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

Joseph Hughes, Rafael Picorel, Michael Seibert, Elmars Krausz

Research output: Contribution to journalArticlepeer-review

Abstract

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.
Original languageAmerican English
Pages (from-to)12345-12357
Number of pages13
JournalBiochemistry
Volume45
Issue number40
DOIs
StatePublished - 2006

NREL Publication Number

  • NREL/JA-270-41014

Keywords

  • hydrogen bonds
  • plants
  • proteins

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