Dynamics of the activity of antioxidant enzymes and the expression of the genes encoding them in wheat after ultrasound exposure
- 作者: Tarasov S.1, Krutova E.1
-
隶属关系:
- Nizhny Novgorod State Agricultural Academy
- 期: 编号 2 (2024)
- 页面: 194-206
- 栏目: PLANT PHYSIOLOGY
- URL: https://journals.rcsi.science/1026-3470/article/view/261357
- DOI: https://doi.org/10.31857/S1026347024020037
- EDN: https://elibrary.ru/WCWGIN
- ID: 261357
如何引用文章
全文:
详细
The effect of ultrasound (5, 10 and 20 min, intensity 25 kW/m2, frequency 26.1 kHz) on the dynamics of the activity of the main antioxidant enzymes: superoxide dismutase, catalase, peroxidase and the expression of the genes encoding them (SOD-1, CAT, POD) was studied in germinating seeds and wheat sprouts. Ultrasound after 1 hour predominantly suppressed the activity of antioxidant enzymes, with subsequent restoration and increase (after 1 and 6 days) of activity. The content of mRNA transcripts of the studied genes predominantly increased 1 hour after exposure, and subsequently (after 1 and 6 days) it was either higher or remained equal to the control. The results obtained apparently indicate that ultrasound triggers eustress mechanisms, i. e. the stimulating effect led to the mobilization of protective processes of cells – hormesis.
全文:
作者简介
S. Tarasov
Nizhny Novgorod State Agricultural Academy
编辑信件的主要联系方式.
Email: tarasov_ss@mail.ru
俄罗斯联邦, 603022, Nizhny Novgorod, Gagarin Ave., 97
E. Krutova
Nizhny Novgorod State Agricultural Academy
Email: tarasov_ss@mail.ru
俄罗斯联邦, 603022, Nizhny Novgorod, Gagarin Ave., 97
参考
- Гланц С. Медико-биологическая статистика. М.: Практика, 1999. 459 с.
- Колупаев, Ю. Е. Антиоксиданты растительной клетки, и их роль в АФК сигналинге и устойчивости растений // Успехи соврем. биол. 2016. Т. 136. С. 181–198.
- Методы биохимического исследования растений / под редакцией А. И. Ермакова. Изд. 3-е, перераб. и доп. Л.: Агропромиздат, 1987 г. 432 с.
- Молекулярно-генетические и биохимические методы в современной биологии растений / под редакцией Вл. В. Кузнецова, В. В. Кузнецова, Г. А. Романова. М.: БИНОМ. Лаборатория знаний. 2011 г. 487 с.
- Пашовкин Т. Н., Шильников Г. В. Регистрация и анализ распределений интенсивностей в ультразвуковых пучках с использованием красителей // Научное приборостроение. 2000. Т. 10. № 3. С. 17–26
- Полесская О. Г., Каширина Е. И., Алехина Н. Д. Изменение активности антиоксидантных ферментов в листьях и корнях пшеницы в зависимости от формы и дозы азота в среде // Физиология растений. 2004. Т. 51. С. 686–691.
- Сиротюк М. Г. Акустическая кавитация. М.: Наука, 2008. 271 с.
