HU176250B - Process for producing mikrobiologically 12-beta-hydroxycardenolide derivatives - Google Patents
Process for producing mikrobiologically 12-beta-hydroxycardenolide derivatives Download PDFInfo
- Publication number
- HU176250B HU176250B HUGO001428A HU176250B HU 176250 B HU176250 B HU 176250B HU GO001428 A HUGO001428 A HU GO001428A HU 176250 B HU176250 B HU 176250B
- Authority
- HU
- Hungary
- Prior art keywords
- mng
- streptomyces
- purpurascens
- blue
- color
- Prior art date
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- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000001089 [(2R)-oxolan-2-yl]methanol Substances 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- PYMYPHUHKUWMLA-VPENINKCSA-N aldehydo-D-xylose Chemical compound OC[C@@H](O)[C@H](O)[C@@H](O)C=O PYMYPHUHKUWMLA-VPENINKCSA-N 0.000 description 1
- 229940024606 amino acid Drugs 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- PYMYPHUHKUWMLA-WDCZJNDASA-N arabinose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C=O PYMYPHUHKUWMLA-WDCZJNDASA-N 0.000 description 1
- 102000006995 beta-Glucosidase Human genes 0.000 description 1
- 108010047754 beta-Glucosidase Proteins 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 229910052799 carbon Inorganic materials 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
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002026 chloroform extract Substances 0.000 description 1
- WORJEOGGNQDSOE-UHFFFAOYSA-N chloroform;methanol Chemical compound OC.ClC(Cl)Cl WORJEOGGNQDSOE-UHFFFAOYSA-N 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000002178 crystalline material Substances 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- WACQKHWOTAEEFS-UHFFFAOYSA-N cyclohexane;ethyl acetate Chemical compound CCOC(C)=O.C1CCCCC1 WACQKHWOTAEEFS-UHFFFAOYSA-N 0.000 description 1
- 235000013681 dietary sucrose Nutrition 0.000 description 1
- 230000029087 digestion Effects 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000000706 filtrate Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 238000004362 fungal culture Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002431 hydrogen Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- BJHIKXHVCXFQLS-UYFOZJQFSA-N keto-D-fructose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)C(=O)CO BJHIKXHVCXFQLS-UYFOZJQFSA-N 0.000 description 1
- 229940049920 malate Drugs 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000005375 photometry Methods 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 238000005201 scrubbing Methods 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- BSYVTEYKTMYBMK-UHFFFAOYSA-N tetrahydrofurfuryl alcohol Chemical compound OCC1CCCO1 BSYVTEYKTMYBMK-UHFFFAOYSA-N 0.000 description 1
- SWGJCIMEBVHMTA-UHFFFAOYSA-K trisodium;6-oxido-4-sulfo-5-[(4-sulfonatonaphthalen-1-yl)diazenyl]naphthalene-2-sulfonate Chemical compound [Na+].[Na+].[Na+].C1=CC=C2C(N=NC3=C4C(=CC(=CC4=CC=C3O)S([O-])(=O)=O)S([O-])(=O)=O)=CC=C(S([O-])(=O)=O)C2=C1 SWGJCIMEBVHMTA-UHFFFAOYSA-K 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 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
- C12P33/00—Preparation of steroids
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)
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HUGO001428 HU176250B (en) | 1978-10-30 | 1978-10-30 | Process for producing mikrobiologically 12-beta-hydroxycardenolide derivatives |
| DD21649079A DD147113A5 (de) | 1978-10-30 | 1979-10-26 | Herstellung von 12 beta-hydroxy-cardenolidderivaten auf mikrobiologischem wege |
| CH962579A CH646995A5 (de) | 1978-10-30 | 1979-10-26 | Verfahren zur herstellung von 12beta-hydroxycardenolidderivaten auf mikrobiologischem wege. |
