Crystalline picrate of the condensation product of ethylenediamine with noradrenaline or with catechol.
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2,4,6-Trinitrophenol (picric acid) is an effective inhibitor of photosynthetic electron transport (pI50 value 6.82). By means of artificial donor and acceptor systems its site of inhibition was located at the reducing side of photosystem II. In addition, picric acid also uncouples photophosphorylation but a much higher concentration is required than for inhibition of electron transport (pI50 value 4.40). By use of radioactivity labelled [U-14C]picric acid (spec. act. 2.1 Ci/mol) a binding constant of 0.25 microM and a number of binding sites of 2.84 nmol/mg chlorophyll was measured. This corresponds to one molecule of picric acid per 394 molecules of chlorophyll or one molecule per electron transport chain. Picric acid is competitively displaced from the thylakoid membrane by 3-(3,4-dichlorophenyl)-1,1-dimethylurea (and functionally related compounds) and phenolic inhibitors as well. In this property picric acid, despite its phenol character, is distinct from other phenolic inhibitors.
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