Free Sterols of Young Needles of Some Species of the Genus Picea during the Period of Active Growth

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Abstract

Using the method of gas chromatography-mass spectrometry, a comparative analysis of the qualitative and quantitative composition of free sterols in the tissues of young growing needles of native (two varieties of Siberian spruce: Picea obovata and P. obovata var. coerulea) and introduced (P. abies, P. pungens) species of the genus Picea growing in the Southern Baikal region was carried out depending on the development phase. The absolute weight of total lipids in the four studied taxa at different growth stages differed and had a species-specific character. It was shown that at the transition boundary between the phases of needle growth (intercalary and cell growth by extension), lipid content increased in all the studied spruce species. Among the free sterols, the main common ∆5-sterols were found, namely β-sitosterol, campesterol, stigmasterol, and cholesterol. The dominant sterol for all the studied taxa was β-sitosterol, its content was 80–95% of the total free sterols. It was shown that for the introduced (non-indigenous) species, the maximum β-sitosterol content occurred during the period of cell growth by stretching, and for the native spruces, the maximum values of β-sitosterol content were found during the period of intercalary growth. It was found that at the beginning of needle formation (intercalary growth), high sterol content is necessary, and it decreases as the needles grow and develop. A decrease in sterol content may be associated with their use as a substrate in the synthesis of other compounds; for example, β-sitosterol and campesterol are precursors of brassinosteroids. In general, the temporal dynamics of sterol composition changes and the progression of active needle growth phases differed between introduced and native spruce species.

About the authors

N. V Semenova

Federal State Budgetary Scientific Institution Siberian Institute of Plant Physiology and Biochemistry, Siberian Branch of the Russian Academy of Sciences

Email: tashasemyonova@mail.ru
Irkutsk, Russia

L. V Dudareva

Federal State Budgetary Scientific Institution Siberian Institute of Plant Physiology and Biochemistry, Siberian Branch of the Russian Academy of Sciences

Irkutsk, Russia

E. V Spiridonova

Federal State Budgetary Scientific Institution Siberian Institute of Plant Physiology and Biochemistry, Siberian Branch of the Russian Academy of Sciences

Irkutsk, Russia

E. G Rudikovskaya

Federal State Budgetary Scientific Institution Siberian Institute of Plant Physiology and Biochemistry, Siberian Branch of the Russian Academy of Sciences

