CH626651A5 - - Google Patents
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- Publication number
- CH626651A5 CH626651A5 CH1010476A CH1010476A CH626651A5 CH 626651 A5 CH626651 A5 CH 626651A5 CH 1010476 A CH1010476 A CH 1010476A CH 1010476 A CH1010476 A CH 1010476A CH 626651 A5 CH626651 A5 CH 626651A5
- Authority
- CH
- Switzerland
- Prior art keywords
- bacterial strains
- poly
- phb
- cbs
- carbon source
- Prior art date
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 33
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 30
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 18
- 230000015572 biosynthetic process Effects 0.000 claims description 18
- 229910052799 carbon Inorganic materials 0.000 claims description 18
- JBKVHLHDHHXQEQ-UHFFFAOYSA-N epsilon-caprolactam Chemical compound O=C1CCCCCN1 JBKVHLHDHHXQEQ-UHFFFAOYSA-N 0.000 claims description 18
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 16
- 230000001580 bacterial effect Effects 0.000 claims description 16
- WHBMMWSBFZVSSR-UHFFFAOYSA-N R3HBA Natural products CC(O)CC(O)=O WHBMMWSBFZVSSR-UHFFFAOYSA-N 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 15
- WHBMMWSBFZVSSR-GSVOUGTGSA-N (R)-3-hydroxybutyric acid Chemical compound C[C@@H](O)CC(O)=O WHBMMWSBFZVSSR-GSVOUGTGSA-N 0.000 claims description 14
- 235000013379 molasses Nutrition 0.000 claims description 14
- 238000003786 synthesis reaction Methods 0.000 claims description 13
- 241000194107 Bacillus megaterium Species 0.000 claims description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 10
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 9
- 230000012010 growth Effects 0.000 claims description 9
- 239000001569 carbon dioxide Substances 0.000 claims description 8
- 241000894006 Bacteria Species 0.000 claims description 6
- 235000015097 nutrients Nutrition 0.000 claims description 6
- 241000589153 Zoogloea ramigera Species 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 4
- 238000002386 leaching Methods 0.000 claims description 4
- 150000002763 monocarboxylic acids Chemical class 0.000 claims description 4
- 239000003471 mutagenic agent Substances 0.000 claims description 4
- YCUVUDODLRLVIC-VPHDGDOJSA-N sudan black b Chemical compound C1=CC(=C23)NC(C)(C)NC2=CC=CC3=C1\N=N\C(C1=CC=CC=C11)=CC=C1\N=N\C1=CC=CC=C1 YCUVUDODLRLVIC-VPHDGDOJSA-N 0.000 claims description 3
- 241000721603 Mycoplana Species 0.000 claims description 2
- 150000001721 carbon Chemical class 0.000 claims description 2
- 230000037149 energy metabolism Effects 0.000 claims description 2
- 230000002349 favourable effect Effects 0.000 claims description 2
- 239000000463 material Substances 0.000 claims description 2
- 235000013619 trace mineral Nutrition 0.000 claims description 2
- 239000011573 trace mineral Substances 0.000 claims description 2
- 241000252867 Cupriavidus metallidurans Species 0.000 claims 1
- 230000001627 detrimental effect Effects 0.000 claims 1
- 239000000243 solution Substances 0.000 description 15
- 229920000642 polymer Polymers 0.000 description 10
- 229920001817 Agar Polymers 0.000 description 8
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 8
- 239000008272 agar Substances 0.000 description 8
- AIYUHDOJVYHVIT-UHFFFAOYSA-M caesium chloride Chemical compound [Cl-].[Cs+] AIYUHDOJVYHVIT-UHFFFAOYSA-M 0.000 description 8
- 239000002028 Biomass Substances 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 241001528539 Cupriavidus necator Species 0.000 description 5
- 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 5
- 238000000605 extraction Methods 0.000 description 5
- 239000008103 glucose Substances 0.000 description 5
- 239000002699 waste material Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 4
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 235000016068 Berberis vulgaris Nutrition 0.000 description 3
- 241000335053 Beta vulgaris Species 0.000 description 3
- 229930091371 Fructose Natural products 0.000 description 3
- 239000005715 Fructose Substances 0.000 description 3
- 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 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 150000001735 carboxylic acids Chemical class 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- MWUXSHHQAYIFBG-UHFFFAOYSA-N nitrogen oxide Inorganic materials O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 241000589152 Azotobacter chroococcum Species 0.000 description 2
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 description 2
- VZUNGTLZRAYYDE-UHFFFAOYSA-N N-methyl-N'-nitro-N-nitrosoguanidine Chemical compound O=NN(C)C(=N)N[N+]([O-])=O VZUNGTLZRAYYDE-UHFFFAOYSA-N 0.000 description 2
- 241000589774 Pseudomonas sp. Species 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- 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 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000011161 development Methods 0.000 description 2
- 230000018109 developmental process Effects 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- -1 ethylene, propylene Chemical group 0.000 description 2
- 238000000855 fermentation Methods 0.000 description 2
- 230000004151 fermentation Effects 0.000 description 2
- 239000000835 fiber Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 230000035772 mutation Effects 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 239000002861 polymer material Substances 0.000 description 2
- 235000010333 potassium nitrate Nutrition 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000013049 sediment Substances 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000005720 sucrose Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 229920001059 synthetic polymer Polymers 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 241000104149 Anystis agilis Species 0.000 description 1
- 241000589151 Azotobacter Species 0.000 description 1
- 241000681683 Azotobacter beijerinckii Species 0.000 description 1
- 241000589149 Azotobacter vinelandii Species 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 229920002160 Celluloid Polymers 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 241000530849 Flavobacterium aquatile LMG 4008 = ATCC 11947 Species 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 241000502617 Hylaeus facilis Species 0.000 description 1
- 239000007836 KH2PO4 Substances 0.000 description 1
- 206010028980 Neoplasm Diseases 0.000 description 1
- 241000589187 Rhizobium sp. Species 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 239000005708 Sodium hypochlorite Substances 0.000 description 1
- 241001246249 Thiocystis violascens Species 0.000 description 1
- YSVZGWAJIHWNQK-UHFFFAOYSA-N [3-(hydroxymethyl)-2-bicyclo[2.2.1]heptanyl]methanol Chemical compound C1CC2C(CO)C(CO)C1C2 YSVZGWAJIHWNQK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000001133 acceleration Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000003698 anagen phase Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 201000011510 cancer Diseases 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000004587 chromatography analysis Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- ALEXXDVDDISNDU-JZYPGELDSA-N cortisol 21-acetate Chemical compound C1CC2=CC(=O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(=O)COC(=O)C)(O)[C@@]1(C)C[C@@H]2O ALEXXDVDDISNDU-JZYPGELDSA-N 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000002255 enzymatic effect Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 238000005188 flotation Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000007789 gas 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
- 230000005484 gravity Effects 0.000 description 1
- XLYOFNOQVPJJNP-ZSJDYOACSA-N heavy water Substances [2H]O[2H] XLYOFNOQVPJJNP-ZSJDYOACSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 239000013067 intermediate product Substances 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 230000000877 morphologic effect Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000010076 replication Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000004071 soot Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
- 239000004416 thermosoftening plastic Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004056 waste incineration Methods 0.000 description 1
Classifications
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/62—Carboxylic acid esters
- C12P7/625—Polyesters of hydroxy carboxylic acids
-
- 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
