SUMMARY: In the presence of pure oxygen at one atmosphere pressure Micromonospora vulgaris is unable to form in liquid media a surface pellicle of growth-bearing aerial mycelium. The production of bottom growth is either unaffected or stimulated by oxygen. Vegetative mycelium which develops from spores in Warburg vessels has an oxygen uptake that is similar in the presence of air or oxygen. Aerial mycelium, harvested from growths in air, shows marked differences as regards oxygen uptake in the presence of air or oxygen; oxygen is inhibitory. Some evidence is presented to show that the effect of oxygen may be connected with the inactivation of essential -SH groups of thiol enzymes.Full and detailed accounts of the isolation, cultivation, temperature/growth relationships and reproduction of the thermophilic actinomycete Micromonospora vulgaris were given by Erikson (1952, 1953a, b). She showed that this organism possesses the most complex reproductive pattern of any actinomycete yet studied, and considers that 'the device of producing a secondary aerial mycelium capable both of further growth and of producing spores, more than doubles the expected life of a mycelial organism a t elevated temperatures'. Erikson & Webley (1953), in a study of the respiration of the different growth phases of this structurally complex organism, found that a high rate of oxygen uptake a t 60" was associated with the presence of aerial mycelium harvested from 1-to %day cultures grown on liquid medium a t 60°, while bottom growth harvested under similar conditions was inactive in this respect. It has now been possible to show that pure oxygen exerts an inhibitory effect on the production of aerial mycelium (in growth experiments) and metabolism of aerial mycelium (respiration experiments; Webley, 1953) of this aerobic organism. The production of vegetative growth is unaffected by these differences in the gas phase.
METHODS
Organism.The experiments presented here were performed with strain H of Micromonospora vulgaris (Erikson, 1953 a).Technique of growth. Material from 2-day-old growth on liquid CPS medium was used throughout (see Erikson & Webley, 1953).Preparation of spore suspensions and aerial mycelium for the Warburg experiments. Spore suspensions were obtained by shaking the pellicle of growth finally obtained, after washing free of medium, in 5 ml. of ~/ 7 5 phosphate buffer (pH 7.0) on a 'Microid' shaker for 5 min. This process resulted in the detachment of a high proportion of the spores which could be separated from