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Year 2018, Volume: 14 Issue: 4, 399 - 404, 28.12.2018
https://doi.org/10.18466/cbayarfbe.410546

Abstract

References

  • 1. Strid, AW, Chow, WS, Anderson, JM, UV-B damage and protection at the molecular level in plants, Photosynthesis Research, 1994, 39, 475-489.
  • 2. Riegger, L, Robinson, D, Photoinduction of UV-absorbing compounds in Antarctic diatoms and Phaeocystis antartica. Marine Ecology Progress Series, 1997 160, 13-25.
  • 3. Bouchereau, A, Aziz, A, Larher, F, Martin-Tanguy, J, Polyamines and environmental challenges, recent development, Plant Science, 1999 140, 103–125.
  • 4. Kramer, GF, Norman, HA, Krizek, DT, Mirecki, RM, Influence of UV-B radiation on polyamines, lipid peroxidation and membrane lipids in cucumber, Phytochemistry, 1991, 30, 2101–2108.
  • 5. Kotzabasis, K, Fotinou, C, Roubelakis-Angelakis, KA, Ghanotakis, D, Polyamines in the photosynthetic apparatus, Photosystem II highly resolved subcomplexes are enriched in spermine, Photosynthesis Research, 1993, 38, 83–88.
  • 6. Bates, LS, Waldren, RP, Tear, ID, Rapid determination of free proline for water-stress studies, Plant Soil, 1973, 39, 205–207.
  • 7. Unal, D, Tuney, I, Sukatar, A, The role of external polyamines on photosynthetic responses, lipid peroxidation, protein and chlorophyll a content under the UV-A (352 nm) stress in Physcia semipinnata, Journal of Photochemistry and Photobiology B, 2008, 90, 64-68.
  • 8. Lütz, C, Navakoudis, E, Seidlitz, HK, Kotzabasis, K, Simulated solar irradiation with enhanced UV-B adjust plastid-and thylakoid-associated polyamine changes for UV-B protection, Biochimica et Biophysica Acta-Bioenergetics, 2005, 1710, 24-33.
  • 9. Demir, Y, Growth and proline content of germinating wheat genotypes under ultraviolet light, Turkish Journal of Botany, 2000, 24, 67-70.
  • 10. Alia, P, Mohanty, P, Matysik, J, Effect of proline on the production of singlet oxygen, Amino Acids, 2001, 21, 195-200.
  • 11. Smirnoff, N, Cumbes, QJ, Hydroxyl radical scavenging activity of compatible solute, Phytochemistry, 1989, 28, 1057–1060.
  • 12. Wang, X, Shi, G, Xu, Q, Hu, J, Exogenous polyamines enhance copper tolerance of Nymphoides peltatum, Journal of Plant Physiology, 2007, 164, 1062-70.
  • 13. Duan, JJ, Li, J, Guo, SR, Kang, YY, Exogenous Spermidine affects polyamine metabolism in salinity-stressed Cucumis sativus roots and enhances short-term salinity tolerance, Journal of Plant Physiology, 2008, 165, 1620-35.
  • 14. Aziz, A, Martin-Tanguy, J, Larher, F, Stress-induced changes in polyamine and tyramine levels can regulate proline accumulation in tomato leaf discs treated with sodiumchloride, Physiologia Plantarum, 1998, 104, 195-202.
  • 15. Tanou, G, Ziogas, V, Belghazi, M, Christou, A, Filippou, P, Job, D, Fotopoulos, V, Molassiotis, A, Polyamines reprogram oxidative and nitrosative status and the proteome of citrus plants exposed to salinity stress, Plant Cell and Environment, 2014, 37,864-885.
  • 16. Kumar, SG, Mattareddy, A, Sudhakar, C, NaCl effects on proline metabolism in two high yielding genotypes of mulberry (Marus alba L.) with contrasting salt tolerance, Plant Science, 2003, 165, 1245-1251.
  • 17. Hoerter, ID, Arnold, AA, Kuczynska, DA, Shibuya, A, Ward, CS, Sauer, MG, Effects of sublethal UVA irradiation on activity levels of oxidative defense enzymes and protein oxidation in Escherichia coli, Journal of Journal of Photochemistry and Photobiology B, 2005, 81, 171–180.
  • 18. Unal, D, Tuney, I, Esiz-Dereboylu, A, Sukatar, A, The effect of UV-A (352 nm) stress on chlorophyll fluorescence, chlorophyll a content, thickness of upper cortex and determinate DNA damage in Physcia semipinnata, Photochemistry and Photobiology, 2009, 94, 71-76.
  • 19. Oh, TJ, Kim, IG, Polyamines protect against DNA strand breaks and aid cell survival against irradiation in Escherichia coli, Biotechnology Techniques, 1998, 12, 755–758.
  • 20. Solheim, B, Zielke, M, Bjerke, JW, Rozema, J, Effects of enhanced UV-B radiation on nitrogen fixation in arctic ecosystems, Plant Ecol, 2006, 182, 109-118.

Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia semipinnata (J. F. Gmel.) Moberg

Year 2018, Volume: 14 Issue: 4, 399 - 404, 28.12.2018
https://doi.org/10.18466/cbayarfbe.410546

Abstract

In this study the protection ability of polyamines on
Photosystem II (PSII), the proline content of the cells and necrosis formation
induced by Ultraviolet-A irradiation were studied. Although 24 h Ultraviolet-A
exposure decreased the photosynthetic quantum yield (Fv/Fm) ratio in Physcia semipinnata (J. F. Gmel.) Moberg,
thalli that treated with 1 mM polyamine, especially spermidine and spermine,
were slightly influenced by the UV-A exposure. It was also found that spd and
spm treated samples had lower proline content than putrescine (put)-treated samples.
Moreover, It was found that the samples that were treated with spd and spm had
lower percentage of DNA damage than put-treated samples and non-treated groups.
In this study, Ultraviolet-A induced DNA damage detected by acridine
orange/ethidium bromide staining assay. The DNA damage in thalli of P. semipinnata
was detected in situ in phycobiont layer after 24 h of Ultraviolet-A exposure,
in contrast, polyamine-treated samples had a lower rate of necrotic cells.

References

  • 1. Strid, AW, Chow, WS, Anderson, JM, UV-B damage and protection at the molecular level in plants, Photosynthesis Research, 1994, 39, 475-489.
  • 2. Riegger, L, Robinson, D, Photoinduction of UV-absorbing compounds in Antarctic diatoms and Phaeocystis antartica. Marine Ecology Progress Series, 1997 160, 13-25.
  • 3. Bouchereau, A, Aziz, A, Larher, F, Martin-Tanguy, J, Polyamines and environmental challenges, recent development, Plant Science, 1999 140, 103–125.
  • 4. Kramer, GF, Norman, HA, Krizek, DT, Mirecki, RM, Influence of UV-B radiation on polyamines, lipid peroxidation and membrane lipids in cucumber, Phytochemistry, 1991, 30, 2101–2108.
  • 5. Kotzabasis, K, Fotinou, C, Roubelakis-Angelakis, KA, Ghanotakis, D, Polyamines in the photosynthetic apparatus, Photosystem II highly resolved subcomplexes are enriched in spermine, Photosynthesis Research, 1993, 38, 83–88.
  • 6. Bates, LS, Waldren, RP, Tear, ID, Rapid determination of free proline for water-stress studies, Plant Soil, 1973, 39, 205–207.
  • 7. Unal, D, Tuney, I, Sukatar, A, The role of external polyamines on photosynthetic responses, lipid peroxidation, protein and chlorophyll a content under the UV-A (352 nm) stress in Physcia semipinnata, Journal of Photochemistry and Photobiology B, 2008, 90, 64-68.
  • 8. Lütz, C, Navakoudis, E, Seidlitz, HK, Kotzabasis, K, Simulated solar irradiation with enhanced UV-B adjust plastid-and thylakoid-associated polyamine changes for UV-B protection, Biochimica et Biophysica Acta-Bioenergetics, 2005, 1710, 24-33.
  • 9. Demir, Y, Growth and proline content of germinating wheat genotypes under ultraviolet light, Turkish Journal of Botany, 2000, 24, 67-70.
  • 10. Alia, P, Mohanty, P, Matysik, J, Effect of proline on the production of singlet oxygen, Amino Acids, 2001, 21, 195-200.
  • 11. Smirnoff, N, Cumbes, QJ, Hydroxyl radical scavenging activity of compatible solute, Phytochemistry, 1989, 28, 1057–1060.
  • 12. Wang, X, Shi, G, Xu, Q, Hu, J, Exogenous polyamines enhance copper tolerance of Nymphoides peltatum, Journal of Plant Physiology, 2007, 164, 1062-70.
  • 13. Duan, JJ, Li, J, Guo, SR, Kang, YY, Exogenous Spermidine affects polyamine metabolism in salinity-stressed Cucumis sativus roots and enhances short-term salinity tolerance, Journal of Plant Physiology, 2008, 165, 1620-35.
  • 14. Aziz, A, Martin-Tanguy, J, Larher, F, Stress-induced changes in polyamine and tyramine levels can regulate proline accumulation in tomato leaf discs treated with sodiumchloride, Physiologia Plantarum, 1998, 104, 195-202.
  • 15. Tanou, G, Ziogas, V, Belghazi, M, Christou, A, Filippou, P, Job, D, Fotopoulos, V, Molassiotis, A, Polyamines reprogram oxidative and nitrosative status and the proteome of citrus plants exposed to salinity stress, Plant Cell and Environment, 2014, 37,864-885.
  • 16. Kumar, SG, Mattareddy, A, Sudhakar, C, NaCl effects on proline metabolism in two high yielding genotypes of mulberry (Marus alba L.) with contrasting salt tolerance, Plant Science, 2003, 165, 1245-1251.
  • 17. Hoerter, ID, Arnold, AA, Kuczynska, DA, Shibuya, A, Ward, CS, Sauer, MG, Effects of sublethal UVA irradiation on activity levels of oxidative defense enzymes and protein oxidation in Escherichia coli, Journal of Journal of Photochemistry and Photobiology B, 2005, 81, 171–180.
  • 18. Unal, D, Tuney, I, Esiz-Dereboylu, A, Sukatar, A, The effect of UV-A (352 nm) stress on chlorophyll fluorescence, chlorophyll a content, thickness of upper cortex and determinate DNA damage in Physcia semipinnata, Photochemistry and Photobiology, 2009, 94, 71-76.
  • 19. Oh, TJ, Kim, IG, Polyamines protect against DNA strand breaks and aid cell survival against irradiation in Escherichia coli, Biotechnology Techniques, 1998, 12, 755–758.
  • 20. Solheim, B, Zielke, M, Bjerke, JW, Rozema, J, Effects of enhanced UV-B radiation on nitrogen fixation in arctic ecosystems, Plant Ecol, 2006, 182, 109-118.
There are 20 citations in total.

