外源尿素缓解烟草生长受铵毒的生物学机制初探
A Preliminary Study on the Biological Mechanisms Underlying the Alleviation of Ammonium Toxicity-Induced Growth Inhibition in Tobacco by Exogenous Urea
DOI: 10.12677/br.2026.153022, PDF,    科研立项经费支持
作者: 彭光莲, 韩 露, 罗齐克:湖南省湘西州农业环境保护管理站,湖南 吉首;彭 滨:湖南省湘西州茶叶产业发展中心,湖南 吉首;刘力筠:湖南省湘西州保靖县农业农村局,湖南 保靖;向禹澄*:中国农业大学资源与环境学院,北京
关键词: 铵毒胁迫烟草外源尿素一氧化氮信号多胺代谢Ammonium Toxicity Stress Tobacco Exogenous Urea Nitric Oxide Signaling Polyamine Metabolism
摘要: 本研究聚焦植物铵毒现象及其作用机理这一农业科学与生物学领域长期关注且亟待突破的基础理论问题。以模式植物烟草为材料,研究发现,在含3 mM N H 4 + 的水培条件下,烟草生长受到显著抑制;而添加微摩尔浓度的外源尿素后,烟草地上部和地下部生物量、侧根数量及总根长均显著增加,表明外源尿素能够有效缓解铵离子对烟草生长造成的胁迫。进一步分析表明,该缓解过程伴随着精氨酸、一氧化氮、精胺和亚精胺等信号物质水平的变化,提示其可能通过调控相关信号代谢网络参与烟草对铵毒胁迫的响应过程。
Abstract: Ammonium toxicity and its underlying mechanisms are long-standing fundamental issues in agricultural science and biology that have attracted sustained attention and urgently require further investigation. Using tobacco as a model plant, this study found that tobacco growth was significantly inhibited under hydroponic conditions containing 3 mM N H 4 + . However, the addition of exogenous urea at micromolar concentrations significantly increased shoot and root biomass, lateral root number, and total root length, indicating that exogenous urea can effectively alleviate the growth stress caused by ammonium in tobacco. Further analysis showed that this alleviating process was accompanied by changes in the levels of signaling molecules such as arginine, nitric oxide, spermine, and spermidine, suggesting that exogenous urea may participate in the tobacco response to ammonium toxicity by regulating related signaling and metabolic networks.
文章引用:彭光莲, 韩露, 罗齐克, 彭滨, 刘力筠, 向禹澄. 外源尿素缓解烟草生长受铵毒的生物学机制初探[J]. 植物学研究, 2026, 15(3): 187-196. https://doi.org/10.12677/br.2026.153022

参考文献

[1] 李婷玉, 姚澜, 钟于秀,等. 绿色发展背景下的中国氮肥需求[J]. 土壤学报, 2025, 62(2): 308-321.
[2] Hu, W.S., Zhang, S.S., Dai, J., Gu, C.M., Yang, L., Li, Y.S., et al. (2025) Nitrate Availability Regulated Leaf Anatomical Structure to Prevent Ammonium Toxicity on Photosynthetic Rate of Brassica napus. Environmental and Experimental Botany, 237, Article ID: 106211. [Google Scholar] [CrossRef
[3] 樊娅萍, 李静祎, 贺苗苗, 等. 硝态氮与铵态氮配合缓解黄瓜苗期铵毒害作用的研究[J]. 中国农学通报, 2024, 40(7): 27-32.
[4] 石楚含, 苏晓晴, 崔萌萌, 等. 过量铵态氮水培处理对烟草幼苗叶片转录组的影响[J]. 贵州农业科学, 2026, 54(1): 38-47.
[5] 范子晗. 柑橘铵毒害产生机制及缓解措施研究[D]: [硕士学位论文]. 重庆: 西南大学, 2021.
[6] Britto, D.T. and Kronzucker, H.J. (2002) NH Toxicity in Higher Plants: A Critical Review. Journal of Plant Physiology, 159, 567-584. [Google Scholar] [CrossRef
[7] Fan, T. F., He, M. J., Li, C. J., Shi, D. X., Yang, C., Chen, Y. Y., et al. (2017) Physiological Dissection Revealed That Both Uptake and Assimilation Are the Major Components Regulating Different Growth Responses of Two Tobacco Cultivars to Nitrogen Nutrition. Plant Biology, 20, 39-49. [Google Scholar] [CrossRef] [PubMed]
[8] Esteban, R., Ariz, I., Cruz, C. and Moran, J.F. (2016) Review: Mechanisms of Ammonium Toxicity and the Quest for Tolerance. Plant Science, 248, 92-101. [Google Scholar] [CrossRef] [PubMed]
[9] Liu, Y. and von Wirén, N. (2017) Ammonium as a Signal for Physiological and Morphological Responses in Plants. Journal of Experimental Botany, 68, 2581-2592. [Google Scholar] [CrossRef] [PubMed]
[10] Rogato, A., D’Apuzzo, E., Barbulova, A., Omrane, S., Parlati, A., Carfagna, S., et al. (2010) Characterization of a Developmental Root Response Caused by External Ammonium Supply in Lotus japonicus. Plant Physiology, 154, 784-795. [Google Scholar] [CrossRef] [PubMed]
[11] Liu, L., Bi, X.Y., Sheng, S., Gong, Y.Y., Pu, W.X. and Ke, J. (2020) Evidence That Exogenous Urea Acts as a Potent Cue to Alleviate Ammonium‐inhibition of Root System Growth of Cotton Plant (Gossypium hirsutum). Physiologia Plantarum, 171, 137-150. [Google Scholar] [CrossRef] [PubMed]
[12] 王学奎. 植物生理生化实验原理和技术[M]. 第2版. 北京: 高等教育出版社, 2006.
