INHIBITION OF PHOTOSYSTEM II ELECTRON-TRANSPORT CHAIN BY AMMONIA AND “DECOUPLING EFFECT”
Abstract and keywords
Abstract (English):
Catalytic center of oxygen-evolving complex (OEC) of photosystem II (PSII) is Mn4CaO5 cluster structure of which is determined now. Ca2+ extraction from OEC is accompanied by decoupling of oxygen evolution and electron transport processes in PSII and by the appearance of a broad EPR signal (so-called “S3” or “split signal”) at low temperatures. These data imply that decoupling and EPR effects can be interdependent. It is interesting that EPR signal «S3» is observed also after treatment of native PSII membranes by fluoride anions, acetate and chloride of ammonia. Previously we found that fluoride anions treatment of PSII like Ca2+ extraction from the OEC provide the appearance of decoupling effect. In the presented work we investigated the effect of ammonia chloride and ammonia nitrate on the functional activity of native PSII membranes to study the effect of anions. We found that ammonia nitrate like ammonia chloride inhibit the oxygen evolution more effectively than the reduction of artificial electron acceptor 2,6- dichlorophenolindophenol that is the action of ammonia decouples these processes. However the inhibition doesn’t depend on the anions. We suggest that ammonia inhibition effect is determined by inactivation of Ca2+ function.

Keywords:
photosystem II, oxygen-evolving complex, ammonia
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References

1. Umena Y., Kawakami K., Shen J.-R., Kamiya N. Crystal structure of oxygen evolving photosystem II at a resolution of 1.9 Å. Nature, 2011, vol. 473, pp. 55-60.

2. Suga M., Akita F., Hirata K., Ueno G., Murakami H., Nakajima Y., Shimizu T., Yamashita K., Yamamoto M., Ago H., Shen J.-R. Native structure of photosystem II at 1.95 Å resolution viewed by femtosecond X-ray pulses. Nature, 2015, vol. 517, pp. 99-103.

3. Cardona T., Murray J.W., Rutherford A.W. Origin and Evolution of Water Oxidation before the Last Common Ancestor of the Cyanobacteria. Mol. Biol. Evol,. 2015, vol. 32, pp. 1310-1328.

4. Ghanotakis D.F., Babcock G.T., Yocum C.F. Calcium reconstitutes high rates of oxygen evolution in polypeptide depleted photosystem II preparations. FEBS Lett., 1984, vol. 167, pp. 127-130.

5. Semin B.K., Davletshina L.N., Ivanov I.I., Rubin A.B., Seibert M. Decoupling of the processes of molecular oxygen synthesis and electron transport in Ca2+-depleted PSII membranes. Photosynth. Res., 2008, vol. 98, pp. 235-249.

6. Semin B.K., Davletshina L.N., Timofeev K.N., Ivanov I.I., Rubin A.B., Seibert M. Production of reactive oxygen species in decoupled, Ca2+-depleted PSII and their use in assigning a function to chloride on both sides of PSII. Photosynth. Res., 2013, vol. 117, pp. 385-399.

7. Ono T., Inoue Y. Abnormal redox reactions in photosynthetic O2-evolving centers in NaCl/EDTA-washed PSII. A dark-stable EPR multiline signal and an unknown positive charge accumulator. Biochim. Biophys. Acta, 1990, vol. 1020, pp. 269-277.

8. Boussac A., Zimmermann J.-L., Rutherford A.W. EPR signals from modified charge accumulation states of the oxygen evolving enzyme in Ca2+-deficient photosystem II. Biochemistry, 1989, vol. 28, pp. 8984-8989.

9. Sivaraja M., Tso J., Dismukes G.C. A calcium-specific site influence the structure and activity of the manganese cluster responsible for photosynthetic water oxidation. Biochemistry, 1989, vol. 28, pp. 9459-9464.

10. Hallahan B.J., Nugent J.H.A., Warden J.T., Evans M.C.W. Investigation of the origin of the "S3" EPR signal from the oxygen-evolving complex of photosystem 2: the role of tyrosine. Z. Biochemistry, 1992, vol. 31, pp. 4562-4573.

11. Baumgarten M., Philo J.S., Dismukes G.C. Mechanism of photoinhibition of photosynthetic water oxidation by chloride depletion and fluoride substitution: oxidation of a protein residue. Biochemistry, 1990, vol. 29, pp. 10814-10822.

12. MacLachlan D.J., Nugent J.H.A. Investigation of the S3 Electron Paramagnetic Resonance Signal from the Oxygen-Evolving Complex of Photosystem 2: Effect of Inhibition of Oxygen Evolution by Acetate. Biochemistry, 1993, vol. 32, pp. 9772-9780.

13. Szalai V.A., Kühne H., Lakshmi K.V., Brudvig G.W. Characterization of the Interaction between Manganese and Tyrosine Z in Acetate-Inhibited Photosystem II. Biochemistry, 1998, vol. 37, pp. 13594-13603.

14. Ghanotakis D.F., Babcock G.T. Hydroxylamine as an inhibitor between Z and P680 in photosystem II. FEBS Lett., 1983, vol. 153, pp. 231-234.

15. Dunahay T.G., Staechelin L.A., Seibert M., Ogilvie P.D., Berg S.P. Structural biochemical and biophysical characterization of four oxygen-evolving Photosystem 2 preparations from spinach. Biochim. Biophys. Acta, 1984, vol. 764, pp. 179-193.

16. Polander B.C., Barry B.A. A hydrogen-bonding network plays a catalytic role in photosynthetic oxygen evolution. Proc. Natl. Acad. Sci. U.S.A., 2012, vol. 109, pp. 6112-6117.

17. Polander B.C., Barry B.A. Detection of an intermediary, protonated water cluster in photosynthetic oxygen evolution. Proc. Natl. Acad. Sci. U.S.A., 2013, vol. 110, pp. 10634-10639.

18. Kuntzleman T., Haddy A. Fluoride inhibition of photosystem II and the effect of removal of the PsbQ subunit. Photosynth. Res., 2009, vol. 102, pp. 7-19.

19. Sandusky P.O., Yocum C.F. The chloride requirement for photosynthetic oxygen evolution: factors affecting nucleophylic displacement of chloride from the oxygen-evolving complex. Biochim. Biophys. Acta, 1986, vol. 849, pp. 85-93.

20. Tsuno M., Suzuki H., Kondo T., Mino H., Noguchi T. Interaction and Inhibitory Effect of Ammonium Cation in the Oxygen Evolving Center of Photosytem II. Biochemistry, 2011, vol. 50, pp. 2506-2514.

21. Sandusky P.O., Yocum C.F. The chloride requirement for photosynthetic oxygen evolution. Analysis of the effects of chloride and other anions on amine inhibition of the oxygen-evolving complex. Biochim. Biophys. Acta, 1984, vol. 766, pp. 603-611.


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