Physiological responses of orchids to prolonged clinorotation

  • N. V. Zaimenko M. M. Gryshko National Botanical Garden of the National Academy of Sciences of Ukraine
  • B. O. Ivanytska M. M. Gryshko National Botanical Garden of the National Academy of Sciences of Ukraine
  • N. V. Rositska M. M. Gryshko National Botanical Garden of the National Academy of Sciences of Ukraine
  • N. P. Didyk M. M. Gryshko National Botanical Garden of the National Academy of Sciences of Ukraine
  • D. Liu United Institute of Modern Technologies (UIoMT)
  • M. Pyzyk United Institute of Modern Technologies (UIoMT)
  • J. Slaski Bio-Industrial Services Division, InnoTech Alberta
Keywords: Cypripedium flavum; Angraecum eburneum; Epidendrum radicans; clinorotation; adaptive reactions.

Abstract

Creation of plant-based bioregenerative life support systems is crucial for future long-duration space exploring missions. Microgravity is one of the major stresses affecting plant growth and development under space flight conditions. Search for higher plant genotypes resilient to microgravity as well as revealing of biological features which could be used as markers of such resilience is rather urgently needed. The objective of this study was to analyze physiological and biochemical responses of three orchid species representing different life forms (terrestrial and epiphytic), growth types (monopodial and sympodial) and pathways of CO2 fixation to long-term (24 months) clinorotation which modeled the combined effect of two stress factors: hermetic conditions and microgravity. Three years old meristematic orchids Cypripedium flavum, Angraecum eburneum, Epidendrum radicans, representing different life forms, types of branching shoot system and pathways of CO2 fixation, were used as test-plants. The microgravity was simulated using three-dimensional (3-D) clinostat equipped with two rotation axes placed at right angles (rotation frequency was 3 rpm) in controlled conditions of air temperature, illumination, air humidity and substrate moisture. The control plants were grown in the similar plastic vessels but not hermetically sealed and without clinorotating in the same environmental conditions. The vital state of the test plants was assessed using characteristics of mineral nutrition, content of photosynthetic pigments, free amino acids, soluble proteins, DNA and RNA, enzymatic and non-enzymatic antioxidants. The results of this study confirmed that orchids grown under simulated microgravity and kept in hermetically-sealed vessels were subjected to oxidative stress, which could be responsible for the observed inhibition of basic physiological processes such as mineral nutrition, metabolism of aminoacids, protein biosynthesis and photosynthesis. Monopodial orchids C. flavum and A. eburneum demonstrated better adaptation to prolonged clinorotation as compared to sympodial E. radicans. In particular, the latter demonstrated some stimulation of mineral nutrition processes (i.e. K, N, Fe, Mn, Zn accumulation), content of photosynthetic pigments, proline and superoxide dismutase activity. Long-lasting clinorotation induced adaptive changes of antioxidant systems in the studied orchids (e.i. increase in carotenoids and proline content and stimulation of superoxide dismutase activity), which helped to maintain the main physiological functions at stable level in the above-mentioned stressful conditions. The following biochemical characteristics in the studied orchids could be considered as markers of resilience to simulated microgravity and hermetic conditions: 1) an increase in the accumulation of non-enzymatic (proline, carotenoids) and enzymatic antioxidants (superoxide dismutase); 2) ability to maintain stable balance of mineral nutrients; 3) increase in the content of photosynthetic pigments; 4) increase in the content of proteinogenic amino acids and soluble proteins; 5) increase in the DNA content or RNA/DNA ratio. Our studies have also demonstrated a correlation between orchid ecomorphological characteristics such as type of branching with their adaptive responses to prolonged clinorotation. We observed no correlation between the studied life form of orchids, ecotype or the pathway of CO2 fixation and their resilience to prolonged clinorotation. This research can be a starting point for studying the relationships between ecomorphological features of various orchids and their resilience to microgravity conditions in the search for biological markers of microgravity tolerance in species of higher plants.