[13] Liu, J.L., Wang, J.Z., Wang, Z.D., Li, M., Liang, C.L., Yang, Y.J., et al. (2022) Alleviation of Iron Deficiency in Pear by Ammonium Nitrate and Nitric Oxide. BMC Plant Biology, 22, Article No. 434. [Google Scholar] [CrossRef] [PubMed]
[14] 黄丽佳, 梁梦洁, 李应郡, 等. 高效液相色谱法测定新鲜烟叶中3种多胺[J]. 理化检验-化学分册, 2020, 56(10): 1079-1084.
[15] 王雪茹, 陈海飞, 张振华. 硝酸盐缓解油菜铵毒害的生理机制[J]. 作物杂志, 2022(6): 124-131.
[16] Zhang, L., Song, H.Y., Li, B.H., Wang, M., Di, D.W., Lin, X.Y., et al. (2021) Induction of s-Nitrosoglutathione Reductase Protects Root Growth from Ammonium Toxicity by Regulating Potassium Homeostasis in Arabidopsis and Rice. Journal of Experimental Botany, 72, 4548-4564. [Google Scholar] [CrossRef] [PubMed]
[17] Hernández-Gómez, E., Valdez-Aguilar, L.A., Cartmill, D.L., Cartmill, A.D. and Alia-Tajacal, I. (2015) Supplementary Calcium Ameliorates Ammonium Toxicity by Improving Water Status in Agriculturally Important Species. AoB Plants, 7, plv105. [Google Scholar] [CrossRef] [PubMed]
[18] 高祖明, 章满芬, 胡雪峰, 等. 有机酸对缓解蔬菜氨中毒的机理[J]. 上海农业学报, 1993, 9(1): 38-43.
[19] Liu, Q., Chen, X.B., Wu, K. and Fu, X.D. (2015) Nitrogen Signaling and Use Efficiency in Plants: What’s New? Current Opinion in Plant Biology, 27, 192-198. [Google Scholar] [CrossRef] [PubMed]
[20] Chen, D., Shao, Q., Yin, L., Younis, A. and Zheng, B. (2019) Polyamine Function in Plants: Metabolism, Regulation on Development, and Roles in Abiotic Stress Responses. Frontiers in Plant Science, 9, Article No. 1945. [Google Scholar] [CrossRef] [PubMed]
[21] Winter, G., Todd, C.D., Trovato, M., Forlani, G. and Funck, D. (2015) Physiological Implications of Arginine Metabolism in Plants. Frontiers in Plant Science, 6, Article No. 534. [Google Scholar] [CrossRef] [PubMed]
[22] Azzawi, T.N.I.A., Khan, M. and Rhie, Y.H. (2026) Nitric Oxide-Based Signaling during Abiotic Stress Responses in Plants: Mechanisms of Tolerance and Applicability in Sustainable Horticultural Crop Management. Plants, 15, Article No. 825. [Google Scholar] [CrossRef
[23] Alcázar, R., Altabella, T., Marco, F., Bortolotti, C., Reymond, M., Koncz, C., et al. (2010) Polyamines: Molecules with Regulatory Functions in Plant Abiotic Stress Tolerance. Planta, 231, 1237-1249. [Google Scholar] [CrossRef] [PubMed]
[24] Sheng, S., Wu, C., Xiang, Y., Pu, W., Duan, S., Huang, P., et al. (2022) Polyamine: A Potent Ameliorator for Plant Growth Response and Adaption to Abiotic Stresses Particularly the Ammonium Stress Antagonized by Urea. Frontiers in Plant Science, 13, Article ID: 783597. [Google Scholar] [CrossRef] [PubMed]
[25] Hasanuzzaman, M., Oku, H., Nahar, K., Bhuyan, M.H.M.B., Mahmud, J.A., Baluska, F., et al. (2018) Nitric Oxide-Induced Salt Stress Tolerance in Plants: ROS Metabolism, Signaling, and Molecular Interactions. Plant Biotechnology Reports, 12, 77-92. [Google Scholar] [CrossRef
[26] Pál, M., Szalai, G., Gondor, O.K. and Janda, T. (2021) Unfinished Story of Polyamines: Role of Conjugation, Transport and Light-Related Regulation in the Polyamine Metabolism in Plants. Plant Science, 308, Article ID: 110923. [Google Scholar] [CrossRef] [PubMed]
[27] Ke, J., Pu, W.-X., Wang, H., Liu, L.-H. and Sheng, S. (2020) Phenotypical Evidence of Effective Amelioration of Ammonium-Inhibited Plant (Root) Growth by Exogenous Low Urea. Journal of Plant Physiology, 255, Article ID: 153306. [Google Scholar] [CrossRef] [PubMed]
[28] Crisp, P.A., Ganguly, D., Eichten, S.R., Borevitz, J.O. and Pogson, B.J. (2016) Reconsidering Plant Memory: Intersections between Stress Recovery, RNA Turnover, and Epigenetics. Science Advances, 2, e1501340. [Google Scholar] [CrossRef] [PubMed]
[29] Kojima, S., Bohner, A. and von Wirén, N. (2006) Molecular Mechanisms of Urea Transport in Plants. The Journal of Membrane Biology, 212, 83-91. [Google Scholar] [CrossRef] [PubMed]