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Trade-off Between Salt Secretion and Gas Exchange by Stomata in the Leaves of Glycyrrhiza uralensis


Affiliations
1 Ministry of Education Key Laboratory of Xinjiang Phytomedicine Resource Utilization, College of Life Sciences, Shihezi University, Xinjiang 832003, China
 

Our previous study found that stomata in the leaves of Glycyrrhiza uralensis (licorice) could secrete salt crystals. In theory, secretion of salt should affect the normal functioning of stomata, thereby affecting the growth and development of G. uralensis; however, its population grows well. We suspect that there may be a trade-off between stomatal salt secretion and gas exchange from the leaves at different positions. Therefore, we compared stomatal salt secretion capacity, chlorophyll content, anatomical structure, net photosynthetic rate and stomatal conductance from the leaves at different positions of licorice. The stomata of lower leaves exhibited strongest salt secretion capacity, whereas the stomata of upper leaves did not secrete any salt. Additionally, the upper and middle leaves had significantly higher chlorophyll content than the lower leaves. The arrangement of mesophyll cells in the upper leaves was densest, and that in the lower leaves was least dense. The net photosynthetic rate and stomatal conductance in the upper leaves were highest, and those in the lower leaves were lowest. We conclude that the stomata of upper leaves are mainly used for gas exchange. In contrast, stomata of lower leaves, showing weak photosynthesis, are responsible for secreting excessive salt to maintain the inner ion balance and ensure normal metabolism in G. uralensis.

Keywords

Licorice, Stomata, Salt Secretion.
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  • Zhang, W., Lan, F. and Hong, X. X., Chinese Pharmacopoeia, China Medical Science and Technology Press, Beijing, 2015.
  • Gafner, S. et al., Isoflavonoids and coumarins from Glycyrrhiza uralensis: antibacterial activity against oral pathogens and conversion of isoflavans into isoflavan-quinones during purification. J. Nat. Prod., 2011, 74, 2514–2519; doi:10.1021/np2004775.
  • Saha, S. et al., Structural features and in vivo antitussive activity of the water extracted polymer from Glycyrrhiza glabra. Int. J. Biol. Macromol., 2011, 48, 634–638; doi:10.1016/j.ijbiomac.2011.02.003.
  • Yazdi, A., Sardari, S. and Sayyah, M., Evaluation of the anticonvulsant activity of the leaves of Glycyrrhiza glabra var. glandulifera grown in Iran, as a possible renewable source for anticonvulsant compounds. IJPR, 2011, 10, 75–82.
  • Wang, J., Chen, X. Q. and Wang, W., Glycyrrhizic acid as the antiviral component of Glycyrrhiza uralensis Fisch. against coxsackievirus A16 and enterovirus 71 of hand foot and mouth disease. J. Ethnopharmacol., 2013, 147, 114–121; doi:10.1016/j.jep.2013.02.017.
  • Kwon, H. J. et al., In vitro anti-rotavirus activity of polyphenol compounds isolated from the ischolar_mains of uralensis. Bioorgan. Med. Chem., 2010, 18, 7668–7674.
  • Shetty, T. K., Satav, J. G. and Nair, C. K. K., Protection of DNA and microsomal membranes in vitro by Glycyrrhiza glabra L. against gamma irradiation. Phytother. Res., 2002, 16, 576–578; doi:10.1002/ptr.927.
  • Cai, H., Chen, X. and Zhang, J. B., 18β -glycyrrhetinic acid inhibits migration and invasion of human gastric cancer cells via the ROS/PKC-α/ERK pathway. J. Nat. Med., 2017, 72, 252–259; doi:10.1007/s11418-017-1145-y.
  • Zhao, K. F. and Feng, L. T., Chinese Halophyte Resources, Science Press, Beijing, 2001.
  • Bhatt, A. and Santo, A., Effects of photoperiod, thermoperiod and salt stress on Gymnocarpos decandrus seeds: potential implications in restoration ecology activities. Botany, 2017, 95, 1093– 1098.
  • Pan, Y., Wu, L. J. and Yu, Z. L., Effect of salt and drought stress on antioxidant enzymes activities and SOD isoenzymes of liquorice (Glycyrrhiza uralensis Fisch). Plant Growth Regul., 2006, 49, 157–165.
  • Belin, C., Thomine, S. and Schroeder, J., Water balance and the regulation of stomatal movements. In Abiotic Stress Adaptation in Plants (eds Pareek, A., Sopory, S. and Bohnert, H.), Springer, The Netherlands, 2009.
  • Melotto, M. et al., Plant stomata function in innate immunity against bacterial invasion. Cell, 2006, 126, 969–980; doi:0.1016/ j.cell.2006.06.054.
  • Liu, M. H. et al., Influence of leaf size of plant on leaf transpiration and temperature in arid regions. Chin. J. Plant Ecol., 2013, 37, 436–442; doi:10.3724/SP.J.1258.2013.00045.
  • Wei, C. X., Wang, J. B. and Chen, Y. F., Epicuticular wax of leaf epidermis: a functional structure for salt excretion in a halophyte Puccinellia tenuiflora. Acta Ecol. Sin., 2004, 24, 2451–2456.
  • Khan, N. A., NaCl-inhibited chlorophyll synthesis and associated changes in ethylene evolution and antioxidative enzyme activities in wheat. Biol. Plantarum., 2003, 47, 437–440; doi:10.1023/ b:biop.0000023890.01126.43.
  • Bao, S. D., Soil Agricultural Chemistry Analysis, China Agricultural Press, Beijing, 2000.
  • Callejas, R. et al., Evaluation of a non-destructive method to estimate the concentration of chlorophyll in leaves of table grape cv. Idesia (Arica), 2013, 31, 19–26.
  • He, N. P. et al., Variation in leaf anatomical traits from tropical to cold-temperate forests and linkage to ecosystem functions. Funct. Ecol., 2017, 32, 10–19; doi:10.1111/1365-2435.12934.
  • Koster, P. et al., The battle of two ions: Ca2+ signalling against Na+ stress. Plant Biol., 2019, 21, 39–48; doi:10.1111/plb.12704.
  • Pritchard, S. G. et al., Calcium sulfate deposits associated with needle substomatal cavities of container-grown longleaf pine (Pinus palustris) seedlings. Int. J. Plant Sci., 2000, 161, 917–923.
  • Michael, F. R. et al., How can stomata contribute to salt tolerance? Ann. Bot-London, 1997, 80, 387–393.
  • Hao, J. B., Zhang, F. S. and Tian, C. Y., Halophytes in Xinjiang, Science Press, Beijing, 2006.
  • Xie, Z. C., Luo, D. and Zhang, W. J., Effects of silicon on cell microscopic structure under salt stress of Glycyrrhiza uralensis. J. Chin. Med. Mater., 2016, 39, 2698–2701; doi:10.13863/ j.issn1001-4454.2016.12.006.
  • Jothiramshekar, S. et al., Responses of selected C3 and C4 halophytes to elevated CO2 concentration under salinity. Curr. Sci., 2018, 115, 129–135.
  • Mehta, P., Jajoo, A. and Mathur, S., Chlorophyll a fluorescence study revealing effects of high salt stress on Photosystem II in wheat leaves. Plant Physiol. Bioch., 2010, 48, 16–20.
  • Joshi, S. C. and Palni, L. M. S., Is dew useful for Himalayan plants? Curr. Sci., 2010, 99, 1434–1439.
  • Wong, S. C., Cowan, I. R. and Farquhar, G. D., Stomatal conductance correlates with photosynthetic capacity. Nature, 1979, 282, 424–426.

