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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.authorStrickler, Melodie A
dc.contributor.authorWalker, Lee M
dc.contributor.authorHillier, Warwick
dc.contributor.authorBritt, R David
dc.contributor.authorDebus, Richard John
dc.date.accessioned2015-12-10T22:14:06Z
dc.date.issued2007
dc.date.updated2015-12-09T08:03:44Z
dc.description.abstractIn 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.issn0006-2960
dc.identifier.urihttp://hdl.handle.net/1885/50105
dc.publisherAmerican Chemical Society
dc.sourceBiochemistry
dc.subjectKeywords: 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.titleNo 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.typeJournal article
local.bibliographicCitation.lastpage3160
local.bibliographicCitation.startpage3151
local.contributor.affiliationStrickler, Melodie A, University of California
local.contributor.affiliationWalker, Lee M, University of California
local.contributor.affiliationHillier, Warwick, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationBritt, R David, University of California
local.contributor.affiliationDebus, Richard John, University of California
local.contributor.authoruidHillier, Warwick, u3465503
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor060199 - Biochemistry and Cell Biology not elsewhere classified
local.identifier.ariespublicationu9204316xPUB197
local.identifier.citationvolume46
local.identifier.doi10.1021/bi062195e
local.identifier.scopusID2-s2.0-33947380152
local.type.statusPublished Version

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