Up to now about 2500 antibiotics produced by Streptomyces have been described, and the greatest part of the clinically applicable substances has been selected from these. Though the probability to find a substance with chemical constitution radically different from those already known has become rather small, there still exists the possibility to isolate new substances which whilst chemically similar to those already described yet might possess favourable pharmaceutical properties. Investigations in this direction have begun in this Institute some years ago, and here an attempt will be made to report, consecutively, on these. I n this part the method of isolating the Streptomyces strains will be dealt with, further, their screening according to their capacity to produce an antibiotic substance will be described.
MethodsT h e isolation of Streptomyces. The colonies of Streptonaycea were isolated from soil samples gathered in Hungary. From these samples sixfold, or thirtysixfold dilutions were made with distilled water and 0.1 ml portions of these suspensions were plated in nutrient media placed in Petri dishes. Composite potato-broth-glucose agar, or meat-extract-peptone agar media were used for this purpose. One group of the media contained no antibiotic, one group contained 2 pg of oxytetracyclin per ml, a third group contained 2 pg of oxytetracyclin and 100 U. of nystatin per ml. The plates were incubated a t 28 "C for two or three days, after the lapse of this time the first isolation of the Streptomycea was carried out. During this short incubation period Streptomyces colonies did not exceed 2 mm nevertheless they were easily discernible as different from bacterial growths. Owing to the filamentous structure of the Streptomyces colonies a slight, moat-like depression is formed around them; the colonies cohere when handled with the point of a needle. These tiny colonies were plated on potato-broth-glucose agar plates and incubated for seven to ten days a t 28 "C, and their growth was noted daily. About 60 to 90 per cent of these growths proved to be pure Streptomyces cultures, the rest was more or less contaminated but could be purified by further platings quite easily. Rarely a few plates were to be found which did not yield a Streptomyces culture. Thus from each soil sample 150 to 200 Streptomyces colonies could be isolated, and compared when their growth process was completed. The colour of the sporiferous aerial sporulating mycelia and the form of sporophores, the colour of the substrate mycelia, and the soluble-pigment yield was investigated. In the course of these investigations from 10 to 30 strains per soil sample were selected.Maintenance of i s o l a t e d s t r a i n s . The maintenance of isolated strains was assured by inoculation every second month to fresh potato-broth-glucose agar plates. Some strains of special interest were kept in lyophilized state. P r o d u c i n g experiments. The experiments were carried out on rotary-shakers (300 r.p.m., 2 cm. diam.) a t 28 "C, using the following media...