References

Ábrahám, E., Cabassa, C., Erdei, L., & Szabados, L. (2010). Methods for determination of proline in plants. Methods in Molecular Biology, 639, 317–331.

Alscher, R., Erturk, N., & Heath, L. S. (2002). Role of superoxide dismutase (SODs) in controlling oxidative stress in plants. Journal of Experimental Botany, 53(372), 1331–1341.

Assimakopoulos, S. F., Mavrakis, A. G., Grintzalis, K., Papapostolou, I., Zervouda-kis, G., Konstantinou, D., Chroni, E., Vagianos, C. E., & Georgiou, C. (2008). Superoxide radical formation in diverse organs of rats with experimentally in-duced obstructive jaundice. Redox Report, 13(4), 179–184.

Batiha, G. E. S., Beshbishy, A. M., Adeyemi, O. S., Nadwa, E. H., Rashwan, E., Kadry, M., Alkazmi, L. M., Elkelish, A. A., & Igarashi, I. (2020). Phytochemi-cal screening and antiprotozoal effects of the methanolic Berberis vulgaris and acetonic Rhuscoriaria extracts. Molecules, 25(3), 550.

Brykov, V., Kovalenko, E. Y., & Ivanytska, B. A. (2018). Microcosm as a perspective model for biological experiment at nanosatellite. Space Science and Technology, 24(2), 55–59.

Buyun, L., Cherevchenko, T., Kovalska, L., & Ivannikov, R. (2015). Reproductive biology of Angraecum eburneum subsp. superbum (Orchidaceae) under glass-house conditions. Environmental and Experimental Biology, 13, 33–39.

Cherevchenko, T. M., Zaimenko, N. V., & Kharitonova, I. P. (2000). Growth and contents of some assimilates inleaves of orchids influenced by the long clinostation. Ukrayinsky Botanichny Zhurnal, 56(l), 83–88 (in Ukrainian).

Cherevchenko, T. M., Zaimenko, N. V., & Martynenko, E. I. (2000). Biokhimichni osoblyvosti epifitnykh ta nazemnykh orkhidey [Biochemical features of epi-phytic and terrestrial orchids]. Fisiologiya i Biokhimiya Kulturnykh Rasteniy, 32(2), 121–127 (in Ukrainian).

Efimov, P. G. (2020). Orchids of Russia: Annotated checklist and geographic distribution. Nature Conservation Research, 5(Suppl. 1), 1–18.

Fabro, G., Kovacs, I., Pavet, V., Szabados, L., & Alvarez, M. E. (2004). Proline accumulation and AtP5CS2 gene activation are induced by plant pathogen in-compatible interactions in Arabidopsis. Molecular Plant-Microbe Interactions Journal, 17, 343–350.

Firmansyah, & Argosubekti, N. (2020). A review of heat stress signaling in plants. IOP Conference Series: Earth and Environmental Science, 484, 012041.

Gholizadeh, A., Saberioon, M., Borůvka L., Wayayok, A., Amin, M., & Soom, M. (2017). Leaf chlorophyll and nitrogen dynamics and their relationship to low-land rice yield for site-specific paddy management. Information Processing in Agriculture, 4(4), 259–268.

Hellmann, H., Funck, D., Rentsch, D., & Frommer, W. B. (2000). Hypersensitivity of an Arabidopsis sugar signaling mutant toward exogenous proline application. Plant Physiology, 122(2), 779–789.

Hiscox, J. D., & Israelstam, C. F. (1979). A method for the extraction of chlorophyll from leaf tissue without maceration. Canadian Journal of Botany, 57, 1332–1334.

Jaleel, C. A., Manivannan, P., Wahid, A., Farooq, M., Al-Juburi, H. J., Somasunda-ram, R., & Panneerselvam, R. (2009). Drought stress in plants: A review on morphological characteristics and pigments composition. International Journal of Agriculture and Biology, 11(1), 100–105.

