Attapulgite clay (AC), which is rich in good adsorption, catalysis, rheology and heat resistance, is an important mineral resource. However, the roles of AC in regulating stress tolerance of plants have not been investigated. In this study, culture pot experiment was used to analyze the effects of AC applied into the soil on growth and physiological metabolism of okra plants. The applied AC significantly enhanced salt and drought tolerance of okra plants. Component analyses showed that the significant increases of ABA, proline, soluble protein, soluble sugar and photosynthetic pigment content, as well as the significant decreases of hydrogen peroxide, superoxide anion radical and malondialdehyde content were observed in okra plants grown in the soil with applied 30 g/kg AC under salt and drought stresses. Enzymatic analyses indicated the activities of 9-cis-epoxycarotenoid dioxygenase, pyrroline-5-carboxylate synthase, superoxide dismutase and peroxidase were also significantly increased under salt and drought stresses. These results demonstrate that the applied AC can alleviate damage caused by salt and drought stresses, leading to the enhanced salt tolerance and drought tolerance of okra plants. The AC has the potential to be used to develop plant growth regulators to enhance the tolerance to abiotic stresses in plants.
Published in | Advances in Biochemistry (Volume 10, Issue 1) |
DOI | 10.11648/j.ab.20221001.11 |
Page(s) | 1-10 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2022. Published by Science Publishing Group |
ABA, Attapulgite Clay, Okra, Proline, Salt and Drought Tolerance
[1] | Wang, F. B., G. L. Ren, F. S. Li, S. T. Qi, Y. Xu, B. W. Wang, Y. L. Yang, Y. X. Ye, Q. Zhou and X. H. Chen. 2018. A chalcone synthase gene AeCHS from Abelmoschus esculentus regulates flavonoids accumulation and abiotic stress tolerance in transgenic Arabidopsis. Acta Physiologiae Plantarum 40: 97. doi: 10.1007/s11738-018-2680-1. |
[2] | Ahmadi, M. and M. K. Souri. 2018. Growth and mineral elements of coriander (Corianderum sativum L.) plants under mild salinity with different salts. Acta Physiologiae Plantarum 40: 94-999. doi: 10.1007/s11738-018-2773-x. |
[3] | Zhang, H., X. R. Gao, Y. H. Zhi, X. Li, Q. Zhang, J. B. Niu, J. Wang, H. Zhai, N. Zhao, J. G. Li, Q. C. Liu and S. Z. He. 2019. A non-tandem CCCH-type zinc-finger protein, IbC3H18, functions as a nuclear transcriptional activator and enhances abiotic stress tolerance in sweet potato. New Phytologist 223: 1918-1936. doi: info:doi/10.1111/nph.15925. |
[4] | Huang, J., S. Sun, D. Xu, H. Lan, H. Sun, Z. Wang, Y. Bao, J. Wang, H. Tang and H. Zhang. 2012. A TFIIIA-type zinc finger protein confers multiple abiotic stress tolerances in transgenic rice (Oryza sativa L.). Plant Molecular Biology 80: 337-350. doi: 10.1007/s11103-012-9955-5. |
[5] | Lang, D., X. Yu, X. Jia, Z. Li and X. Zhang. 2020. Methyl jasmonate improves metabolism and growth of NaCl-stressed Glycyrrhiza uralensis seedlings. Scientia Horticulturae 266: 109287. doi: 10.1016/j.scienta.2020.109287. |
[6] | Zhu, J. K. 2016. Abiotic stress signaling and responses in plants. Cell 167: 313-324. doi: 10.1016/j.cell.2016.08.029. |
[7] | Ahmadi, M. and M. K. Souri. 2019. Nutrient uptake, proline content and antioxidant enzymes activity of pepper (Capsicum annuum L.) under higher electrical conductivity of nutrient solution created by nitrate and chloride salts of potassium and calcium. Acta Scientiarum Polonorum-Hortorum Cultus 18: 113-122. doi: 10.24326/asphc.2019.5.11. |