Irkutsk, Russia

References

  1. Громадин А.В. 2010. Дендрология: учебное пособие. М.: Изд-во РГАУ – МСХА имени К.А. Тимирязева. 848 с.
  2. Farjon A. 2018. The kew review: Conifers of the world. Kew Bulletin. 73 (1), 1–16.
  3. Алексеев В.А., Связева О.А. 2009. Древесные растения лесов России. Список видов и государственный учет биоразнообразия лесных ресурсов. Красноярск: СО РАН, Институт леса им. В.Н. Сукачева. 182 с.
  4. Рысин Л.П. 2012. Хвойные леса России. Изв. Самарского научного центра РАН. 14 (1(4)), 1106–1109.
  5. Робакидзе Е.А., Патов А.И. 2011. Рост хвои ели сибирской (Picea obovata Ledeb.) в зависимости от экологических факторов. Лесной журн. 3, 7–14.
  6. Бенькова А.В., Шашкин А.В. 2003. Фотосинтез сосны и лиственницы и его связь с радиальным приростом. Лесоведение. 5, 38–43.
  7. Силкина О.В., Винокурова Р.И. 2009. Сезонная динамика содержания хлорофиллов и микроэлементов в формирующейся хвое Abies sibirica и Picea abies. Физюл. растений. 56 (6), 864–870.
  8. Алаудинова Е.В., Поваляева В.А., Миронов П.В. 2010. Липиды меристем лесообразующих хвойных пород центральной сибири в условиях низкотемпературной адаптации. 3. Особенности обмена нейтральных липидов меристем почек Larix sibirica Ledeb., Picea obovata L. и Pinus sylvestris L. Химия растит. сырья. 1, 67–74.
  9. Нохсоров В.В., Дударева Л.В., Петров К.А. 2019. Состав и содержание липидов и их жирных кислот в хвое Pinus sylvestris L. и Picea obovata Ledeb. при закаливании к низкой температуре в условиях криолитозоны Якутии. Физюл. растений. 66 (4), 286–294.
  10. Jablonsky M., Vernarecová M., Ház A., Dubinyová L., Skulcova A., Sladková A., Surina I. 2015. Extraction of phenolic and lipophilic compounds from spruce (Picea abies) bark using accelerated solvent extraction by ethanol. Wood Res. 60 (4), 583–590.
  11. Kreis W., Muller-Uri F. 2010. Biochemistry of sterols, cardiac glycosides, brassinosteroids, phytoecdysteroids and steroid saponins. Annu. Plant Rev. 40, 304–363. https://www.doi.org/10.1002/9781119312994.apr0428
  12. Carland F.M., Fujioka S., Takatsuto S., Yoshida S., Nelson T. 2002. The identification of CVP1 reveals a role for sterols in vascular patterning. Plant Cell. 14, 2045–2058. https://www.doi.org/10.1105/tpc.003939
  13. Qian P., Han B., Forestier E., Hu Z., Gao N., Lu W., Shaller H., Li J., Hou, S. 2013. Sterols are required for cell-fate commitment and maintenance of the stomatal lineage in Arabidopsis. Plant J. 74 (6), 1029–1044. https://www.doi.org/10.1111/tpj.12190
  14. Shahzad R., Ewas M., Harlina P.W., Khan S.U., Zhenyuan P., Nie X., Nishawy E. 2021. β-Sitosterol differentially regulates key metabolites for growth improvement and stress tolerance in rice plants during prolonged UV-B stress. J. Genet. Eng. Biotechnol. 19 (1), 79–95. https://www.doi.org/10.1186/s43141-021-00183-6
  15. Du Y., Fu X., Chu Y., Wu P., Liu Y., Ma L., Tian H., Zhu B. 2022. Biosynthesis and the role of plant sterols in development and stress responses. Int. J. Mol. Sci. 23, 2332–2354. https://www.doi.org/10.3390/ijms23042332
  16. Семенова Н.В., Шмаков В.Н., Константинов Ю.М., Дударева Л.В. 2023. Сравнительный анализ состава стеринов эмбриогенных и неэмбриогенных клеточных линий Larix sibirica Ledeb. Физюл. растений. 70 (2), 181–191.
  17. Сулкарнаева А.Г., Валитова Ю.Н., Мухитова Ф.К., Минибаева Ф.В. 2014. Стресс-индуцированные изменения мембранных стеринов в корнях пшеницы. ДАН. 455 (2), 229–231.
  18. Willmann M. R. 2000. Sterols as regulators of plant embryogenesis. Trends Plant Sci. 5 (10), 416.
  19. Валитова Ю.Н., Сулкарнаева А.Г., Минибаева Ф.В. 2016. Растительные стерины: многообразие, биосинтез, физиологические функции. Биохимия. 81 (8), 1050–1068.
  20. Hartmann M.A. 1998. Plant sterols and the membrane environment. Trends Plant Sci. 3 (5), 170–175. https://www.doi.org/10.1016/S1360-1385(98)01233-3
  21. Bajguz A., Chmur M., Gruszka D. 2020. Comprehensive overview of the Brassinosteroid biosynthesis pathways: Substrates, products, inhibitors, and connections. Front. Plant Sci. 11, 1034–1043. https://www.doi.org/10.3389/fpls.2020.01034
