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Femtosecond Spectroscopic Studies on the Red Light‐Absorbing Form of Oat Phytochrome and 2,3‐Dihydrobiliverdin
Author(s) -
Rentsch Sabine,
Hermann Gudrun,
Bischoff Mark,
Strehlow Dietmar,
Rentsch Manfred
Publication year - 1997
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.1751-1097.1997.tb03193.x
Subject(s) - excited state , picosecond , femtosecond , excitation , absorption (acoustics) , ultrafast laser spectroscopy , ground state , chemistry , chromophore , phytochrome , population , absorption spectroscopy , atomic physics , photochemistry , laser , optics , red light , physics , botany , demography , quantum mechanics , sociology , biology
— The excited state behavior of the red light‐absorbing form of phytochrome (Pr) was studied on the femtosecond time scale. After excitation of Pr with 75 fs laser pulses at 616 nm the kinetics of the transient absorption changes was recorded at selected wavelengths probing mainly the bleaching of the Pr ground‐state absorption and the stimulated emission. The kinetic data obtained indicate the population of an excited state with a 3 ps lifetime immediately after excitation. This state precedes the formation of another excited state with a 32 ps lifetime. The decay of the latter state is followed by the appearance of a first product state that is assumed to represent lunii‐R. In addition, 2,3‐dihydrobiliverdin, which is considered to be an adequate model of the Pr chro‐mophore, was included in the femtosecond studies. The absorption difference spectra recorded at various delay times show an immediate bleaching of the ground‐state absorption. Simultaneously with bleaching a broad transient absorption appears between 410 and 525 nm. The data analysis yields similar kinetic components as they were observed in the decay of Pr. It is suggested from this finding that within the first tens of picoseconds after excitation the excited‐state properties of Pr are mainly determined by the properties of the chromophore itself.