JPS5946596B2 - 不溶性酵素の製造方法 - Google Patents
不溶性酵素の製造方法Info
- Publication number
- JPS5946596B2 JPS5946596B2 JP51032673A JP3267376A JPS5946596B2 JP S5946596 B2 JPS5946596 B2 JP S5946596B2 JP 51032673 A JP51032673 A JP 51032673A JP 3267376 A JP3267376 A JP 3267376A JP S5946596 B2 JPS5946596 B2 JP S5946596B2
- Authority
- JP
- Japan
- Prior art keywords
- ions
- enzyme
- bound
- activity
- polymer
- 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
Links
- 108090000790 Enzymes Proteins 0.000 title claims description 20
- 102000004190 Enzymes Human genes 0.000 title claims description 20
- 238000004519 manufacturing process Methods 0.000 title claims description 6
- 229920000642 polymer Polymers 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 11
- 230000000694 effects Effects 0.000 claims description 7
- 150000002500 ions Chemical class 0.000 claims description 6
- 239000007800 oxidant agent Substances 0.000 claims description 5
- -1 potassium ferricyanide Chemical compound 0.000 claims description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical group NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 3
- 125000003277 amino group Chemical group 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 239000000203 mixture Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 230000002411 adverse Effects 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- DJHGAFSJWGLOIV-UHFFFAOYSA-K Arsenate3- Chemical class [O-][As]([O-])([O-])=O DJHGAFSJWGLOIV-UHFFFAOYSA-K 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 150000001879 copper Chemical class 0.000 claims 1
- 230000001590 oxidative effect Effects 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- 229940088598 enzyme Drugs 0.000 description 15
- 150000001875 compounds Chemical class 0.000 description 13
- 229910021538 borax Inorganic materials 0.000 description 7
- 235000010339 sodium tetraborate Nutrition 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- 108090000631 Trypsin Proteins 0.000 description 6
- 102000004142 Trypsin Human genes 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000004328 sodium tetraborate Substances 0.000 description 6
- 239000012588 trypsin Substances 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000000178 monomer Substances 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 4
- 108010038061 Chymotrypsinogen Proteins 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- 108010015776 Glucose oxidase Proteins 0.000 description 3
- 239000004366 Glucose oxidase Substances 0.000 description 3
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 229920001577 copolymer Polymers 0.000 description 3
- 230000008878 coupling Effects 0.000 description 3
- 238000010168 coupling process Methods 0.000 description 3
- 238000005859 coupling reaction Methods 0.000 description 3
- 239000012153 distilled water Substances 0.000 description 3
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 3
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Chemical compound CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 3
- 229940116332 glucose oxidase Drugs 0.000 description 3
- 235000019420 glucose oxidase Nutrition 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 description 2
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 2
- 108090000317 Chymotrypsin Proteins 0.000 description 2
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000008351 acetate buffer Substances 0.000 description 2
- 238000005903 acid hydrolysis reaction Methods 0.000 description 2
- 238000001042 affinity chromatography Methods 0.000 description 2
- 239000000872 buffer Substances 0.000 description 2
- 229960002376 chymotrypsin Drugs 0.000 description 2
