Damage and protection of the photosynthetic apparatus from UV-B radiation. II. Effect of quercetin at different pH

Journal of Plant Physiology

Volumn 184, Issue , 2015, Pages 98-105

  Dobrikova, Anelia G ^a   Apostolova, Emilia L ^a  

^a INSTITUTE OF BIOPHYSICS AND BIOMEDICAL ENGINEERING   (Bulgaria)

Author keywords

Low temperature chlorophyll fluorescence; Pea thylakoid membranes; Photosynthetic oxygen evolution; Quercetin; UV B radiation

Indexed keywords

PISUM SATIVUM;

ANTIOXIDANT; PHOTOSYSTEM II; QUERCETIN;

DRUG EFFECTS; METABOLISM; PEA; PH; PHOTOSYNTHESIS; PHOTOSYSTEM II; RADIATION RESPONSE; THYLAKOID; ULTRAVIOLET RADIATION;

ANTIOXIDANTS; HYDROGEN-ION CONCENTRATION; PEAS; PHOTOSYNTHESIS; PHOTOSYSTEM II PROTEIN COMPLEX; QUERCETIN; THYLAKOIDS; ULTRAVIOLET RAYS;

EID: 84939547919     PISSN: 01761617     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jplph.2015.06.008     Document Type: Article

References (59)

