4.6 Article

Natural Variants of Photosystem II Subunit D1 Tune Photochemical Fitness to Solar Intensity

Journal

JOURNAL OF BIOLOGICAL CHEMISTRY
Volume 288, Issue 8, Pages 5451-5462

Publisher

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC
DOI: 10.1074/jbc.M112.394668

Keywords

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Funding

  1. Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences of the United States Department of Energy [DE-FG02-10ER16195]
  2. Air Force Office of Scientific Research Grant [FA9550-10-1-0052]
  3. Department of Energy [DE-EE0003373]
  4. Consortium for Algal Biofuels Commercialization (CAB-COMM)
  5. Department of Defense, Army Research Office, National Defense Science and Engineering Graduate Fellowship [32CFR168a]
  6. National Science Foundation Graduate Research Fellowship [DGE-0937373]

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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 Mn4CaO5 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.

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