journal article·2022-10Open access

Effect of TiO2 nanoparticles on the thermal stability of native DNA under UV irradiation

Evgeniya Usenko, Alexander Glamazda, Vladimir Valeev, Anastasiia Svidzerska, Anna Laguta, Sergey Petrushenko, Victor Karachevtsev

Applied Physics A· Volume 128· Issue 10

Abstract

$TiO2$ nanoparticles (NPs) are widely used in the environmental engineering, medicine, chemical and food industries due to their unique photocatalytic and biocidal properties. NPs may generate reactive oxygen species and, hence, have the toxic effect on the living cells via oxidative stress. An external UV irradiation may magnify the photocatalytic properties of $TiO2$ NPs. In this regard, we have analyzed the influence of $TiO2$ NPs on the conformation and thermal stability of native DNA in a buffer solution without and under UV irradiation exploiting absorption spectroscopy with DNA thermal denaturation in the range of 20-94 degrees Celsius. Upon DNA heating from about 25 to 44 degrees Celsius, we have observed the stabilization of DNA duplex in the presence of $TiO2$ NPs. This additional biopolymer stabilization indicates that partial DNA unwinding appears as a result of the direct binding of the biopolymer to NPs. We showed that the performed UV treatment of DNA during 3 hours leads to partial unwinding of the biopolymer structure. The NPs injection to the biopolymer solution induced the additional effect on the DNA thermal stability under UV irradiation. The performed analysis of the experimental data suggests that the nature of the impact of NPs on the biopolymer is complex.
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Research context

OpenAlex topics: TiO2 Photocatalysis and Solar Cells · Nanoparticles: synthesis and applications · Chemistry and Chemical Engineering

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (36)