- ATDGTVJJHBUTRL-UHFFFAOYSA-N cyanogen bromide Chemical compound BrC#N ATDGTVJJHBUTRL-UHFFFAOYSA-N 0.000 description 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 2
- YAGKRVSRTSUGEY-UHFFFAOYSA-N ferricyanide Chemical compound [Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] YAGKRVSRTSUGEY-UHFFFAOYSA-N 0.000 description 2
- 239000002609 medium Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 239000012429 reaction media Substances 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 239000000758 substrate Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- ZWZVWGITAAIFPS-UHFFFAOYSA-N thiophosgene Chemical compound ClC(Cl)=S ZWZVWGITAAIFPS-UHFFFAOYSA-N 0.000 description 2
- 229920002818 (Hydroxyethyl)methacrylate Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- 229910004835 Na2B4O7 Inorganic materials 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 102000057297 Pepsin A Human genes 0.000 description 1
- 108090000284 Pepsin A Proteins 0.000 description 1
- 108091006587 SLC13A5 Proteins 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000012472 biological sample Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000969 carrier Substances 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- JBDSSBMEKXHSJF-UHFFFAOYSA-N cyclopentanecarboxylic acid Chemical compound OC(=O)C1CCCC1 JBDSSBMEKXHSJF-UHFFFAOYSA-N 0.000 description 1
- 239000012954 diazonium Substances 0.000 description 1
- 150000001989 diazonium salts Chemical class 0.000 description 1
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 1
- AJFXNBUVIBKWBT-UHFFFAOYSA-N disodium;boric acid;hydrogen borate Chemical group [Na+].[Na+].OB(O)O.OB(O)O.OB(O)O.OB([O-])[O-] AJFXNBUVIBKWBT-UHFFFAOYSA-N 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000007863 gel particle Substances 0.000 description 1
- 229960000789 guanidine hydrochloride Drugs 0.000 description 1
- PJJJBBJSCAKJQF-UHFFFAOYSA-N guanidinium chloride Chemical compound [Cl-].NC(N)=[NH2+] PJJJBBJSCAKJQF-UHFFFAOYSA-N 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 239000008241 heterogeneous mixture Substances 0.000 description 1
- 229920001480 hydrophilic copolymer Polymers 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- GTLFLKPYMGGXKO-UHFFFAOYSA-N n-[4-[ethyl-(4-methyl-3-oxopent-4-enyl)amino]phenyl]acetamide Chemical compound CC(=C)C(=O)CCN(CC)C1=CC=C(NC(C)=O)C=C1 GTLFLKPYMGGXKO-UHFFFAOYSA-N 0.000 description 1
- 229940111202 pepsin Drugs 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000012798 spherical particle Substances 0.000 description 1
- 238000003756 stirring 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
- 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
- C12N11/087—Acrylic polymers
-
- 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
- Y10S436/00—Chemistry: analytical and immunological testing
- Y10S436/815—Test for named compound or class of compounds
- Y10S436/817—Steroids or hormones
Landscapes
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- Enzymes And Modification Thereof (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CS7500002132A CS181417B1 (en) | 1975-03-27 | 1975-03-27 | Method for preparing insoluble biologically active compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS51117784A JPS51117784A (en) | 1976-10-16 |
| JPS5946596B2 true JPS5946596B2 (ja) | 1984-11-13 |
Family
ID=5357554
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP51032673A Expired JPS5946596B2 (ja) | 1975-03-27 | 1976-03-26 | 不溶性酵素の製造方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US4085005A (enExample) |
| JP (1) | JPS5946596B2 (enExample) |
| CA (1) | CA1054081A (enExample) |
| CS (1) | CS181417B1 (enExample) |
| DE (1) | DE2613011A1 (enExample) |
| FR (1) | FR2305441A1 (enExample) |
| GB (1) | GB1499357A (enExample) |