[8] | Debouba, M., H. Gouia, A. Suzuki and M. H. Ghorbel. 2006. NaCl stress effects on enzymes involved in nitrogen assimilation pathway in tomato ‘Lycopersicon esculentum’ seedlings. Journal of Plant Physiology 163: 1247-1258. doi: 10.1016/j.jplph.2005.09.012. |
[9] | Penna, S. 2003. Building stress tolerance through over-producing trehalose in transgenic plants. Trends in Plant Science 8: 353-357. doi: 10.1016/S1360-1385(03)00159-6. |
[10] | Guan, Y., C. Song, Y. Gan and F. Li. 2014. Increased maize yield using slow-release attapulgite-coated fertilizers. Agronomy for Sustainable Development 34: 657-665. doi: 10.1007/s13593-013-0193-2. |
[11] | Murray, H. 2000. Traditional and new applications for kaolin, smectite, and palygorskite: a general overview. Applied Clay Science 17: 207-221. doi: 10.1016/S0169-1317(00)00016-8. |
[12] | Ye, B., Y. H. Li, F. X. Qiu, C. Sun, Z. Zhao, T. Ma and D. Yang. 2013. Production of biodiesel from soybean oil catalyzed by attapulgite loaded with C4H5O6KNa catalyst. The Korean Journal of Chemical Engineering 1-8. |
[13] | Xie, L. H., M. Z. Liu, B. L. Ni and Y. Wang. 2010. Slow-release nitrogen and boron fertilizer from a functional superabsorbent formulation based on wheat straw and attapulgite. Chemical Engineering Journal 167; 342-348. doi: 10.1016/j.cej.2010.12.082. |
[14] | Yang, J. J., W. D. Cheng, H. M. Lin, X. Z. Liu and Y. Hu. 2010. Effect of palygorskite adding NPK fertilizer on plant dry matter accumulation and polysaccharide content of Radix Hedysari. Medicinal Plant 1: 1-4. doi: CNKI:SUN:MDPT.0.2010-04-004. |
[15] | Wang, F. B., W. L. Kong, G. Wong, L. F. Fu, R. H. Peng, Z. J. Li and Q. H. Yao. 2016. AtMYB12 regulates flavonoids accumulation and abiotic stress tolerance in transgenic Arabidopsis thaliana. Molecular Genetics and Genomics 291: 1545-1559. doi: 10.1007/s00438-016-1203-2. |
[16] | Zhai, H., F. B. Wang, Z. Z. Si, J. X. Huo, L. Xing, Y. Y. An, S. Z. He and Q. C. Liu. 2016. A myo-inositol-1-phosphate synthase gene, IbMIPS1, enhances salt and drought tolerance and stem nematode resistance in transgenic sweetpotato. Plant Biotechnology Journal 14: 592-602. doi: 10.1111/pbi.12402. |
[17] | Lichtenthaler, H. K. and C. Buschmann. 2001. Chlorophylls and carotenoids: measurement and characterization by UV-VIS spectroscop. Current Protocols in Food Analytical Chemistry 1. |
[18] | Gao, S., L. Yuan, H. Zhai, C. L. Liu, S. Z. He and Q. C. Liu. 2011. Transgenic sweetpotato plants expressing an LOS5 gene are tolerant to salt stress. Plant Cell, Tissue and Organ Culture 107: 205-213. doi: 10.1007/s11240-011-9971-1. |
[19] | Hatami, E., A. A. Shokouhian, A. R. Ghanbari and L. A. Naseri. 2018. Alleviating salt stress in almond rootstocks using of humic acid. Scientia Horticulturae 237; 296-302. doi: 10.1016/j.scienta.2018.03.034. |
[20] | Jiang, Y., Y. Qiu, Y. Hu and D. Yu. 2016. Heterologous expression of AtWRKY57 confers drought tolerance in Oryza sativa. Frontiers in Plant Science 7: 145. doi: 10.3389/fpls.2016.00145. |
[21] | Hayzer, D. J. and T. Leisinger. 1980. The gene-enzyme relationships of proline biosynthesis in Escherichia coli. Journal of General and Applied Microbiology 118; 287-293. doi: 10.1099/00221287-118-2-287. |
[22] | Feng, Y., X. Chen, Y. He, X. Kou and Z. Xue. 2019. Effects of exogenous trehalose on the metabolism of sugarand abscisic acid in tomato seedlings under salt stress. Transactions of Tianjin University 25: 451-471. doi: 10.1007/s12209-019-00214-x. |
