<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Tóth SZ</dc:creator>
  <dc:creator>Schansker G</dc:creator>
  <dc:creator>Strasser RJ</dc:creator>
  <dc:date>2007</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">The plastoquinone (PQ) pool of the photosynthetic electron transport chain becomes reduced under anaerobic conditions. Here, anaerobiosis was used as a tool to manipulate the PQ-pool redox state in darkness and to study the effects of the PQ-redox state on the Chl-a fluorescence (OJIP) kinetics in pea leaves (Pisum sativum L.). It is shown that the F(J) (fluorescence intensity at 3 ms) is linearly related to the area above the OJ-phase (first 3 ms) representing the reduction of the acceptor side of photosystem II (PSII) and F(J) is also linearly related to the area above the JI-phase (3-30 ms) that parallels the reduction of the PQ-pool. This means that F(J) depends on the availability of oxidized PQ-molecules bound to the Q(B)-site. The linear relationships between F(J) and the two areas indicate that F(J) is not sensitive to energy transfer between PSII-antennae (connectivity). It is further shown that a approximately 94% reduced PQ-pool is in equilibrium with a approximately 19% reduction of Q(A) (primary quinone acceptor of PSII). The non-linear relationship between the initial fluorescence value (F(20 micros)) and the area above the OJ-phase supports the idea that F(20 mus )is sensitive to connectivity. This is reinforced by the observation that this non-linearity can be overcome by transforming the F(20 micros)-values into [Q(A) (-)]-values. Based on the F(J)-value of the OJIP-transient, a simple method for the quantification of the redox state of the PQ-pool is proposed.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://sonar.ch/global/documents/271796</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1007/s11120-007-9179-8</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/17487568</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:source>Photosynthesis research. - 2007</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Anaerobiosis</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Biological Assay</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Chlorophyll</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Chlorophyll A</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Fluorescence</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Light</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Oxidation-Reduction</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Peas</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Plastoquinone</dc:subject>
  <dc:title xmlns:ns10="xml" ns10:lang="en">A non-invasive assay of the plastoquinone pool redox state based on the OJIP-transient.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
