No evidence from FTIR Difference Spectroscopy That Aspartate-342 of the D1 Polypeptide Ligates a Manganese Ion That Undergoes Oxidation during the S0 to S1, S1 to S2, or S2 to S3 Transitions in Photosystem II
| dc.contributor.author | Strickler, Melodie A | |
| dc.contributor.author | Walker, Lee M | |
| dc.contributor.author | Hillier, Warwick | |
| dc.contributor.author | Britt, R David | |
| dc.contributor.author | Debus, Richard John | |
| dc.date.accessioned | 2015-12-10T22:14:06Z | |
| dc.date.issued | 2007 | |
| dc.date.updated | 2015-12-09T08:03:44Z | |
| dc.description.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 → S 1, 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 → S 1, S1 → S2, or S2 → S 3 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 α-COO - group of D1-Ala344 and (2) any increase in positive charge that develops on the Mn4 cluster during the S0 → S 1 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 α-COO- group of D1-Ala344. | |
| dc.identifier.issn | 0006-2960 | |
| dc.identifier.uri | http://hdl.handle.net/1885/50105 | |
| dc.publisher | American Chemical Society | |
| dc.source | Biochemistry | |
| dc.subject | Keywords: Bacteria; Fourier transform infrared spectroscopy; Manganese; Metal ions; Oxidation; X ray crystallography; Cyanobacterium Synechocystis; Photosystem II; Polypeptide ligates; State transitions; Polypeptides; aspartic acid; manganese; article; Cyanobacteri | |
| dc.title | No evidence from FTIR Difference Spectroscopy That Aspartate-342 of the D1 Polypeptide Ligates a Manganese Ion That Undergoes Oxidation during the S0 to S1, S1 to S2, or S2 to S3 Transitions in Photosystem II | |
| dc.type | Journal article | |
| local.bibliographicCitation.lastpage | 3160 | |
| local.bibliographicCitation.startpage | 3151 | |
| local.contributor.affiliation | Strickler, Melodie A, University of California | |
| local.contributor.affiliation | Walker, Lee M, University of California | |
| local.contributor.affiliation | Hillier, Warwick, College of Medicine, Biology and Environment, ANU | |
| local.contributor.affiliation | Britt, R David, University of California | |
| local.contributor.affiliation | Debus, Richard John, University of California | |
| local.contributor.authoruid | Hillier, Warwick, u3465503 | |
| local.description.embargo | 2037-12-31 | |
| local.description.notes | Imported from ARIES | |
| local.identifier.absfor | 060199 - Biochemistry and Cell Biology not elsewhere classified | |
| local.identifier.ariespublication | u9204316xPUB197 | |
| local.identifier.citationvolume | 46 | |
| local.identifier.doi | 10.1021/bi062195e | |
| local.identifier.scopusID | 2-s2.0-33947380152 | |
| local.type.status | Published Version |
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