The donor side of Photosystem II as the copper-inhibitory binding site

We have measured, under Cu (II) toxicity conditions, the oxygen-evolving capacity of spinach PS II particles in the Hill reactions H2O -> SiMo (in the presence and absence of DCMU) and H2O -> PPBQ, as well as the fluorescence induction curve of Tris-washed spinach PS II particles. Cu (II) inhi...

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Detalles Bibliográficos
Autores: Arellano, Juan B., Lázaro, Juan J., López Gorgé, Julio, Barón Ayala, Matilde
Tipo de recurso: artículo
Fecha de publicación:1995
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/17225
Acceso en línea:http://hdl.handle.net/10261/17225
Access Level:acceso abierto
Palabra clave:Copper toxicity
Photosystem II
Spinacia oleracea
Descripción
Sumario:We have measured, under Cu (II) toxicity conditions, the oxygen-evolving capacity of spinach PS II particles in the Hill reactions H2O -> SiMo (in the presence and absence of DCMU) and H2O -> PPBQ, as well as the fluorescence induction curve of Tris-washed spinach PS II particles. Cu (II) inhibits both Hill reactions and, in the first case, the DCMU-insensitive H2O -> SiMo activity. In addition, the variable fluorescence is lowered by Cu (II). We have interpreted our results in terms of a donor side inhibition close to the reaction center. The same polarographic and fluorescence measurements carried out at different pHs indicate that Cu (II) could bind to amino acid residues that can be protonated and deprotonated. In order to reverse the Cu (II) inhibition by a posterior EDTA treatment, in experiments of preincubation of PS II particles with Cu (II) in light we have demonstrated that light is essential for the damage due to Cu (II) and that this furthermore is irreversible.