ArticleBiochemistry2007
No evidence from FTIR difference spectroscopy that aspartate-342 of the D1 polypeptide ligates a Mn ion that undergoes oxidation during the S0 to S1, S1 to S2, or S2 to S3 transitions in photosystem II.
Article in Biochemistry, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.
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19 citing papers in PubMed, 105 citations in OpenAlex.
- Does Serial Femtosecond Crystallography Depict State-Specific Catalytic Intermediates of the Oxygen-Evolving Complex?Journal of the American Chemical Society · 2023Article
- Post-translational amino acid conversion in photosystem II as a possible origin of photosynthetic oxygen evolution.Nature communications · 2022Article
- Substitution of the D1-AsnThe Journal of biological chemistry · 2018Article
- Quantum mechanics/molecular mechanics simulation of the ligand vibrations of the water-oxidizing MnProceedings of the National Academy of Sciences of the United States of America · 2016Article
- Warwick Hillier: a tribute.Photosynthesis research · 2014Article
- Fourier transform infrared difference spectroscopy for studying the molecular mechanism of photosynthetic water oxidation.Frontiers in plant science · 2013Article
- Ligation of D1-His332 and D1-Asp170 to the manganese cluster of photosystem II from Synechocystis assessed by multifrequency pulse EPR spectroscopy.Biochemistry · 2011Article
- Altered structure of the Mn4Ca cluster in the oxygen-evolving complex of photosystem II by a histidine ligand mutation.The Journal of biological chemistry · 2011Article
- Participation of glutamate-354 of the CP43 polypeptide in the ligation of manganese and the binding of substrate water in photosystem II.Biochemistry · 2011Article
- Article
- Computational insights into the O2-evolving complex of photosystem II.Photosynthesis research · 2008Review
- A model of the oxygen-evolving center of photosystem II predicted by structural refinement based on EXAFS simulations.Journal of the American Chemical Society · 2008Article
- Glutamate-354 of the CP43 polypeptide interacts with the oxygen-evolving Mn4Ca cluster of photosystem II: a preliminary characterization of the Glu354Gln mutant.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2008Article
- On the structure of the manganese complex of photosystem II: extended-range EXAFS data and specific atomic-resolution models for four S-states.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2008Article
- Protein Ligation of the Photosynthetic Oxygen-Evolving Center.Coordination chemistry reviews · 2008Article
- Oxidative photosynthetic water splitting: energetics, kinetics and mechanism.Photosynthesis research · 2007Review
- Spectral properties of the CP43-deletion mutant of Synechocystis sp. PCC 6803.Photosynthesis researchArticle
- Fourier transform infrared (FTIR) spectroscopy.Photosynthesis researchReview
- Substrate water binding and oxidation in photosystem II.Photosynthesis researchReview
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5 authors at 3 institutions in 2 countries.
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Abstract
In the recent X-ray crystallographic structural models of photosystem II, Asp342 of the D1 polypeptide is assigned as a ligand of the oxygen-evolving Mn4 cluster. To determine if D1-Asp342 ligates a Mn ion that undergoes oxidation during one or more of the S0 --> S1, S1 --> S2, and S2 --> S3 transitions, the FTIR difference spectra of the individual S state transitions in D1-D342N mutant PSII particles from the cyanobacterium Synechocystis sp. PCC 6803 were compared with those in wild-type PSII particles. Remarkably, the data show that the mid-frequency (1800-1200 cm-1) FTIR difference spectra of wild-type and D1-D342N PSII particles are essentially identical. Importantly, the mutation alters none of the carboxylate vibrational modes that are present in the wild-type spectra. The absence of significant mutation-induced spectral alterations in D1-D342N PSII particles shows that the oxidation of the Mn4 cluster does not alter the frequencies of the carboxylate stretching modes of D1-Asp342 during the S0 --> S1, S1 --> S2, or S2 --> S3 transitions. One explanation of these data is that D1-Asp342 ligates a Mn ion that does not increase its charge or oxidation state during any of these S state transitions. However, because the same conclusion was reached previously for D1-Asp170, and because the recent X-ray crystallographic structural models assign D1-Asp170 and D1-Asp342 as ligating different Mn ions, this explanation requires that (1) the extra positive charge that develops on the Mn4 cluster during the S1 --> S2 transition be localized on the Mn ion that is ligated by the alpha-COO- group of D1-Ala344 and (2) any increase in positive charge that develops on the Mn4 cluster during the S0 --> S1 and S2 --> S3 transitions be localized on the one Mn ion that is not ligated by D1-Asp170, D1-Asp342, or D1-Ala344. In separate experiments that were conducted with l-[1-13C]alanine, we found no evidence that D1-Asp342 ligates the same Mn ion that is ligated by the alpha-COO- group of D1-Ala344.
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