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      Formation of the early photoproduct lumi-R of cyanobacterial phytochrome cph1 observed by ultrafast mid-infrared spectroscopy.

      Journal of the American Chemical Society
      Bacterial Proteins, chemistry, Isomerism, Photochemistry, Phytochrome, Protein Kinases, Spectrophotometry, Infrared, methods, Synechocystis, metabolism

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          Abstract

          The photoreactions of the Pr ground state of cyanobacterial phytochrome Cph1 from Synechocystis PCC 6803 have been investigated by picosecond time-resolved mid-infrared spectroscopy at ambient temperature. With femtosecond excitation of the Pr state at 640 nm, the photoisomerized Lumi-R product state is generated with kinetics and associated difference spectra indicative of vibrational cooling with tau(1) = 3 ps time constant and excited state decay with tau(1) = 3 ps, tau(2) = 14 ps, and tau(3) = 134 ps time constants. The Lumi-R state is characterized by downshifted absorption of three C=C modes assigned to C(15)=C(16), C(4)=C(6), and a delocalized C=C mode, in addition to the downshifted C(19)=O mode. The Lumi-R minus Pr difference spectrum is indicative of global restructuring of the chromophore on the ultrafast timescale, which is discussed in light of C(15) Z/E photoisomerization in addition to changes near C(5), which could be low bond order torsional angle changes.

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          Author and article information

          Journal
          17199291
          10.1021/ja0660709

          Chemistry
          Bacterial Proteins,chemistry,Isomerism,Photochemistry,Phytochrome,Protein Kinases,Spectrophotometry, Infrared,methods,Synechocystis,metabolism

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