| SE (1) | SE430069B (enExample) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4180629A (en) * | 1974-10-30 | 1979-12-25 | Ceskoslovenska Akademie Ved | Polymers containing a reactive aromatic system based on p-phenylenediamine derivatives |
| US4530963A (en) * | 1982-08-20 | 1985-07-23 | Devoe-Holbein International, N.V. | Insoluble chelating compositions |
| GB8334499D0 (en) * | 1983-12-24 | 1984-02-01 | Beecham Group Plc | Derivatives |
| US4952519A (en) * | 1988-05-02 | 1990-08-28 | E. I. Du Pont De Nemours And Company | Protein immobilization with poly(ethyleneimine) derivatized with a hydroprobic group |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3706633A (en) * | 1970-04-10 | 1972-12-19 | Monsanto Co | Preparation of water-insoluble enzyme derivatives |
| US3745088A (en) * | 1970-12-23 | 1973-07-10 | Us Agriculture | Active water-insoluble enzymes |
| US3970521A (en) * | 1974-08-07 | 1976-07-20 | Exxon Research And Engineering Company | Immobilized glycoenzymes |
-
1975
- 1975-03-27 CS CS7500002132A patent/CS181417B1/cs unknown
-
1976
- 1976-03-24 US US05/669,866 patent/US4085005A/en not_active Expired - Lifetime
- 1976-03-25 GB GB12042/76A patent/GB1499357A/en not_active Expired
- 1976-03-25 SE SE7603640A patent/SE430069B/xx not_active IP Right Cessation
- 1976-03-26 JP JP51032673A patent/JPS5946596B2/ja not_active Expired
- 1976-03-26 DE DE19762613011 patent/DE2613011A1/de not_active Withdrawn
- 1976-03-26 FR FR7608802A patent/FR2305441A1/fr active Granted
- 1976-03-26 CA CA249,108A patent/CA1054081A/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2613011A1 (de) | 1976-10-07 |
| GB1499357A (en) | 1978-02-01 |
| CS181417B1 (en) | 1978-03-31 |
| CA1054081A (en) | 1979-05-08 |
| SE430069B (sv) | 1983-10-17 |
| FR2305441B1 (enExample) | 1980-03-28 |
| US4085005A (en) | 1978-04-18 |
| SE7603640L (sv) | 1976-09-28 |
| FR2305441A1 (fr) | 1976-10-22 |
| JPS51117784A (en) | 1976-10-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4101380A (en) | Process for the cross-linking of proteins | |
| US5252714A (en) | Preparation and use of polyethylene glycol propionaldehyde | |
| US4141857A (en) | Support matrices for immobilized enzymes | |
| EP0008100B1 (de) | Verfahren zur Herstellung eines makroporösen polymeren Trägermaterials zur kovalenten Bindung von Proteinen | |
| JPH0791313B2 (ja) | サッカライド変性された水溶性の蛋白質−複合体 | |
| JPH0458311B2 (enExample) | ||
| JPS59105005A (ja) | ビニレンカ−ボネ−ト重合体およびその製法 | |
| US4088639A (en) | Macromolecular adenine nucleotide derivatives | |
| JPS5946596B2 (ja) | 不溶性酵素の製造方法 | |
| US5310786A (en) | Reversibly precipitable, water-soluble polymer conjugates | |
| US4206259A (en) | Support matrices for immobilized enzymes | |
| US4193910A (en) | Preparation of support matrices for immobilized enzymes | |
| JPS6368618A (ja) | 生物学的に活性な物質の固定化用担体 | |
| JP2719047B2 (ja) | 担体固定化ペニシリンｇアミダーゼ、グルタリル−７−ａｃａアシラーゼ又はｄ−アミノ酸オキシダーゼ | |
| US4767620A (en) | Crosslinked polymers with carbonate ester groups, and a process for their preparation | |
| Coughlin et al. | Preparation and properties of soluble–insoluble nicotinamide coenzymes | |
| CA1301686C (en) | Enzyme reactor with cofactor immobilized on a polymer | |
| CA2058194A1 (en) | Immobilized d-amino acid oxidase and its use for the preparation of medicaments | |
| US5543310A (en) | Immobilized phosphorylase | |
| JPS6049480B2 (ja) | ベタイン型ポリマ−による酵素または菌体の固定化方法 | |
| JPS63304000A (ja) | 生体由来物質の固定化方法 | |
| CA1336893C (en) | Reversibly precipitable, water-soluble polymer conjugates, their preparation and use in homogeneous catalysis | |
| Kennedy et al. | [8] Immobilization of enzymes on transition metal-activated support | |
| JPH02164831A (ja) | 酸化物の製造方法および酸化用触媒 | |
| JPS6148919B2 (enExample) |