GB692066A - Improvements in or relating to antibiotics and the preparation thereof - Google Patents

Improvements in or relating to antibiotics and the preparation thereof

Info

Publication number
GB692066A
GB692066A GB9375/51A GB937551A GB692066A GB 692066 A GB692066 A GB 692066A GB 9375/51 A GB9375/51 A GB 9375/51A GB 937551 A GB937551 A GB 937551A GB 692066 A GB692066 A GB 692066A
Authority
GB
United Kingdom
Prior art keywords
antibiotic
neutral
broth
water
solvents
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
GB9375/51A
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.)
Pfizer Inc
Original Assignee
Pfizer Inc
Charles Pfizer and Co Inc
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 Pfizer Inc, Charles Pfizer and Co Inc filed Critical Pfizer Inc
Publication of GB692066A publication Critical patent/GB692066A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07GCOMPOUNDS OF UNKNOWN CONSTITUTION
    • C07G11/00Antibiotics

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)

Abstract

An antibiotic thiolutin is produced by cultivating in a nutrient medium a strain of Streptomyces albus, the cultural characteristics of which are described, or a mutant thereof. The antibiotic is effective against bacteria and fungi, neutral, slightly soluble in water, contains the elements carbon, hydrogen, oxygen, nitrogen and sulphur, and the mineral oil suspension shows characteristic absorption bands in the infra red region of the spectrum especially at 3295, 3220, 3110, 1680, 1645, 1607, 1551, 1439, 1322, 1239, 1138, 1091, 1060, 1039, 975, 875, 825, 800, 740, 729. The ultra-violet absorption spectrum is characteristic. It is soluble in organic solvents such as butanol, methanol, ethanol, acetone, methyl isobutyl ketone, glacial acetic acid, dimethylformamide, chloroform, pyridine and isopropanol; less so in petroleum ether, benzene and hexane. The antibiotic is produced by growing the micro organism in a nutrient medium containing (a) carbohydrate, e.g. sugars, starch and glycerol, (b) organic nitrogen source, e.g. soybean meal, cotton seed meal, peanut meal, corn steep liquor and N-Z-Amine B (enzymatic digest of casein), (c) mineral salts, e.g. sodium chloride, sodium nitrate, magnesium sulphate and potassium phosphate, (d) buffer, e.g. calcium carbonate and potassium dihydrogen phosphate, (e) antifoaming agent, e.g. vegetable or animal oil. The pH is adjusted to 6 to 7, the temperature is 23 DEG to 32 DEG C., and preferably 26 DEG to 30 DEG C., the duration of treatment 2 to 7 days with agitation and aeration at the rate of 1/2 to 2 volumes air per volume of broth per minute. The antibiotic is recovered from the clarified broth by (a) solvent extraction with water-immiscible organic solvents at acid, neutral or basic pH, but preferably at acid or neutral pH. Alcohols, esters, ketones, hydrocarbons, ethers and chlorinated solvents may be used, and in particular butanol, ethyl acetate, methyl isobutyl ketone, benzene and chloroform; (b) absorption on, e.g. activated carbon followed by elution with a solvent. The broth is clarified by driect filtration with a filler aid, or after acidification to preferably pH2 and heating to 70-90 DEG C. for 10 to 60 minutes. The antibiotic may be crystallized from solvents such as alcohols, e.g. methyl alcohol, ketones, dimethylformamide or mixtures thereof with water. Suspensions of the antibiotic in peanut oil or sesame oil when injected into mice were less toxic than when the antibiotic was taken by mouth.
GB9375/51A 1950-05-03 1951-04-23 Improvements in or relating to antibiotics and the preparation thereof Expired GB692066A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US692066XA 1950-05-03 1950-05-03

Publications (1)

Publication Number Publication Date
GB692066A true GB692066A (en) 1953-05-27

Family

ID=22087415

Family Applications (1)

Application Number Title Priority Date Filing Date
GB9375/51A Expired GB692066A (en) 1950-05-03 1951-04-23 Improvements in or relating to antibiotics and the preparation thereof

Country Status (1)

Country Link
GB (1) GB692066A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2173499A (en) * 1985-02-04 1986-10-15 Ici Plc Fungicidal dithiolopyrrolones
CN114317338A (en) * 2021-12-21 2022-04-12 北京工商大学 Streptomyces and application thereof in preparation of antibacterial drugs
CN115261422A (en) * 2022-06-30 2022-11-01 塔里木大学 Preparation method and application of new species thiolutin

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2173499A (en) * 1985-02-04 1986-10-15 Ici Plc Fungicidal dithiolopyrrolones
CN114317338A (en) * 2021-12-21 2022-04-12 北京工商大学 Streptomyces and application thereof in preparation of antibacterial drugs
CN115261422A (en) * 2022-06-30 2022-11-01 塔里木大学 Preparation method and application of new species thiolutin

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