Abstract

In the presence of ferredoxin and NADP, DBMIB abolishes the fast-relaxing portion of P-700 together with the reduction of NADP. The slow-relaxing portion is inhibited at much higher concentrations. Qualitatively similar results have been observed with DNP-INT. However, its action appears to be a light-dependent process. The slow, cyclic turnover of P-700 in the presence of DCMU, ferredoxin and NADPH is inhibited by DBMIB but only slightly by DNP-INT. The data suggest that the inhibitors act at different sites of the electron-transport system.

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