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INVARIABLE TRAPPING TIMES IN PHOTOSYSTEM I UPON EXCITATION OF MINOR LONG‐WAVELENGTH‐ABSORBING PIGMENTS
Author(s) -
Trissl H.W.,
Hecks B.,
Wulf K.
Publication year - 1993
Publication title -
photochemistry and photobiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.818
H-Index - 131
eISSN - 1751-1097
pISSN - 0031-8655
DOI - 10.1111/j.1751-1097.1993.tb02264.x
Subject(s) - trapping , excitation , wavelength , picosecond , chemistry , photosystem i , excited state , analytical chemistry (journal) , molecular physics , materials science , atomic physics , photosystem ii , optics , optoelectronics , photosynthesis , laser , physics , ecology , biochemistry , quantum mechanics , chromatography , biology
The primary charge separation in photosystem (PS) I was measured on stacked pea thylakoids using the light‐gradient photovoltage technique. Upon 532 nm excitation with picosecond flashes, a trapping time of 80 ± 10 ps for PS I was found, which is in close agreement with literature data. In the wavelength range between 700 nm and 717 nm the trapping time was essentially the same although there was an indication for a slight decrease. To further analyze the data we performed a spectral decomposition of PS I with Chi a and b solvent spectra. This procedure yielded bands at around 682 nm, 690 nm, 705 nm and 715 nm. According to this decomposition, a selective excitation of long‐wavelength antenna pigments at wavelengths Λ > 710 nm is possible, because the direct excitation of the main 682 nm band is small compared to the excitation of the two most red‐shifted bands. The invariability of the trapping time of the excitation wavelength suggests thermal equilibration of the excitation energy among all antenna pigments according to their excited state energy levels and their abundance. Hence, we conclude that trapping in PS I is essentially rate‐limited by the primary charge separation much as it is the case in PS II. Then, according to our spectral decomposition in a time constant of2–3 ps is predicted for the primary charge separation in PS I.