What Are the Oxidation States of Manganese Required To Catalyze Photosynthetic Water Oxidation?
| dc.contributor.author | Kolling, Derrick R. J | |
| dc.contributor.author | Cox, Nicholas | |
| dc.contributor.author | Ananyev, Gennady | |
| dc.contributor.author | Pace, Ronald | |
| dc.contributor.author | Dismukes, G. Charles | |
| dc.date.accessioned | 2016-03-24T03:01:33Z | |
| dc.date.available | 2016-03-24T03:01:33Z | |
| dc.date.issued | 2012 | |
| dc.date.updated | 2016-06-14T09:17:53Z | |
| dc.description.abstract | Photosynthetic O₂ production from water is catalyzed by a cluster of four manganese ions and a tyrosine residue that comprise the redox-active components of the water-oxidizing complex (WOC) of photosystem II (PSII) in all known oxygenic phototrophs. Knowledge of the oxidation states is indispensable for understanding the fundamental principles of catalysis by PSII and the catalytic mechanism of the WOC. Previous spectroscopic studies and redox titrations predicted the net oxidation state of the S₀ state to be (Mn(III))₃Mn(IV). We have refined a previously developed photoassembly procedure that directly determines the number of oxidizing equivalents needed to assemble the Mn₄Ca core of WOC during photoassembly, starting from free Mn(II) and the Mn-depleted apo-WOC complex. This experiment entails counting the number of light flashes required to produce the first O₂ molecules during photoassembly. Unlike spectroscopic methods, this process does not require reference to synthetic model complexes. We find the number of photoassembly intermediates required to reach the lowest oxidation state of the WOC, S₀, to be three, indicating a net oxidation state three equivalents above four Mn(II), formally (Mn(III))₃Mn(II), whereas the O₂ releasing state, S₄, corresponds formally to (Mn(IV))₃Mn(III). The results from this study have major implications for proposed mechanisms of photosynthetic water oxidation. | |
| dc.description.sponsorship | This work was supported by the Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the U.S. Department of Energy through grant DE-FG02-10ER16195. D.R.J.K. was supported by an American Chemical Society Alternative Energy postdoctoral fellowship and the Dreyfus postdoctoral fellowship in environmental chemistry. | en_AU |
| dc.identifier.issn | 0006-3495 | en_AU |
| dc.identifier.uri | http://hdl.handle.net/1885/100883 | |
| dc.publisher | Biophysical Society | |
| dc.rights | © 2012 by the Biophysical Society. | |
| dc.source | Biophysical Journal | |
| dc.subject | apoproteins | |
| dc.subject | catalysis | |
| dc.subject | computer simulation | |
| dc.subject | iron | |
| dc.subject | kinetics | |
| dc.subject | lasers | |
| dc.subject | manganese | |
| dc.subject | markov chains | |
| dc.subject | models, molecular | |
| dc.subject | oxidation-reduction | |
| dc.subject | oxygen | |
| dc.subject | photosystem ii protein complex | |
| dc.subject | spinacia oleracea | |
| dc.subject | water | |
| dc.subject | photosynthesis | |
| dc.title | What Are the Oxidation States of Manganese Required To Catalyze Photosynthetic Water Oxidation? | |
| dc.type | Journal article | |
| local.bibliographicCitation.issue | 2 | en_AU |
| local.bibliographicCitation.lastpage | 322 | en_AU |
| local.bibliographicCitation.startpage | 313 | en_AU |
| local.contributor.affiliation | Kolling, Derrick R J, Princeton University, United States of America | en_AU |
| local.contributor.affiliation | Cox, Nicholas, College of Physical and Mathematical Sciences, CPMS Research School of Chemistry, RSC General, The Australian National University | en_AU |
| local.contributor.affiliation | Ananyev, Gennady M, Rutgers University, United States of America | en_AU |
| local.contributor.affiliation | Pace, Ronald, College of Physical and Mathematical Sciences, CPMS Research School of Chemistry, RSC General, The Australian National University | en_AU |
| local.contributor.affiliation | Dismukes, G Charles, Rutgers University, United States of America | en_AU |
| local.contributor.authoruid | u3286768 | en_AU |
| local.description.notes | Imported from ARIES | en_AU |
| local.identifier.absfor | 030606 | en_AU |
| local.identifier.absseo | 970103 | en_AU |
| local.identifier.ariespublication | u8302325xPUB10 | en_AU |
| local.identifier.citationvolume | 103 | en_AU |
| local.identifier.doi | 10.1016/j.bpj.2012.05.031 | en_AU |
| local.identifier.essn | 1542-0086 | en_AU |
| local.identifier.scopusID | 2-s2.0-84864765524 | |
| local.identifier.thomsonID | 000306522300019 | |
| local.publisher.url | http://www.biophysics.org/ | en_AU |
| local.type.status | Published Version | en_AU |