Hydrogen Sulfide Led to a Modification in the Structure of Mitochondrial Membrane of Epicotyls of Pea Seedlings Pisum sativum L. under Water Deficit Conditions
- Authors: Gerasimov N.Y.1, Nevrova O.V1, Zhigacheva I.V1, Generozova I.P1,2, Goloshchapov A.N1
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Affiliations:
- N.M.Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
- K.A. Timiryazev Institute of Plant Physiology, Russian Academy of Sciences
- Issue: Vol 69, No 2 (2024)
- Pages: 277-285
- Section: Articles
- URL: https://journals.rcsi.science/0006-3029/article/view/257576
- DOI: https://doi.org/10.31857/S0006302924020086
- EDN: https://elibrary.ru/OUUKKR
- ID: 257576
Cite item
Abstract
About the authors
N. Yu Gerasimov
N.M.Emanuel Institute of Biochemical Physics, Russian Academy of Sciences
Email: n.yu.gerasimov@gmail.com
Moscow, Russia
O. V Nevrova
N.M.Emanuel Institute of Biochemical Physics, Russian Academy of SciencesMoscow, Russia
I. V Zhigacheva
N.M.Emanuel Institute of Biochemical Physics, Russian Academy of SciencesMoscow, Russia
I. P Generozova
N.M.Emanuel Institute of Biochemical Physics, Russian Academy of Sciences; K.A. Timiryazev Institute of Plant Physiology, Russian Academy of SciencesMoscow, Russia; Moscow, Russia
A. N Goloshchapov
N.M.Emanuel Institute of Biochemical Physics, Russian Academy of SciencesMoscow, Russia
References
- Nxele X., Klein A., and Ndimba B. K. Drought and salinity stress alters ROS accumulation, water retention, and osmolyte content in sorghum plants. S. Afr. J. Bot., 108, 261–266 (2017). doi: 10.1016/j.sajb.2016.11.003
- Bamagoos A., Alharby H., and Fahad S. Biochar coupling with phosphorus fertilization modifies antioxidant activity, osmolyte accumulation and reactive oxygen species synthesis in the leaves and xylem sap of rice cultivars under high-temperature stress. Physiol. Mol. Biol. Plants, 27 (9), 2083–2100 (2021). DOI: 10.1007%2Fs12298-021-01062-7
- Hetherington A. M., Hunter M. I. S., and Crawford R. M. M. Contrasting effects of anoxia on rhizome lipids in Iris species. Phytochemistry, 21 (6), 1275–1278 (1982). doi: 10.1016/0031-9422(82)80125-8
- Abbas S. R., Ahmad S. D., Sabir S. M., and Shah A.H. Detection of drought tolerant sugarcane genotypes (Saccharum officinarum) using lipid peroxidation, antioxidant activity, glycine-betaine and proline contents. J. Soil Sci. Plant Nutr., 14 (1), 233–243 (2014). doi: 10.4067/S0718-95162014005000019
- Ma D., Ding H., Wang C., Qin H., Han Q., Hou J., Lu H., Xie Y., and Guo T. Alleviation of drought stress by hydrogen sulfide is partially related to the abscisic acid signaling pathway in wheat. PLoS One, 11 (9), e0163082 (2016). doi: 10.1371/journal.pone.0163082
- Zhou Z.-H., Wang Y., Ye X.-Y., and Li Z.-G. Signaling molecule hydrogen sulfide improves seed germination and seedling growth of maize (Zea mays L.) under high temperature by inducing antioxidant system and osmolyte biosynthesis. Front. Plant Sci., 9, 1288 (2018). doi: 10.3389/fpls.2018.01288
- Cheng T., Shi J., Dong Y., Ma Y., Peng Y., Hu X., and Chen J. Hydrogen sulfide enhances poplar tolerance to high-temperature stress by increasing S-nitrosoglutathione reductase (GSNOR) activity and reducing reactive oxygen/nitrogen damage. Plant Growth Reg., 84 (1), 11–23 (2018). DOI: 10. 1007/s10725-017-0316-x
- Liu Z., Li Y., Cao C., Liang S., Ma Y., Liu X., and Pei Y. The role of H2S in low temperature-induced cucurbitacin C increases in cucumber. Plant Mol. Biol., 99 (6), 535–544 (2019). doi: 10.1007/s11103-019-00834-w
- Zhu C. Q., Zhang J. H., Sun L.M., Zhu L. F., Abliz B., Hu W. J., Zhong C., Bai Z. G., Sajid H., Cao X. C., and Jin Q. Y. Hydrogen sulfide alleviates aluminum toxicity via decreasing apoplast and symplast Al contents in rice. Front. Plant Sci., 9, 294 (2018). doi: 10.3389/fpls.2018.00294
- Tang X., An B., Cao D., Xu R., Wang S., Zhang Z., Liu X., and Sun X. Improving photosynthetic capacity, alleviating photosynthetic inhibition and oxidative stress under low temperature stress with exogenous hydrogen sulfide in blueberry seedlings. Front. Plant Sci., 11, 108 (2020). doi: 10.3389/fpls.2020.00108
- Bindu D. P., Solomon H. S., and Khosrow K. Effects of hydrogen sulfide on mitochondrial function and cellular bioenergetics. Redox Biol., 38, 101772 (2021). doi: 10.1016/j.redox.2020.101772
- Koch M. S. and Erskine J. M. Sulfide as a phytotoxin to the tropical seagrass Thalassia testudinum: interactions with light, salinity and temperature. J. Ex. Mar. Biol. Ecol., 266 (1), 81–95 (2001). doi: 10.1016/S0022-0981(01)00339-2
- Koch M. S., Mendelssohn I. A., and McKee K. L. Mechanism for the hydrogen sulphide-induced growth limitation in wetland macrophytes. Limnol. and Oceanogr., 35 (2), 399–408 (1990). doi: 10.4319/lo.1990.35.2.0399
- Li Z. G. Hydrogen sulfide: a multifunctional gaseous molecule in plants. Rus. J. Plant Physiol., 60 (6), 733– 740 (2013). doi: 10.1134/S1021443713060058
- Hancock J. T. and Whiteman M. Hydrogen sulfide signaling: interactions with nitric oxide and reactive oxygen species. Ann. N. Y. Acad. Sci., 1365 (1), 5–14 (2016). doi: 10.1111/nyas.12733
- Huo J., Huang D., Zhang J., Fang, H., Wang B., Wang C., and Liao W. Hydrogen sulfide: a gaseous molecule in postharvest freshness. Front. Plant Sci., 9, 1172 (2018). doi: 10.3389/fpls.2018.01172
- Kim J. Y., Lee H. J., Jung H. J., Maruyama K., Suzuki N., and Kang H. Overexpression of microRNA395c or 395e affects differently the seed germination of Arabidopsis thaliana under stress conditions. Planta, 232 (6), 1447–1454 (2010). doi: 10.1007/s00425-010-1267-x
- Sadeghian S. Y. and Yavari N. Effect of water‐deficit stress on germination and early seedling growth in sugar beet. J. Agron. Crop Sci., 190 (2), 138–144 (2004). doi: 10.1111/j.1439-037X.2004.00087.x
- Chen Z., Huang Y., Yang W., Chang G., Li P., Wei J., Yuan X., Huang J., and Hu X. The hydrogen sulfide signal enhances seed germination tolerance to high temperatures by retaining nuclear COP1 for HY5 degradation. Plant Sci., 285, 34–43 (2019). doi: 10.1016/j.plantsci.2019.04.024
- Zhao M., Liu Q., Zhang Y., Yang N., Wu G., Li Q., and Wang W. Alleviation of osmotic stress by H2S is related to regulated PLDα1 and suppressed ROS in Arabidopsis thaliana. J. Plant Res., 133 (3), 393–407 (2020). doi: 10.1007/s10265-020-01182-3
- Christou A., Filippou P., Manganaris G. A., and Fotopoulos V. Sodium hydrosulfide induces systemic thermotolerance to strawberry plants through transcriptional regulation of heat shock proteins and aquaporin. BMC Plant Biol., 14 (1), 42 (2014). doi: 10.1186/1471-2229-14-42
- Hu L. Y., Hu S.-L., Wu J, Li Y.-H., Zheng J.-L., Wei Z.-J., Liu J., Wang H.-L., Liu Y.-S., and Zhang H. Hydrogen sulfide prolongs postharvest shelf life of strawberry and plays an antioxidative role in fruits. J. Agric. Food Chem., 60 (35), 8684–8693 (2012). doi: 10.1021/jf300728h
- Li S.-P., Hu K.-D., Hu L.-Y., Li Y.-H., Jiang A.-M., Xiao F., Han Y., Liu Y.-S., and Zhang H. Hydrogen sulfide alleviates postharvest senescence of broccoli by modulating antioxidant defense and senescence-related gene expression. J. Agric. Food Chem., 62 (5), 1119–1129 (2014). doi: 10.1021/jf4047122