Jiao, S., Hilaire, E., Paulsen, A. Q., & Guikema, J. A. (2004). Brassica rapa plants adapted to microgravity with reduced photosystem I and its photochemical ac-tivity. Physiologia Plantarum, 122(2), 281–290.

Khapugin, A. A. (2020). A global systematic review on orchid data in protected areas. Nature Conservation Research, 5(Suppl. 1), 19–33.

Khodadad, C. L., Hummerick, M. E., Spencer, L. E., Dixit, A. R., Richards, J. T., Romeyn, M. W., Smith, T. M., Wheeler, R. M., & Massa, G. D. (2020). Mi-crobiological and nutritional analysis of lettuce crops grown on the International Space Station. Frontiers in Plant Science, 11, 199.

Kibinza, S., Bazin, J., Bailly, C., Farrant, J. M., Corbineau, F., & El-Maarouf-Bouteau, H. (2011). Catalase is a key enzyme in seed recovery from ageing during priming. Plant Science, 181(3), 309–315.

Kirillova, I. A., & Kirillov, D. V. (2021). Reproductive success of orchids at the northern border of their distribution areas (North-East of European Russia). Nature Conservation Research, 6(1), 17–27.

Kiss J. Z., Wolverton, C., Wyatt, S. E., Hasenstein, K. H., & van Loon, J. (2019). Comparison of microgravity analogs to spaceflight in studies of plant growth and development. Frontiers in Plant Science, 10, 1577.

Kochubey, S. M., Adamchuk, N. I., Kordyum, E. I., & Guikema, J. A. (2004). Microgravity affects the photosynthetic apparatus of Brassica rapa. Plant Biosystems, 138, 1–9.

Li, J., Cang, Z., Jiao, F., Bai, X., Zhang, D., & Zhai, R. (2015). Influence of drought stress on photosynthetic characteristics and protective enzymes of potato at seedling stage. Journal of the Saudi Society of Agricultural Sciences, 16(1), 82–88.

McElroy, J. S., & Kopsell, D. A. (2009). Physiological role of carotenoids and other antioxidants in plants and application to turfgrass stress management. New Zealand Journal of Crop and Horticultural Science, 37(4), 327–333.

Moreno-Villanueva, M., Wong, M., & Wu, H. (2017). Interplay of space radiation and microgravity in DNA damage and DNA damage response. npj Micro-gravity, 3, 14.

Muthukumar, T., & Shenbagam, M. (2017). Vegetative anatomical adaptations of Epidendrum radicans (Epidendroideae, Orchidaceae) to epiphytic conditions of growth. Modern Phytomorphology, 11, 117–130.

Oluwafemi, F. A., & Olubiyi, R. A. (2019). Investigation of corn seeds growth under simulated microgravity. Arid Zone Journal of Engineering, Technology and Environment, 15, 110–115.

Ovchinnikov, Y. A. (1974). Novye metody analisa aminokislot, peptidov, proteinov [New methods of analysis of aminoacids, peptides, proteins]. Mir, Moscow (in Russian).

Paul, A.-L., Sing, N. J., Zupanska, A. K., Krishnamurthy, A., Schultz, E. R., & Ferl, R. J. (2017). Genetic dissection of the Arabidopsis spaceflight transcriptome: Are some responses dispensable for the physiological adaptation of plants to spaceflight? PLoS One, 12(6), e0180186.

Pratelli, R., & Pilot, G. (2014). Regulation of amino acid metabolic enzymes and transporters in plants. Journal of Experimental Botany, 65, 5535–5556.

Sadak, S. H. M., Abdelhamid, M. T., & Schmidhalter, U. (2015). Effect of foliar application of aminoacids on plant yield and physiological parameters in bean plants irrigated with seawater. Acta Biologica Colombiana, 20(1), 141–152.

Scandalios, J. G. (1993). Oxygen stress and superoxide dismutases. Plant Physiology, 101(1), 7–12.

Sharma, S. S., & Dietz, K. J. (2009). Review. The relationship between metal toxicity and cellular redox imbalance. Trends in Plant Science, 14(1), 43–50.