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/85—Flavobacterium
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Biological Depolymerization Polymers (AREA)
Priority Applications (13)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1010476A CH626651A5 (fr) | 1976-08-06 | 1976-08-06 | |
| DE19772733203 DE2733203A1 (de) | 1976-08-06 | 1977-07-22 | Verfahren zur gewinnung von bakterienstaemmen fuer die herstellung von poly-(d-3-hydroxybuttersaeure) |
| NL7708517A NL7708517A (nl) | 1976-08-06 | 1977-08-02 | Werkwijze voor het verkrijgen van bacteriestam- men voor de bereiding van poly-(d-3-hydroxyboter- zuur). |
| SE7708844A SE7708844L (sv) | 1976-08-06 | 1977-08-03 | Utvinning av bakteriestammar for framstellning av poly-(d-3-hydroxismorsyra |
| BE179923A BE857493A (fr) | 1976-08-06 | 1977-08-04 | Procede d'obtention de souches bacteriennes |
| GB32783/77A GB1535632A (en) | 1976-08-06 | 1977-08-04 | Bacterial production of poly-(d-3-hydroxybutyric acid) |
| AU27660/77A AU510376B2 (en) | 1976-08-06 | 1977-08-05 | Bacterial production of poly-(D-3-hydroxybutyric acid |
| FR7724203A FR2360667A1 (fr) | 1976-08-06 | 1977-08-05 | Procede d'obtention de souches bacteriennes |
| DK351877A DK351877A (da) | 1976-08-06 | 1977-08-05 | Fremgangsmade til udvinding af bakteriestammer som danner poly-(d-3-hydroxysmorsyre |
| IT68816/77A IT1082252B (it) | 1976-08-06 | 1977-08-05 | Procedimento per la produzione di ceppi batterici per la preparazione dell acido poli d 3 idrossibutirrico |
| JP9458077A JPS5320478A (en) | 1976-08-06 | 1977-08-06 | Production of polyy*dd33 hydroxybutyric acid* producing strain |
| US05/822,756 US4138291A (en) | 1976-08-06 | 1977-08-08 | Microbiological methods |
| CA284,313A CA1098463A (fr) | 1976-08-06 | 1977-08-08 | Production d'un acide poly-d-3-hydrobutyrique par une souche de bacteries |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH1010476A CH626651A5 (fr) | 1976-08-06 | 1976-08-06 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH626651A5 true CH626651A5 (fr) | 1981-11-30 |
Family
ID=4359387
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH1010476A CH626651A5 (fr) | 1976-08-06 | 1976-08-06 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US4138291A (fr) |
| JP (1) | JPS5320478A (fr) |
| AU (1) | AU510376B2 (fr) |
| BE (1) | BE857493A (fr) |
| CA (1) | CA1098463A (fr) |
| CH (1) | CH626651A5 (fr) |
| DE (1) | DE2733203A1 (fr) |
| DK (1) | DK351877A (fr) |
| FR (1) | FR2360667A1 (fr) |
| GB (1) | GB1535632A (fr) |
| IT (1) | IT1082252B (fr) |
| NL (1) | NL7708517A (fr) |
| SE (1) | SE7708844L (fr) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2446859A1 (fr) * | 1979-01-22 | 1980-08-14 | Solvay | Procede de separation de poly-b-hydroxybutyrates d'une biomasse |
| DE3063405D1 (en) * | 1979-02-21 | 1983-07-07 | Ici Plc | Microbiological process for the production of poly (beta-hydroxybutyric acid) and micro-organisms for use therein |
| DE2948023A1 (de) * | 1979-11-29 | 1981-06-04 | Bayer Ag, 5090 Leverkusen | (beta)-hydroxibuttersaeure-polyester, verfahren zu ihrer herstellung und ihre verwendung als lackrohstoffe |
| US4358583A (en) * | 1980-08-13 | 1982-11-09 | Imperial Chemical Industries Plc | Extraction of poly(β-hydroxy butyric acid) |
| AU560653B2 (en) * | 1981-07-07 | 1987-04-16 | Monsanto Company | 3-hydroxybutyrate polymers |
| US4477654A (en) * | 1981-07-07 | 1984-10-16 | Imperial Chemical Industries Plc | 3-Hydroxybutyrate polymers |
| US4480038A (en) * | 1982-04-30 | 1984-10-30 | E. I. Dupont De Nemours And Company | Density separation of protein overproducing bacteria |
| EP0145233B2 (fr) * | 1983-11-23 | 1991-11-06 | Imperial Chemical Industries Plc | Procédé de séparationpour un polymerede butyrate-3-hydroxy |
| DE3343576A1 (de) * | 1983-12-01 | 1985-06-13 | Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München | Verfahren zur biotechnologischen herstellung von poly-d(-)-3-hydroxybuttersaeure |
| DE3343551A1 (de) * | 1983-12-01 | 1985-06-13 | Lentia GmbH Chem. u. pharm. Erzeugnisse - Industriebedarf, 8000 München | Verfahren zur biotechnologischen herstellung von poly-d(-)-3-hydroxybuttersaeure |
| US5266470A (en) * | 1985-05-28 | 1993-11-30 | Imperial Chemical Industries Plc | Copolymer production |
