GB708159A - A new antibiotic (erythromycin) and a process for preparing same - Google Patents

A new antibiotic (erythromycin) and a process for preparing same

Info

Publication number
GB708159A
GB708159A GB11470/52A GB1147052A GB708159A GB 708159 A GB708159 A GB 708159A GB 11470/52 A GB11470/52 A GB 11470/52A GB 1147052 A GB1147052 A GB 1147052A GB 708159 A GB708159 A GB 708159A
Authority
GB
United Kingdom
Prior art keywords
per cent
erythromycin
soluble
chloroform
absorption spectrum
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
GB11470/52A
Inventor
Robert Levi Bunch
James Myrlin Mcguire
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.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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 Eli Lilly and Co filed Critical Eli Lilly and Co
Priority to GB11470/52A priority Critical patent/GB708159A/en
Publication of GB708159A publication Critical patent/GB708159A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H17/00Compounds containing heterocyclic radicals directly attached to hetero atoms of saccharide radicals
    • C07H17/04Heterocyclic radicals containing only oxygen as ring hetero atoms
    • C07H17/08Hetero rings containing eight or more ring members, e.g. erythromycins
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N1/00Microorganisms, 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
    • C12N1/20Bacteria; Culture media therefor
    • C12N1/205Bacterial isolates
    • 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
    • C12P19/00Preparation of compounds containing saccharide radicals
    • C12P19/44Preparation of O-glycosides, e.g. glucosides
    • C12P19/60Preparation of O-glycosides, e.g. glucosides having an oxygen of the saccharide radical directly bound to a non-saccharide heterocyclic ring or a condensed ring system containing a non-saccharide heterocyclic ring, e.g. coumermycin, novobiocin
    • C12P19/62Preparation of O-glycosides, e.g. glucosides having an oxygen of the saccharide radical directly bound to a non-saccharide heterocyclic ring or a condensed ring system containing a non-saccharide heterocyclic ring, e.g. coumermycin, novobiocin the hetero ring having eight or more ring members and only oxygen as ring hetero atoms, e.g. erythromycin, spiramycin, nystatin
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12RINDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
    • C12R2001/00Microorganisms ; Processes using microorganisms
    • C12R2001/01Bacteria or Actinomycetales ; using bacteria or Actinomycetales
    • C12R2001/465Streptomyces