[23] | Moradi, F. and A. M. Ismail. 2007. Responses of photosynthesis, chlorophyll fluorescence and ROS-scavenging systems to salt stress during seedling and reproductive stages in rice. Annals of Botany 99: 1161-1173. doi: 10.1093/aob/mcm052. |
[24] | Krasensky, J. and C. Jonak 2012. Drought, salt, and temperature stress-induced metabolic rearrangements and regulatory networks. Journal of Experimental Botany 63: 1593-1608. doi: 10.1093/jxb/err460. |
[25] | Liu, Y., X. Ji, X. Nie, M. Qu, L. Zheng, Z. Tan, H. Zhao, L. Huo, S. Liu, B. Zhang and Y. Wang. 2015. Arabidopsis AtbHLH112 regulates the expression of genes involved in abiotic stress tolerance by binding to their E-box and GCG-box motifs. New Phytologist 207: 692-709. doi: 10.1111/nph.13387. |
[26] | Apel, K. and H. Hirt. 2004. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annual Review of Plant Biology 55: 373-399. doi: 10.1146/annurev.arplant.55.031903.141701. |
[27] | Chen, T. H. H. and N. Murata. 2002. Enhancement of tolerance of abiotic stress by metabolic engineering of betaines and other compatible solutes. Current Opinion in Plant Biology 5: 250-257. doi: 10.1016/S1369-5266(02)00255-8. |
[28] | Di Martino, C., S. Delfine, R. Pizzuto, F. Loreto and A. Fuggi. 2003. Free amino acids and glycine betaine in leaf osmoregulation of spinach responding to increasing salt stress. New Phytologist 158: 455-463. doi: 10.1046/j.1469-8137.2003.00770.x. |
[29] | Mostofa, M. G., M. A. Hossain and M. Fujita. 2015. Trehalose pretreatment induces salt tolerance in rice (Oryza sativa L.) seedlings: oxidative damage and co-induction of antioxidant defense and glyoxalase systems. Protoplasma 252: 461-475. doi: 10.1007/s00709-014-0691-3. |
[30] | Zhu, J. K. 2002. Salt and drought stress signal transduction in plants. Annual Review of Plant Biology 53; 247-273. doi: 10.1146/annurev.arplant.53.091401.143329. |
[31] | Li, J., Y. Li, Z. Yin, J. Jiang, M. Zhang, X. Guo, Z. Ye, Y. Zhao, H. Xiong, Z. Zhang, Y. Shao, C. Jiang, H. Zhang, G. An, N. C. Paek, J. Ali and Z. Li. 2017. OsASR5 enhances drought tolerance through a stomatal closure pathway associated with ABA and H2O2 signalling in rice. Plant Biotechnology Journal 15: 183-196. doi: 10.1111/pbi.12601. |
[32] | Li, G., Y. X. Ye, X. Q. Ren, M. Y. Qi, H. Y. Zhao, Q. Zhou, X. H. Chen, J. Wang, C. Y. Yuan and F. B. Wang. 2020. The rice Aux/IAA transcription factor gene OsIAA18 enhances salt and osmotic tolerance in Arabidopsis. Biologia Plantarum 64: 454-464. doi: 10.32615/bp.2019.069. |
[33] | Sripinyowanich, S., P. Klomsakul, B. Boonburapong, T. Bangyeekhun, T. Asami, H. Gu, T. Buaboocha and S. Chadchawan. 2013. Exogenous ABA induces salt tolerance in indica rice (Oryza sativa L.): The role of OsP5CS1 and OsP5CR gene expression during salt stress. Environmental and Experimental Botany 86: 94-105. doi: org/10.1016/j.envexpbot.2010.01.009. |
[34] | Zhu, M. D., M. Zhang, D. J. Gao, K. Zhou and Y. M. Lv. 2020. Rice OsHSFA3 gene improves drought tolerance by modulating polyamine biosynthesis depending on abscisic acid and ROS levels. International Journal of Molecular Sciences 21: 1857. doi: 10.3390/ijms21051857. |
[35] | Li, J., X. Guo, M. Zhang, X. Wang, Y. Zhao, Z. Yin, Z. Zhang, Y. Wang, H. Xiong, H. Zhang, E. Todorovskac and Z. Li. 2018. OsERF71 confers drought tolerance via modulating aba signaling and proline biosynthesis. Plant Science 270: 131-139. doi: 10.1016/j.plantsci.2018.01.017. |
