CA1198698A - Process for the stabilisation of aqueous solutions of cholesterol esterase from pseudomonas - Google Patents
Process for the stabilisation of aqueous solutions of cholesterol esterase from pseudomonasInfo
- Publication number
- CA1198698A CA1198698A CA000417722A CA417722A CA1198698A CA 1198698 A CA1198698 A CA 1198698A CA 000417722 A CA000417722 A CA 000417722A CA 417722 A CA417722 A CA 417722A CA 1198698 A CA1198698 A CA 1198698A
- Authority
- CA
- Canada
- Prior art keywords
- buffer
- litre
- process according
- mmol
- active agent
- 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
- 102000000019 Sterol Esterase Human genes 0.000 title claims abstract description 43
- 108010055297 Sterol Esterase Proteins 0.000 title claims abstract description 43
- 238000000034 method Methods 0.000 title claims abstract description 27
- 241000589516 Pseudomonas Species 0.000 title claims abstract description 24
- 239000007864 aqueous solution Substances 0.000 title claims abstract description 15
- 230000006641 stabilisation Effects 0.000 title claims abstract description 7
- 239000000872 buffer Substances 0.000 claims abstract description 29
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 claims abstract description 21
- 229910001425 magnesium ion Inorganic materials 0.000 claims abstract description 21
- 239000004094 surface-active agent Substances 0.000 claims abstract description 20
- 239000000243 solution Substances 0.000 claims description 22
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 18
- -1 aralkyl alcohol Chemical compound 0.000 claims description 11
- 239000011777 magnesium Substances 0.000 claims description 6
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 5
- 229910052749 magnesium Inorganic materials 0.000 claims description 5
- 229940091250 magnesium supplement Drugs 0.000 claims description 5
- 108090000371 Esterases Proteins 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 229920000151 polyglycol Polymers 0.000 claims description 2
- 239000010695 polyglycol Substances 0.000 claims description 2
- 239000012736 aqueous medium Substances 0.000 claims 1
- 235000001055 magnesium Nutrition 0.000 claims 1
- 238000011105 stabilization Methods 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 abstract description 18
- 108090000790 Enzymes Proteins 0.000 abstract description 18
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 23
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 15
- 239000007983 Tris buffer Substances 0.000 description 13
- 230000000694 effects Effects 0.000 description 13
- 239000003153 chemical reaction reagent Substances 0.000 description 11
- 235000012000 cholesterol Nutrition 0.000 description 11
- 239000008363 phosphate buffer Substances 0.000 description 7
- 210000002966 serum Anatomy 0.000 description 7
- 229910019142 PO4 Inorganic materials 0.000 description 6
- 239000013543 active substance Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 159000000003 magnesium salts Chemical class 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 150000003626 triacylglycerols Chemical class 0.000 description 5
- ITRHZTGVVSWIDC-UHFFFAOYSA-N 11-methyl-1-(11-methyldodecoxy)dodecane Chemical class CC(C)CCCCCCCCCCOCCCCCCCCCCC(C)C ITRHZTGVVSWIDC-UHFFFAOYSA-N 0.000 description 4
- 229920004890 Triton X-100 Polymers 0.000 description 4
- 239000013504 Triton X-100 Substances 0.000 description 4
- 230000002255 enzymatic effect Effects 0.000 description 4
- 230000000813 microbial effect Effects 0.000 description 4
- 235000021317 phosphate Nutrition 0.000 description 4
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 241000589540 Pseudomonas fluorescens Species 0.000 description 3
- 239000012190 activator Substances 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 150000001840 cholesterol esters Chemical class 0.000 description 3
- 238000001514 detection method Methods 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical group 0.000 description 3
- 150000002500 ions Chemical class 0.000 description 3
- 239000000523 sample Substances 0.000 description 3
- 230000003019 stabilising effect Effects 0.000 description 3
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 3
- JKMHFZQWWAIEOD-UHFFFAOYSA-N 2-[4-(2-hydroxyethyl)piperazin-1-yl]ethanesulfonic acid Chemical compound OCC[NH+]1CCN(CCS([O-])(=O)=O)CC1 JKMHFZQWWAIEOD-UHFFFAOYSA-N 0.000 description 2
