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. 1999 May;120(1):217–226. doi: 10.1104/pp.120.1.217

Figure 1.

Figure 1

Inhibition of ATP synthesis of tobacco cell cultures by SA. A, Separation and identification of ATP and 32Pi on TLC plates. Separations were for supernatants from untreated cell cultures (lane 1) or the same supernatants that had been incubated at 30°C for 30 min in the presence (lane 2) or absence (lane 3) of 10 units of the ATP-hydrolyzing apyrase. B, Time course of inhibition of ATP synthesis by 1 mm SA. C, Concentration curve for inhibition of ATP synthesis after incubation for 10 min with 20 to 500 μm SA. The first two lanes in A and B are commercially purchased [γ-32P]ATP and 32Pi used as the standards.