Details

Primary Language English
Subjects Engineering
Journal Section Articles
Authors

Dilek Ünal

İnci Tüney Kızılkaya

Publication Date December 28, 2018
Published in Issue Year 2018 Volume: 14 Issue: 4

Cite

APA Ünal, D., & Tüney Kızılkaya, İ. (2018). Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia semipinnata (J. F. Gmel.) Moberg. Celal Bayar Üniversitesi Fen Bilimleri Dergisi, 14(4), 399-404. https://doi.org/10.18466/cbayarfbe.410546
AMA Ünal D, Tüney Kızılkaya İ. Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia semipinnata (J. F. Gmel.) Moberg. CBUJOS. December 2018;14(4):399-404. doi:10.18466/cbayarfbe.410546
Chicago Ünal, Dilek, and İnci Tüney Kızılkaya. “Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia Semipinnata (J. F. Gmel.) Moberg”. Celal Bayar Üniversitesi Fen Bilimleri Dergisi 14, no. 4 (December 2018): 399-404. https://doi.org/10.18466/cbayarfbe.410546.
EndNote Ünal D, Tüney Kızılkaya İ (December 1, 2018) Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia semipinnata (J. F. Gmel.) Moberg. Celal Bayar Üniversitesi Fen Bilimleri Dergisi 14 4 399–404.
IEEE D. Ünal and İ. Tüney Kızılkaya, “Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia semipinnata (J. F. Gmel.) Moberg”, CBUJOS, vol. 14, no. 4, pp. 399–404, 2018, doi: 10.18466/cbayarfbe.410546.
ISNAD Ünal, Dilek - Tüney Kızılkaya, İnci. “Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia Semipinnata (J. F. Gmel.) Moberg”. Celal Bayar Üniversitesi Fen Bilimleri Dergisi 14/4 (December 2018), 399-404. https://doi.org/10.18466/cbayarfbe.410546.
JAMA Ünal D, Tüney Kızılkaya İ. Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia semipinnata (J. F. Gmel.) Moberg. CBUJOS. 2018;14:399–404.
MLA Ünal, Dilek and İnci Tüney Kızılkaya. “Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia Semipinnata (J. F. Gmel.) Moberg”. Celal Bayar Üniversitesi Fen Bilimleri Dergisi, vol. 14, no. 4, 2018, pp. 399-04, doi:10.18466/cbayarfbe.410546.
Vancouver Ünal D, Tüney Kızılkaya İ. Exogenous Polyamine Treatment Prevents UV-A Induced Cellular Damage and Photoinhibition of Photosystem II in Lichen Physcia semipinnata (J. F. Gmel.) Moberg. CBUJOS. 2018;14(4):399-404.