Biochemical Prophage Induction Assay: A Rapid Test for Antitumor Agents That Interact with DMA1

A biochemical (colorimetrie) assay of bacteriophage A induction was utilized in the detection, identification, and purification of DMA-interacting natural products with potential antitumor activ ity. A set of 142 standard antibiotics, composed principally of natural products with established antitumor activity and/or de fined mechanisms of action, was tested in the assay. As ex pected, most inducers were direct inhibitors of DNA synthesis. A few other types of inducer, with probable indirect effects on DNA synthesis, were found after prolonged incubation: one class of RNA synthesis inhibitor, a dihydrofolate reductase inhibitor; and two inhibitors of bacterial cell wall synthesis. The biochemical induction assay was semiautomated for use as a prescreen in the search for novel antitumor agents in 10,724 actinomycete fermentation broths. Approximately 1% of the cultures produced compounds that were active in the assay; some appear to be novel. None required metabolic activation (via rat liver 89) for inducing activity. The biochemical induction assay was adapted for bioautography (the detection of inducing chemicals chromatographed on thin-layer plates) and for strain improvement programs (selection of isolates with enhanced inducing activity). The speed of the assay (2 to 5 hr) made it useful for monitoring antitumor agent production and purification. The sensitivity of the assay could be varied, depending on the length of the incubation period. Mi crobes, nutrients, and toxic solvents did not usually interfere with the detection of inducing activity.