Show source-provided references
1. A.A. Dayem, M.K. Hossain, S.B. Lee, K. Kim, S.K. Saha, G.-M. Yang, H.Y. Choi, S.-G. Cho, Int. J. Mol. Sci. 18, 1 (2017)
2. C.L. de Dicastillo, M.G. Correa, F.B. Martínez, C. Streitt, M.J. Galotto, Antimicrobial effect of titanium dioxide nanoparticles, in Antimicrobial Resistance - A One Health Perspective. ed. by M. Mare, S.H.E. Lim, K. Lai, R. Cristina (IntechOpen, London, UK, 2020). https://doi.org/10.5772/intechopen.9089110.5772/intechopen.90891 ↗
3. K. McNamara, S.A. Tofail, Adv. Phys.: X 2(1), 54 (2017)
4. H. Wang, Y. Yao, G. Wu, Q. Sun, M. Wang, X. Chen, J. Wanget, A room temperature oxygen gas sensor based on hierarchical TiO2, IEEE International Conference on manipulation, manufacturing and measurement on the nanoscale (3M-NANO), 199 (2016)10.1109/3M-NANO.2016.7824936 ↗
5. Yu. Zhu, K. Yan, Z. Xu, J. Zhangz, J. Electrochem. Soc. 163(9), B526 (2016)10.1149/2.1291609jes ↗
6. M. Ghadiry, M. Gholami, L. Choon Kong, C. Wu Yi, H. Ahmad, Y. Alias, Sensors 16, 39 (2016)10.3390/s16010039 ↗
7. S. Jafari, B. Mahyad, H. Hashemzadeh, S. Janfaza, T. Gholikhani, L. Tayebi, Int J Nanomed. 14(150), 3447 (2020)10.2147/IJN.S249441 ↗
8. R. Vian, H. Salehi, M. Lapierre, F. Cuisinier, V. Cavaillès, S. Balme, Food Chem. 360, 130003 (2021)10.1016/j.foodchem.2021.130003 ↗
9. Characterising the potential risks posed by engineered nanoparticles: a second UK government research report. Department of Environment, Food and Rural Affairs (DEFRA, London, UK, 2007)
10. EU nanotechnology R&D in the field of health and environmental impact of nanoparticles (Compiled by PilarAguar and José Juan Murcia Nicolás, Unit G4 Nano and Converging Sciences and Technologies European Commission, Research DG, 2008)
11. V. Aruoja, H.C. Dubourguier, K. Kasemets, A. Kahru, Sci. Total Environ. 407(4), 1461 (2009)10.1016/j.scitotenv.2008.10.053 ↗
12. I. Velzeboer, A.J. Hendriks, A.M.J. Ragas, D. Van de Meent, Environ. Toxicol. Chem. 27(9), 1942 (2008)10.1897/07-509.1 ↗
13. C. Blaise, F. Gagne, J.F. Ferard, P. Eullaffroy, Environ. Toxicol. 23, 591 (2008)10.1002/tox.20402 ↗
14. S. Patel, P. Patel, S.R. Bakshi, Cytotechnology 69(2), 245 (2017)10.1007/s10616-016-0054-3 ↗
15. R.P. Rastogi, Richa, A. Kumar, M.B. Tyagi, R.P. Sinha, J. Nucleic Acids 2010, 592980 (2010)10.4061/2010/592980 ↗
16. N. González, M. del Àngels Custal, D. Rodríguez, J.-R. Riba, E. Armelin, Mater. Res. 20(4), 1082 (2017)10.1590/1980-5373-mr-2017-0178 ↗
17. T.A. Egerton, Molecules 19, 18192 (2014)10.3390/molecules191118192 ↗
18. X. Zhang, F. Wang, B. Liu, E.Y. Kelly, M.R. Servos, J. Liu, Langmuir 30(3), 839 (2014)10.1021/la404633p ↗
19. K. Li, S. Du, S. Van Ginkel, Y. Chen, Atomic force microscopy study of the interaction of DNA and nanoparticles, in Nanomaterial, Advances in Experimental Medicine and Biology, vol. 811, ed. by D.G. Capco, Y. Chen (Springer, Dordrecht, 2014), pp.93–109
20. S. Patel, P. Patel, S.B. Undre, Sh.R. Pandya, M. Singh, S. Bakshi, J. Mol. Liq. 213, 304 (2016)10.1016/j.molliq.2015.11.002 ↗
21. K.S. El-said, E.M. Ali, K. Kanehira, A. Taniguchi, J. Nanobiotechnol. 12, 48 (2014)10.1186/s12951-014-0048-2 ↗
22. DNA Replication: From Old Principles to New Discoveries (Advances in Experimental Medicine and Biology Book 1042) 1st ed. 2017 Edition, Kindle Edition
23. V.A. Sorokin, V.A. Valeev, E.L. Usenko, V.V. Andrushchenko, Int. J. Biol. Macromol. 50(3), 854 (2012)10.1016/j.ijbiomac.2011.11.011 ↗
24. K. Higasi, H. Baba, A. Rembaum, Quantum Organic Chemistry (Interscience (A division John Wiley & Sons), New York, 1965)
25. E.L. Usenko, V.A. Valeev, AYu. Glamazda, V.A. Karachevtsev, J. Spectrosc. (2020). https://doi.org/10.1155/2020/885021410.1155/2020/8850214 ↗
26. M.V. Karachevtsev, O.S. Lytvyn, S.G. Stepanian, V.S. Leontiev, L. Adamowicz, V.A. Karachevtsev, J. Nanosci. Nanotech. 8(3), 1473 (2008)10.1166/jnn.2008.18214 ↗
27. C. Cascio, O. Geiss, F. Franchini, I. Ojea-Jimenez, F. Rossi, D. Gilliland, L. Calzolai, J. Anal. At. Spectrom 30, 1255 (2015)10.1039/C4JA00410H ↗
28. I. de la Calle, M. Menta, M. Kleina, B. Maxit, F. Séby, SpectrochimicaActa Part B 147, 28 (2018)10.1016/j.sab.2018.05.012 ↗
29. B. Krause, T. Meyer, H. Sieg, C. Kästner, P. Reichardt, J. Tentschert, H. Jungnickel, I. Estrela-Lopis, A. Burele, S. Chevance, F. Gauffre, P. Jalili, J. Meijer, L. Boehmert, A. Braeuning, A.F. Thünemann, F. Emmerling, V. Fessard, P. Laux, A. Lampen, A. Luch, RSC Adv. 8, 14377 (2018)10.1039/C8RA00205C ↗
30. T.G.F. Souza, V.S.T. Ciminelli, N.D.S. Mohallem, J. Phys.: Conf. Ser. 733, 012039 (2016)
31. Th. Dasri, P. Chaiyachate, S. Audtarat, P. Charee, A. Chingsungnoen, J. Met. Mater. Miner. 30(3), 30 (2020)10.55713/jmmm.v30i3.679 ↗
32. J. Kiefer, Effects of ultraviolet radiation on DNA, in Chromosomal Alterations: Methods, Results and Importance in Human Health. ed. by G. Obe, Vijayalaxmi (Springer, Berlin Heidelberg, 2007), pp.39–5310.1007/978-3-540-71414-9_3 ↗
33. A.P. Sarapultsev, S.V. Rempel, J.V. Kuznetsova, G.P. Sarapultsev, J. Ural Med. Acad. Sci. (2016). https://doi.org/10.22138/2500-0918-2016-15-3-97-11110.22138/2500-0918-2016-15-3-97-111 ↗
34. N.S. Leonenko, O.B. Leonenko, Innov. Biosyst. Bioeng. 4(2), 75 (2020)10.20535/ibb.2020.4.2.192810 ↗
35. H.M. Ali, H. Babar, T.R. Shah, M.U. Sajid, M.A. Qasim, S. Javed, Appl. Sci. 8(4), 587 (2018)10.3390/app8040587 ↗
36. N.A. Kasyanenko, A.A. Andreeva, A.V. Baryshev, V.M. Bakulev, M.N. Likhodeeva, P.N. Vorontsov-Velyaminov, J. Phys. Chem. B 123, 9557 (2019)10.1021/acs.jpcb.9b07341 ↗