[36] | Li, Z. J., X. Y. Fu, Y. S. Tian, J. Xu, J. J. Gao, B. Wang, H. J. Han, L. J. Wang, F. J. Zhang, Y. M. Zhu, Y. N. Huang, R. H. Peng and Q. H. Yao. 2019. Overexpression of a trypanothione synthetase gene from Trypanosoma cruzi, TcTrys, confers enhanced tolerance to multiple abiotic stresses in rice. Gene 710: 279-290. doi: 10.1016/j.gene.2019.06.018. |
[37] | Xiong, H., J. Li, P. Liu, J. Duan, Y. Zhao, X. Guo, Y. Li, H. Zhang, J. Ali and Z. Li. 2014. Overexpression of OsMYB48-1, a novel MYB-related transcription factor, enhances drought and salinity tolerance in rice. PLoS ONE 9: e92913. doi: 10.1371/journal.pone.0092913. |
[38] | Kang, C., S. Z. He, H. Zhai, R. J. Li, N. Zhao and Q. C. Liu. 2018. A sweetpotato auxin response factor gene (IbARF5) is involved in carotenoid biosynthesis and salt and drought tolerance in transgenic Arabidopsis. Frontiers in Plant Science 9; 1307. doi: 10.3389/fpls.2018.01307. |
[39] | Liu, D. G., S. Z. He, H. Zhai, L. J. Wang, Y. Zhao, B. Wang, R. J. Li and Q. C. Liu. 2014. Overexpression of IbP5CR enhances salt tolerance in transgenic sweetpotato. Plant Cell, Tissue and Organ Culture 117: 1-16. doi: 10.1007/s11240-013-0415-y. |
[40] | Zhang, H., Y. X. Liu, Y. Xu, S. Chapman, A. J. Love and T. Xia. 2012. A newly isolated Na+/H+ antiporter gene, DmNHX1, confers salt tolerance when expressed transiently in Nicotiana benthamiana or stably in Arabidopsis thaliana. Plant Cell, Tissue and Organ Culture 110: 189-200. doi: 10.1007/s11240-012-0142-9. |
[41] | Liang, W. J., X. L. Ma, P. Wan and L. Liu. 2018. Plant salt-tolerance mechanism: a review. Biochemical and Biophysical Research Communications 495: 286-291. doi: 10.1016/j.bbrc.2017.11.043. |
[42] | Parihar, P., S. Singh, R. Singh, V. P. Singh and S. M. Prasad. 2015. Effect of salinity stress on plants and its tolerance strategies: a review. Environmental Science and Pollution Research 22: 4056-4075. doi: 10.1007/s11356-014-3739-1. |
[43] | James, R. A., A. R. Rivelli, R. Munns and S. V. Caemmerer. 2002. Factors affecting CO2 assimilation, leaf injury and growth in salt-stressed durum wheat. Functional Plant Biology 29: 1393-1403. doi: 10.1071/FP02069. |
[44] | Lawlor, D. W. 2002. Limitation to photosynthesis in water-stressed leaves: stomata vs. metabolism and the role of ATP. Annals of Botany 89: 871-885. doi: org/10.1093/aob/mcf110. |
[45] | Parida, A. K. and A. B. Das. 2005. Salt tolerance and salinity effects on plants: a review. Ecotoxicology and Environmental Safety 60: 324-349. doi: 10.1016/j.ecoenv.2004.06.010. |
[46] | Tuteja, N. 2007. Abscisic acid and abiotic stress signaling. Plant Signaling and Behavior 2: 135-138. doi: 10.4161/psb.2.3.4156. |
[47] | Alia, P. Mohanty and J. Matysik. 2001. Effect of proline on the production of singlet oxygen. Amino Acids 21: 195-200. doi: 10.1007/s007260170026. |
[48] | De Ronde, J. A., W. A. Cress, G. H. J. Krüger. R. J. Strasser and J. Van Staden. 2004. Photosynthetic response of transgenic soybean plants, containing an Arabidopsis P5CR gene, during heat and drought stress. Journal of Plant Physiology 161; 1211-1224. doi: 10.1016/j.jplph.2004.01.014. |
[49] | Sevengor, S., F. Yasar, S. Kusvuran and S. Ellialtioglu. 2011. The effect of salt stress on growth, chlorophyll content, lipid peroxidation and antioxidative enzymes of pumpkin seedling. African Journal of Agricultural Research 6: 4920-4924. doi: 10.2485/jhtb.20.37. |
