dc.contributor.author
Klauss, André
dc.contributor.author
Sikora, Thomas
dc.contributor.author
Süss, Björn
dc.contributor.author
Dau, Holger
dc.date.accessioned
2018-06-08T03:47:08Z
dc.date.available
2014-09-04T11:35:14.673Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/15913
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-20100
dc.description.abstract
The Mn complex of photosystem II (PSII) cycles through 4 semi-stable states
(S0 to S3). Laser-flash excitation of PSII in the S2 or S3 state induces
processes with time constants around 350 ns, which have been assigned
previously to energetic relaxation of the oxidized tyrosine (YZox). Herein we
report monitoring of these processes in the time domain of hundreds of
nanoseconds by photoacoustic (or ‘optoacoustic’) experiments involving
pressure-wave detection after excitation of PSII membrane particles by ns-
laser flashes. We find that specifically for excitation of PSII in the S2
state, nuclear rearrangements are induced which amount to a contraction of
PSII by at least 30 Å3 (time constant of 350 ns at 25 °C; activation energy of
285 +/− 50 meV). In the S3 state, the 350-ns-contraction is about 5 times
smaller whereas in S0 and S1, no volume changes are detectable in this time
domain. It is proposed that the classical S2 = > S3 transition of the Mn
complex is a multi-step process. The first step after YZox formation involves
a fast nuclear rearrangement of the Mn complex and its protein–water
environment (~ 350 ns), which may serve a dual role: (1) The Mn‐ complex
entity is prepared for the subsequent proton removal and electron transfer by
formation of an intermediate state of specific (but still unknown) atomic
structure. (2) Formation of the structural intermediate is associated
(necessarily) with energetic relaxation and thus stabilization of YZox so that
energy losses by charge recombination with the QA− anion radical are
minimized. The intermediate formed within about 350 ns after YZox formation in
the S2-state is discussed in the context of two recent models of the S2 = > S3
transition of the water oxidation cycle. This article is part of a Special
Issue entitled: Photosynthesis Research for Sustainability: From Natural to
Artificial.
en
dc.rights.uri
http://www.elsevier.com/open-access/userlicense/1.0/
dc.subject
Oxygen evolution
dc.subject
Photosynthesis
dc.subject
Photosystem II
dc.subject
Water oxidation
dc.subject.ddc
500 Naturwissenschaften und Mathematik::530 Physik
dc.title
Fast structural changes (200–900 ns) may prepare the photosynthetic manganese
complex for oxidation by the adjacent tyrosine radical
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Biochimica et Biophysica Acta (BBA) - Bioenergetics. - 1817 (2012), 8, S.
1196-1207
dc.identifier.sepid
24276
dcterms.bibliographicCitation.doi
10.1016/j.bbabio.2012.04.017
dcterms.bibliographicCitation.url
http://dx.doi.org/10.1016/j.bbabio.2012.04.017
refubium.affiliation
Physik
de
refubium.affiliation.other
Institut für Experimentalphysik
refubium.mycore.fudocsId
FUDOCS_document_000000020891
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000003865
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
00052728