SK278790B6 - Mikrobiologický spôsob výroby kyseliny6-hydroxypyr - Google Patents
Mikrobiologický spôsob výroby kyseliny6-hydroxypyr Download PDFInfo
- Publication number
- SK278790B6 SK278790B6 SK2660-92A SK266092A SK278790B6 SK 278790 B6 SK278790 B6 SK 278790B6 SK 266092 A SK266092 A SK 266092A SK 278790 B6 SK278790 B6 SK 278790B6
- Authority
- SK
- Slovakia
- Prior art keywords
- acid
- salts
- carboxylic acid
- microorganisms
- hydroxypyrazinecarboxylic
- Prior art date
Links
- LHXIGTYJDLGWRO-UHFFFAOYSA-N 6-oxo-1h-pyrazine-2-carboxylic acid Chemical compound OC(=O)C1=CN=CC(O)=N1 LHXIGTYJDLGWRO-UHFFFAOYSA-N 0.000 title claims abstract description 15
- 238000013048 microbiological method Methods 0.000 title 1
- 150000003839 salts Chemical class 0.000 claims abstract description 23
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims abstract description 17
- 238000000034 method Methods 0.000 claims abstract description 14
- 244000005700 microbiome Species 0.000 claims abstract description 14
- 241000588986 Alcaligenes Species 0.000 claims abstract description 3
- 239000000758 substrate Substances 0.000 claims description 10
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 229940081066 picolinic acid Drugs 0.000 claims description 8
- NIPZZXUFJPQHNH-UHFFFAOYSA-N pyrazine-2-carboxylic acid Chemical compound OC(=O)C1=CN=CC=N1 NIPZZXUFJPQHNH-UHFFFAOYSA-N 0.000 claims description 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229910052757 nitrogen Inorganic materials 0.000 claims description 3
- 230000002906 microbiologic effect Effects 0.000 claims description 2
- 239000002609 medium Substances 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 241000588813 Alcaligenes faecalis Species 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical group [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002253 acid Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 235000010755 mineral Nutrition 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 239000002028 Biomass Substances 0.000 description 2
- 229940005347 alcaligenes faecalis Drugs 0.000 description 2
- 230000036983 biotransformation Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000006698 induction Effects 0.000 description 2
- 238000002955 isolation Methods 0.000 description 2
- IPEHBUMCGVEMRF-UHFFFAOYSA-N pyrazinecarboxamide Chemical compound NC(=O)C1=CN=CC=N1 IPEHBUMCGVEMRF-UHFFFAOYSA-N 0.000 description 2
- 229910052709 silver Inorganic materials 0.000 description 2
- 239000004332 silver Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- MFLUBKYTRLCODV-UHFFFAOYSA-M sodium;pyrazine-2-carboxylate Chemical compound [Na+].[O-]C(=O)C1=CN=CC=N1 MFLUBKYTRLCODV-UHFFFAOYSA-M 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000006228 supernatant Substances 0.000 description 2
- VRCWSYYXUCKEED-UHFFFAOYSA-N 6-Hydroxypicolinic acid Chemical compound OC(=O)C1=CC=CC(=O)N1 VRCWSYYXUCKEED-UHFFFAOYSA-N 0.000 description 1
- RSIRAMVPQSGCGG-UHFFFAOYSA-N 6-oxo-1h-pyrazine-2-carboxylic acid;sodium Chemical compound [Na].OC(=O)C1=CN=CC(=O)N1 RSIRAMVPQSGCGG-UHFFFAOYSA-N 0.000 description 1
- 241000193798 Aerococcus Species 0.000 description 1
- 241000193830 Bacillus <bacterium> Species 0.000 description 1
- 229910021591 Copper(I) chloride Inorganic materials 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- WDIHJSXYQDMJHN-UHFFFAOYSA-L barium chloride Chemical compound [Cl-].[Cl-].[Ba+2] WDIHJSXYQDMJHN-UHFFFAOYSA-L 0.000 description 1
- 229910001626 barium chloride Inorganic materials 0.000 description 1
- PWHCIQQGOQTFAE-UHFFFAOYSA-L barium chloride dihydrate Chemical compound O.O.[Cl-].[Cl-].[Ba+2] PWHCIQQGOQTFAE-UHFFFAOYSA-L 0.000 description 1
- 159000000009 barium salts Chemical class 0.000 description 1
