A treatment procedure using lysozyme and ethylenediaminetetracetic acid gave intact but permeable cells (permeaplasts) of Anacystis nidulans. Rates of electron transport from water to carbon dioxide, ferricyanide, 2, 6-dichlorophenol indo. phenol, benzoquinone, and methyl viologen, and from reduced indophenol to methyl viologen were measured as a function of treatment time. Rates of oxygen evolution in complete photosynthesis and electron flow from water to methyl viologen showed rapid and parallel decline with treatment time. Electron flow from water to ferricyanide and from reduced indophenol to methyl viologen increased during the first half hour of treatment (phase 1) to 60 to 80% of the original photosynthetic rate. Longer treatment (phase 2) resulted in decreased rate of ferricyanide reduction but not in rate of methyl viologen reduction from indophenol. Electron flow from water to quinone was two to three times higher than for complete photosynthesis in intact cells. It remained high during phase 1 and declined during phase 2. Phase 1 permeaplasts apparently retain high activity for photosystems 1 and 2 photoreactions. This alga is less sensitive to lysozyme than others examined and is easily manipulated. Cultures were grown in medium C (7), modified by doubled concentrations of iron and microelements, in a continuous culture chamber (11) at 30 C, and aerated with 1% CO, in air. At 100 ft-c from tungsten lamps and a cell concentration of 2.5 [l cells/ml, the specific growth rate was about 0.9/day.A standard permeaplast preparation was obtained by the following procedure. A harvested cell suspension was centrifuged at 12,000g for 5 to 10 min at 0 C, and the cells were resuspended in 50 mm TES buffer at pH 7.3 to give 7 to 10 1d cells/ml. Lysozyme (Worthington Biochemicals, 2X recrystallized) was added to give 1.5 to 2.0 mg/lA cells, and Na4EDTA was added to give 1.0 mm. Cell suspensions were incubated in 15-ml tubes, about 5 ml/tube at 35 C in room light with occasional stirring by a Vortex mixer. After desired time of treatment, aliquots of suspension were diluted in several volumes of cold TES buffer, centrifuged for 5 to 10 min at 12,000g at 0 C, washed in TES buffer, and resuspended in room temperature TES to give cell concentrations of 0.5 to 2.0 /il/ml for assay. Most preparations gave relatively stable activities for about 1 hr when maintained at room temperature after the initial centrifugation.Oxygen exchange was measured by a Beckman oxygen macroelectrode in a cuvette of about 1.5 ml (12) or by a YSI 5331 electrode in a 1.6-ml cuvette at 25 C (17