NZ196164A - Production of immobilized glucose isomerase - Google Patents
Production of immobilized glucose isomeraseInfo
- Publication number
- NZ196164A NZ196164A NZ196164A NZ19616481A NZ196164A NZ 196164 A NZ196164 A NZ 196164A NZ 196164 A NZ196164 A NZ 196164A NZ 19616481 A NZ19616481 A NZ 19616481A NZ 196164 A NZ196164 A NZ 196164A
- Authority
- NZ
- New Zealand
- Prior art keywords
- glucose isomerase
- solution
- cells
- glucose
- microorganism
- Prior art date
Links
- 108700040099 Xylose isomerases Proteins 0.000 title claims description 126
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 230000000694 effects Effects 0.000 claims description 28
- 238000000034 method Methods 0.000 claims description 22
- 150000004676 glycans Chemical class 0.000 claims description 18
- 229920001282 polysaccharide Polymers 0.000 claims description 18
- 239000005017 polysaccharide Substances 0.000 claims description 18
- 244000005700 microbiome Species 0.000 claims description 16
- 239000003456 ion exchange resin Substances 0.000 claims description 13
- 229920003303 ion-exchange polymer Polymers 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- NWUYHJFMYQTDRP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene;1-ethenyl-2-ethylbenzene;styrene Chemical compound C=CC1=CC=CC=C1.CCC1=CC=CC=C1C=C.C=CC1=CC=CC=C1C=C NWUYHJFMYQTDRP-UHFFFAOYSA-N 0.000 claims description 10
- 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 10
- 150000001720 carbohydrates Chemical class 0.000 claims description 10
- 239000008103 glucose Substances 0.000 claims description 10
- 230000007928 solubilization Effects 0.000 claims description 8
- 238000005063 solubilization Methods 0.000 claims description 8
- 229920001429 chelating resin Polymers 0.000 claims description 6
- 238000012258 culturing Methods 0.000 claims description 6
- 239000002736 nonionic surfactant Substances 0.000 claims description 6
- 239000007900 aqueous suspension Substances 0.000 claims description 5
- 239000002244 precipitate Substances 0.000 claims description 5
- 239000006228 supernatant Substances 0.000 claims description 5
- 238000010908 decantation Methods 0.000 claims description 4
- 230000003381 solubilizing effect Effects 0.000 claims description 3
- 241000187134 Streptomyces olivochromogenes Species 0.000 claims description 2
- JXASPPWQHFOWPL-UHFFFAOYSA-N Tamarixin Natural products C1=C(O)C(OC)=CC=C1C1=C(OC2C(C(O)C(O)C(CO)O2)O)C(=O)C2=C(O)C=C(O)C=C2O1 JXASPPWQHFOWPL-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 description 58
- 210000004027 cell Anatomy 0.000 description 37
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 22
- 238000003756 stirring Methods 0.000 description 18
- 238000001179 sorption measurement Methods 0.000 description 14
- 238000005342 ion exchange Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 10
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 8
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 238000006317 isomerization reaction Methods 0.000 description 7
- 229920002125 Sokalan® Polymers 0.000 description 6
- 239000000969 carrier Substances 0.000 description 6
- 239000006285 cell suspension Substances 0.000 description 6
- 239000003960 organic solvent Substances 0.000 description 6
- 102000004190 Enzymes Human genes 0.000 description 5
- 108090000790 Enzymes Proteins 0.000 description 5
- 229940088598 enzyme Drugs 0.000 description 5
- 238000001914 filtration Methods 0.000 description 5
- 208000035404 Autolysis Diseases 0.000 description 4
- 206010057248 Cell death Diseases 0.000 description 4
- 229930091371 Fructose Natural products 0.000 description 4
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 4
- 239000005715 Fructose Substances 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 238000005119 centrifugation Methods 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 238000001816 cooling Methods 0.000 description 4
- 239000000706 filtrate Substances 0.000 description 4
- 229910001629 magnesium chloride Inorganic materials 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000028043 self proteolysis Effects 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 210000002421 cell wall Anatomy 0.000 description 2