Soliman, M. H., Alayafi, A. A. M., El Kelish, A. A., & Abu-Elsaoud, A. M. (2018). Acetylsalicylic acid enhance tolerance of Phaseolus vulgaris L. to chilling stress, improving photosynthesis, antioxidants and expression of cold stress res-ponsive genes. Botanical Studies, 59(1), 6.

Stutte, G. W., Monje, O., HatWeld, R. D., Paul, A.-L., Ferl, R. J., & Simone, C. G. (2006). Microgravity effects on leaf morphology, cell structure, carbon metabolism and mRNA expression of dwarf wheat. Planta, 224, 1038–1049.

Tang, W., & Newton, R. (2005). Polyamines reduce salt-induced oxidative damage by increasing the activities of antioxidant enzymes and decreasing lipid peroxi-dation in Virginia pine. Plant Growth Regulation, 46, 31–43.

Tay, S., He, J., & Yam, T. W. (2019). CAM plasticity in epiphytic tropical orchid species responding to environmental stress. Botanical Studies, 60(7), 1–15.

Wang, H. F., & Zhan, H. J. (2009). The research progress in determination of cata-lase activity. Science and Technology Innovation Herald, 19, 7–8.

Weber, H., Chetelat, A., Reymond, P., & Farmer, E. E. (2004). Selective and power-ful stress gene expression in Arabidopsis in response to malondialdehyde. The Plant Journal, 37(6), 877–888.

Wolff, S., Coelho, L., Zabrodina, M., & Brinckmann, E. (2013). Plant mineral nutrition, gas exchange and photosynthesis in space: A review. Advances in Space Research, 51, 465–475.

Wolff, S., Palma, C., Marcelis, L. F. M., Jost, A.-I., & van Delden, S. (2018). Testing new concepts for crop cultivation in space: Effects of rooting volume and nitrogen availability. Life, 8(4), 45.

Wyszkowski, M. (1996). Sklad aminokwsowy bialka bulwczterechodmianziemniaka w zaleznosci od nawozenia azotem. Acta Academiae Agriculturae ac Technicae Olstenensis, Agricultura, 63, 129–138.

Yang, L. Y., Yang, S. L., Li, J. Y., Ma, J. H., Pang, T., Zou, C. M., He, B., & Gong, M. (2018). Effects of different growth temperatures on growth, development, and plastid pigments metabolism of tobacco (Nicotiana tabacum L.) plants. Botanical Studies, 59, 5.

Zabel, P., Bamseya, M., Schubert, D., & Tajmar, M. (2016). Review and analysis of over 40 years of space plant growth systems. Life Sciences in Space Research, 10, 1–16.

Zaimenko, N. V. (1999). Effect of clinostating on physiological-biochemical processes in tropical orchids. Ukrainian Botanical Journal, 56(2), 174–179.

Zaimenko, N. V., Didyk, N. P., Ellanska, N. E., Ivanytska, B. O., Pavluchenko, N. A., Rakhmetov, D. B., & Kharytonova, I. P. (2016). Implementation of new technique for phyto and chemical melioration of acidic and saline soils. Science and Innovation, 12(1), 58–68.

Zaimenko, N. V., Didyk, N. P., Pavliuchenko, N. A., Ivanytska, B. O., Kharytonova, I. P., & Rositska, N. V. (2018). Natural silicates mixed with organic fertilizers enhance corn adaptation to salt stress and improve physical characteristics of sandy soil. Journal of Crop Improvement, 20, 188–207.

Zhao, Q., Li, J., & Liu, M. (2002). Effects of simulated microgravity on characteris-tics of photosynthesis in plant seedling. Space Medicine and Medical Engineer-ing (Beijing), 15(2), 79–83.

Zheng, H. Q., Han, F., & Le, J. (2015). Higher plants in space: Microgravity perception, response, and adaptation. Microgravity Science and Technology, 27, 377–386.

Published
2021-10-27
Section
Articles

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