CH626651A5 - - Google Patents

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Info

Publication number: CH626651A5
Authority: CH; Switzerland
Prior art keywords: bacterial strains; poly; phb; cbs; carbon source
Prior art date: 1976-08-06

Application number

CH1010476A

Other languages

German (de)

English (en)

Inventor

Robert M Lafferty

Original Assignee

Agroferm Ag

Priority date (The priority date 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 date listed.)

1976-08-06

Filing date

1976-08-06

Publication date

1981-11-30

1976-08-06 Application filed by Agroferm Ag filed Critical Agroferm Ag

1976-08-06 Priority to CH1010476A priority Critical patent/CH626651A5/de

1977-07-22 Priority to DE19772733203 priority patent/DE2733203A1/de

1977-08-02 Priority to NL7708517A priority patent/NL7708517A/xx

1977-08-03 Priority to SE7708844A priority patent/SE7708844L/xx

1977-08-04 Priority to BE179923A priority patent/BE857493A/xx

1977-08-04 Priority to GB32783/77A priority patent/GB1535632A/en

1977-08-05 Priority to AU27660/77A priority patent/AU510376B2/en

1977-08-05 Priority to IT68816/77A priority patent/IT1082252B/it

1977-08-05 Priority to DK351877A priority patent/DK351877A/da

1977-08-05 Priority to FR7724203A priority patent/FR2360667A1/fr

1977-08-06 Priority to JP9458077A priority patent/JPS5320478A/ja

1977-08-08 Priority to CA284,313A priority patent/CA1098463A/en

1977-08-08 Priority to US05/822,756 priority patent/US4138291A/en

1981-11-30 Publication of CH626651A5 publication Critical patent/CH626651A5/de

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
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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
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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
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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
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239000008103 glucose Substances 0.000 description 5
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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
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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
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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
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238000010790 dilution Methods 0.000 description 2
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238000000855 fermentation Methods 0.000 description 2
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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
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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
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239000005720 sucrose Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
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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
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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
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238000005119 centrifugation Methods 0.000 description 1
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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
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238000005886 esterification reaction Methods 0.000 description 1
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238000002474 experimental method Methods 0.000 description 1
239000002360 explosive Substances 0.000 description 1
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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)

CH1010476A 1976-08-06 1976-08-06 CH626651A5 (ko)

Priority Applications (13)

Application Number	Priority Date	Filing Date	Title
CH1010476A CH626651A5 (ko)	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
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
DK351877A DK351877A (da)	1976-08-06	1977-08-05	Fremgangsmade til udvinding af bakteriestammer som danner poly-(d-3-hydroxysmorsyre
FR7724203A FR2360667A1 (fr)	1976-08-06	1977-08-05	Procede d'obtention de souches bacteriennes
JP9458077A JPS5320478A (en)	1976-08-06	1977-08-06	Production of polyydd33 hydroxybutyric acid producing strain
CA284,313A CA1098463A (en)	1976-08-06	1977-08-08	Microbial production of poly-(d-3-hydroxybutyric acid)
US05/822,756 US4138291A (en)	1976-08-06	1977-08-08	Microbiological methods

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1010476A CH626651A5 (ko)	1976-08-06	1976-08-06

Publications (1)

Publication Number	Publication Date
CH626651A5 true CH626651A5 (ko)	1981-11-30

Family

ID=4359387

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1010476A CH626651A5 (ko)	1976-08-06	1976-08-06

Country Status (13)

Country	Link
US (1)	US4138291A (ko)
JP (1)	JPS5320478A (ko)
AU (1)	AU510376B2 (ko)
BE (1)	BE857493A (ko)
CA (1)	CA1098463A (ko)
CH (1)	CH626651A5 (ko)
DE (1)	DE2733203A1 (ko)
DK (1)	DK351877A (ko)
FR (1)	FR2360667A1 (ko)
GB (1)	GB1535632A (ko)
IT (1)	IT1082252B (ko)
NL (1)	NL7708517A (ko)
SE (1)	SE7708844L (ko)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
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
EP0015669B1 (en) *	1979-02-21	1983-05-25	Imperial Chemical Industries 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)
US4477654A (en) *	1981-07-07	1984-10-16	Imperial Chemical Industries Plc	3-Hydroxybutyrate polymers
AU560653B2 (en) *	1981-07-07	1987-04-16	Monsanto Company	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 (en) *	1983-11-23	1991-11-06	Imperial Chemical Industries Plc	Separation processfor a 3-hydroxybutyrate polymer
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
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
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 (en) *	1988-11-07	1993-01-26	William J. Page	Hyperproduction of poly-.beta.-hydroxybutyrate during exponential growthby mutant strains of azotobacter vinelandii
US5147791A (en) *	1989-04-06	1992-09-15	University Of New Mexico	Enzyme catalyzed synthesis of polyesters
US5334520A (en) *	1990-05-25	1994-08-02	Center For Innovative Technology	Production of poly-beta-hydroxybutyrate in transformed escherichia coli
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
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 (en) *	1997-03-17	2016-07-13	BTG International Limited	Therapeutic compositions comprising ketone bodies or their precursors
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

