Protochlorophyllide a: A Comprehensive Photophysical Picture

被引:48
|
作者
Dietzek, Benjamin [1 ,2 ]
Tschierlei, Stefanie [1 ]
Hermann, Gudrun [3 ]
Yartsev, Arkady [4 ]
Pascher, Torbjoern [4 ]
Sundstrom, Villy [4 ]
Schmitt, Michael [1 ]
Popp, Juergen [1 ,2 ]
机构
[1] Univ Jena, Inst Phys Chem, D-07743 Jena, Germany
[2] Inst Photon Technol, D-07702 Jena, Germany
[3] Univ Jena, Inst Biochem & Biophys, D-07743 Jena, Germany
[4] Lund Univ, Dept Chem Phys, S-22100 Lund, Sweden
关键词
enzyme catalysis; photophysics; porphyrins; transient absorption spectroscopy; UV/Vis spectroscopy; TIME-RESOLVED ABSORPTION; EXCITED-STATE PROCESSES; CHLOROPHYLL BIOSYNTHESIS; ZINC TETRAPHENYLPORPHINE; ULTRAFAST DYNAMICS; OXIDOREDUCTASE; SPECTROSCOPY; DEPENDENCE; EVOLUTION; PERIDININ;
D O I
10.1002/cphc.200800536
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The photochemistry of protochlorophyllide a, a precursor in the biosynthesis of chlorophyll and substrate of the light regulated enzyme protochlorophyllide oxidoreductase, is investigated by pump-probe spectroscopy. Upon excitation into the lowest lying Q-band the light induced changes ore recorded over a wide range of probe wavelengths in the visible and near-IR region between 500 and 1000 nm. Following excitation, an initial ultrafast 450 Is process is observed related to the motion out of the Franck-Condon region on the excited state surface; thus directly unraveling previous suggestions based on time-resolved fluorescence measurements (ChemPhysChem 2006, 7, 1727-1733). Furthermore, the data reveals a previously concealed photointermediate, whose formation on a nanosecond timescale matches the overall fluorescence decay and is assigned to a triplet state. The implications of this finding with respect to the photochemistry of NADPH.-protochlorophyllide oxidoreductase (POR) ore discussed.
引用
收藏
页码:144 / 150
页数:7
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