Photophysical Behavior and Assignment of the Low-Energy Chlorophyll States in the CP43 Proximal Antenna Protein of Higher Plant Photosystem II

Joseph L. Hughes,* Rafael Picorel,§ Michael Seibert,§ and Elmars Krausz
Research School of Chemistry, The Australian National University, Canberra, ACT 0200, Australia, National Renewable Energy Laboratory, Golden, Colorado 80401-3393, and Estacin Experimental de Aula Dei, CSIC, Apdo. 202, 50080 Zaragoza, Spain
Biochemistry, 2006, 45 (40), pp 12345–12357
DOI: 10.1021/bi0614683
Publication Date (Web): September 16, 2006
Copyright © 2006 American Chemical Society

 M.S. and R.P. appreciate support from the Energy Biosciences Division, Basic Energy Sciences, Office of Science, U.S. Department of Energy. R.P. also acknowledges the MYCT in Spain (Grant BMC2005-07422-C02-01).

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*

 Corresponding author. Telephone:  +61-2-6125-3577. Fax:  +61-2-6125-0750. E-mail:  hughes@rsc.anu.edu.au.

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 The Australian National University.

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§

 National Renewable Energy Laboratory.

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 Estación Experimental de Aula Dei, CSIC.

Abstract

Abstract Image

We have employed absorption, circular dichroism (CD), and persistent spectral hole-burning measurements at 1.7 K to study the photoconversion properties and exciton coupling of low-energy chlorophylls (Chls) in the CP43 proximal antenna light-harvesting subunit of photosystem II (PSII) isolated from spinach. These 683 nm states act as traps for excitation energy in isolated CP43. They “bleach” at 683 nm upon illumination and photoconvert to a form absorbing in the range 660−680 nm. We present new data that show the changes in the CD spectrum due to the photoconversion process. These changes occur in parallel with those in absorption, providing evidence that the feature undergoing the apparent bleach is a component of a weakly exciton-coupled system. From our photoconversion difference spectra, we assign four states in the Chl long-wavelength region of CP43, two of which are the known trap states and are both highly localized on single Chls. The other two states are associated with weak exciton coupling (maximally 50 cm-1) to one of these traps. We propose a mechanism for photoconversion that involves Chl−protein hydrogen bonding. New hole-burning data are presented that indicate this mechanism is distinct to that for narrow-band spectral hole burning in CP43. We discuss the photophysical behavior of the Chl trap states in isolated CP43 compared to their behavior in intact PSII preparations. The latter represent a more intact, physiological complex, and we find no clear evidence that they exhibit the photoconversion process reported here.

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History

  • Published In Issue October 10, 2006
  • Received July 19, 2006
    Revised Manuscript Received August 15, 2006

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