| GB7937475A GB2034716B (en) | 1978-10-30 | 1979-10-29 | Microbiological method for the preparation of 12-hydroxy-cardenolide compounds |
| NL7907937A NL7907937A (nl) | 1978-10-30 | 1979-10-29 | Nieuw microbiologisch procede voor de bereiding van 12 beta-hydroxycardenolideverbindingen. |
| DE19792943817 DE2943817A1 (de) | 1978-10-30 | 1979-10-30 | Bei gaerung in submerser kultur zur einfuehrung der 12 beta -hydroxygruppe und ggf. 7 beta -hydroxygruppe in den aglykonteil von herzglykosiden bzw. in deren aglykone selbst und zur abspaltung der d- glucosegruppe und acetylgruppe von primaeren digitalisglykosiden, der d-glucosegruppe von purpureaglykosiden und der acetylgruppe von acetylderivaten von sekundaeren digitalisglykosiden faehige aus boeden erhaeltliche mikroorganismenstaemme und verfahren zur mikrobiologischen herstellung von 12 beta -hydroxycardenolidverbindungen |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| HUGO001428 HU176250B (en) | 1978-10-30 | 1978-10-30 | Process for producing mikrobiologically 12-beta-hydroxycardenolide derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU176250B true HU176250B (en) | 1981-01-28 |
Family
ID=10996878
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HUGO001428 HU176250B (en) | 1978-10-30 | 1978-10-30 | Process for producing mikrobiologically 12-beta-hydroxycardenolide derivatives |
Country Status (6)
| Country | Link |
|---|---|
| CH (1) | CH646995A5 (enrdf_load_stackoverflow) |
| DD (1) | DD147113A5 (enrdf_load_stackoverflow) |
| DE (1) | DE2943817A1 (enrdf_load_stackoverflow) |
| GB (1) | GB2034716B (enrdf_load_stackoverflow) |
| HU (1) | HU176250B (enrdf_load_stackoverflow) |
| NL (1) | NL7907937A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU190784B (en) * | 1981-09-28 | 1986-11-28 | Richter Gedeon Vegyeszeti Gyar Rt,Hu | Process for the intensification of the microbiological transformation of steroid compounds |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU175474B (hu) * | 1978-05-23 | 1980-08-28 | Gyogyszerkutato Intezet | Novyjj mikrobiologicheskijj sposob poluchenija proizvodnykh kardenolida soderzhahhikh gruppu 12-beta-gidroksila |
| HU175601B (hu) * | 1978-08-11 | 1980-09-28 | Gyogyszerkutato Intezet | Mikrobiologocheskij sposob poluchenija vtorichnykh gljukozidov iz pervichnykh digitalis gljukozidov |
| CA2037985A1 (en) * | 1990-03-23 | 1991-09-24 | Robert C. Gmelin | Economical air separator |
| EP0449448B1 (en) * | 1990-03-29 | 1997-01-22 | The Boc Group, Inc. | Process for producing oxygen enriched product stream |
| ZA911499B (en) * | 1990-03-30 | 1991-12-24 | Boc Group Inc | Purifying fluids by adsorption |
| JPH04222611A (ja) * | 1990-12-21 | 1992-08-12 | Matsushita Electric Ind Co Ltd | フィルター装置 |
| JPH04224498A (ja) * | 1990-12-26 | 1992-08-13 | Kayseven Co Ltd | 船灯状態異常の警報装置 |
-
1978
- 1978-10-30 HU HUGO001428 patent/HU176250B/hu not_active IP Right Cessation
-
1979
- 1979-10-26 CH CH962579A patent/CH646995A5/de not_active IP Right Cessation
- 1979-10-26 DD DD21649079A patent/DD147113A5/de not_active IP Right Cessation
- 1979-10-29 GB GB7937475A patent/GB2034716B/en not_active Expired
- 1979-10-29 NL NL7907937A patent/NL7907937A/nl not_active Application Discontinuation
- 1979-10-30 DE DE19792943817 patent/DE2943817A1/de active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| DE2943817C2 (enrdf_load_stackoverflow) | 1988-01-14 |
| GB2034716B (en) | 1983-01-12 |
| NL7907937A (nl) | 1980-05-02 |
| DE2943817A1 (de) | 1980-05-14 |
| CH646995A5 (de) | 1984-12-28 |
| GB2034716A (en) | 1980-06-11 |
| DD147113A5 (de) | 1981-03-18 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 | ||
| HMM4 | Cancellation of final prot. due to non-payment of fee |