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) 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.

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Main Authors: Arellano, Juan B., Lázaro, Juan J., López Gorgé, Julio, Barón Ayala, Matilde
Format: artículo biblioteca
Language:English
Published: Springer 1995-08
Subjects:Copper toxicity, Photosystem II, Spinacia oleracea,
Online Access:http://hdl.handle.net/10261/17225
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spelling dig-irnasa-es-10261-172252016-05-24T10:05:52Z The donor side of Photosystem II as the copper-inhibitory binding site Arellano, Juan B. Lázaro, Juan J. López Gorgé, Julio Barón Ayala, Matilde Copper toxicity Photosystem II Spinacia oleracea 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. This work was supported by a grant from the Spanish DGICYT (PB94-0116). J.B. Arellano was the recipient of a fellowship from the Spanish Science and Education Ministry. Peer reviewed 2009-09-29T07:01:57Z 2009-09-29T07:01:57Z 1995-08 artículo http://purl.org/coar/resource_type/c_6501 Photosynthesis Research (1995) 45:127-134 http://hdl.handle.net/10261/17225 10.1007/BF00032584 en http://www.springerlink.com/content/l750136238114824/fulltext.pdf open 295011 bytes application/pdf Springer
institution IRNASA ES
collection DSpace
country España
countrycode ES
component Bibliográfico
access En linea
databasecode dig-irnasa-es
tag biblioteca
region Europa del Sur
libraryname Biblioteca del IRNASA España
language English
topic Copper toxicity
Photosystem II
Spinacia oleracea
Copper toxicity
Photosystem II
Spinacia oleracea
spellingShingle Copper toxicity
Photosystem II
Spinacia oleracea
Copper toxicity
Photosystem II
Spinacia oleracea
Arellano, Juan B.
Lázaro, Juan J.
López Gorgé, Julio
Barón Ayala, Matilde
The donor side of Photosystem II as the copper-inhibitory binding site
description 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.
format artículo
topic_facet Copper toxicity
Photosystem II
Spinacia oleracea
author Arellano, Juan B.
Lázaro, Juan J.
López Gorgé, Julio
Barón Ayala, Matilde
author_facet Arellano, Juan B.
Lázaro, Juan J.
López Gorgé, Julio
Barón Ayala, Matilde
author_sort Arellano, Juan B.
title The donor side of Photosystem II as the copper-inhibitory binding site
title_short The donor side of Photosystem II as the copper-inhibitory binding site
title_full The donor side of Photosystem II as the copper-inhibitory binding site
title_fullStr The donor side of Photosystem II as the copper-inhibitory binding site
title_full_unstemmed The donor side of Photosystem II as the copper-inhibitory binding site
title_sort donor side of photosystem ii as the copper-inhibitory binding site
publisher Springer
publishDate 1995-08
url http://hdl.handle.net/10261/17225
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