- 239000007995 HEPES buffer Substances 0.000 description 2
- 239000007993 MOPS buffer Substances 0.000 description 2
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229940024606 amino acid Drugs 0.000 description 2
- 150000001413 amino acids Chemical class 0.000 description 2
- 229940099352 cholate Drugs 0.000 description 2
- BHQCQFFYRZLCQQ-OELDTZBJSA-N cholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(O)=O)C)[C@@]2(C)[C@@H](O)C1 BHQCQFFYRZLCQQ-OELDTZBJSA-N 0.000 description 2
- 239000000306 component Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 230000003301 hydrolyzing effect Effects 0.000 description 2
- 235000019626 lipase activity Nutrition 0.000 description 2
- 229960001983 magnesium aspartate Drugs 0.000 description 2
- RXMQCXCANMAVIO-CEOVSRFSSA-L magnesium;(2s)-2-amino-4-hydroxy-4-oxobutanoate Chemical compound [H+].[H+].[Mg+2].[O-]C(=O)[C@@H](N)CC([O-])=O.[O-]C(=O)[C@@H](N)CC([O-])=O RXMQCXCANMAVIO-CEOVSRFSSA-L 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920002113 octoxynol Polymers 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 2
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 2
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 description 1
- GJMPSRSMBJLKKB-UHFFFAOYSA-N 3-methylphenylacetic acid Chemical compound CC1=CC=CC(CC(O)=O)=C1 GJMPSRSMBJLKKB-UHFFFAOYSA-N 0.000 description 1
- ZVZFHCZCIBYFMZ-UHFFFAOYSA-N 6-methylheptoxybenzene Chemical compound CC(C)CCCCCOC1=CC=CC=C1 ZVZFHCZCIBYFMZ-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 239000004254 Ammonium phosphate Substances 0.000 description 1
- MOKFEALJVTYTSM-UHFFFAOYSA-N C(CCCCCCCCCC(C)C)C=1NC=CN1 Chemical compound C(CCCCCCCCCC(C)C)C=1NC=CN1 MOKFEALJVTYTSM-UHFFFAOYSA-N 0.000 description 1
- 108010089254 Cholesterol oxidase Proteins 0.000 description 1
- 102000003976 Esterases Human genes 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 244000228957 Ferula foetida Species 0.000 description 1
- 241000589774 Pseudomonas sp. Species 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 229910000148 ammonium phosphate Inorganic materials 0.000 description 1
- 235000019289 ammonium phosphates Nutrition 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 210000000941 bile Anatomy 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 238000003759 clinical diagnosis Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 150000001991 dicarboxylic acids Chemical class 0.000 description 1
- 239000003248 enzyme activator Substances 0.000 description 1
- CCIVGXIOQKPBKL-UHFFFAOYSA-N ethanesulfonic acid Chemical compound CCS(O)(=O)=O CCIVGXIOQKPBKL-UHFFFAOYSA-N 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910001629 magnesium chloride Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 208000035278 mandibuloacral dysplasia progeroid syndrome Diseases 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 210000000496 pancreas Anatomy 0.000 description 1
- 210000001819 pancreatic juice Anatomy 0.000 description 1
- 239000008055 phosphate buffer solution Substances 0.000 description 1
- 229940085991 phosphate ion Drugs 0.000 description 1
- 238000005375 photometry Methods 0.000 description 1
- 239000008057 potassium phosphate buffer Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- WBWWGRHZICKQGZ-HZAMXZRMSA-N taurocholic acid Chemical compound C([C@H]1C[C@H]2O)[C@H](O)CC[C@]1(C)[C@@H]1[C@@H]2[C@@H]2CC[C@H]([C@@H](CCC(=O)NCCS(O)(=O)=O)C)[C@@]2(C)[C@@H](O)C1 WBWWGRHZICKQGZ-HZAMXZRMSA-N 0.000 description 1
- 229940117957 triethanolamine hydrochloride Drugs 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
- C12N9/96—Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/60—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving cholesterol
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)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Immunology (AREA)
- Physics & Mathematics (AREA)
- Biophysics (AREA)
- Analytical Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Biomedical Technology (AREA)
- Measuring Or Testing Involving Enzymes Or Micro-Organisms (AREA)
- Enzymes And Modification Thereof (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Steroid Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Saccharide Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Fats And Perfumes (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Detergent Compositions (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEP3200274.2 | 1982-01-07 | ||
| DE19823200274 DE3200274A1 (de) | 1982-01-07 | 1982-01-07 | Verfahren zur stabilisierung waessriger loesungen von cholesterinesterase aus pseudomonaden |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1198698A true CA1198698A (en) | 1985-12-31 |
Family
ID=6152717
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA000417722A Expired CA1198698A (en) | 1982-01-07 | 1982-12-15 | Process for the stabilisation of aqueous solutions of cholesterol esterase from pseudomonas |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US4476223A (enExample) |
| EP (1) | EP0084684B1 (enExample) |
| JP (1) | JPS58175488A (enExample) |
| AT (1) | ATE12659T1 (enExample) |
| AU (1) | AU553593B2 (enExample) |
| CA (1) | CA1198698A (enExample) |
| DD (1) | DD208824A5 (enExample) |
| DE (2) | DE3200274A1 (enExample) |
| DK (1) | DK163527C (enExample) |
| ES (1) | ES518694A0 (enExample) |
| FI (1) | FI77262C (enExample) |
| ZA (1) | ZA8367B (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6030680A (ja) * | 1983-07-30 | 1985-02-16 | Amano Pharmaceut Co Ltd | リパ−ゼにエステラ−ゼ活性を付加する方法 |
| DE3447390A1 (de) * | 1984-12-24 | 1986-07-03 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren zur gewinnung von cholesterinesterase |
| EP0218083A1 (en) * | 1985-09-03 | 1987-04-15 | Abbott Laboratories | Stabilized cholesterol reagent and method for determining total cholesterol using the reagent |
| DK145090D0 (da) * | 1990-06-14 | 1990-06-14 | Novo Nordisk As | Cellulasepraeparat og anvendelse deraf |
| US5460944A (en) * | 1991-10-28 | 1995-10-24 | Boehringer Mannheim Gmbh | Storable protein solution |
| DK99492D0 (da) * | 1992-08-07 | 1992-08-07 | Novo Nordisk As | Nyt enzym |
| EP3722418A1 (en) * | 2019-04-08 | 2020-10-14 | AB Enzymes Oy | Solution stable enzyme composition |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR891187A (fr) * | 1942-09-25 | 1944-02-29 | Procédé de conservation de la présure | |
| US3884764A (en) * | 1974-03-25 | 1975-05-20 | Eastman Kodak Co | Method and composition for blood serum cholesterol analysis |
| DE2911284C2 (de) * | 1979-03-22 | 1982-01-28 | Boehringer Mannheim Gmbh, 6800 Mannheim | Verfahren und Reagenz zur Aktivierung der Cholesterinesterase |
| DE2933646A1 (de) * | 1979-08-20 | 1981-03-26 | Boehringer Mannheim Gmbh, 68305 Mannheim | Verfahren zur gewinnung von cholesterinesterase |
| DE2933648A1 (de) * | 1979-08-20 | 1981-03-26 | Boehringer Mannheim Gmbh, 68305 Mannheim | Verfahren zur gewinnung von cholesterinesterase |
| US4409326A (en) * | 1980-07-10 | 1983-10-11 | Modrovich Ivan Endre | Stabilized enzymatic solutions and method for determining total cholesterol in human serum |
-
1982
- 1982-01-07 DE DE19823200274 patent/DE3200274A1/de not_active Withdrawn
- 1982-12-15 CA CA000417722A patent/CA1198698A/en not_active Expired
- 1982-12-20 AU AU91668/82A patent/AU553593B2/en not_active Ceased
- 1982-12-23 US US06/452,690 patent/US4476223A/en not_active Expired - Lifetime
- 1982-12-30 ES ES518694A patent/ES518694A0/es active Granted
- 1982-12-31 DE DE8282112129T patent/DE3263043D1/de not_active Expired
- 1982-12-31 AT AT82112129T patent/ATE12659T1/de not_active IP Right Cessation
- 1982-12-31 EP EP82112129A patent/EP0084684B1/de not_active Expired
-
1983
- 1983-01-03 DK DK000283A patent/DK163527C/da not_active IP Right Cessation
- 1983-01-05 DD DD83247040A patent/DD208824A5/de unknown
- 1983-01-06 FI FI830036A patent/FI77262C/fi not_active IP Right Cessation
- 1983-01-06 ZA ZA8367A patent/ZA8367B/xx unknown
- 1983-01-07 JP JP58000568A patent/JPS58175488A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FI830036L (fi) | 1983-07-08 |
| DE3263043D1 (en) | 1985-05-15 |
| DK283D0 (da) | 1983-01-03 |
| US4476223A (en) | 1984-10-09 |
| DD208824A5 (de) | 1984-04-11 |
| FI77262B (fi) | 1988-10-31 |
| JPS6121076B2 (enExample) | 1986-05-24 |
| AU9166882A (en) | 1983-07-14 |
| AU553593B2 (en) | 1986-07-24 |
| FI830036A0 (fi) | 1983-01-06 |
| DE3200274A1 (de) | 1983-07-14 |
| ZA8367B (en) | 1983-10-26 |
| JPS58175488A (ja) | 1983-10-14 |
| EP0084684B1 (de) | 1985-04-10 |
| DK163527B (da) | 1992-03-09 |
| FI77262C (fi) | 1989-02-10 |
| ATE12659T1 (de) | 1985-04-15 |
| EP0084684A1 (de) | 1983-08-03 |
| DK163527C (da) | 1992-08-03 |
| DK283A (da) | 1983-07-08 |
| ES8402347A1 (es) | 1984-02-16 |
| ES518694A0 (es) | 1984-02-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |