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Cyanobacterial in vivo solar hydrogen production using a photosystem I–hydrogenase (PsaD-HoxYH) fusion complex

Abstract

Photosynthetically produced hydrogen is an attractive, sustainable fuel. Semiartificial in vitro techniques have been successfully implemented in which hydrogenases were attached to isolated photosystems for hydrogen production. However, in vitro systems are in general short lived as metabolic processes that support self-repair and maintenance are missing. So far, photosystem–hydrogenase fusions have been tested in vitro only. Here, we report photosynthetic hydrogen production using a photosystem I–hydrogenase fusion in vivo. The NiFe-hydrogenase HoxYH of the cyanobacterium Synechocstis sp. PCC 6803 was fused to its photosystem I subunit PsaD in close proximity to the 4Fe4S cluster FB, which ordinarily donates electrons to ferredoxin. The resultant psaD-hoxYH mutant grows photoautotrophically, achieves a high concentration of photosynthetically produced hydrogen of 500 μM under anaerobic conditions in the light and does not take up the generated hydrogen. Our data indicate that photosynthetic hydrogen production in psaD-hoxYH is most likely based on both oxygenic and anoxygenic photosynthesis.

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Fig. 1: Hydrogen production in WT and Δhox/hoxYH related to the optical density at 750 nm (OD750) of the cultures.
Fig. 2: Strategy for the in vivo fusion of the Hox hydrogenase (HoxYH) of Synechocystis to its PSI by fusing the hydrogenase moiety hoxY to a truncated version of the PSI subunit psaD.
Fig. 3: Growth, hydrogenase activity, localization of the hydrogenase in WT and psaD-hoxYH (which is a ΔhoxΔpsaD/psaD-hoxYH mutant) and immunoblot analyses.
Fig. 4: Transitory in vivo photoH2 and O2 production in WT and psaD-hoxYH in darkness and upon illumination under anaerobic conditions in the absence and presence of DCMU.
Fig. 5: Assumed photosynthetic electron flow to the hydrogenase (HoxYH) in the psaD-hoxYH mutant.
Fig. 6: Lasting in vivo photoH2 production in WT and psaD-hoxYH under anaerobic conditions in continuous light in the absence and presence of DCMU.
Fig. 7: Light dependence of lasting photoH2 production in WT and psaD-hoxYH under anaerobic conditions in continuous light.
Fig. 8: Glucose dependence of lasting photoH2 production in WT and psaD-hoxYH in the presence of DCMU.

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Data availability

The authors declare that all data supporting the findings of this study are available within the paper and the supplementary file. Source data for Figs. 1, 3a–c, 4a–f, 6a–f, 7a–d and 8a–d and for Supplementary Fig. 5 are provided with the paper.

References

  1. Gutekunst, K. et al. The bidirectional NiFe-hydrogenase in Synechocystis sp. PCC 6803 is reduced by flavodoxin and ferredoxin and is essential under mixotrophic, nitrate-limiting conditions. J. Biol. Chem. 289, 1930–1937 (2014).

    Article  Google Scholar 

  2. Gutthann, F., Egert, M., Marques, A. & Appel, J. Inhibition of respiration and nitrate assimilation enhances photohydrogen evolution under low oxygen concentrations in Synechocystis sp. PCC 6803. Biochim. Biophys. Acta Bioenerg. 1767, 161–169 (2007).

    Article  Google Scholar 

  3. McIntosh, C. L., Germer, F., Schulz, R., Appel, J. & Jones, A. K. The [NiFe]-hydrogenase of the cyanobacterium Synechocystis sp. PCC 6803 works bidirectionally with a bias to H2 production. J. Am. Chem. Soc. 133, 11308–11319 (2011).

    Article  Google Scholar 

  4. Cournac, L., Guedeney, G., Peltier, G. & Vignais, P. M. Sustained photoevolution of molecular hydrogen in a mutant of Synechocystis sp. strain PCC 6803 deficient in the type I NADPH-dehydrogenase complex. J. Bacteriol. 186, 1737–1746 (2004).

    Article  Google Scholar 

  5. Peden, E. A. et al. Identification of global ferredoxin interaction networks in Chlamydomonas reinhardtii. J. Biol. Chem. 288, 35192–35209 (2013).

    Article  Google Scholar 

  6. Sawyer, A. & Winkler, M. Evolution of Chlamydomonas reinhardtii ferredoxins and their interactions with [FeFe]-hydrogenases. Photosynth. Res. 134, 307–316 (2017).

    Article  Google Scholar 

  7. Dutta, I. & Vermaas, W. F. J. The electron transfer pathway upon H2 oxidation by the NiFe bidirectional hydrogenase of Synechocystis sp. PCC 6803 in the light shares components with the photosynthetic electron transfer chain in thylakoid membranes. Int. J. Hydrogen Energy 41, 11949–11959 (2016).

    Article  Google Scholar 

  8. Appel, J., Phunpruch, S., Steinmüller, K. & Schulz, R. The bidierctional hydrogenase of Synechocystis sp. PCC 6803 works as an electron valve during photosynthesis. Arch. Microbiol. 173, 333–338 (2000).

    Article  Google Scholar 

  9. Nagy, V. et al. Water-splitting-based, sustainable and efficient H2 production in green algae as achieved by substrate limitation of the Calvin–Benson–Bassham cycle. Biotechnol. Biofuels 11, 1–16 (2018).

  10. Melis, A., Zhang, L., Forestier, M., Ghirardi, M. L. & Seibert, M. Sustained photobiological hydrogen gas production upon reversible inactivation of oxygen evolution in the green AlgaChlamydomonas reinhardtii. Plant Physiol. 122, 127–136 (2000).

    Article  Google Scholar 

  11. Ducat, D. C., Sachdeva, G. & Silver, P. A. Rewiring hydrogenase-dependent redox circuits in cyanobacteria. Proc. Natl Acad. Sci. USA 108, 3941–3946 (2011).

    Article  Google Scholar 

  12. Reisner, E., Powell, D. J., Cavazza, C., Fontecilla-Camps, J. C. & Armstrong, F. A. Visible light-driven H2 production by hydrogenases attached to dye-sensitized TiO2 nanoparticles. J. Am. Chem. Soc. 131, 18457–18466 (2009).

    Article  Google Scholar 

  13. Wilker, M. B. et al. Electron transfer kinetics in CdS nanorod–[FeFe]-hydrogenase complexes and implications for photochemical H2 generation. J. Am. Chem. Soc. 136, 4316–4324 (2014).

    Article  Google Scholar 

  14. Hambourger, M. et al. [FeFe]-hydrogenase-catalyzed H2 production in a photoelectrochemical biofuel cell. J. Am. Chem. Soc. 130, 2015–2022 (2008).

    Article  Google Scholar 

  15. Sokol, K. P. et al. Bias-free photoelectrochemical water splitting with photosystem II on a dye-sensitized photoanode wired to hydrogenase. Nat. Energy 3, 944–951 (2018).

    Article  Google Scholar 

  16. Mersch, D. et al. Wiring of photosystem II to hydrogenase for photoelectrochemical water splitting. J. Am. Chem. Soc. 137, 8541–8549 (2015).

    Article  Google Scholar 

  17. Yacoby, I. et al. Photosynthetic electron partitioning between [FeFe]-hydrogenase and ferredoxin:NADP+-oxidoreductase (FNR) enzymes in vitro. Proc. Natl Acad. Sci. USA 108, 9396–9401 (2011).

  18. Lubner, C. E. et al. Solar hydrogen-producing bionanodevice outperforms natural photosynthesis. Proc. Natl Acad. Sci. USA 108, 20988–20991 (2011).

    Article  Google Scholar 

  19. Ihara, M. et al. Light-driven hydrogen production by a hybrid complex of a [NiFe]-hydrogenase and the cyanobacterial photosystem I. Photochem. Photobiol. 82, 676–682 (2006).

    Article  Google Scholar 

  20. Krassen, H. et al. Photosynthetic hydrogen production by a hybrid complex of photosystem I and [NiFe]-hydrogenase. ACS Nano 3, 4055–4061 (2009).

    Article  Google Scholar 

  21. Lubner, C. E., Grimme, R., Bryant, D. A. & Golbeck, J. H. Wiring photosystem I for direct solar hydrogen production. Biochemistry 49, 404–414 (2010).

    Article  Google Scholar 

  22. Utschig, L. M., Soltau, S. R. & Tiede, D. M. Light-driven hydrogen production from photosystem I-catalyst hybrids. Curr. Opin. Chem. Biol. 25, 1–8 (2015).

    Article  Google Scholar 

  23. Ihara, M., Nakamoto, H., Kamachi, T., Okura, I. & Maedal, M. Photoinduced hydrogen production by direct electron transfer from photosystem I cross-linked with cytochrome c 3 to [NiFe]-hydrogenase. Photochem. Photobiol. 82, 1677–1685 (2006).

    Article  Google Scholar 

  24. Aubert-Jousset, E. C., Cano M., Guedeney, G., Richaud, P. & Cournac, L. Role of HoxE subunit in Synechocystis PCC6803 hydrogenase. FEBS J. 4035–4043 (2011).

  25. Schmitz, O. et al. Molecular biological analysis of a bidirectional hydrogenase from cyanobacteria. Eur. J. Biochem. 233, 266–276 (1995).

    Article  Google Scholar 

  26. Serebryakova, L. T. & Sheremetieva, M. E. Characterization of catalytic properties of hydrogenase isolated from the unicellular cyanobacterium Gloeocapsa alpicola CALU 743. Biochem. (Mosc.) 71, 1370–1376 (2006).

    Article  Google Scholar 

  27. Page, C. C., Moser, C. C., Chen, X. & Dutton, P. L. Natural engineering principles of electron tunnelling in biological oxidation–reduction. Nature 402, 47–52 (1999).

    Article  Google Scholar 

  28. Grotjohann, I. & Fromme, P. Structure of cyanobacterial photosystem I. Photosynth. Res. 85, 51–72 (2005).

    Article  Google Scholar 

  29. Kubota-Kawai, H. et al. X-ray structure of an asymmetrical trimeric ferredoxin–photosystem I complex. Nat. Plants 4, 218–224 (2018).

    Article  Google Scholar 

  30. Fromme, P., Bottin, H., Krauss, N. & Sétif, P. Crystallization and electron paramagnetic resonance characterization of the complex of photosystem I with its natural electron acceptor ferredoxin. Biophys. J. 83, 1760–1773 (2002).

    Article  Google Scholar 

  31. Fromme, P., Jordan, P. & Krauß, N. Structure of photosystem I. Biochim. Biophys. Acta 1507, 5–31 (2001).

    Article  Google Scholar 

  32. Jordan, P. et al. Three-dimensional structure of cyanobbacterial photosystem I at 2.5 Å resolution. Nature 441, 909–917 (2001).

    Article  Google Scholar 

  33. Shomura, Y. et al. Structural basis of the redox switches in the NAD-reducing soluble [NiFe]-hydrogenase. Science 357, 928–932 (2017).

  34. Chitnis, V. P., Ke, A. & Chitnis, P. R. The PsaD subunit of photosystem I (mutations in the basic domain reduce the level of PsaD in the membranes). Plant Physiol. 115, 1699–1705 (1997).

    Article  Google Scholar 

  35. Schuller, J. M. et al. Structural adaptations of photosynthetic complex I enable ferredoxin-dependent electron transfer. Science 363, 257–260 (2019).

  36. Kothari, A., Potrafka, R. & Garcia-Pichel, F. Diversity in hydrogen evolution from bidirectional hydrogenases in cyanobacteria from terrestrial, freshwater and marine intertidal environments. J. Biotechnol. 162, 105–114 (2012).

    Article  Google Scholar 

  37. Iwuchukwu, I. J. et al. Self-organized photosynthetic nanoparticle for cell-free hydrogen production. Nat. Nanotechnol. 5, 73–79 (2009).

    Article  Google Scholar 

  38. Millsaps, J. F., Bruce, B. D., Lee, J. W. & Greenbaum, E. Nanoscale photosynthesis: photocatalytic production of hydrogen by plantinized photosystem I reaction centers. Photochem. Photobiol. 73, 630–635 (2001).

    Article  Google Scholar 

  39. Gibson, D. G. et al. Enzymatic assembly of DNA molecules up to several hundred kilobases. Nat. Methods 6, 343–345 (2009).

  40. Noskov, V. N. et al. Defining the minimal length of sequence homology required for selective gene isolation by TAR cloning. Nucleic Acids Res. 29, 1–6 (2001).

  41. Shanks, R. M. Q., Caiazza, N. C., Hinsa, S. M., Toutain, C. M. & O’Toole, G. A. Saccharomyces cerevisiae-based molecular tool kit for manipulation of genes from gram-negative bacteria. Appl. Environ. Microbiol. 72, 5027–5036 (2006).

    Article  Google Scholar 

  42. Gietz, R. D. & Schiestl, R. H. High-efficiency yeast transformation using the LiAc/SS carrier DNA/PEG method. Nat. Protoc. 2, 31–34 (2007).

    Article  Google Scholar 

  43. Williams, J. G. K. Construction of specific mutations in photosystem II photosynthetic reaction center by genetic engineering methods in synechocystis 6803. Methods Enzymol. 167, 766–778 (1988).

    Article  Google Scholar 

  44. Gutekunst, K. et al. In-vivo turnover frequency of the cyanobacterial NiFe-hydrogenase during photohydrogen production outperforms in-vitro systems. Sci. Rep. 8, 1–10 (2018).

  45. Eckert, C. et al. Genetic analysis of the Hox hydrogenase in the cyanobacterium synechocystis sp. PCC 6803 reveals subunit roles in association, assembly, maturation, and function. J. Biol. Chem. 287, 43502–43515 (2012).

    Article  Google Scholar 

  46. Wittenberg, G. et al. Identification and characterization of a stable intermediate in photosystem I assembly in tobacco. Plant J. 90, 478–490 (2017).

    Article  Google Scholar 

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Acknowledgements

We thank R. Schulz for giving us a scientific home. HoxH and HoxY antibodies were provided by P. Nixon. This study was financed by grants from the Bundesministerium für Bildung und Forschung (BMBF, FP3 09) and the Deutsche Forschungsgemeinschaft (GU1522/2-1).

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J.A. and K.G. conceived the research. J.A. and V.H. constructed and characterized the mutants. M.B. performed the immunoblot analysis. J.A., V.H., M.B. and K.G. analysed data. K.G. wrote the manuscript and supervised the work.

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Correspondence to Kirstin Gutekunst.

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Appel, J., Hueren, V., Boehm, M. et al. Cyanobacterial in vivo solar hydrogen production using a photosystem I–hydrogenase (PsaD-HoxYH) fusion complex. Nat Energy 5, 458–467 (2020). https://doi.org/10.1038/s41560-020-0609-6

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