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Spectral characteristic of fluorescence induction in a model cyanobacterium, Synechococcus sp. (PCC 7942)
Authors:Radek Kaňa  Ond?ej Prášil  Ond?ej Komárek  George C Papageorgiou
Institution:a Laboratory of Photosynthesis, Institute of Microbiology, Academy of Sciences Czech Republic, T?eboň, Czech Republic
b Institute of Physical Biology and Faculty of Biology, University of South Bohemia in ?eské Budějovice, Czech Republic
c National Center for Scientific Research Demokritos, Institute of Biology, 153 10 Athens, Greece
d Department of Plant Biology, Department of Biochemistry and Center of Biophysics and Computational Biology, University of Illinois at Urbana-Champaign, 265 Morrill Hall, 505 South Goodwin Avenue, Urbana, IL 61801-3707, USA
e Institute of System Biology and Ecology, Academy of Sciences Czech Republic, Nové Hrady 136, 37 333, Czech Republic
Abstract:We present here three-dimensional time-wavelength-intensity displays of changes in variable fluorescence, during the O(JI)PSMT transient, observed in cyanobacterium at room temperature. We were able to measure contributions of individual chromophores to fluorescence spectra at various times of fluorescence induction (FI). The method was applied to a freshwater cyanobacterium, Synechococcus sp. (PCC 7942). Analysis of our experimental results provides the following new conclusions: (i) the main chlorophyll (Chl) a emission band at ∼ 685 nm that originates in Photosystem (PS) II exhibits typical fast (OPS) and slow (SMT) FI kinetics with both orange (622 nm) and blue (464 nm) excitation. (ii) Similar kinetics are exhibited for its far-red emission satellite band centered at ∼ 745 nm, where the PS II contribution predominates. (iii) A significant OPS-SMT-type kinetics of C-phycocyanin emission at ∼ 650 nm are observed with the blue light excitation, but not with orange light excitation where the signal rose only slightly to a maximum. The induction of F650 was not caused by an admixture of the F685 fluorescence and thus our data show light-inducible and dark-reversible changes of phycobilin fluorescence in vivo. We discuss possible interpretations of this new observation.
Keywords:Fluorescence induction  Cyanobacterium  PCC 7942  Phycobilisome  State transition
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