Ahmed Gharib, Yanze Su, Zhihao Zuo, Rujia Chen, Hanyao Wang, Tianyun Tao, Mingli Chuan, Qing Bu, Yanmo Luo, Yaoqing Li, Shuting Wang, Yu Hua, Yi Ji, Jianheng Ding, Wei Liu, Shuihua He, Pengcheng Li, Yang Xu, Chenwu Xu, Yue Lu, Zefeng Yang
{"title":"Melatonin enhances metal oxide nanoparticles tolerance in rice seedlings through dual regulation of antioxidant defense and photosynthetic efficiency.","authors":"Ahmed Gharib, Yanze Su, Zhihao Zuo, Rujia Chen, Hanyao Wang, Tianyun Tao, Mingli Chuan, Qing Bu, Yanmo Luo, Yaoqing Li, Shuting Wang, Yu Hua, Yi Ji, Jianheng Ding, Wei Liu, Shuihua He, Pengcheng Li, Yang Xu, Chenwu Xu, Yue Lu, Zefeng Yang","doi":"10.1111/ppl.70020","DOIUrl":null,"url":null,"abstract":"<p><p>The growing utilization of metal oxide nanoparticles (MONPs) presents novel and potential hazards to plants. However, the impacts of MONPs on plants and the mechanisms underlying their tolerance to MONPs remain unclear. In this study, we demonstrated that both CuO and ZnO nanoparticles hindered plant growth and triggered oxidative damage in rice seedlings. The role of melatonin in rice tolerance to MONPs was elucidated through a comprehensive analysis of OsCOMT mutant and overexpression plants, which showed melatonin deficiency and sufficiency, respectively. Our results revealed that the melatonin-deficient OsCOMT mutant plants exhibited hypersensitivity to MONPs, while the melatonin-sufficient OsCOMT overexpression plants showed enhanced MONPs tolerance. Physiological assessments further indicated that melatonin counteracted rice oxidative damage triggered by MONPs by increasing the activities of antioxidative enzymes, including superoxide dismutase, peroxidase, catalase, and glutathione reductase. Moreover, melatonin was found to foster rice growth under MONP stress by positively regulating the maximum photochemical efficiency, reducing non-photochemical fluorescence quenching, and promoting the biosynthesis of sucrose and starch. These findings not only highlight the hazardous effects of MONPs on plants, but also underscore the pivotal role of melatonin in bolstering plant resilience against MONPs.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"176 6","pages":"e70020"},"PeriodicalIF":5.4000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70020","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
Melatonin enhances metal oxide nanoparticles tolerance in rice seedlings through dual regulation of antioxidant defense and photosynthetic efficiency.
The growing utilization of metal oxide nanoparticles (MONPs) presents novel and potential hazards to plants. However, the impacts of MONPs on plants and the mechanisms underlying their tolerance to MONPs remain unclear. In this study, we demonstrated that both CuO and ZnO nanoparticles hindered plant growth and triggered oxidative damage in rice seedlings. The role of melatonin in rice tolerance to MONPs was elucidated through a comprehensive analysis of OsCOMT mutant and overexpression plants, which showed melatonin deficiency and sufficiency, respectively. Our results revealed that the melatonin-deficient OsCOMT mutant plants exhibited hypersensitivity to MONPs, while the melatonin-sufficient OsCOMT overexpression plants showed enhanced MONPs tolerance. Physiological assessments further indicated that melatonin counteracted rice oxidative damage triggered by MONPs by increasing the activities of antioxidative enzymes, including superoxide dismutase, peroxidase, catalase, and glutathione reductase. Moreover, melatonin was found to foster rice growth under MONP stress by positively regulating the maximum photochemical efficiency, reducing non-photochemical fluorescence quenching, and promoting the biosynthesis of sucrose and starch. These findings not only highlight the hazardous effects of MONPs on plants, but also underscore the pivotal role of melatonin in bolstering plant resilience against MONPs.
期刊介绍:
Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.