S U M M A R YClostridium perfringens type A ( A T C C I~ 124) was grown in bottles (static culture) and in fermenters (batch and continuous culture) in a proteose peptone medium supplemented with phosphate, cysteine, vitamins and different carbohydrates. The lag phase was shorter and the growth rate higher when the medium was pre-reduced. The final yields of bacteria, phospholipase C, and theta-haemolysin were also significantly higher in the pre-reduced medium. The optimum pH for maximum bacterial yield was 7.0 and the optimum temperature for growth was 37 "C. The formation of phospholipase C was optimum between pH 6.0 and 7-0 and for thetahaemolysin between pH 7.0 and 7.5. The optimum temperature for synthesis of both phospholipase C and theta-haemolysin was 37 "C. Culture under controlled conditions gave more reproducible production of these two proteins than experiments in bottles. The cultures reached the stationary phase before phospholipase C activity started to decline, while theta-haemolysin activity was stable. The strain was also grown in continuous cuIture at a dilution rate of 0.4 h-I, at pH 7-0 and 37 "C, with a yield of I ~2 mg dry wt/ml in the complex medium supplemented with glucose (5 g/l). After the continuous feed was started the activity of phospholipase C declined very rapidly to zero, while theta-haemolysin continued to be produced at a constant level. Thus continuous culture offered no benefit over batch culture for reproducible laboratory-scale production of phospholipase C.