- Ampofo J. O., Ngadi M. Ultrasonic assisted phenolic elicitation and antioxidant potential of common bean (Phaseolus vulgaris) sprouts // Ultrason Sonochem. 2020. № 64. Р. 104–974. https://doi.org/10.1016/j.ultsonch.2020.104974
- Biswas B., Sit N. Effect of ultrasonication on functional properties of tamarind seed protein isolates // J Food Sci Technol. 2020. V. 57. № 6. Р. 2070–2078. https://doi.org/10.1007/s13197-020-04241-8
- Bobrovskikh A., Zubairova U., Kolodkin A., Doroshkov A. Subcellular compartmentalization of the plant antioxidant system: an integrated overview. PeerJ. 2020. V. 8. https://doi.org/10.7717/peerj.9451
- Cabassa-Hourton C., Schertl P., Bordenave-Jacquemin M., Saadallah K., Guivarc’h A., Lebreton S., Planchais S., Klodmann J., Eubel H., Crilat E., Lefebvre-De Vos D., Ghelis T., Richard L., Abdelly C., Carol P., Braun H. P., Savouré A. Proteomic and functional analysis of proline dehydrogenase 1 link proline catabolism to mitochondrial electron transport in Arabidopsis thaliana // Biochem J. 2016. V. 473. № 17. Р.2623–2634. https://doi.org/10.1042/bcj20160314
- Calabrese E. J. Hormesis: Path and Progression to Significance. Int J Mol Sci. 2018. V. 19. № . 10. P. 28–71. https://doi.org/10.3390/ijms19102871
- Cao W., Wang P., Yang L., Fang Z., Zhang Y., Zhuang M., Lv H., Wang Y., Ji J. Carotenoid Biosynthetic Genes in Cabbage: Genome-Wide Identification, Evolution, and Expression Analysis // Genes (Basel). 2021. V. 12. № 12. P. 20–27. doi: 10.3390/genes12122027
- de Klerk E., AC’t Hoen P. A. Alternative mRNA transcription, processing, and translation: insights from RNA sequencing // Trends Genet. 2015. V. 31. № 3. P. 128–139. https://doi.org/10.1016/j.tig.2015.01.001
- Demidchik V. Mechanisms of oxidative stress in plants: From classical chemistry to cell biology // Environ. Expt. Bot. 2015. № 109. Р. 212–228. https://doi.org/10.1016/j.envexpbot.2014.06.021
- Deng X., Ma Y., Lei Y., Zhu X., Zhang L., Hu L., Lu S., Guo X., Zhang J. Ultrasonic structural modification of myofibrillar proteins from Coregonus peled improves emulsification properties // Ultrason Sonochem. 2021. № 76. Р. 105–659. https://doi.org/10.1016/j.ultsonch.2021.105659
- Ding Q., Tian G., Wang X., Deng W., Mao K., Sang Y. Effect of ultrasonic treatment on the structure and functional properties of mantle proteins from scallops (Patinopecten yessoensis) // Ultrason Sonochem. 2021. № 79. Р. 105–770. https://doi.org/10.1016/j.ultsonch.2021.105770
- Dixon D. P., Lapthorn A. Edwards R. Plant glutathione transferases // Genome Biol. 2002. V. 3. № . 3 REVIEWS3004.1–30004–10. https://doi.org/10.1186/gb-2002-3-3-reviews3004
- Dobránszki J., Hidvégi N., Gulyás A., Tóth B., Teixeira da Silva J. A. Abiotic stress elements in in vitro potato (Solanum tuberosum L.) exposed to air-based and liquid-based ultrasound: A comparative transcriptomic assessment // Prog Biophys Mol Biol. 2020. V. 158. P. 47–56. https://doi.org/10.1016/j.pbiomolbio.2020.09.001
- Ercan S. S., Soysal C. Effect of ultrasound and temperature on tomato peroxidase // Ultrason Sonochem. 2011. V. 18. № 2. P. 689–695. https://doi.org/10.1016/j.ultsonch.2010.09.014
- Ermakov A., Bobrovskikh A., Zubairova U., Konstantinov D., Doroshkov A. Stress-induced changes in the expression of antioxidant system genes for rice (Oryza sativa L.) and bread wheat (Triticum aestivum L.) // PeerJ. 2019. V. 7. https://doi.org/10.7717/peerj.7791
- Fritsche S., Wang X., Jung C. Recent Advances in our Understanding of Tocopherol Biosynthesis in Plants: An Overview of Key Genes, Functions, and Breeding of Vitamin E Improved Crops // Antioxidants (Basel). 2017. V. 6. № 4. P. 99. https://doi.org/10.3390/antiox6040099
- Gallegos J. Alternative Splicing Plays a Major Role in Plant Response to Cold Temperatures // Plant Cell. 2018. V. 30. № 7. P. 1378–1379. https://doi.org/10.1105/tpc.18.00430
- Gebicka L., Gebicki J. L. The effect of ultrasound on heme enzymes in aqueous solution // J Enzyme Inhib. 1997 V. 12. № 2. P. 133–141. https://doi.org/10.3109/14756369709035814
- Chavan P., Sharma P., Sharma S. R., Mittal T. C., Jaiswal A. K. Application of High-Intensity Ultrasound to Improve Food Processing Efficiency: A Review // Foods. 2022. V. 11. № 1. P. 122. https://doi.org/10.3390/foods11010122
