In order to characterize the reactions catalyzed by nitrogenase in the Azolla-Anabaena association, '5N2 fixation, C2H2 reduction, and ATPdependent H2 production were measured in both the Azolla-Anabaena complex and in the alga isolated from the complex.The rate of reduction of substrates and of ATP-dependent H2 evolution was determined at varous partial pressures of C2H2 and N2. A pC2H2 of 0.1 atm was nearly optimal for C2H4 production and inhibited H2 production by 95%. The ratio of C2H2 reduced to N2 fixed was determined as a function of constant pC2H2 (0.1 atm) and variable pN2. This ratio decreased with increasing pN2 and the decrease was correlated with less H2 production. Ratios obtained at N2 partial pressures of approximately 0.3, 0.6, and 0.8 atm, respectively, were 3.2, 2.0, and 1.7 for the association and 4.4, 3.0, and 2.5 for the isolated symbiont.Rates obtained for C2H2 reduction, N2 fixation, and H2 production were used to obtain an expression of the electron balance in vivo.Azolla is a genus of small aquatic ferns which, under natural conditions, invariably contain the heterocystous blue-green alga, Anabaena azollae, as a symbiont in an enclosed chamber in the dorsal leaf lobes (10,12). In the intact association, the alga can provide the Azolla plant with its total nitrogen requirement. Previous studies showed that the symbiont contained nitrogenase and was capable of C2H2 reduction, ATP-dependent H2 evolution, and excretion of ammonia (10,11,13).Although C2H2 reduction is a simple and sensitive assay of nitrogenase activity, C2H2 is not the biologically important substrate, and the assay is an indirect measurement of nitrogen fixation. Since the reduction of N2 to 2NH3 requires six electrons while reduction of C2H2 to C2H4 requires two electrons, a theoretical conversion factor of 3C2H2 reduced per N2 fixed is frequently used in estimating nitrogen fixation from C2H2 reduction assays. Studies on isolated nitrogenase have shown that when provided with a source of ATP and reductant the rate of electron flow through the enzyme is independent of the substrate (7,20). Moreover, while normal assay levels of C2H2 almost totally suppress H2 production, some electrons continue to be utilized in reducing protons to H2 when N2 is the substrate and employed at saturating levels (16,20). Thus, the C2H2/N2 ratio is usually closer to 4 for nitrogenase in vitro. However, in vivo studies have produced a range of ratios from less than 2 to greater than 8 (8), and it would appear that the ratio may be dependent upon both the organism and experimental conditions employed. This is a report on 15N2 fixation by the fern-algal association and the symbiont isolated directly from the leaf cavities. In order to determine whether a specific conversion factor can be used, and to assess some factors capable of affecting it, the effect of pN2 on N2 fixation and ATP-dependent H2 evolution was determined in parallel with measurements of C2H2 reduction. Ratios of C2H2 reduction to N2 fixation and the effect of H2 evoluti...