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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 BE BE179923A patent/BE857493A/xx not_active IP Right Cessation
- 1977-08-04 GB GB32783/77A patent/GB1535632A/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
- 1977-08-05 AU AU27660/77A patent/AU510376B2/en not_active Expired
- 1977-08-05 FR FR7724203A patent/FR2360667A1/fr active Granted
- 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/en not_active Expired

Also Published As

Publication number	Publication date
JPS5320478A (en)	1978-02-24
BE857493A (fr)	1978-02-06
SE7708844L (sv)	1978-02-07
AU510376B2 (en)	1980-06-19
FR2360667B3 (ko)	1980-06-06
DK351877A (da)	1978-02-07
US4138291A (en)	1979-02-06
GB1535632A (en)	1978-12-13
CA1098463A (en)	1981-03-31
DE2733203A1 (de)	1978-02-09
IT1082252B (it)	1985-05-21
NL7708517A (nl)	1978-02-08
AU2766077A (en)	1979-02-08
FR2360667A1 (fr)	1978-03-03

Legal Events

Date	Code	Title	Description
1985-04-30	PL	Patent ceased

Publication	Publication Date	Title
CH626651A5 (ko)	1981-11-30
Andrady	1994	Assessment of environmental biodegradation of synthetic polymers
DE3789377T2 (de)	1994-07-28	Verfahren zur Herstellung von Polyestern durch Fermentation, Verfahren zur Herstellung von optisch-aktiven Karbonsäuren und -estern, und Polyester enthaltende Produkte.
DE60217202T2 (de)	2008-03-13	Polyhydroxyalkanoat-Polyester die Vinylphenylgruppen in der Seitenkette enthalten und Verfahren zu dessen Herstellung
DE60034543T2 (de)	2007-12-27	Polyhydroxyalkanoate und ein Verfahren zu ihrer Herstellung mittels Mikroorganismen
DE3688163T2 (de)	1993-09-30	Verfahren zur Rückgewinnung von extrazellulären Enzymen aus gesamten Fermentationsbrühen.
Herron et al.	1978	Recovery of poly-β-hydroxybutyrate from estuarine microflora
DE2808932A1 (de)	1978-09-07	Herstellung von aethanol aus cellulose
DE4200878A1 (de)	1992-08-20	Gleichzeitige verzuckerung und fermentation (ssf) unter verwendung von cellobiose-fermentierender hefe brettanomyces custersil (cbs 5512)
DE3230197A1 (de)	1983-04-07	Methangaerungsverfahren
DE2633076A1 (de)	1977-02-17	Verfahren zur durchfuehrung von enzymatischen reaktionen unter verwendung von in einer polymerisatmatrix eingeschlossenen mikroorganismen
Maheswari et al.	2011	Production of bioplastic using Spirulina platensis and comparison with commercial plastic
EP0222302B1 (de)	1992-05-27	Aureobasidium-pullulans-Stamm, Herstellungsverfahren und Verwendung
Xavier et al.	1994	Sugar-cane pressmud as a novel and inexpensive substrate for production of lactic acid in a solid-state fermentation system
DE69005623T2 (de)	1994-05-11	Mikrobiologische herstellung von polyestern.
EP0593975A1 (de)	1994-04-27	Verwendung thermoplastischer Poly(ester-urethane) als kompostierbare Kunststoffe
CA1313158C (en)	1993-01-26	Hyperproduction of poly-.beta.-hydroxybutyrate during exponential growthby mutant strains of azotobacter vinelandii
CN111378254B (zh)	2024-02-20	盐单胞菌Halomonas sp ZY-1利用秸秆和地沟油廉价合成生物可降解地膜
EP0082814A1 (de)	1983-06-29	Mikroorganismen des Genus Pseudomonas und Verfahren zum Abbau von Methylgruppen-haltigen Verbindungen in wässrigen Lösungen
EP0082114A1 (de)	1983-06-22	Mikroorganismen des Genus Hyphomicrobium und Verfahren zum Abbau von Methylgruppen-haltigen Verbindungen in wässrigen Lösungen
DE69021613T2 (de)	1996-02-08	Polymer-Herstellung.
DE2150375A1 (de)	1972-04-20	Verfahren zur biotechnischen Herstellung rhamnosehaltiger Glycolipide
DE2152039B2 (de)	1973-10-31	Verfahren zur Herstellung von Baktenenzellmasse
DE3781699T2 (de)	1993-03-11	Verfahren zur herstellung von l-sorbose.
DE1926178B2 (de)	1974-06-20	Mikrobiologisches Verfahren zur Herstellung von D-Arabit