The mechanism for proton-coupled electron transfer from tyrosine in a model complex and comparisons with Y-z oxidation in photosystem II

M Sjodin, Stenbjörn Styring, B Akermark, LC Sun

Research output: Contribution to journalArticlepeer-review

Abstract

In the water-oxidizing reactions of photosystem II (PSII), a tyrosine residue plays a key part as an intermediate electron-transfer reactant between the primary donor chlorophylls (the pigment P-680) and the water-oxidizing Mn cluster. The tyrosine is deprotonated upon oxidation, and the coupling between the proton reaction and electron transfer is of great mechanistic importance for the understanding of the water-oxidation mechanism. Within a programme on artificial photosynthesis, we have made and studied the proton-coupled tyrosine oxidation in a model system and been able to draw mechanistic conclusions that we use to interpret the analogous reactions in PSII.
Original languageEnglish
Pages (from-to)1471-1478
JournalPhilosophical Transactions of the Royal Society B: Biological Sciences
Volume357
Issue number1426
DOIs
Publication statusPublished - 2002

Subject classification (UKÄ)

  • Biological Sciences

Free keywords

  • tyrosine
  • photosystem II
  • proton-coupled electron transfer
  • photochemistry
  • ruthenium

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