- Huang Y., Mei G., Fu X., Wang Y., Ruan X., Cao D. Ultrasonic Waves Regulate Antioxidant Defense and Gluconeogenesis to Improve Germination from Naturally Aged Soybean Seeds // Front Plant Sci. 2022. № 13. Р. 833–858. https://doi.org/10.3389/fpls.2022.833858
- Hasanuzzaman M., Bhuyan M., Parvin K., Bhuiyan T. F., Anee T. I., Nahar K., Hossen M. S., Zulfiqar F., Alam M. M., Fujita M. Regulation of ROS Metabolism in Plants under Environmental Stress: A Review of Recent Experimental Evidence // Int J Mol Sci. 2020. V. 21. № 22. P. 86–95. https://doi.org/10.3390/ijms21228695
- Hassan S., Imran M., Ahmad N., Khan M. K. Lipids characterization of ultrasound and microwave processed germinated sorghum // Lipids Health Dis. 2017. № 16. № 1. Р. 125. https://doi.org/10.1186/s12944-017-0516-4
- Hidvégi N., Gulyás A., Dobránszki J. Ultrasound, as a hypomethylating agent, remodels DNA methylation and alters mRNA transcription in winter wheat (Triticum aestivum L.) seedlings // Physiol Plant. 2022. V. 174. № 5. https://doi.org/10.1111/ppl.13777
- Jacome Burbano M.S, Gilson E. The Power of Stress: The Telo-Hormesis Hypothesis // Cells. 2021. V. 10. № 5. P. 11–56. https://doi.org/10.3390/cells10051156
- Jalal B., McNally R.J., Elias J. A., Potluri S., Ramachandran V. S. “Fake it till You Make it”! Contaminating Rubber Hands (“Multisensory Stimulation Therapy”) to Treat Obsessive-Compulsive Disorder // Front Hum Neurosci. 2020. V. 13. P. 414. https://doi.org/10.3389/fnhum.2019.00414
- Jiang W., Yang L., He Y., Zhang H., Li W., Chen H., Ma D., Yin J. Genome-wide identification and transcriptional expression analysis of superoxide dismutase (SOD) family in wheat (Triticum aestivum) // PeerJ. 2019. V. 7. https://doi.org/10.7717/peerj.8062
- John S., Olas J. J., Mueller-Roeber B. Regulation of alternative splicing in response to temperature variation in plants // J Exp Bot. 2021. V. 72. № 18. P. 6150–6163. https://doi.org/10.1093/jxb/erab232
- Karthikesh M. S., Yang X. The effect of ultrasound cavitation on endothelial cells // Exp Biol Med (Maywood). 2021. V. 246. № 7. P. 758–770. https://doi.org/10.1177/1535370220982301
- Kashkooli H. A., Rooney J. A., Roxby R. Effects of ultrasound on catalase and malate dehydrogenase // J Acoust Soc Am. 1980. V. 67. № 5. P. 1798–1801. https://doi.org/10.1121/1.384309
- Kawakami D., Yoshida T., Kanemaru Y., Huarhua Zaquinaula M. H., Mizukami T., Arimoto M., Shibata T., Goto A., Enami Y., Amano H., Teraoka T., Komatsu K., Arie T. Induction of resistance to diseases in plant by aerial ultrasound irradiation // J Pestic Sci. 2019. V. 44. № 1. P. 41–47. https://doi.org/10.1584/jpestics.d18-064
- Lam P. Y., Wang L., Lo C., Zhu F. Y. Alternative Splicing and Its Roles in Plant Metabolism // Int J Mol Sci. 2022. V. 23. № 13. P. 73–55. https://doi.org/10.3390/ijms23137355
- Li Q. Q., Liu Z., Lu W., Liu M. Interplay between Alternative Splicing and Alternative Polyadenylation Defines the Expression Outcome of the Plant Unique OXIDATIVE TOLERANT-6 Gene // Sci Rep. 2017. V. 7. № 1. P. 20–52. https://doi.org/10.1038/s41598-017-02215-z
- Li Y., Cheng Y., Zhang Z., Wang Y., Mintah B. K., Dabbour M., Jiang H., He R., Ma H. Modification of rapeseed protein by ultrasound-assisted pH shift treatment: Ultrasonic mode and frequency screening, changes in protein solubility and structural characteristics // Ultrason Sonochem. 2020. № 69. Р. 105–240. https://doi.org/10.1016/j.ultsonch.2020.105240
- Liu J., Wang Q., Karagić Đ., Liu X., Cui J., Gui J., Gu M., Gao W. Effects of ultrasonication on increased germination and improved seedling growth of aged grass seeds of tall fescue and Russian wildrye // Sci Rep. 2016. № 6. https://doi.org/10.1038/srep22403
- López-Ribera I., Vicient C. M. Use of ultrasonication to increase germination rates of Arabidopsis seeds // Plant Methods. 2017. V. 13. P. 31. https://doi.org/10.1186/s13007-017-0182-6
- Lowry, O.N., Rosenbrough N. J., Tarr A. L., Randall R. J. Protein measurement with the Folin phenol reagent // J. Biol. Chem. 1951. V. 193. № 1. P. 265–275.
- Lv S., Taha A., Hu H., Lu Q., Pan S. Effects of Ultrasonic-Assisted Extraction on the Physicochemical Properties of Different Walnut Proteins // Molecules. 2019. V. 24. № 23. Р. 4260. https://doi.org/10.3390/molecules24234260
- Maresca D., Lakshmanan A., Abedi M., Bar-Zion A., Farhadi A., Lu G. J., Szablowski J. O., Wu D., Yoo S., Shapiro M. G. Biomolecular Ultrasound and Sonogenetics // Annu Rev Chem Biomol Eng. 2018. V. 9. P. 229–252. https://doi.org/10.1146/annurev-chembioeng-060817-084034
- Naumenko N., Potoroko I., Kalinina I. Stimulation of antioxidant activity and γ-aminobutyric acid synthesis in germinated wheat grain Triticum aestivum L. by ultrasound: Increasing the nutritional value of the product // Ultrason Sonochem. 2022. V. 86. P. 106–000. https://doi.org/10.1016/j.ultsonch.2022.106000
- Patterson B. D., Payne L. A., Chen Y. Z., Graham D. An inhibitor of catalase induced by cold in chilling-sensitive plants. Plant Physiol. 1984. V. 76. № 4. P. 1014–1018. https://doi.org/10.1104/pp.76.4.1014
- Pesti-Asbóth G., Molnár-Bíróné P., Forgács I., Remenyik J., Dobránszki J. Ultrasonication affects the melatonin and auxin levels and the antioxidant system in potato in vitro // Front Plant Sci. 2022. V. 13. P. 979–141. https://doi.org/10.3389/fpls.2022.979141
- Pfannschmidt T., Bräutigam K., Wagner R., Dietzel L., Schröter Y., Steiner S., Nykytenko A. Potential regulation of gene expression in photosynthetic cells by redox and energy state: approaches towards better understanding // Ann Bot. 2009. V. 103. № 4. P. 599–607. https://doi.org/10.1093/aob/mcn081
- Ratnikova T. A., Podila R., Rao A. M., Taylor A. G. Tomato Seed Coat Permeability to Selected Carbon Nanomaterials and Enhancement of Germination and Seedling Growth // ScientificWorldJournal. 2015. V. 2015. Р. 419–215. https://doi.org/10.1155/2015/419215
- Reyes A., Huber W. Alternative start and termination sites of transcription drive most transcript isoform differences across human tissues // Nucleic Acids Res. 2018. V. 46. № 2. P. 582–592. https://doi.org/10.1093/nar/gkx1165
- Saini A., Rohila J. S., Govindan G., Li Y. F., Sunkar R. Splice Variants of Superoxide Dismutases in Rice and Their Expression Profiles under Abiotic Stresses // Int J Mol Sci. 2021. V. 22. № 8 P .39–97. https://doi.org/10.3390/ijms22083997
- Schmittgen T. D., Zakrajsek B. A., Mills A. G., Gorn V., Singer M. J., Reed M. W. Quantitative reverse transcription-polymerase chain reaction to study mRNA decay: comparison of endpoint and real-time methods // Anal Biochem. 2000. V. 285. № 2. P. 194–204. https://doi.org/10.1006/abio.2000.4753
- Seo P. J., Park M. J., Park C. M. Alternative splicing of transcription factors in plant responses to low temperature stress: mechanisms and functions // Planta. 2013. V. 237. № 6. P. 1415–1424. https://doi.org/10.1007/s00425-013-1882-4
- Smolikova G., Medvedev S. Seed-to-Seedling Transition: Novel Aspects // Plants (Basel). 2022. V. 11. № 15. P. 19–88. https://doi.org/10.1007/s00425-013-1882-4
- Su J., Cavaco-Paulo A. Effect of ultrasound on protein functionality // Ultrason Sonochem. 2021. № . 76. Р. 105–653. https://doi.org/10.1016/j.ultsonch.2021.105653
- Sun Z., Li S., Chen W., Zhang J., Zhang L., Sun W., Wang Z. Plant Dehydrins: Expression, Regulatory Networks, and Protective Roles in Plants Challenged by Abiotic Stress // Int J Mol Sci. 2021. V. 22. № 23 https://doi.org/10.3390/ijms222312619
