GB712547A - Antibiotic and methods of obtaining same - Google Patents
Antibiotic and methods of obtaining sameInfo
- Publication number
- GB712547A GB712547A GB7415/52A GB741552A GB712547A GB 712547 A GB712547 A GB 712547A GB 7415/52 A GB7415/52 A GB 7415/52A GB 741552 A GB741552 A GB 741552A GB 712547 A GB712547 A GB 712547A
- Authority
- GB
- United Kingdom
- Prior art keywords
- methanol
- water
- antibiotic
- culture
- medium
- 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.)
- Expired
Links
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
- C12P1/00—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes
- C12P1/06—Preparation of compounds or compositions, not provided for in groups C12P3/00 - C12P39/00, by using microorganisms or enzymes by using actinomycetales
-
- 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
- C12N1/00—Microorganisms, e.g. protozoa; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
- C12N1/205—Bacterial isolates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/465—Streptomyces
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Biomedical Technology (AREA)
- Virology (AREA)
- Medicinal Chemistry (AREA)
- Mycology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Compounds Of Unknown Constitution (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
An antibiotic sistomycosin is produced by inoculating a nutrient medium with Streptomyces viridosporus NRRL 2414, which is described, incubating the inoculated medium under aerobic conditions at a temperature of 20-35 DEG C. for 1 to 8 days and isolating the antibiotic so produced from the culture mixture. The medium may be liquid or solid, the culture submerged or surface. It is preferred to use an aqueous nutrient containing a source of assimilable carbon, proteinaceous material and mineral salts, having initial pH 6-8.2, especially 7.3-7.7, and submerged culture with aeration by air, oxygen, or an oxygen-containing gas at 25-28 DEG C. for 1-4 days. Light should be excluded. The air may be injected into the medium, or the medium may be sprayed into the sterile air. Suitable carbon sources are arabinose, fructose, galactose, lactose, maltose, rhamnose, xylose, glycerol, mannitol and glucose, starch, dextrin, fermentation and distillers' slops, corn steep water solids, corn steep liquor and fermentation residues, e.g. of butanol-acetone. Suitable proteinaceous materials are beef extract, acid hydrolysed casein, beef peptone, soybean oil meal, dried fermentation residues; water-soluble, defatted and partially hydrolysed soybean meal, mixed amino acids, urea and purines. Minerals are sodium chloride, calcium carbonate, monopotassium hydrogen phosphate and di-potassium hydrogen phosphate. The antibiotic is obtained from (a) the liquid culture by first filtering off the mycelium, and from (b) the solid culture by first extracting with a solvent such as water or methanol. The liquids so obtained are extracted with a water-immiscible alcohol, e.g. n-butanol, the solvent removed and the solid extract treated with a fat solvent such as chloroform. The residue is extracted with chloroform containing 10 per cent methanol, and the solution so formed passed down a column of a silicate ion-exchanger. The column is washed with chloroform-methanol of increasing methanol content, and then eluted with methanol. The residue after the removal of the methanol is extracted with water, and the antibiotic recovered by freeze drying. Sistomycosin is a neutral substance, effective in inhibiting the growth of eumycetes and having no effect on the growth of most gram-negative and gram-positive bacteria, and containing only C, H, O and N. It is soluble in water and methanol, less soluble in wet acetone and aqueous alcohols containing more than one carbon atom per molecule; insoluble in chloroform, diethyl ether, ethyl acetate, benzene and petroleum ether. Decomposed by light, it reduces cold aqueous potassium permanganate solution and boiling Benedict's solution; gives a positive Molisch test, a negative ferric chloride test, imparts a deep cherry-red-to-chocolate colour to warm concentrated sulphuric acid, no colour with hydrochloric acid and thymol. In water, it exhibits characteristic maximum and minimum absorption bands in the ultra-violet region of the spectrum. In a hydrocarbon oil, it shows a characteristic infra-red absorption spectrum.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US1057122XA | 1951-03-26 | 1951-03-26 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB712547A true GB712547A (en) | 1954-07-28 |
Family
ID=22307386
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB7415/52A Expired GB712547A (en) | 1951-03-26 | 1952-03-21 | Antibiotic and methods of obtaining same |
Country Status (5)
Country | Link |
---|---|
CH (1) | CH298331A (en) |
DE (1) | DE916574C (en) |
DK (1) | DK87962C (en) |
FR (1) | FR1057122A (en) |
GB (1) | GB712547A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3240787A (en) * | 1962-01-23 | 1966-03-15 | Inst Medical Res | Alpha-hydroxymethyl-n-[omega-hydroxamic-acid-ethylene-carbonylamino-methylene-carbonyl]-pyrrolidine and process for its production |
FR2777571A1 (en) * | 1998-04-21 | 1999-10-22 | Revico | Fermentative production of compounds of economic interest, especially flavors such as gamma-decalactone |
US6518050B1 (en) | 1998-04-21 | 2003-02-11 | Revico | Process for producing and extracting aromatic compounds |
WO2009138994A1 (en) * | 2008-05-14 | 2009-11-19 | Biocon Limited | A fermentation process for the production of secondary metabolites |
-
1952
- 1952-03-21 GB GB7415/52A patent/GB712547A/en not_active Expired
- 1952-03-22 FR FR1057122D patent/FR1057122A/en not_active Expired
- 1952-03-25 DE DEP7337A patent/DE916574C/en not_active Expired
- 1952-03-26 DK DK100452AA patent/DK87962C/en active
- 1952-03-26 CH CH298331D patent/CH298331A/en unknown
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3240787A (en) * | 1962-01-23 | 1966-03-15 | Inst Medical Res | Alpha-hydroxymethyl-n-[omega-hydroxamic-acid-ethylene-carbonylamino-methylene-carbonyl]-pyrrolidine and process for its production |
FR2777571A1 (en) * | 1998-04-21 | 1999-10-22 | Revico | Fermentative production of compounds of economic interest, especially flavors such as gamma-decalactone |
US6518050B1 (en) | 1998-04-21 | 2003-02-11 | Revico | Process for producing and extracting aromatic compounds |
WO2009138994A1 (en) * | 2008-05-14 | 2009-11-19 | Biocon Limited | A fermentation process for the production of secondary metabolites |
Also Published As
Publication number | Publication date |
---|---|
DK87962C (en) | 1959-10-12 |
DE916574C (en) | 1954-10-11 |
CH298331A (en) | 1954-04-30 |
FR1057122A (en) | 1954-03-05 |
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