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  • Trade-off Between Salt Secretion and Gas Exchange by Stomata in the Leaves of Glycyrrhiza uralensis

Abstract Views: 150  |  PDF Views: 88

Authors

Peng You Chen
Ministry of Education Key Laboratory of Xinjiang Phytomedicine Resource Utilization, College of Life Sciences, Shihezi University, Xinjiang 832003, China
Miao Ma
Ministry of Education Key Laboratory of Xinjiang Phytomedicine Resource Utilization, College of Life Sciences, Shihezi University, Xinjiang 832003, China
Ling yu Shi
Ministry of Education Key Laboratory of Xinjiang Phytomedicine Resource Utilization, College of Life Sciences, Shihezi University, Xinjiang 832003, China

Abstract


Our previous study found that stomata in the leaves of Glycyrrhiza uralensis (licorice) could secrete salt crystals. In theory, secretion of salt should affect the normal functioning of stomata, thereby affecting the growth and development of G. uralensis; however, its population grows well. We suspect that there may be a trade-off between stomatal salt secretion and gas exchange from the leaves at different positions. Therefore, we compared stomatal salt secretion capacity, chlorophyll content, anatomical structure, net photosynthetic rate and stomatal conductance from the leaves at different positions of licorice. The stomata of lower leaves exhibited strongest salt secretion capacity, whereas the stomata of upper leaves did not secrete any salt. Additionally, the upper and middle leaves had significantly higher chlorophyll content than the lower leaves. The arrangement of mesophyll cells in the upper leaves was densest, and that in the lower leaves was least dense. The net photosynthetic rate and stomatal conductance in the upper leaves were highest, and those in the lower leaves were lowest. We conclude that the stomata of upper leaves are mainly used for gas exchange. In contrast, stomata of lower leaves, showing weak photosynthesis, are responsible for secreting excessive salt to maintain the inner ion balance and ensure normal metabolism in G. uralensis.

Keywords


Licorice, Stomata, Salt Secretion.

References





DOI: https://doi.org/10.18520/cs%2Fv116%2Fi7%2F1212-1217