- Tovoli F., Cantisani V., Schiavone C., Piscaglia F. What Future for Ultrasound in Medicine? // Ultraschall Med. 2018. V. 39. № 1. P. 7–10. https://doi.org/10.1055/s-0043-125421
- Tyagi S., Shumayla, Verma P. C., Singh K., Upadhyay S. K. Molecular characterization of ascorbate peroxidase (APX) and APX-related (APX-R) genes in Triticum aestivum L. // Genomics. 2020. V. 112. № 6. Р. 4208–4223. https://doi.org/10.1016/j.ygeno.2020.07.023
- Vodeneev V., Akinchits E., Sukhov V. Variation potential in higher plants: Mechanisms of generation and propagation // Plant Signal Behav. 2015. V. 10. № 9. https://doi.org/10.1080/15592324.2015.1057365
- Wang Q., Chen G., Yersaiyiti H., Liu Y., Cui J., Wu C., Zhang Y., He X. Modeling analysis on germination and seedling growth using ultrasound seed pretreatment in switchgrass. PLoS One. 2012. V. 7. № 10. https://doi.org/10.1371/journal.pone.0047204
- Wang W., Zhang X., Deng F., Yuan R., Shen F. Genome-wide characterization and expression analyses of superoxide dismutase (SOD) genes in Gossypium hirsutum // BMC Genomics. 2017. V. 18. № 1. P. 376. https://doi.org/10.1186/s12864-017-3768-5
- Winkel-Shirley B. Flavonoid biosynthesis. A colorful model for genetics, biochemistry, cell biology, and biotechnology // Plant Physiol. 2001 V. 126. № 2. P. 485–493. https://doi.org/10.1104/pp.126.2.485
- Wong K. S., Lee L., Yeo L. Y., Tan M. K. Enhancing rate of water absorption in seeds via a miniature surface acoustic wave device // R Soc Open Sci. 2019. № 6. № 3. Р. 181560–181571. https://doi.org/10.1098/rsos.181560
- Yang X., Jia Z., Pu Q., Tian Y., Zhu F., Liu Y. ABA Mediates Plant Development and Abiotic Stress via Alternative Splicing // Int J Mol Sci. 2022. V. 23. № 7. P. 37–96. https://doi.org/10.3390/ijms23073796
- Yu M., Zhou Y., Wang X., Xie M., Zhang B., Yu H., Sun Z. Effect of ultrasonic pre-treatment on Ara h 1 in peanut sprouts // Ultrason Sonochem. 2021. № 75. Р. 105–607. https://doi.org/10.1016/j.ultsonch.2021.105607
- Zhang Y., Zheng L., Yun L., Ji L., Li G., Ji M., Shi Y., Zheng X. Catalase (CAT) Gene Family in Wheat (Triticum aestivum L.): Evolution, Expression Pattern and Function Analysis // Int J Mol Sci. 2022a. V. 23. № 1. P. 542. https://doi.org/10.3390/ijms23010542
- Zhang G.., Xu J, Wang Y., Sun X., Huang S., Huang L., Liu Y., Liu H., Sun J. Combined transcriptome and metabolome analyses reveal the mechanisms of ultrasonication improvement of brown rice germination. Ultrason Sonochem. 2022b. № 91. Р. 106–239. https://doi.org/10.1016/j.ultsonch.2022.106239
- Zhao F., Liu X., Ding X., Dong H., Wang W. Effects of High-Intensity Ultrasound Pretreatment on Structure, Properties, and Enzymolysis of Soy Protein Isolate // Molecules. 2019. V. 24. № 20. Р. 36–37. https://doi.org/10.3390/molecules24203637
- Zhao P., Huo S., Fan J., Chen J., Kiessling F., Boersma A. J., Göstl R., Herrmann A. Activation of the Catalytic Activity of Thrombin for Fibrin Formation by Ultrasound // Angew Chem Int Ed Engl. 2021. № 60. № 26. Р. 14707–14714. https://doi.org/10.1002/anie.202105404
- Zhiguo, E., Wang L., Zhou J. Splicing and alternative splicing in rice and humans // BMB Rep. 2013. V. 46. № 9. P. 439–447. https://doi.org/10.5483/bmbrep.2013.46.9.161
- Zhu L., Zhu L., Murtaza A., Liu Y., Liu S., Li J., Iqbal A., Xu X., Pan S., Hu W. Ultrasonic Processing Induced Activity and Structural Changes of Polyphenol Oxidase in Orange (Citrus sinensis Osbeck) // Molecules. 2019. № 24. № 10. Р. 1922. https://doi.org/10.3390/molecules24101922