Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

What Are the Oxidation States of Manganese Required To Catalyze Photosynthetic Water Oxidation?

dc.contributor.authorKolling, Derrick R. J
dc.contributor.authorCox, Nicholas
dc.contributor.authorAnanyev, Gennady
dc.contributor.authorPace, Ronald
dc.contributor.authorDismukes, G. Charles
dc.date.accessioned2016-03-24T03:01:33Z
dc.date.available2016-03-24T03:01:33Z
dc.date.issued2012
dc.date.updated2016-06-14T09:17:53Z
dc.description.abstractPhotosynthetic 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.sponsorshipThis 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.issn0006-3495en_AU
dc.identifier.urihttp://hdl.handle.net/1885/100883
dc.publisherBiophysical Society
dc.rights© 2012 by the Biophysical Society.
dc.sourceBiophysical Journal
dc.subjectapoproteins
dc.subjectcatalysis
dc.subjectcomputer simulation
dc.subjectiron
dc.subjectkinetics
dc.subjectlasers
dc.subjectmanganese
dc.subjectmarkov chains
dc.subjectmodels, molecular
dc.subjectoxidation-reduction
dc.subjectoxygen
dc.subjectphotosystem ii protein complex
dc.subjectspinacia oleracea
dc.subjectwater
dc.subjectphotosynthesis
dc.titleWhat Are the Oxidation States of Manganese Required To Catalyze Photosynthetic Water Oxidation?
dc.typeJournal article
local.bibliographicCitation.issue2en_AU
local.bibliographicCitation.lastpage322en_AU
local.bibliographicCitation.startpage313en_AU
local.contributor.affiliationKolling, Derrick R J, Princeton University, United States of Americaen_AU
local.contributor.affiliationCox, Nicholas, College of Physical and Mathematical Sciences, CPMS Research School of Chemistry, RSC General, The Australian National Universityen_AU
local.contributor.affiliationAnanyev, Gennady M, Rutgers University, United States of Americaen_AU
local.contributor.affiliationPace, Ronald, College of Physical and Mathematical Sciences, CPMS Research School of Chemistry, RSC General, The Australian National Universityen_AU
local.contributor.affiliationDismukes, G Charles, Rutgers University, United States of Americaen_AU
local.contributor.authoruidu3286768en_AU
local.description.notesImported from ARIESen_AU
local.identifier.absfor030606en_AU
local.identifier.absseo970103en_AU
local.identifier.ariespublicationu8302325xPUB10en_AU
local.identifier.citationvolume103en_AU
local.identifier.doi10.1016/j.bpj.2012.05.031en_AU
local.identifier.essn1542-0086en_AU
local.identifier.scopusID2-s2.0-84864765524
local.identifier.thomsonID000306522300019
local.publisher.urlhttp://www.biophysics.org/en_AU
local.type.statusPublished Versionen_AU

Downloads

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
1-s2.0-S000634951200611X-main.pdf
Size:
927.34 KB
Format:
Adobe Portable Document Format

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
884 B
Format:
Item-specific license agreed upon to submission
Description: