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. 1981 May;78(5):2957–2961. doi: 10.1073/pnas.78.5.2957

Monomeric chlorophyll a enol: Evidence for its possible role as the primary electron donor in photosystem I of plant photosynthesis

Michael R Wasielewski 1, James R Norris 1, Lester L Shipman 1, Chih-Ping Lin 1, Walter A Svec 1
PMCID: PMC319478  PMID: 16593015

Abstract

The chlorophyll a (Chl a) special-pair model of the primary donor of photosystem I (P700) does not account in a completely adequate fashion for the magnetic resonance properties observed for P700+. Moreover, P700 is at least 420 mV easier to oxidize than is Chl a in vitro. Neither Chl a dimer formation nor selective ligation of Chl a can account for this potential difference. Enolization of the Chl a ring V β-keto ester results in a very different π electronic structure. The Chl a enol can be trapped as a silyl enol ether. In addition, the enol analog 9-desoxo-9,10-dehydro-Chl a can be prepared. Both the trapped enol and its 9-H analog are ≈350 mV easier to oxidize than Chl a. The ESR spectrum of the cation radical consists of a single 6.1-G gaussian line that is line narrowed relative to that of Chl a+ in a manner similar to P700+. Electron-nuclear double resonance (ENDOR) spectroscopy resolves only a 3.5-MHz hyperfine splitting for the 3-methyl-group. The remaining splittings are all less than 3.5 MHz. The second moment of the ESR line of fully 13C-enriched 9-desoxo-9,10-dehydro-Chl a+ agrees with that of [13C]P700+ to within 10%. Application of the special-pair model to the [13C]P700+ second-moment data yields a 100% error. Ab initio molecular orbital calculations on ethyl chlorophyllide a enol cation bear out the ESR and ENDOR data. We conclude that a monomeric Chl a enol model provides a better description of the magnetic resonance parameters and oxidation potential of P700 than a Chl a special-pair model.

Keywords: ESR, redox potential, cation radical, electronic structure

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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