| AT390068B (de) * | 1988-07-07 | 1990-03-12 | Danubia Petrochemie | Extraktionsmittel fuer poly-d(-)-3-hydroxybuttersaeure |
| CA1313158C (fr) * | 1988-11-07 | 1993-01-26 | William J. Page | Hyperproduction de poly-.beta.-hydroxybutyrate durant une croissance exponentielle par des souches mutantes d'azobacter vinelandii |
| US5147791A (en) * | 1989-04-06 | 1992-09-15 | University Of New Mexico | Enzyme catalyzed synthesis of polyesters |
| US5518907A (en) * | 1989-06-07 | 1996-05-21 | Center For Innovative Technology | Cloning and expression in Escherichia coli of the Alcaligenes eutrophus H16 poly-beta-hydroxybutyrate biosynthetic pathway |
| US5334520A (en) * | 1990-05-25 | 1994-08-02 | Center For Innovative Technology | Production of poly-beta-hydroxybutyrate in transformed escherichia coli |
| DE4040158A1 (de) * | 1990-12-15 | 1992-06-17 | Danubia Petrochem Deutschland | Flaechenfoermiger gegenstand aus einer mit polyhydroxyalkanoat-dispersion beschichteten traegerschicht |
| NL9201803A (nl) * | 1992-10-16 | 1994-05-16 | Inst Voor Agrotech Onderzoek | PHB-producerend microorganisme, werkwijze voor het verkrijgen van een PHB-producerend microorganisme, werkwijze voor het produceren van PHB en werkwijze voor het verwijderen van glycerol uit een glycerol bevattend medium. |
| US5302525A (en) * | 1992-11-23 | 1994-04-12 | National Research Council Of Canada | Methylobacterium extorquwns microorganism useful for the preparation of poly-β-hydroxybutyric acid polymers |
| JPH0790003A (ja) * | 1993-03-01 | 1995-04-04 | Teika Corp | 新規多糖類、その製造方法、新規多糖類の用途およびアゾトバクター・ベイジェリンキィーｔｎｍ１株 |
| EP2283834B1 (fr) * | 1997-03-17 | 2016-07-13 | BTG International Limited | Compositions thérapeutiques contenants des corps kétoniques ou leurs précurseurs |
| US6808907B2 (en) * | 2001-03-27 | 2004-10-26 | Canon Kabushiki Kaisha | Method and apparatus for producing polyhydroxyalkanoate |
| BRPI0600782A (pt) * | 2006-02-24 | 2007-11-20 | Phb Ind Sa | composição para preparo de poliol poliéster degradável, processo para obtenção de poliol poliéster, de elastÈmero, de espumas, de tintas e de adesivos, e espuma degradável de um poliol poliéster |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2439572A (en) * | 1944-03-15 | 1948-04-13 | Levin Samuel Baruch | Apparatus and process for the cultivation of microorganisms |
| US3071518A (en) * | 1960-02-09 | 1963-01-01 | Cons Lab Inc | Method of increasing metabolic product yield of organisms |
| US3044942A (en) * | 1960-09-27 | 1962-07-17 | Grace W R & Co | Process for preparing poly-beta-hydroxybutyric acid |
| US3072538A (en) * | 1960-12-30 | 1963-01-08 | Grace W R & Co | Isolation of bacteria |
-
1976
- 1976-08-06 CH CH1010476A patent/CH626651A5/de not_active IP Right Cessation
-
1977
- 1977-07-22 DE DE19772733203 patent/DE2733203A1/de not_active Withdrawn
- 1977-08-02 NL NL7708517A patent/NL7708517A/xx not_active Application Discontinuation
- 1977-08-03 SE SE7708844A patent/SE7708844L/xx not_active Application Discontinuation
- 1977-08-04 GB GB32783/77A patent/GB1535632A/en not_active Expired
- 1977-08-04 BE BE179923A patent/BE857493A/fr not_active IP Right Cessation
- 1977-08-05 FR FR7724203A patent/FR2360667A1/fr active Granted
- 1977-08-05 AU AU27660/77A patent/AU510376B2/en not_active Expired
- 1977-08-05 DK DK351877A patent/DK351877A/da not_active Application Discontinuation
- 1977-08-05 IT IT68816/77A patent/IT1082252B/it active
- 1977-08-06 JP JP9458077A patent/JPS5320478A/ja active Pending
- 1977-08-08 US US05/822,756 patent/US4138291A/en not_active Expired - Lifetime
- 1977-08-08 CA CA284,313A patent/CA1098463A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE857493A (fr) | 1978-02-06 |
| SE7708844L (sv) | 1978-02-07 |
| DK351877A (da) | 1978-02-07 |
| AU2766077A (en) | 1979-02-08 |
| JPS5320478A (en) | 1978-02-24 |
| AU510376B2 (en) | 1980-06-19 |
| DE2733203A1 (de) | 1978-02-09 |
| IT1082252B (it) | 1985-05-21 |
| US4138291A (en) | 1979-02-06 |
| GB1535632A (en) | 1978-12-13 |
| FR2360667A1 (fr) | 1978-03-03 |
| FR2360667B3 (fr) | 1980-06-06 |
| NL7708517A (nl) | 1978-02-08 |
| CA1098463A (fr) | 1981-03-31 |
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| PL | Patent ceased |