GB744540A - Amino acid compounds and methods for producing the same - Google Patents

Amino acid compounds and methods for producing the same

Info

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
Application number
GB776753A
Inventor
John Ehrlich
Mildred Penner Knudsen
Quentin Royal Bartz
Salvatore Anthony Fusari
Theodore Herbert Haskell
James Alexander Moore
Roger Dean Westland
Ernest D Nicolaides
John Raymond Dice
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Parke Davis and Co LLC
Original Assignee
Parke Davis and Co LLC
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.)
Filing date
Publication date
Application filed by Parke Davis and Co LLC filed Critical Parke Davis and Co LLC
Priority to GB776753A priority Critical patent/GB744540A/en
Priority to NL178004A priority patent/NL79734C/xx
Priority to FR1088178D priority patent/FR1088178A/en
Priority to BE519968D priority patent/BE519968A/xx
Publication of GB744540A publication Critical patent/GB744540A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C245/00Compounds containing chains of at least two nitrogen atoms with at least one nitrogen-to-nitrogen multiple bond
    • C07C245/12Diazo compounds, i.e. compounds having the free valencies of >N2 groups attached to the same carbon atom
    • C07C245/14Diazo 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
    • C07C245/18Diazo 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
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/04Alpha- or beta- amino acids
    • C12P13/06Alanine; 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.
GB776753A 1953-03-20 1953-03-20 Amino acid compounds and methods for producing the same Expired GB744540A (en)

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)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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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