- Yao G.-F., Wei Z.-Z., Li T.-T., Tang J., Huang Z.-Q., Yang F., Li Y.-H., Han Z., Hu F., Hu L.-Y., Hu K.-D., and Zhang H. Modulation of enhanced antioxidant activity by hydrogen sulfide antagonization of ethylene in tomato fruit ripening. J. Agric. Food Chem., 66 (40), 10380–10387 (2018). doi: 10.1021/acs.jafc.8b03951
- Joshi N. C., Yadav D., Ratneret K., Kamara I., AvivSharon E., Irihimovitch V., and Charuvi D. Sodium hydrosulfide priming improves the response of photosynthesis to overnight frost and day high light in avocado (Persea americana Mill, cv.‘Hass’). Physiol. Plant., 168 (2), 394–405 (2020). doi: 10.1111/ppl.13023
- Ni Z.-J., Hu K.-D., Song C.-B., Ma R.-H., Li Z.-R., Zheng J.-L., Fu L.-H., Wei Z.-J., and Zhang H. Hydrogen sulfide alleviates postharvest senescence of grape by modulating the antioxidant defenses. Oxid. Med. Cell. Longev., 2016, 4715651 (2016). doi: 10.1155/2016/4715651
- Ge Y., Hu K.-D., Wang S.-S., Hu L.-Y., Chen X.-Y., Li Y.-H., Yang Y., Yang F., and Zhang H. Hydrogen sulfide alleviates postharvest ripening and senescence of banana by antagonizing the effect of ethylene. PLoS One, 12 (6), e0180113 (2017). doi: 10.1371/journal.pone.0180113
- Liu D., Li J., Li Z., and Pei Y. Hydrogen sulfide inhibits ethylene-induced petiole abscission in tomato (Solanum lycopersicum L.). Hort. Res., 7 (1), 14 (2020). doi: 10.1038/s41438-019-0237-0
- Бинюков В. И., Борунова С. Ф., Гольдфельд М. Г., Жукова И. Г., Кудлай Д. Г., Кузнецов А. Н., Шапиро А. Б. и Островский Д. Н. Исследование структурных переходов в биологических мембранах методом спинового зонда; температурные изменения мембран бактерий. Биохимия, 36 (6), 1149–1155 (1971).
- Вассерман А. М., Бучаченко А. Л., Коварский А. Л. и Нейман М. Б. Исследование молекулярных движений в полимерах методом парамагнитного зонда. Высокомолекуляр. соединения, 10А (8), 1930–1936 (1968).
- Lowry O. H., Rosebrough N. J., Farr A. L., and Randall R. J. Protein measurement with the Folin phenol reagent. J. Biol. Chem., 193 (1), 265–275 (1951).
- Комов В. П. и Шведова В. Н. Биохимия: учебник для вузов (Юрайт, М., 2021).
- Гендель Л. Я., Гольдфельд М. Г., Кольтовеp В. К., Розанцев Э. Г. и Сускина В. И. Исследование конформационных переходов в биомембранах методом слабо связанного парамагнитного зонда. Биофизика, 13 (6), 1114–1116 (1968).
- Герасимов Н. Ю., Неврова О. В., Жигачева И. В., Генерозова И. П. и Голощапов А. Н. Действие антиоксидантной системы «ресвератрол – серанитрозильный комплекс железа натрий-μ2-дитиосульфатотетранитрозилдиферрат» тетрагидрат на митохондрии эпикотилей проростков гороха in vitro». Биофизика, 68 (4), 653–659 (2023). doi: 10.31857/S000630292304004X
- Миль Е. М., Бинюков В. И., Жигачева И. В., Албантова А. А., Фаттахов С. Г., Коновалов А. И., Заиков Г. Е. и Тунакова Ю. А. Изучение влияния стрессовых воздействий и регулятора роста растений мелафена на митохондрии проростков гороха методом АСМ. Вестн. КНИТУ, 16 (13), 141–144 (2013).
- Конов К. Б. Исследование методами ЭПР воздействия криопротекторов сахарозы, трегалозы, глицерина и сорбита на структуру и динамику модельной липидной мембраны. Дис. к-та физ.-мат. наук (Каз. физ.-тех. инст. им. Е. К. Завойского, Казань, 2016).
- Ganong W. F. Review of Medical Physiology (McGrawHill Med., Minneapolis, 2005).
- Коваль И. В. Тиолы как синтоны. Rus. Chem. Rev., 62 (8), 769–786 (1993). DOI: 10.1070/ RC1993v062n08ABEH000046