Titration of Photophosphorylation in Spinach Chloroplasts with 3‐(3,4‐dichlorophenyl)‐1,1‐dimethylurea (DCMU)

Abstract The kinetics of the inhibition of photophosphorylation in chloroplasts from spinach (Spinacia oleracea) was investigated with 3‐(3,4‐dichlorophenyl)‐1,1‐dimethylurea (DCMU) in small concentration intervals, starting at 10‐7M. Plots of the reciprocal of photophosphorylation against concentration of DCMU gave essentially the same straight line with 2 mM nicotinamide adenine dinucleotide phosphate (NADP) together with saturating amounts of ferredoxin or with 4 mM K3Fe(CN)6 as the final acceptors for electrons. Practically complete inhibition was obtained at 3 x 10‐6M DCMU. With 0.1 mM flavin mononucleotide (FMN) and ferredoxin, the inhibition between 10‐7M and 10‐6M DCMU was a little slower than in the other two cases. At 10‐6M DCMU a break occurred to a new straight line in the plots, indicating that another reaction was inhibited. Total photophosphorylation without DCMU was about 77 μmol ATP per mg chlorophyll and hour. At the breaking point 20% remained, and inhibition was not complete even at 8 x 10‐6M DCMU. The inhibitor constant for the high‐DCMU reaction was in the order of 2 x 10‐5M; for the low‐DCMU reaction some complication made the “constant” appear negative. With phenazine methosulfate (PMS) added, DCMU was without effect on photophosphorylation. – As earlier shown by us, titration curves for intact cells of the microalga Scenedesmus show the break at 10‐6M DCMU; and above 6 x 10‐6M photophosphorylation in the algae is not further decreased by DCMU. The data are compared and their possible significance is discussed.