  22. Clouse S.D. 2011. Brassinosteroid signal transduction: from receptor kinase activation to transcriptional networks regulating plant development. Plant Cell. 23 (4), 1219–1230. https://www.doi.org/10.1105/tpc.111.084475
  23. Tian X., Xuan L., Liu B., Hu T., Wang C., Wang X. 2018. Effects of heterologous expression of Populus euphratica brassinosteroids biosynthetic enzyme genes CPD (PeCPD) and DWF4 (PeDWF4) on tissue dedifferentiation and growth of Arabidopsis thaliana seedlings. PCTOC. 132 (1), 111–121. https://www.doi.org/10.1007/s11240-017-1316-2
  24. Zhiponova M.K., Vanhoutte I., Boudolf V., Betti C., Dhondt S., Coppens F., Mylle E., Maes S., Gonzalez-Garcia M.P., Cano-Delgano A.I., Inze D., Beemster G.T.S., De Veylder L., Russinova E. 2013. Brassinosteroid production and signaling differentially control cell division and expansion in the leaf. New Phytol. 197 (2), 490–502. https://www.doi.org/10.1111/nph.12036
  25. Ермошин А.А., Киселева И.С., Борцова С.А., Санаева Ю.В., Алексеева В.В. 2016. Морфологические особенности побега трансгенных растений табака, экспрессирующих ген синтеза 3-окси-3-метилглутарил-КоА редуктазы (HMG1) в прямой и обработанной ориентациях относительно промотора. Онтогенез. 47 (4), 244–250.
  26. Кищенко И.Т. 2020. Динамика содержания азотистых веществ и липидов в хвое интродуцированных видов Picea A. Dietr. в таежной зоне (Карелия). Вестник Пермского университета. Сер. биол. 1, 4–12.
  27. Valitova J., Renkova A., Beckett R., Minibayeva F. 2024. Stigmasterol: An enigmatic plant stress sterol with versatile functions. Int. J. Mol. Sci. 25, 8122–8141. https://www.doi.org/10.3390/ijms25158122
  28. Li Z., Cheng B., Yong B., Liu T., Peng Y., Zhang X., Ma X., Huang L., Liu W., Nie G. 2019. Metabolomics and physiological analyses reveal β-sitosterol as an important plant growth regulator inducing tolerance to water stress in white clover. Planta. 250, 2033–2046. https://www.doi.org/10.1007/s00425-019-03277-1
  29. Ines C., Corbacho J., Paredes M.A., Labrador J., Cordeiro A.M., Gomez-Jimenez M.C. 2019. Regulation of sterol content and biosynthetic gene expression during flower opening and early fruit development in olive. Physiol. Plant. 167 (4), 526–539. https://www.doi.org/10.1111/ppl.12969
  30. Deng S., Wei T., Tan K., Hu M., Li F., Zhai Y., Ye S., Xiao Y., Hou L., Pei Y., Luo M. 2016. Phytosterol content and the campesterol: Sitosterol ratio influence cotton fiber development: role of phytosterols in cell elongation. Sci. China Life Sci. 59 (2), 183–193. https://www.doi.org/10.1007/s11427-015-4992-3
  31. Jang J.C., Fujioka S., Tasaka M., Seto H., Takatsuto S., Ishii A., Aida M., Yoshida S., Sheen J. 2000. A critical role of sterols in embryonic patterning and meristem programming revealed by the fackel mutants of Arabidopsis thaliana. Genes Dev. 14 (12), 1485–1497.
  32. Diener C.A., Li H., Zhou W.X., Whoriskey W.J., Nes W.D., Fink G.R. 2000. Sterol methyltransferase 1 controls the level of cholesterol in plants. Plant Cell. 12, 853–870. https://www.doi.org/10.1105/tpc.12.6.853
  33. Nakamoto M., Schmit A.C., Heintz D., Schaller H., Ohta D. 2015. Diversification of sterol methyltransferase enzymes in plants and a role for β-sitostero in oriented cell plate formation and polarized growth. Plant J. 84 (5), 860–874. https://www.doi.org/10.1111/tpj.13043
  34. Niu Q., Tan K., Zang Z., Xiao Z., Chen K., Hu M., Luo M. 2019. Modification of phytosterol composition influences cotton fiber cell elongation and secondary cell wall deposition. BMC Plant. Biol. 19, 208. https://www.doi.org/10.1186/s12870-019-1830-y
  35. Aboobucker S.I., Suza W.P. 2019. Why do plants convert sitosterol to stigmasterol? Front. Plant Sci. 10, 354. https://www.doi.org/10.3389/fpls.2019.00354
  36. Stalleart V.M., Geuns J.M.C. 1994. Phospholipids and free sterol composition of hypocotyl plasma membranes of ageing munq bean seedlings. Phytochemistry. 36 (5), 1177–1180. https://www.doi.org/10.1016/S0031-9422(00)89633-8
  37. Hõll W., Goller I. 1982. Free sterols and steryl esters in the trunkwood of Picea abies (L.) Karst. Z. Pflanzenphysiol. 106 (5), 409–418.

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