1. Agati G., Azzarello E., Pollastri S., Tattini M. Flavonoids as antioxidants in plants: location and functional significance. Plant Sci. 2012, 196:67-76.
2. Agati G., Biricolti S., Guidi L., Ferrini F., Fini A., Tattini M. The biosynthesis of flavonoids is enhanced similarly by UV radiation and root zone salinity in L. vulgare leaves. J. Plant Physiol. 2011, 168:204-212.
3. Agati G., Brunetti C., Ferdinando M.D., Ferrini F., Pollastri S., Tattini M. Functional roles of flavonoids in photoprotection: new evidence, lessons from the past. Plant Physiol. Biochem. 2013, 72:35-45.
4. Agati G., Tattini M. Multiple functional roles of flavonoids in photoprotection. New Phytol. 2010, 186:786-793.
5. Apostolova E.L., Dobrikova A.G., Ivanova P.I., Petkanchin I.B., Taneva S.G. Relationship between the organization of the PSII supercomplex and the functions of the photosynthetic apparatus. J. Photochem. Photobiol. B 2006, 83:114-122.
6. Arntzen C.J., Falkenthal S.V., Bobick S. Inhibition of photophosphorylation by kaempferol. Plant Physiol. 1974, 53:304-306.
7. Barber J., Chow W.S., Scoufflaire C., Lannoye R. The relationship between thylakoid stacking and salt induced chlorophyll fluorescence change. Biochim. Biophys. Acta 1980, 591:92-103.
8. Barber J., Ford R.C., Mitchell R.A.C., Millner P.A. Chloroplast thylakoid membrane fluidity and its sensitivity to temperature. Planta 1984, 161:375-380.
9. Barta C., Kálai T., Hideg K., Vass I., Hideg É. Differences in the ROS generating efficacy of various ultraviolet wavelengths in detached spinach leaves. Funct. Plant Biol. 2004, 31:23-28.
10. Bornman J.F., Reuber S., Cen Y.P., Weissenbock G. Ultraviolet radiation as a stress factor and the role of protective pigments. Plants and UV-B: Responses to Environmental Change 1997, 156-168. Cambridge University Press. P. Lumsden (Ed.).
11. Brandle J.R., Campbell W.F., Sisson W.B., Caldwell M.M. Net photosynthesis, electron transport capacity and ultra structure of P. sativum L. exposed to ultraviolet-B radiation. Plant Physiol. 1977, 60:165-168.
12. Carlberg I., Bingsmark S., Vennigerholz F., Larsson U.K., Andersson B. Low temperature effects on thylakoid protein phosphorilation and membrane dynamics. Biochim. Biophys. Acta 1992, 1099:111-117.
13. Chanhan N.P., Fatma T., Mishra R.K. Protection of wheat chloroplasts from lipid peroxidation and loss of photosynthetic pigments by quercetin under strong illumination. J. Plant Physiol. 1992, 140:409-413.
14. Delrieu M.-J., Hung S.P.N., de Kouchkovsky F. pH dependence of the S2→S3 transition associated with O2 evolution in inside-out thylakoids. FEBS Lett. 1985, 187:321-326.
15. Dobrikova A., Apostolova E. Protective effects of naringin on the photosynthetic apparatus against UV-B radiation. C R Acad. Bulg. Sci. 2014, 67:675-682.
16. Dobrikova A.G., Morgan R.M., Ivanov A.G., Apostolova E., Petkanchin I., Huner N.P.A., Taneva S.G. Electric properties of thylakoid membranes from pea mutants with modified carotenoid and chlorophyll-protein complexes composition. Photosynth. Res. 2000, 65:165-174.
17. Dobrikova A.G., Tuparev N.P., Krasteva I., Buscheva M.H., Velitchkova M.Y. Artificial alterations of fluidity of pea thylakoid membranes and its effect on energy distribution between both photosystems. Z. Naturforsch. 1997, 52c:475-480.
18. Dobrikova A.G., Krasteva V., Apostolova E.L. Damage and protection of the photosynthetic apparatus from UV-B radiation. I. Effect of ascorbate. J. Plant Physiol. 2013, 170:251-257.
19. Erlejman A.G., Verstraeten S.V., Fraga C.G., Oteiza P.I. The interaction of flavonoids with membranes: potential determinant of flavonoid antioxidant effects. Free Radic. Res. 2004, 38:1311-1320.
20. Gao Q., Zhang L. Ultraviolet-B-induced oxidative stress and antioxidant defense system responses in ascorbate-deficient vtc1 mutants of Arabidopsis thaliana. J. Plant Physiol. 2008, 165:138-148.
21. Garstka M., Jagielski A. Peroxidative reactions attenuate oxygen effect on spectroscopic properties of isolated chloroplasts. J. Photochem. Photobiol. B. 2001, 64:82-92.
22. Harborne J.B. Nature distribution and function of plant flavonoids. Prog. Clin. Biol. Res. 1986, 213:15-24.
23. Hideg E., Vass I. UV-B induced free radical production in plant leaves and isolated thylakoid membranes. Plant Sci. 1996, 115:25l-260.
24. Horton P., Ruban A.V., Rees D., Pascal A.A., Noctor G., Young A.J. Control of the light-harvesting function of chloroplast membranes by aggregation of the LHCII chlorophyll-protein complex. FEBS Lett. 1991, 292:1-4.
25. Huner N.P.A., Krol M., Williams J.P., Maissan E., Low P.S., Roberts D., Thompson J.E. Low temperature development induces a specific decrease in trans-δ3-hexadecenoic acid content which influences LHCII organization. Plant Physiol. 1987, 84:12-18.
26. Ivanova P.I., Dobrikova A.G., Taneva S.G., Apostolova E.L. Sensitivity of the photosynthetic apparatus to UV-A radiation: a role of light-harvesting complex II-photosystem II supercomplex organization. Radiat. Environ. Biophys. 2008, 7:169-177.
27. Kataria S., Jajoo A., Guruprasad K.N. Impact of increasing ultraviolet-B (UV-B) radiation on photosynthetic processes. J. Photochem. Photobiol. B . 2014, 137:55-66.
28. Kok B., Forbush B., McGloin M. Co-operation of charges in photosynthetic O2 evolution. I. A linear four step mechanism. Photochem. Photobiol. 1970, 11:457-475.
29. Krause G.H., Weis E. Chlorophyll fluorescence and photosynthesis: the basics. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1991, 42:313-349.
