Production, Isolation, and Properties of Azetomycins

Author:

Formica Joseph V.1,Apple Martin A.1

Affiliation:

1. Cancer Research Institute, University of California Medical School, San Francisco, California 94143

Abstract

Streptomyces antibioticus synthesizes five actinomycins that differ in the “proline site” of the molecule. When cultured in the presence of azetidine-2-carboxylic acid (AzC), antibiotic synthesis was stimulated 40 to 50%, synthesis of actinomycin IV was inhibited, and one or both prolines were replaced by AzC. AzC incorporation could not be reversed by concomitant supplementation with proline or sarcosine, and only pipecolic acid affected a minor reversal of AzC incorporation. AzC-containing actinomycins were isolated and designated azet-I and azet-II; a third unresolved component or mixture was called azet-III. The molar ratio of AzC to proline was: azet-I, 1:1; azet-II, 2:0. Azet-III was equivocal. These azetidine actinomycins (azetomycins) were found to be potently inhibitory to the growth of selected gram-positive but not as potent to the growth of gram-negative organisms. The relative inhibitory affect against growth and ribonucleic acid synthesis in Bacillus subtilis was: actinomycin IV azet-I > azet-II >>> azet-III. Protein synthesis was affected similarly; however, kinetic studies with B. subtilis revealed that ribonucleic acid synthesis was inhibited rapidly followed by an inhibition of protein synthesis. At concentrations less than 1 μg/ml, deoxyribonucleic acid synthesis was stimulated by these actinomycins.

Publisher

American Society for Microbiology

Subject

Infectious Diseases,Pharmacology (medical),Pharmacology

Reference20 articles.

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2. Uber den Threoningehalt der Actinomycine;Brockman H. H. G.;Naturwissenschaften,1955

3. A study on the conditions and mechanism of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid;Burton K.;Biochem. J.,1956

4. Isolation, purification and characterization of pipecolic acid-containing actinomycins;Formica J. V.;Pip 2, Pip la, and Pip 1p. J. Biol. Chem.,1973

5. Actinomycin analogues containing pipecolic acid: relationship of structure to biological activity;Formica J. V.;J. Bacteriol.,1968

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