Abstract

An antibiotic, erythromycin, active against gram positive and gram negative microorganisms, Rickettsial bodies and large viruses is produced by cultivating an erythromycinproducing strain of Streptomyces erythreus, which is described, or a mutant thereof, in a culture medium containing assimilable sources of carbohydrate, nitrogen and inorganic salts. Cultivation is either surface (5-10 days) or submerged (2-5 days) with aeration at 25-37 DEG C., preferably 26-30 DEG C. The medium is adjusted to pH 6.0-7.5, preferably 6.5. Specified carbohydrates are starch, glucose, sucrose, and molasses. Nitrogen sources are corn steep solids, soybean meal, distillers' solubles, casein, amino acid mixtures, brewers' yeast and peptones, nitrates and ammonium salts. Inorganic salts are such as yield the ions sodium, potassium, calcium, phosphate, chloride, sulphate and cobalt. Erythromycin is isolated by (a) extraction with substantially water-immiscible solvents, e.g. alkyl esters of fatty acids, e.g. ethyl acetate and amyl acetate, chlorinated hydrocarbons, e.g. chloroform and ethylene dichloride, alcohols such as butyl alcohol, ketones such as methyl ethyl ketone, and ethers such as diethyl ether and dibutyl ether; and by (b) adsorption on, e.g., activated alumina, silica gel, magnesium aluminium silicate and activated carbon (which has been pretreated with acetic acid to reduce the bonding between the antibiotic and the carbon), and elution therefrom with a solvent such as 50 per cent methanol in benzene. Extraction or adsorption is at pH 9.0-10.0, preferably 9.5. Below this pH erythromycin complex forms. Salts are prepared by treating an aqueous solution of erythromycin with the appropriate acid. Specified salts are the hydrochloride, sulphate, citrate, mandelate, oleate, palmitate, myristate, stearate and oxalate. Erythromycin base has the analysis: C=60.4 per cent, H=9.26 per cent, N=2.07 per cent, and O= 28.27 per cent. It is a crystalline nitrogenous base, melting at 136-140 DEG C., having molecular weight of 725; [a ]25D=-78 DEG (C=1.99 ethanol); soluble in alcohol, acetone, chloroform, acetonitrile and ethyl acetate, less soluble in water, ether, ethylene dichloride and amyl acetate; pKa=8.8 when titrated in 2 : 1-dimethyl formamide-water solution; refractive indices in sodium light at 27 DEG C., n1=1.452, n2=1.473; ultra-violet-absorption spectrum characterized by a single broad peak-of-intensity having a maximum at 280 mm at pH 6.3; X-ray diffraction pattern and infra-red absorption spectrum given. Erythromycin hydrochloride forms needles melting at 170-173 DEG C., very soluble in water and alcohols, sparingly soluble in ether, amyl acetate and chloroform, has characteristic infra-red absorption spectrum. Erythromycin complex forms needles melting at 82-83.5 DEG C.; soluble in acetone, alcohols, chloroform and ethylene dichloride; slightly soluble in ketones and ethers; molecular weight 1130; [a ]25D= - 47 (C=2 per cent ethanol); contains C=64.71 per cent, H=10.23 per cent; N=1.35 per cent, O=23.71 per cent; ultraviolet absorption spectrum shows one maximum at 274 mm <FORM:0708159/IV (b)/1> =1.07; refractive indices in sodium light at 25 DEG C., n1=1.509, n2=1.499; X-ray diffraction pattern and infra-red absorption spectrum in chloroform is given. Specified strains of erythromycin-producing S. erythreus are NRRL-2338, NRRL 2359, NRRL 2360 and NRRL 2361.
GB11470/52A 1952-05-06 1952-05-06 A new antibiotic (erythromycin) and a process for preparing same Expired GB708159A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB11470/52A GB708159A (en) 1952-05-06 1952-05-06 A new antibiotic (erythromycin) and a process for preparing same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB11470/52A GB708159A (en) 1952-05-06 1952-05-06 A new antibiotic (erythromycin) and a process for preparing same

Publications (1)

Publication Number Publication Date
GB708159A true GB708159A (en) 1954-04-28

Family

ID=9986855

Family Applications (1)

Application Number Title Priority Date Filing Date
GB11470/52A Expired GB708159A (en) 1952-05-06 1952-05-06 A new antibiotic (erythromycin) and a process for preparing same

Country Status (1)

Country Link
GB (1) GB708159A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1114499B (en) * 1959-06-27 1961-10-05 Lilly Co Eli Process for the preparation of alkyl sulfate salts of the erythromycin and erythromycin B esters
EP1266905A1 (en) * 2000-03-22 2002-12-18 Chugai Seiyaku Kabushiki Kaisha Process for producing purified erythromycin
CN103484407A (en) * 2013-09-26 2014-01-01 宁夏启元药业有限公司 Culturing medium and fermentation method for producing erythrocin through fermentation of streptomyces erythreus

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1114499B (en) * 1959-06-27 1961-10-05 Lilly Co Eli Process for the preparation of alkyl sulfate salts of the erythromycin and erythromycin B esters
EP1266905A1 (en) * 2000-03-22 2002-12-18 Chugai Seiyaku Kabushiki Kaisha Process for producing purified erythromycin
EP1266905A4 (en) * 2000-03-22 2003-05-07 Chugai Pharmaceutical Co Ltd Process for producing purified erythromycin
US6767998B2 (en) 2000-03-22 2004-07-27 Chugai Seiyaku Kabushiki Kaisha Method for preparing purified erythromycin
CN103484407A (en) * 2013-09-26 2014-01-01 宁夏启元药业有限公司 Culturing medium and fermentation method for producing erythrocin through fermentation of streptomyces erythreus
CN103484407B (en) * 2013-09-26 2015-08-19 宁夏启元药业有限公司 A kind of substratum of streptomyces erythareus fermentative production erythromycin and fermentation process

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