30. Lichtenthaler H.K. Chlorophyll and carotenoids: pigments of photosynthetic biomembranes. Methods Enzym. 1987, 148:350-382.
31. Lin Z.F., Liu N., Lin G.Z., Peng C.L. Factors altering the membrane fluidity of spinach thylakoid as determined by fluorescence polarization. Acta Physiol. Plant 2011, 33:1019-1024.
32. Majer P., Neugart S., Krumbein A., Schreiner M., Hideg É. Singlet oxygen scavenging by leaf flavonoids contributes to sunlight acclimation in Tilia platyphyllos. Environ. Exp. Bot. 2014, 100:1-9.
33. Messinger J., Renger G. Analyses of pH-induced modifications of the period four oscillation of flash-induced oxygen evolution reveal distinct structural changes of the photosystem II donor side at characteristic pH values. Biochemistry 1994, 33:10896-10905.
34. Mittler R. Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci. 2002, 7:405-410.
35. Moreland D.E., Novitzki W.P. Interference by luteolin, quercetin and taxifolin with chloroplast-mediated electron transport and phosphorylation. Plant Soil 1987, 98:145-159.
36. Movileanu L., Neagoe I., Flonta M.L. Interaction of the antioxidant flavonoid quercetin with planar lipid bilayers. Int. J. Pharm. 2000, 205:135-146.
37. Nedunchezhian N., Kulandaivelu G. Evidence for the ultraviolet-B (280-320nm) radiation induced structural reorganization and damage of photosystem II polypeptides in isolated chloroplasts. Physiol. Plant. 1991, 81:558-562.
38. Ollila F., Halling K., Vuorela P., Vuorela H., Slotte J.P. Characterization of flavonoid-biomembrane interactions. Arch. Biochem. Biophys. 2002, 399(1):103-108.
39. Oteiza P.I., Erlejman A.G., Verstraeten S.V., Keen C.L., Fraga C.G. Flavonoid-membrane interactions: a protective role of flavonoids at the membrane surface. Clin. Dev. Immunol. 2005, 12:19-25.
40. Pawlikowska-Pawlega B., Gruszecki W.I., Misiak L., Paduch R., Piersiak T., Zarzyka B., Pawelec J., Gawron A. Modification of membranes by quercetin, a naturally occurring flavonoid, via its incorporation in the polar head group. Biochim. Biophys. Acta 2007, 1768:2195-2204.
41. Plijter J.J., de Groot A., van Dijk M.A., van Gorkom H.J. Destabilization by high pH of the S1-state of the oxygen-evolving complex in photosystem II particles. FEBS Lett. 1986, 195:313-318.
42. Poklar U.N., Ota A., Sentjurc M., Kure S., Abram V. Flavonoids and cell membrane fluidity. Food Chem. 2010, 121:78-84.
43. Renger G., Voss M., Gräber P., Schulze A. Effect of UV irradiation on different partial reactions of the primary processes of photosynthesis. Stratospheric Ozone Reduction, Solar Ultraviolet Radiation and Plant Life 1986, 171-184. Springer-Verlag, Berlin. C. Worrest, M.M. Caldwell (Eds.).
44. Rodrigues G.C., Jansen M.A.K., van den Noort M.E., van Rensen J.J.S. Evidence for the semireduced primary quinone electron acceptor of photosystem II being a photosensitizer for UVB damage to the photosynthetic apparatus. Plant Sci. 2006, 170:283-290.
45. Ruelland E., Zachowski A. How plants sense temperature. Environ. Exp. Bot. 2010, 69:225-232.
46. Saunders J.A., McClure J.W. The distribution of flavonoids in chloroplasts of twenty five species of vascular plants. Phytochemistry 1976, 15:809-810.
47. Selvaraj S., Krishnaswamy S., Devashya V., Sethuraman S., Krishnan U.M. Influence of membrane lipid composition on flavonoid-membrane interactions: implications on their biological activity. Prog. Lipid Res. 2014, 58C:1-13.
48. Singh A.K., Singhal G.S. Specific degradation of D1 protein during exposure of thylakoid membranes to high temperature in the dark. Photosynthetica 1999, 36:433-440.
49. Shutilova N., Semenova G., Klimov V., Shnyrov V. Temperature-induced functional and structural transformations of the photosystem II oxygen-evolving complex in spinach subchloroplast preparations. Biochem. Mol. Biol. Int. 1995, 35:1233-1243.
50. Takahama U. Supression of lipid photoperoxidation by quercctin and its glycosides in spinach chloroplasts. Photochem. Photobiol. 1983, 38:363-367.
51. Takahama U. Hydrogen peroxide-dependent oxidation of flavonols by intact spinach chloroplasts. Plant Physiol. 1984, 74:852-855.
52. Tevini M., Braun J., Fieser G. The protective function of the epidermal layer of rye seedlings againts ultraviolet-B radiation. Photochem. Photobiol. 1991, 53:329-333.
53. Tournaire C., Croux S., Maurette M.T., Beck I., Hocquaux M., Braun A.M., Oliveros E. Antioxidant activity of flavonoids: efficiency of singlet oxygen (1 delta g) quenching. J. Photochem. Photobiol. B 1993, 19:205-215.
54. Vass I., Sass L., Spetea C., Bakou A., Ghanotakis D.F., Petrouleas V. UV-B-induced inhibition of photosystem II electron transport studied by EPR and chlorophyll fluorescence. Impairment of donor and acceptor side components. Biochemistry 1996, 35:8964-8973.
55. Vass I., Szilárd A., Sicora C. Adverse effects of UV-B light on the structure and function of the photosynthetic apparatus. Handbook of Photosynthesis 2005, 827-843. CRC Press, Taylor and Francis Group, Boca Raton, FL. 2nd ed. M. Pessarakli (Ed.).
56. Yu S.-G., Björn L.O. Differences in UV-B sensitivity between PSII from grana lamellae and stroma lamellae. J. Photochem. Photobiol. B 1996, 34:35-38\.
57. Zaprometov M.N., Nikolaeva T.N. Chloroplasts isolated from kidney bean leaves are capable of phenolic compound biosynthesis. Russ. J. Plant Physiol. 2003, 50:623-626.
58. Zeinalov Y. Existence of two different ways for oxygen evolution in photosynthesis and photosynthetic unit concept. Photosynthetica 1982, 16:27-35.
59. Zeinalov Y. An equipment for investigations of photosynthetic oxygen production reactions. Bulg. J. Plant Physiol. 2002, 28:57-67.