[50] | Yasar, S., F. Ellialtioglu and K. Yildiz. 2008. Effect salt stress on antioxidant defense systems, lipid peroxidation, and chlorophyll content in green bean. Russian Journal of Plant Physiology 55: 782-786. doi: 10.1134/S1021443708060071. |
[51] | Saha, P., P. Chatterjee and A. K. Biswas. 2010. NaCl pretreatment alleviates salt stress by enhancement of antioxidant defense system and osmolyte accumulation in mungbean (Vigina radiate L. Wilczek). Indian Journal of Experimental Biology 48: 593-600. doi: hdl.handle.net/123456789/9073. |
[52] | Qin, J., W. Y. Dong, K. N. He, Y. Yu, G. D. Tan, L. Han, M. Dong, Y. Y. Zhang, D. Zhang, A. Z. Li and Z. L. Wang. 2010. NaCl salinity-induced changes in water status, ion contents and photosynthetic properties of Shepherdia argentea (Pursh) Nutt. seedlings. Plant Soil and Environment 56: 325-332. doi: 10.1007/s11104-009-9988-y. |
[53] | Poor, P., K. Gemes, F. Horvath, A. Szepesi, M. L. Simon and I. Tari. 2011. Salicylic acid treatment via the rooting medium interferes with stomatal response, CO2 fixation rate and carbohydrate metabolism in tomato, and decreases harmful effects of subsequent salt stress. Plant Biology 13: 105-114. doi: 10.1111/j.1438-8677.2010.00344.x. |
[54] | Hussain, H. A., S. Men, S. Hussain, Y. Chen, S. Ali, S. Zhang, K. Zhang, Y. Li, Q. Xu, C. Liao and L. Wang. 2019. Interactive effects of drought and heat stresses on morpho-physiological attributes, yield, nutrient uptake and oxidative status in maize hybrids. Scientific Reports 9: 3890. doi: 10.1038/s41598-019-40362-7. |
[55] | Munns, R. and M. Tester. 2008. Mechanisms of salinity tolerance. Annual Review of Plant Biology 59: 651-681. doi: 10.1146/annurev.arplant.59.032607.092911. |
[56] | Zhao, Q., L. Zhou, J. Liu, X. Du, M. A. Asad, F. Huang, G. Pan and F. Cheng. 2018. Relationship of ROS accumulation and superoxide dismutase isozymes in developing anther with floret fertility of rice under heat stress. Plant Physiology and Biochemistry 122: 90-101. doi: 10.1016/j.plaphy.2017.11.009. |
[57] | Gill, S. S. and N. Tuteja. 2010. Reactive oxygen species and antioxidant machinery in abiotic stress tolerance in crop plants. Plant Physiology and Biochemistry 48: 909-930. doi: 10.1016/j.plaphy.2010.08.016. |
APA Style
Hengpeng Li, Shasha Yang, Wenya Wu, Chunyan Wang, Yanyang Li, et al. (2022). Physiological and Biochemical Mechanisms of Improving Salt and Drought Tolerance in Okra Plants Based on Applied Attapulgite Clay. Advances in Biochemistry, 10(1), 1-10. https://doi.org/10.11648/j.ab.20221001.11
ACS Style
Hengpeng Li; Shasha Yang; Wenya Wu; Chunyan Wang; Yanyang Li, et al. Physiological and Biochemical Mechanisms of Improving Salt and Drought Tolerance in Okra Plants Based on Applied Attapulgite Clay. Adv. Biochem. 2022, 10(1), 1-10. doi: 10.11648/j.ab.20221001.11
AMA Style
Hengpeng Li, Shasha Yang, Wenya Wu, Chunyan Wang, Yanyang Li, et al. Physiological and Biochemical Mechanisms of Improving Salt and Drought Tolerance in Okra Plants Based on Applied Attapulgite Clay. Adv Biochem. 2022;10(1):1-10. doi: 10.11648/j.ab.20221001.11
