Cationic state distribution over the P700 chlorophyll pair in photosystem I

Biophys J. 2011 Oct 19;101(8):2018-25. doi: 10.1016/j.bpj.2011.09.010.

Abstract

The primary electron donor P700 in photosystem I is composed of two chlorophylls, P(A) and P(B). P700 forms the cationic [P(A)/P(B)](•+) state as a result of light-induced electron transfer. We obtained a P(A)(•+)/P(B)(•+) ratio of 28:72 and a spin distribution of 22:78 for the entire PSI protein-pigment complex. By considering the influence of the protein components on the redox potential for one-electron oxidation of P(A)/P(B) monomers, we found that the following three factors significantly contributed to a large P(B)(•+) population relative to P(A)(•+): 1), Thr-A743 forming a H-bond with P(A); 2), P(A) as a chlorophyll a epimer; and 3), a conserved PsaA/PsaB pair, the Arg-A750/Ser-B734 residue. In addition, 4), the methyl-ester groups of the accessory chlorophylls A(-1A)/A(-1B) significantly stabilized the cationic [P(A)/P(B)](•+) state and 5), the methyl-ester group orientations were completely different in A(-1A) and A(-1B) as seen in the crystal structure. When the methyl-ester group was rotated, the spin-density distribution over P(A)/P(B) ranged from 22:78 to 15:85.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Chlorophyll / chemistry*
  • Chlorophyll / metabolism
  • Coenzymes / metabolism
  • Crystallography, X-Ray
  • Cyanobacteria / enzymology
  • Dimerization
  • Electron Transport
  • Hydrogen Bonding
  • Models, Molecular
  • Molecular Conformation
  • Molecular Sequence Data
  • Photosystem I Protein Complex / chemistry*
  • Photosystem I Protein Complex / metabolism
  • Protein Subunits / chemistry
  • Protein Subunits / metabolism
  • Quantum Theory
  • Stereoisomerism
  • Thermodynamics

Substances

  • Coenzymes
  • Photosystem I Protein Complex
  • Protein Subunits
  • Chlorophyll
  • chlorophyll P 700