GB744540A - Amino acid compounds and methods for producing the same - Google Patents
Amino acid compounds and methods for producing the sameInfo
- Publication number
- GB744540A GB744540A GB776753A GB776753A GB744540A GB 744540 A GB744540 A GB 744540A GB 776753 A GB776753 A GB 776753A GB 776753 A GB776753 A GB 776753A GB 744540 A GB744540 A GB 744540A
- Authority
- GB
- United Kingdom
- Prior art keywords
- water
- serine
- aqueous
- glycyl
- nitrite
- 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
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C245/00—Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
- C07C245/12—Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom
- C07C245/14—Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom having diazo groups bound to acyclic carbon atoms of a carbon skeleton
- C07C245/18—Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom having diazo groups bound to acyclic carbon atoms of a carbon skeleton the carbon skeleton being further substituted by carboxyl groups
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/06—Alanine; Leucine; Isoleucine; Serine; Homoserine
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (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)
Abstract
The invention comprises O-diazoacetyl-l- and -dl-serine and their metal salts, and the preparation thereof by (a) reacting a mono-acid addition salt of O-glycyl-l- or -dl-serine with a diazotizing agent, followed, if desired, by reaction of the product with a hydroxide, carbonate, bicarbonate, oxide, alkoxide or amide of an alkali or alkaline-earth metal, or (b) in the case of O-diazoacetyl-l-serine, inoculating a suitable sterile aqueous nutrient medium, having a pH of 5.0-8.5 (preferably 6.5-7.0) and containing carbon and nitrogen sources and inorganic salts, with Streptomyces fragilis, incubating the mixture under aerobic conditions at about 20-35 DEG C. (preferably 23-29 DEG C), removing solid material present in the culture mixture, and isolating the product from the aqueous liquid. Process (a) is advantageously effected below about 30 DEG C. in an aqueous reaction medium of pH 3-6 (preferably 4.0-5.5), suitable diazotizing agents being nitrous acid (which may be formed in situ from an inorganic nitrite and a mineral acid), alkyl nitrites, and nitrosyl compounds. The starting materials are obtainable by the processes of Specifications 744,584, 744,585, 744,586, 744,587 and 744,588. The product of (b) may be isolated by concentrating the culture liquid to a small volume, adding 3-10 volumes of a water-miscible organic solvent (e.g. acetone) and separating insoluble impurities, or evaporating the culture liquid to dryness, and extracting the residue with a water-miscible organic solvent containing less than 50 per cent of water, and in either case passing the resulting solution through an adsorption column containing alumina of pH 5-8 or solid sodium aluminium silicate, discarding the percolate, eluting with water or an aqueous water-miscible organic solvent mixture containing more than 50 per cent of water, removing the solvents from the eluate, dissolving the residue in a small amount of water, passing the solution through an adsorption column containing activated carbon, discarding the percolate, eluting with water containing 1-25 per cent of a water-miscible organic solvent (e.g. acetone), concentrating the eluate to a small volume and precipitating the O-diazoacetyl-l-serine by the addition of a water-miscible organic solvent (e.g. ethanol). The products are useful for therapeutic purposes. In examples: (1) and (2) O-glycyl-l- and -dl-serine monohydrochlorides are treated with sodium nitrite in aqueous solution in the cold; (3) O-glycyl-dl-serine monohydrochloride is treated with silver nitrite in aqueous solution at room temperature; (4) the sodium nitrite in (2) is replaced by nitrous acid; (5) O-glycyl-l-serine monohydrochloride is treated with amyl nitrite in aqueous ethanol in the cold; (6) O-glycyl-dl- or -l-serine monosulphate (produced in situ from the disulphate and caustic soda) is treated as in (1); (7) the amyl nitrite in (5) is replaced by butyl nitrite; (8) nitrogen trioxide fumes are bubbled through an aqueous solution of O-glycyl-l-serine monohydrochloride; the products of the foregoing examples may be treated with sodium bicarbonate, potassium hydroxide or calcium hydroxide to produce the corresponding metal salts; (9) an aqueous medium containing glucose, soybean expeller oil meal, acid hydrolysed casein, debittered yeast and sodium chloride is adjusted to pH 7.5 with caustic soda, a trace of calcium carbonate is added and the medium is sterilized (after which the pH is 6.85) and fermented with S. fragilis at 27 DEG C., the resulting culture being used to ferment a further medium containing the same ingredients plus ammonium nitrate; (10) a similar medium, with the addition of lard as antifoam, is subjected to a single stage fermentation with S. fragilis; (11) in the process of (9) the first medium contains a mixture of lard and mineral oil as antifoam, whilst the ammonium nitrate is omitted from the second; (12) an aqueous medium containing glucose, saline extracted hog stomach, ammonium chloride, sodium hydroxide (to pH 7.5) and calcium carbonate is sterilized (after which the pH is 6.8-7.2) and fermented with S. fragilis; (13) an aqueous medium containing glucose, soybean expeller oil meal, saline extracted hog stomach, sodium chloride, ammonium chloride and calcium carbonate is fermented as in (11); the products of (9)-(11) and (13) are worked up by the first of the methods outlined above.
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB776753A GB744540A (en) | 1953-03-20 | 1953-03-20 | Amino acid compounds and methods for producing the same |
NL178004A NL79734C (en) | 1953-03-20 | 1953-05-01 | |
FR1088178D FR1088178A (en) | 1953-03-20 | 1953-05-02 | Manufacture of o-diazoacetylserines |
BE519968D BE519968A (en) | 1953-03-20 | 1953-05-15 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB776753A GB744540A (en) | 1953-03-20 | 1953-03-20 | Amino acid compounds and methods for producing the same |
Publications (1)
Publication Number | Publication Date |
---|---|
GB744540A true GB744540A (en) | 1956-02-08 |
Family
ID=9839329
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB776753A Expired GB744540A (en) | 1953-03-20 | 1953-03-20 | Amino acid compounds and methods for producing the same |
Country Status (4)
Country | Link |
---|---|
BE (1) | BE519968A (en) |
FR (1) | FR1088178A (en) |
GB (1) | GB744540A (en) |
NL (1) | NL79734C (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0285085A2 (en) * | 1987-03-30 | 1988-10-05 | Fujisawa Pharmaceutical Co., Ltd. | Amino acid derivatives, process for the preparation thereof and pharmaceutical composition comprising the same |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2996500A (en) * | 1956-06-06 | 1961-08-15 | Parke Davis & Co | Diazoacetylserine compounds and methods for producing the same |
US3030388A (en) * | 1958-06-23 | 1962-04-17 | Parke Davis & Co | Amino acid compounds and methods for producing the same |
-
1953
- 1953-03-20 GB GB776753A patent/GB744540A/en not_active Expired
- 1953-05-01 NL NL178004A patent/NL79734C/xx active
- 1953-05-02 FR FR1088178D patent/FR1088178A/en active Active
- 1953-05-15 BE BE519968D patent/BE519968A/xx unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0285085A2 (en) * | 1987-03-30 | 1988-10-05 | Fujisawa Pharmaceutical Co., Ltd. | Amino acid derivatives, process for the preparation thereof and pharmaceutical composition comprising the same |
EP0285085A3 (en) * | 1987-03-30 | 1990-05-16 | Fujisawa Pharmaceutical Co., Ltd. | Amino acid derivatives, process for the preparation thereof and pharmaceutical composition comprising the same |
Also Published As
Publication number | Publication date |
---|---|
NL79734C (en) | 1955-11-15 |
BE519968A (en) | 1955-05-27 |
FR1088178A (en) |
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