10-19 | Mcneil-Ppc, Inc. | Preparation of inulin products |
| US6423833B1 (en) * | 1998-05-05 | 2002-07-23 | Steven J. Catani | Functional sugar polymers from inexpensive sugar sources and apparatus for preparing same |
| US5998177A (en) * | 1998-11-19 | 1999-12-07 | Neose Technologies, Inc. | Process for processing sucrose into glucose |
-
1999
- 1999-05-04 US US09/305,788 patent/US6423833B1/en not_active Expired - Lifetime
- 1999-05-04 EP EP99920336A patent/EP1076716A1/fr not_active Ceased
- 1999-05-04 AU AU37858/99A patent/AU759465B2/en not_active Ceased
- 1999-05-04 BR BR9911012-1A patent/BR9911012A/pt not_active IP Right Cessation
- 1999-05-04 WO PCT/US1999/009752 patent/WO1999057300A1/fr active IP Right Grant
-
2000
- 2000-11-03 NO NO20005545A patent/NO325114B1/no not_active IP Right Cessation
-
2002
- 2002-04-23 US US10/127,462 patent/US20030044942A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| EP1076716A1 (fr) | 2001-02-21 |
| US6423833B1 (en) | 2002-07-23 |
| US20030044942A1 (en) | 2003-03-06 |
| NO20005545D0 (no) | 2000-11-03 |
| AU759465B2 (en) | 2003-04-17 |
| AU3785899A (en) | 1999-11-23 |
| WO1999057300A1 (fr) | 1999-11-11 |
| NO20005545L (no) | 2000-11-03 |
| BR9911012A (pt) | 2001-02-06 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |