DE3924446A1 - Verfahren zum einschliessen von mikroorganismen oder teilen davon, die in fermentationsverfahren brauchbar sind, in ein gel - Google Patents
Verfahren zum einschliessen von mikroorganismen oder teilen davon, die in fermentationsverfahren brauchbar sind, in ein gelInfo
- Publication number
- DE3924446A1 DE3924446A1 DE3924446A DE3924446A DE3924446A1 DE 3924446 A1 DE3924446 A1 DE 3924446A1 DE 3924446 A DE3924446 A DE 3924446A DE 3924446 A DE3924446 A DE 3924446A DE 3924446 A1 DE3924446 A1 DE 3924446A1
- Authority
- DE
- Germany
- Prior art keywords
- microorganisms
- gel
- parts
- organic solvent
- solvent
- 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.)
- Withdrawn
Links
- 244000005700 microbiome Species 0.000 title claims abstract description 31
- 229920001817 Agar Polymers 0.000 title claims abstract description 24
- 239000008272 agar Substances 0.000 title claims abstract description 18
- 239000003960 organic solvent Substances 0.000 title claims description 3
- 239000000499 gel Substances 0.000 claims abstract description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 16
- 238000000855 fermentation Methods 0.000 claims abstract description 13
- 230000004151 fermentation Effects 0.000 claims abstract description 13
- 239000002904 solvent Substances 0.000 claims abstract description 5
- 238000000034 method Methods 0.000 claims description 24
- 239000007788 liquid Substances 0.000 claims description 15
- 239000000203 mixture Substances 0.000 claims description 14
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000003791 organic solvent mixture Substances 0.000 claims description 10
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 claims description 6
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 claims description 6
- BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 claims description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 4
- XYIBRDXRRQCHLP-UHFFFAOYSA-N ethyl acetoacetate Chemical compound CCOC(=O)CC(C)=O XYIBRDXRRQCHLP-UHFFFAOYSA-N 0.000 claims description 3
- 229940093858 ethyl acetoacetate Drugs 0.000 claims description 3
- 235000019445 benzyl alcohol Nutrition 0.000 claims description 2
- 238000009835 boiling Methods 0.000 claims description 2
- 206010067482 No adverse event Diseases 0.000 claims 1
- 239000011877 solvent mixture Substances 0.000 claims 1
- 239000007863 gel particle Substances 0.000 abstract description 7
- 230000009931 harmful effect Effects 0.000 abstract description 3
- 239000011324 bead Substances 0.000 description 12
- 210000004027 cell Anatomy 0.000 description 11
- 239000002609 medium Substances 0.000 description 11
- 239000000725 suspension Substances 0.000 description 11
- 239000001963 growth medium Substances 0.000 description 10
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 7
- 239000012153 distilled water Substances 0.000 description 7
- 229920002401 polyacrylamide Polymers 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 108090000790 Enzymes Proteins 0.000 description 4
- 102000004190 Enzymes Human genes 0.000 description 4
- 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 description 4
- 238000001879 gelation Methods 0.000 description 4
- 239000008103 glucose Substances 0.000 description 4
- 230000001954 sterilising effect Effects 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- 241000187747 Streptomyces Species 0.000 description 3
- 239000011942 biocatalyst Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000011780 sodium chloride Substances 0.000 description 3
- 241000588724 Escherichia coli Species 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000007836 KH2PO4 Substances 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
- ZRWPUFFVAOMMNM-UHFFFAOYSA-N Patulin Chemical compound OC1OCC=C2OC(=O)C=C12 ZRWPUFFVAOMMNM-UHFFFAOYSA-N 0.000 description 2
- JGSARLDLIJGVTE-MBNYWOFBSA-N Penicillin G Chemical compound N([C@H]1[C@H]2SC([C@@H](N2C1=O)C(O)=O)(C)C)C(=O)CC1=CC=CC=C1 JGSARLDLIJGVTE-MBNYWOFBSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 230000003115 biocidal effect Effects 0.000 description 2
- 235000010410 calcium alginate Nutrition 0.000 description 2
- 239000000648 calcium alginate Substances 0.000 description 2
- 229960002681 calcium alginate Drugs 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 235000010216 calcium carbonate Nutrition 0.000 description 2
- OKHHGHGGPDJQHR-YMOPUZKJSA-L calcium;(2s,3s,4s,5s,6r)-6-[(2r,3s,4r,5s,6r)-2-carboxy-6-[(2r,3s,4r,5s,6r)-2-carboxylato-4,5,6-trihydroxyoxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,4,5-trihydroxyoxane-2-carboxylate Chemical compound [Ca+2].O[C@@H]1[C@H](O)[C@H](O)O[C@@H](C([O-])=O)[C@H]1O[C@H]1[C@@H](O)[C@@H](O)[C@H](O[C@H]2[C@H]([C@@H](O)[C@H](O)[C@H](O2)C([O-])=O)O)[C@H](C(O)=O)O1 OKHHGHGGPDJQHR-YMOPUZKJSA-L 0.000 description 2
- 229940041514 candida albicans extract Drugs 0.000 description 2
- 239000006285 cell suspension Substances 0.000 description 2
- HOKIDJSKDBPKTQ-GLXFQSAKSA-N cephalosporin C Chemical compound S1CC(COC(=O)C)=C(C(O)=O)N2C(=O)[C@@H](NC(=O)CCC[C@@H](N)C(O)=O)[C@@H]12 HOKIDJSKDBPKTQ-GLXFQSAKSA-N 0.000 description 2
- 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 2
- BNIILDVGGAEEIG-UHFFFAOYSA-L disodium hydrogen phosphate Chemical compound [Na+].[Na+].OP([O-])([O-])=O BNIILDVGGAEEIG-UHFFFAOYSA-L 0.000 description 2
- 229910000397 disodium phosphate Inorganic materials 0.000 description 2
- 235000019800 disodium phosphate Nutrition 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 2
- 229910000359 iron(II) sulfate Inorganic materials 0.000 description 2
- 235000013372 meat Nutrition 0.000 description 2
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 2
- 235000019796 monopotassium phosphate Nutrition 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 239000012138 yeast extract Substances 0.000 description 2
- NGHVIOIJCVXTGV-ALEPSDHESA-N 6-aminopenicillanic acid Chemical compound [O-]C(=O)[C@H]1C(C)(C)S[C@@H]2[C@H]([NH3+])C(=O)N21 NGHVIOIJCVXTGV-ALEPSDHESA-N 0.000 description 1
- NGHVIOIJCVXTGV-UHFFFAOYSA-N 6beta-amino-penicillanic acid Natural products OC(=O)C1C(C)(C)SC2C(N)C(=O)N21 NGHVIOIJCVXTGV-UHFFFAOYSA-N 0.000 description 1
- 241000194110 Bacillus sp. (in: Bacteria) Species 0.000 description 1
- 244000063299 Bacillus subtilis Species 0.000 description 1
- 235000014469 Bacillus subtilis Nutrition 0.000 description 1
- 108010001478 Bacitracin Proteins 0.000 description 1
- OLFQLEJXIHEDEJ-UHFFFAOYSA-N CCCCC(CC)CO.CC(C)CCCCCO Chemical compound CCCCC(CC)CO.CC(C)CCCCCO OLFQLEJXIHEDEJ-UHFFFAOYSA-N 0.000 description 1
- 108010089254 Cholesterol oxidase Proteins 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 241000589344 Methylomonas Species 0.000 description 1
- 241000218919 Micromonospora inyonensis Species 0.000 description 1
- 229930184499 Nikkomycin Natural products 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- 241001149507 Penicillium urticae Species 0.000 description 1
- 241000222350 Pleurotus Species 0.000 description 1
- 241000187562 Rhodococcus sp. Species 0.000 description 1
- 241000219289 Silene Species 0.000 description 1
- 235000019764 Soybean Meal Nutrition 0.000 description 1
- 241000187433 Streptomyces clavuligerus Species 0.000 description 1
- 241000142915 Streptomyces diastatochromogenes Species 0.000 description 1
- 241000187389 Streptomyces lavendulae Species 0.000 description 1
- 229930194936 Tylosin Natural products 0.000 description 1
- 239000004182 Tylosin Substances 0.000 description 1
- 235000010443 alginic acid Nutrition 0.000 description 1
- 229920000615 alginic acid Polymers 0.000 description 1
- 229960003071 bacitracin Drugs 0.000 description 1
- 229930184125 bacitracin Natural products 0.000 description 1
- CLKOFPXJLQSYAH-ABRJDSQDSA-N bacitracin A Chemical compound C1SC([C@@H](N)[C@@H](C)CC)=N[C@@H]1C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H]1C(=O)N[C@H](CCCN)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H](CC=2C=CC=CC=2)C(=O)N[C@@H](CC=2N=CNC=2)C(=O)N[C@H](CC(O)=O)C(=O)N[C@@H](CC(N)=O)C(=O)NCCCC1 CLKOFPXJLQSYAH-ABRJDSQDSA-N 0.000 description 1
- 238000009395 breeding Methods 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 210000003850 cellular structure Anatomy 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000011261 inert gas Substances 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000001057 ionotropic effect Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- WWJFFVUVFNBJTN-UHFFFAOYSA-N neopolyoxin C Natural products C=1C=C(O)C=NC=1C(O)C(C)C(N)C(=O)NC(C(O)=O)C(C(C1O)O)OC1N1C=CC(=O)NC1=O WWJFFVUVFNBJTN-UHFFFAOYSA-N 0.000 description 1
- WWJFFVUVFNBJTN-VHDFTHOZSA-N nikkomycin Z Chemical compound N1([C@@H]2O[C@@H]([C@H]([C@H]2O)O)[C@H](NC(=O)[C@@H](N)[C@H](C)[C@H](O)C=2N=CC(O)=CC=2)C(O)=O)C=CC(=O)NC1=O WWJFFVUVFNBJTN-VHDFTHOZSA-N 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 229940056360 penicillin g Drugs 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000008363 phosphate buffer Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 210000001938 protoplast Anatomy 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 230000009528 severe injury Effects 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229940005741 sunflower lecithin Drugs 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- WBPYTXDJUQJLPQ-VMXQISHHSA-N tylosin Chemical compound O([C@@H]1[C@@H](C)O[C@H]([C@@H]([C@H]1N(C)C)O)O[C@@H]1[C@@H](C)[C@H](O)CC(=O)O[C@@H]([C@H](/C=C(\C)/C=C/C(=O)[C@H](C)C[C@@H]1CC=O)CO[C@H]1[C@@H]([C@H](OC)[C@H](O)[C@@H](C)O1)OC)CC)[C@H]1C[C@@](C)(O)[C@@H](O)[C@H](C)O1 WBPYTXDJUQJLPQ-VMXQISHHSA-N 0.000 description 1
- 229960004059 tylosin Drugs 0.000 description 1
- 235000019375 tylosin Nutrition 0.000 description 1
- 238000004383 yellowing 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
- C12N9/0004—Oxidoreductases (1.)
- C12N9/0006—Oxidoreductases (1.) acting on CH-OH groups as donors (1.1)
-
- 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
- C12N11/04—Enzymes or microbial cells immobilised on or in an organic carrier entrapped within the carrier, e.g. gel or hollow fibres
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Wood Science & Technology (AREA)
- Microbiology (AREA)
- Biotechnology (AREA)
- Biomedical Technology (AREA)
- Biochemistry (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Medicinal Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
HU883987A HU202579B (en) | 1988-07-27 | 1988-07-27 | Process for closing in gel microorganisma or parts of microorganisma utilizable in fermentations |
Publications (1)
Publication Number | Publication Date |
---|---|
DE3924446A1 true DE3924446A1 (de) | 1990-02-01 |
Family
ID=10966373
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE3924446A Withdrawn DE3924446A1 (de) | 1988-07-27 | 1989-07-24 | Verfahren zum einschliessen von mikroorganismen oder teilen davon, die in fermentationsverfahren brauchbar sind, in ein gel |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPH0276581A (fr) |
DE (1) | DE3924446A1 (fr) |
FR (1) | FR2634785A1 (fr) |
HU (1) | HU202579B (fr) |
IT (1) | IT1230999B (fr) |
SU (1) | SU1760985A3 (fr) |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4208482A (en) * | 1976-04-23 | 1980-06-17 | Anheuser-Busch, Incorporated | Immobilization of glucose isomerase |
US4399219A (en) * | 1981-01-29 | 1983-08-16 | Massachusetts Institute Of Technology | Process for isolating microbiologically active material |
NL8103168A (nl) * | 1981-07-01 | 1983-02-01 | Tno | Werkwijze voor het uitvoeren van een enzymatische reaktie. |
SE441009B (sv) * | 1982-03-08 | 1985-09-02 | Kjell Nilsson | Sett att immobilisera levande biomaterial i perlformiga polymerer |
JPS61260883A (ja) * | 1985-05-15 | 1986-11-19 | Kikuchi Keiji | 生酵母菌包括寒天ビ−ズの製造法ならびにアルコ−ルの連続製造法 |
PT83746B (pt) * | 1985-11-15 | 1988-08-17 | Gist Brocades Nv | Processo para a preparacao de novos biocatalisadores imobilizados e para a producao de etanol por fermentacao |
-
1988
- 1988-07-27 HU HU883987A patent/HU202579B/hu not_active IP Right Cessation
-
1989
- 1989-07-06 JP JP1175394A patent/JPH0276581A/ja active Pending
- 1989-07-24 DE DE3924446A patent/DE3924446A1/de not_active Withdrawn
- 1989-07-25 FR FR8909979A patent/FR2634785A1/fr active Pending
- 1989-07-26 IT IT8921320A patent/IT1230999B/it active
- 1989-07-26 SU SU894614585A patent/SU1760985A3/ru active
Also Published As
Publication number | Publication date |
---|---|
IT1230999B (it) | 1991-11-08 |
HUT50866A (en) | 1990-03-28 |
FR2634785A1 (fr) | 1990-02-02 |
SU1760985A3 (ru) | 1992-09-07 |
JPH0276581A (ja) | 1990-03-15 |
IT8921320A0 (it) | 1989-07-26 |
HU202579B (en) | 1991-03-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2721829C3 (de) | Verfahren zur Herstellung eines immobilisierte mikrobielle Zellen enthaltenden hydrophilen komplexen Xerogels | |
DE4480132C2 (de) | Verfahren und Rhodococcus rhodochrous-Stamm zur Herstellung von Amiden aus Nitrilen | |
DD274631A5 (de) | Verfahren zur biologischen herstellung von amiden | |
DE3517629A1 (de) | Verfahren zur herstellung von hyaluronsaeure durch fermentation | |
DE2415461A1 (de) | Verfahren zum erzeugen von algenzellen | |
DE3018767C2 (fr) | ||
DE2614114B2 (de) | Verfahren zur Herstellung von Kreatininamidohydrolase | |
DE2502706A1 (de) | Verfahren zur herstellung von 7-amino-cephem-verbindungen | |
EP0502525B1 (fr) | Procédé biotechnologique pour la production de S-(+)-2,2-diméthylcyclopropanecarboxamide et acide R-(-)-2,2-diméthylcyclopropanecarboxylique | |
CH662582A5 (de) | Verfahren zur erhoehung der antibiotikum-produktion durch in vivo genetische rekombination. | |
DE2811303C3 (de) | Enzymatische Komplexe, die zur Umwandlung racemischer Hydantoine in optisch aktive Aminosäuren geeignet sind, sowie deren Anwendung | |
DE3924446A1 (de) | Verfahren zum einschliessen von mikroorganismen oder teilen davon, die in fermentationsverfahren brauchbar sind, in ein gel | |
EP0371408B1 (fr) | Biocatalyseurs et leur procédé de préparation | |
DE4316646A1 (de) | Lävansucraseenzym, Verfahren zu dessen Herstellung, Mikroorganismen, die es produzieren und Zusammensetzungen, die es enthalten | |
DE2363285A1 (de) | Verfahren zur herstellung von lapfelsaeure durch mikrobiologische fermentation und mittel zur durchfuehrung des verfahrens | |
DE3019254C2 (fr) | ||
DE2241091C3 (fr) | ||
DE2058371A1 (de) | Verfahren zur Herstellung von 6-Aminopenicillansaeure | |
EP0014364A2 (fr) | Procédé pour la dégradation microbiologique de l'acrylonitrile en dispersions aqueuses | |
DE3018584A1 (de) | Verfahren zur herstellung von d- alpha -aminosaeuren | |
DE2108760B2 (de) | Verfahren zur mikrobiologischen herstellung von jodinin | |
DE3831396C1 (en) | Process and biologically active substances for the microbiological breakdown of acetonitrile in mobile phases from high pressure liquid chromatography | |
DE2241091B2 (de) | Verfahren zur herstellung von 7- (d-alpha-aminophenylacetoamido)-desace- toxy-cephalosporansaeure | |
DE2044513C (de) | Verfahren zur Herstellung von alkalischer Amylase | |
RU2157841C1 (ru) | Штамм бактерий aсetobacter pasterianus абз-2 гкм визр n 102 для окисления углеводородов нефти и нефтепродуктов |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
8139 | Disposal/non-payment of the annual fee |