Abstract

Photosystem II (PSII) is composed of six core polypeptides that make up the minimal unit capable of performing the primary photochemistry of light-driven charge separation and water oxidation in all oxygenic phototrophs. The D1 subunit of this complex contains most of the ligating amino acid residues for the Mn(4)CaO(5) core of the water-oxidizing complex (WOC). Most cyanobacteria have 3-5 copies of the psbA gene coding for at least two isoforms of D1, whereas algae and plants have only one isoform. Synechococcus elongatus PCC 7942 contains two D1 isoforms; D1:1 is expressed under low light conditions, and D1:2 is up-regulated in high light or stress conditions. Using a heterologous psbA expression system in the green alga Chlamydomonas reinhardtii, we have measured growth rate, WOC cycle efficiency, and O(2) yield as a function of D1:1, D1:2, or the native algal D1 isoform. D1:1-PSII cells outcompete D1:2-PSII cells and accumulate more biomass in light-limiting conditions. However, D1:2-PSII cells easily outcompete D1:1-PSII cells at high light intensities. The native C. reinhardtii-PSII WOC cycles less efficiently at all light intensities and produces less O(2) than either cyanobacterial D1 isoform. D1:2-PSII makes more O(2) per saturating flash than D1:1-PSII, but it exhibits lower WOC cycling efficiency at low light intensities due to a 40% faster charge recombination rate in the S(3) state. These functional advantages of D1:1-PSII and D1:2-PSII at low and high light regimes, respectively, can be explained by differences in predicted redox potentials of PSII electron acceptors that control kinetic performance.

Highlights

  • Cyanobacteria use multiple Photosystem II (PSII)-D1 isoforms to adapt to environmental conditions

  • The D1 protein of PSII is one of six core polypeptides that make up the minimal unit performing the primary photochemistry of light-driven charge separation and water oxidation in all oxygenic phototrophs

  • The OD730 nm of D1:1-PSII cultures was significantly higher than C. reinhardtii-PSII or D1:2-PSII, indicative of more cells or more absorbance per cell

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Summary

Background

Cyanobacteria use multiple PSII-D1 isoforms to adapt to environmental conditions. Results: D1:2 achieves higher quantum efficiency of water oxidation and biomass accumulation rate at high light versus D1:1; the latter is more efficient at low light due to less charge recombination. The D1 protein of PSII is one of six core polypeptides that make up the minimal unit performing the primary photochemistry of light-driven charge separation and water oxidation in all oxygenic phototrophs It provides most of the ligating amino acid residues for the WOC manganese core as well as binding pockets for the P680 chlorophyll-a (Chl-a) special pair, pheophytin (Pheo), and the secondary PQ acceptor. We show that when compared with the D1:2 and algal isoforms, D1:1 has higher WOC cycling efficiency at low light intensities, which is supported by the observation of a more stable S3 WOC intermediate We attribute this improved efficiency to fewer competing PSII-cyclic electron transfers from native cofactors (including QAϪ and cyt b559)

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