- 238000004113 cell culture Methods 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 238000001311 chemical methods and process Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 239000012737 fresh medium Substances 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- ZTAQCRRTNOJVIU-UHFFFAOYSA-N methyl 4-oxidopyrazin-4-ium-2-carboxylate Chemical compound COC(=O)C1=C[N+]([O-])=CC=N1 ZTAQCRRTNOJVIU-UHFFFAOYSA-N 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 229960005206 pyrazinamide Drugs 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- -1 sodium pyrazinecarboxylic acid sodium salt Chemical compound 0.000 description 1
- RLEBKHAOAHYZHT-UHFFFAOYSA-M sodium;pyridine-2-carboxylate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=N1 RLEBKHAOAHYZHT-UHFFFAOYSA-M 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 239000000814 tuberculostatic agent Substances 0.000 description 1
- 238000000870 ultraviolet spectroscopy 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
- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/10—Nitrogen as only ring hetero atom
- C12P17/12—Nitrogen as only ring hetero atom containing a six-membered hetero ring
-
- 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
- Y10S435/829—Alcaligenes
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)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH255691 | 1991-08-30 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK278790B6 true SK278790B6 (sk) | 1998-02-04 |
| SK266092A3 SK266092A3 (en) | 1998-02-04 |
Family
ID=4236458
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK2660-92A SK266092A3 (en) | 1991-08-30 | 1992-08-28 | Microbiological method of producing 6-hydroxypyrazinecarboxylic acid |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US5238829A (cs) |
| EP (1) | EP0529653B1 (cs) |
| JP (1) | JPH05252968A (cs) |
| AT (1) | ATE144554T1 (cs) |
| CA (1) | CA2077133A1 (cs) |
| CZ (1) | CZ279296B6 (cs) |
| DE (1) | DE59207418D1 (cs) |
| DK (1) | DK0529653T3 (cs) |
| ES (1) | ES2093156T3 (cs) |
| MX (1) | MX9204902A (cs) |
| SK (1) | SK266092A3 (cs) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3275353B2 (ja) * | 1992-02-26 | 2002-04-15 | 三菱化学株式会社 | ６−ヒドロキシ含窒素６員環化合物の製造方法 |
| CZ282939B6 (cs) * | 1992-03-04 | 1997-11-12 | Lonza A.G. | Mikrobiologický způsob hydroxylace dusíkatých heterocyklických karboxylových kyselin |
| JP3319628B2 (ja) * | 1992-07-08 | 2002-09-03 | ロンザ リミテッド | ５−ヒドロキシピラジンカルボン酸を製造するための微生物学的方法 |
| AU2002220603A1 (en) * | 2000-10-06 | 2002-04-15 | Lonza A.G. | Biotechnological method for preparing carboxylic acids with a hydroxy-nitrogen heterocycle |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IN170700B (cs) * | 1989-12-20 | 1992-05-02 | Lonza Ag | |
| JP3275353B2 (ja) * | 1992-02-26 | 2002-04-15 | 三菱化学株式会社 | ６−ヒドロキシ含窒素６員環化合物の製造方法 |
-
1992
- 1992-08-25 MX MX9204902A patent/MX9204902A/es unknown
- 1992-08-27 JP JP4228579A patent/JPH05252968A/ja not_active Withdrawn
- 1992-08-27 US US07/936,201 patent/US5238829A/en not_active Expired - Fee Related
- 1992-08-28 SK SK2660-92A patent/SK266092A3/sk unknown
- 1992-08-28 DK DK92114746.8T patent/DK0529653T3/da active
- 1992-08-28 ES ES92114746T patent/ES2093156T3/es not_active Expired - Lifetime
- 1992-08-28 CZ CS922660A patent/CZ279296B6/cs unknown
- 1992-08-28 EP EP92114746A patent/EP0529653B1/de not_active Expired - Lifetime
- 1992-08-28 AT AT92114746T patent/ATE144554T1/de not_active IP Right Cessation
- 1992-08-28 DE DE59207418T patent/DE59207418D1/de not_active Expired - Fee Related
- 1992-08-28 CA CA002077133A patent/CA2077133A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CZ279296B6 (cs) | 1995-04-12 |
| CZ266092A3 (en) | 1993-03-17 |
| ES2093156T3 (es) | 1996-12-16 |
| EP0529653A3 (en) | 1994-07-06 |
| DK0529653T3 (da) | 1996-11-18 |
| EP0529653B1 (de) | 1996-10-23 |
| ATE144554T1 (de) | 1996-11-15 |
| MX9204902A (es) | 1993-05-01 |
| CA2077133A1 (en) | 1993-03-01 |
| SK266092A3 (en) | 1998-02-04 |
| JPH05252968A (ja) | 1993-10-05 |
| DE59207418D1 (de) | 1996-11-28 |
| EP0529653A2 (de) | 1993-03-03 |
| US5238829A (en) | 1993-08-24 |
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