- 210000004748 cultured cell Anatomy 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- OQUKIQWCVTZJAF-UHFFFAOYSA-N phenol;sulfuric acid Chemical compound OS(O)(=O)=O.OC1=CC=CC=C1 OQUKIQWCVTZJAF-UHFFFAOYSA-N 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
- 241000186361 Actinobacteria <class> Species 0.000 description 1
- 241000269031 Armatimonadetes bacterium Species 0.000 description 1
- 241000193749 Bacillus coagulans Species 0.000 description 1
- 229920002261 Corn starch Polymers 0.000 description 1
- GUBGYTABKSRVRQ-WFVLMXAXSA-N DEAE-cellulose Chemical compound OC1C(O)C(O)C(CO)O[C@H]1O[C@@H]1C(CO)OC(O)C(O)C1O GUBGYTABKSRVRQ-WFVLMXAXSA-N 0.000 description 1
- 239000004471 Glycine Substances 0.000 description 1
- 108010093096 Immobilized Enzymes Proteins 0.000 description 1
- 240000001929 Lactobacillus brevis Species 0.000 description 1
- 235000013957 Lactobacillus brevis Nutrition 0.000 description 1
- 102000016943 Muramidase Human genes 0.000 description 1
- 108010014251 Muramidase Proteins 0.000 description 1
- 108010062010 N-Acetylmuramoyl-L-alanine Amidase Proteins 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 240000007930 Oxalis acetosella Species 0.000 description 1
- 235000008098 Oxalis acetosella Nutrition 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- 241000187747 Streptomyces Species 0.000 description 1
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 1
- 229940054340 bacillus coagulans Drugs 0.000 description 1
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000008120 corn starch Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 238000000502 dialysis Methods 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- -1 for example 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
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229960000274 lysozyme Drugs 0.000 description 1
- 239000004325 lysozyme Substances 0.000 description 1
- 235000010335 lysozyme Nutrition 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 238000000527 sonication Methods 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- 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
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/90—Isomerases (5.)
- C12N9/92—Glucose isomerase (5.3.1.5; 5.3.1.9; 5.3.1.18)
-
- 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
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation 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
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/08—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer
- C12N11/082—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a synthetic polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/10—Enzymes or microbial cells immobilised on or in an organic carrier the carrier being a carbohydrate
- C12N11/12—Cellulose or 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
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/14—Enzymes or microbial cells immobilised on or in an inorganic carrier
-
- 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
- C12P19/24—Preparation of compounds containing saccharide radicals produced by the action of an isomerase, e.g. fructose
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/814—Enzyme separation or purification
- Y10S435/815—Enzyme separation or purification by sorption
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- Enzymes And Modification Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1211180A JPS56109586A (en) | 1980-02-05 | 1980-02-05 | Production of fixed glucoseisomerase |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ196164A true NZ196164A (en) | 1984-03-16 |
Family
ID=11796446
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ196164A NZ196164A (en) | 1980-02-05 | 1981-02-02 | Production of immobilized glucose isomerase |
Country Status (15)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA1195270A (en) * | 1982-07-22 | 1985-10-15 | Edward Katz | Immobilized glucose isomerase and process |
