Phagolessin A58, an antibiotic produced by an unidentified strain of Streptomycetes sp. was described in a previous publication (1). The antibiotic is not yet available in crystalline form and the most active fractions contain considerable amounts of impurities. Despite this, the antibiotic was considered sufficiently interesting to justify a more detailed study of its antiphage properties.Phagolessin A58 is moderately active against a number of gram-positive and gram-negative bacteria, and against a wide range of bacterial viruses. Out of 60 viruses examined, 50 proved to be sensitive to a greater or lesser degree. The antiphage action is of the direct phagicidal type, the antibiotic causing an apparently irreversible inactivation of free phage particles after a relatively short contact. This inactivation of phage particles by phagolessin A58 is inhibited by desoxyribose nucleic acid, and to a lesser extent by ribose nucleic acid.The phages included in this present study comprise the seven coli-phages of the T system (2), acting on their common host Escherichia coli strain B. The authors are indebted to Dr. Max Delbriick who supplied the phages and their host strain. The r mutants (3) of phages T4 and T6 were used in place of the wild types.
Materials and MethodsPhagolessin ASg.--Extracts of the antibiotic used in this work were methyl alcohol solutions of lyophilized material and contained variable amounts of impurities. Concentrations were expressed in units per milliliter. A solution having an antiphage activity at a dilution of 1:40,000 against cholera phage C, the standard phage for this antibiotic, was considered to contain 40,000 units per ml. Weekly serial dilutions were run against the standard phage in order to detect any loss in antiphage activity in the preparation in current use. Since this antibiotic is highly unstable at neutral or alkaline reaction, dilutions of the active material into neutral medium were made immediately before being used in experiments.Med/a.--The nutrient broth used in all experiments contained 0.8 per cent Dffco nutrient broth and 0.5 per cent sodium chloride. Agar plates were prepared by adding Difco bacto agar to the nutrient broth, 2.0 per cent agar being used to plate phages T1, T3, and T7, and 1.2 per cent agar for phages T2, T4r, T5, and T6r. This procedure made clearing counts considerably easier.