@article{10.11648/j.ab.20221001.11, author = {Hengpeng Li and Shasha Yang and Wenya Wu and Chunyan Wang and Yanyang Li and Chenzhong Wan and Yuxiu Ye and Xinhong Chen and Zunxin Wang and Laibao Hu and Feibing Wang}, title = {Physiological and Biochemical Mechanisms of Improving Salt and Drought Tolerance in Okra Plants Based on Applied Attapulgite Clay}, journal = {Advances in Biochemistry}, volume = {10}, number = {1}, pages = {1-10}, doi = {10.11648/j.ab.20221001.11}, url = {https://doi.org/10.11648/j.ab.20221001.11}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ab.20221001.11}, abstract = {Attapulgite clay (AC), which is rich in good adsorption, catalysis, rheology and heat resistance, is an important mineral resource. However, the roles of AC in regulating stress tolerance of plants have not been investigated. In this study, culture pot experiment was used to analyze the effects of AC applied into the soil on growth and physiological metabolism of okra plants. The applied AC significantly enhanced salt and drought tolerance of okra plants. Component analyses showed that the significant increases of ABA, proline, soluble protein, soluble sugar and photosynthetic pigment content, as well as the significant decreases of hydrogen peroxide, superoxide anion radical and malondialdehyde content were observed in okra plants grown in the soil with applied 30 g/kg AC under salt and drought stresses. Enzymatic analyses indicated the activities of 9-cis-epoxycarotenoid dioxygenase, pyrroline-5-carboxylate synthase, superoxide dismutase and peroxidase were also significantly increased under salt and drought stresses. These results demonstrate that the applied AC can alleviate damage caused by salt and drought stresses, leading to the enhanced salt tolerance and drought tolerance of okra plants. The AC has the potential to be used to develop plant growth regulators to enhance the tolerance to abiotic stresses in plants.}, year = {2022} }
TY - JOUR T1 - Physiological and Biochemical Mechanisms of Improving Salt and Drought Tolerance in Okra Plants Based on Applied Attapulgite Clay AU - Hengpeng Li AU - Shasha Yang AU - Wenya Wu AU - Chunyan Wang AU - Yanyang Li AU - Chenzhong Wan AU - Yuxiu Ye AU - Xinhong Chen AU - Zunxin Wang AU - Laibao Hu AU - Feibing Wang Y1 - 2022/01/08 PY - 2022 N1 - https://doi.org/10.11648/j.ab.20221001.11 DO - 10.11648/j.ab.20221001.11 T2 - Advances in Biochemistry JF - Advances in Biochemistry JO - Advances in Biochemistry SP - 1 EP - 10 PB - Science Publishing Group SN - 2329-0862 UR - https://doi.org/10.11648/j.ab.20221001.11 AB - Attapulgite clay (AC), which is rich in good adsorption, catalysis, rheology and heat resistance, is an important mineral resource. However, the roles of AC in regulating stress tolerance of plants have not been investigated. In this study, culture pot experiment was used to analyze the effects of AC applied into the soil on growth and physiological metabolism of okra plants. The applied AC significantly enhanced salt and drought tolerance of okra plants. Component analyses showed that the significant increases of ABA, proline, soluble protein, soluble sugar and photosynthetic pigment content, as well as the significant decreases of hydrogen peroxide, superoxide anion radical and malondialdehyde content were observed in okra plants grown in the soil with applied 30 g/kg AC under salt and drought stresses. Enzymatic analyses indicated the activities of 9-cis-epoxycarotenoid dioxygenase, pyrroline-5-carboxylate synthase, superoxide dismutase and peroxidase were also significantly increased under salt and drought stresses. These results demonstrate that the applied AC can alleviate damage caused by salt and drought stresses, leading to the enhanced salt tolerance and drought tolerance of okra plants. The AC has the potential to be used to develop plant growth regulators to enhance the tolerance to abiotic stresses in plants. VL - 10 IS - 1 ER -