| US4933284A (en) * | 1986-05-07 | 1990-06-12 | Uop | Regenerable dialkylaminoalkyl cellulose support matrix for immobilizing biologically active materials |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2224133B2 (de) * | 1972-05-17 | 1974-06-20 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verwendung von bestimmten Mikroorganismen-Stämmen zur Gewinnung von Cholesterinoxydase, welche Cholesterin mit O tief 2 zu Cholestenon + H tief 2 O tief 2 oxydiert |
| IE38174B1 (en) * | 1972-07-07 | 1978-01-18 | Snam Progetti | Process for purifying an enzyme |
| DE2418978A1 (de) * | 1974-04-19 | 1975-10-30 | Boehringer Mannheim Gmbh | Steroid-delta-isomerase |
| US4113568A (en) * | 1977-03-24 | 1978-09-12 | Mitsubishi Chemical Industries, Ltd. | Process for the renewal of an insolubilized glucose isomerase |
| JPS54147992A (en) * | 1978-05-12 | 1979-11-19 | Cpc International Inc | Production of fixed glucose isomerase |
-
1980
- 1980-02-05 JP JP1211180A patent/JPS56109586A/ja active Granted
- 1980-12-19 US US06/217,976 patent/US4343902A/en not_active Expired - Fee Related
-
1981
- 1981-01-28 AU AU66650/81A patent/AU544815B2/en not_active Ceased
- 1981-01-30 AR AR284151A patent/AR227172A1/es active
- 1981-01-30 GB GB8102956A patent/GB2068974B/en not_active Expired
- 1981-02-02 NZ NZ196164A patent/NZ196164A/en unknown
- 1981-02-02 CA CA000369911A patent/CA1159785A/en not_active Expired
- 1981-02-03 DE DE3103573A patent/DE3103573A1/de not_active Withdrawn
- 1981-02-04 ES ES499092A patent/ES8202585A1/es not_active Expired
- 1981-02-04 IN IN127/CAL/81A patent/IN154089B/en unknown
- 1981-02-04 DK DK48481A patent/DK48481A/da not_active Application Discontinuation
- 1981-02-04 FR FR8102153A patent/FR2475062A1/fr not_active Withdrawn
- 1981-02-05 NL NL8100565A patent/NL8100565A/nl not_active Application Discontinuation
- 1981-02-05 IT IT19533/81A patent/IT1135318B/it active
-
1985
- 1985-12-30 MY MY116/85A patent/MY8500116A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| NL8100565A (nl) | 1981-09-01 |
| US4343902A (en) | 1982-08-10 |
| GB2068974B (en) | 1983-09-07 |
| IT1135318B (it) | 1986-08-20 |
| ES499092A0 (es) | 1982-02-01 |
| IN154089B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1984-09-15 |
| JPS56109586A (en) | 1981-08-31 |
| FR2475062A1 (fr) | 1981-08-07 |
| CA1159785A (en) | 1984-01-03 |
| AR227172A1 (es) | 1982-09-30 |
| JPH0211232B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1990-03-13 |
| DK48481A (da) | 1981-08-06 |
| DE3103573A1 (de) | 1982-02-11 |
| MY8500116A (en) | 1985-12-31 |
| AU544815B2 (en) | 1985-06-13 |
| GB2068974A (en) | 1981-08-19 |
| AU6665081A (en) | 1981-08-13 |
| ES8202585A1 (es) | 1982-02-01 |
| IT8119533A0 (it) | 1981-02-05 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE2703615C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| US3868304A (en) | Method of making fructose with immobilized glucose isomerase | |
| JPS609797B2 (ja) | イソマルチユロ−スの製造法 | |
| US4390627A (en) | Immobilization of the sucrose mutase in whole cells of protaminobacter rubrum | |
| US4208482A (en) | Immobilization of glucose isomerase | |
| EP0096547B1 (en) | Process for preparing uridine diphosphate-n-acetylgalactosamine | |
| EP0307158B1 (en) | Process for the preparation of branched fructooligosaccharides | |
| US5314810A (en) | Fructose transferring enzyme absorbed on a granular carrier for production of fructooligosaccharides | |
| JP3202365B2 (ja) | オリゴマンヌロン酸を重合度によって分離する方法 | |
| JP3523285B2 (ja) | 糖分解酵素の製造法 | |
| US4263400A (en) | Immobilized enzymes | |
| US4008124A (en) | Process for the isomerization of glucose into fructose | |
| JPH0556957B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | ||
| NZ196164A (en) | Production of immobilized glucose isomerase | |
| US4250263A (en) | Method of purification of thermally stable enzymes | |
| EP0032987B1 (en) | Thermophilic aspartase, processes for producing, culture used, and l-aspartic acid preparation process using the same | |
| US4081327A (en) | Preparation of d-fructose | |
| JP3235904B2 (ja) | 耐熱性マンノースイソメラーゼ及びその製造法並びにこれを用いたマンノースの製造法 | |
| JP3252927B2 (ja) | レバンサッカラーゼ酵素、その製造方法、それを産生する微生物およびそれを含む組成物 | |
| US3033758A (en) | Preparation of levans | |
| US3589982A (en) | Production of l-asparaginase | |
| JPS5849234B2 (ja) | グルコ−スイソメラ−ゼの固定化法 | |
| JPH06237782A (ja) | マンノースの分離取得方法 | |
| KR870001148B1 (ko) | 고착글루코오스 이성화 효소의 제조방법 | |
| JP3482454B2 (ja) | 高純度キシログルカンオリゴ７糖の製造方法 |