{"title":"Soluble sugars maintain redox homeostasis and accelerate the growth of cultured Malva neglecta cells under 2D-clinorotation","authors":"Somayeh Alikhani , Faezeh Ghanati , Zahra Hajebrahimi , Maryam Soleimani , Naba Najar , Elham Khalili","doi":"10.1016/j.jplph.2025.154489","DOIUrl":null,"url":null,"abstract":"<div><div>In addition to their nutritional role, carbohydrates play essential roles in metabolism, growth, development, and response to the environment. In the present study, the effects of clinorotation on structural and soluble sugar metabolism and the redox system were investigated in cultured <em>Malva neglecta</em> cells. A rapidly growing cell line was established from leaf explants of <em>M. neglecta</em> on a solidified LS medium, and the cells were exposed to 2D-clinostat for 7 days. Clinorotation significantly increased monosaccharide content, including glucose, fructose, rhamnose, mannose, and xylose, while reducing sucrose levels compared to control groups. The activities of pectin methylesterase (PME) and β-1, 3-glucanase increased, whereas those of covalently wall-bound peroxidase (CPO) and polyphenol oxidase (PPO) decreased. This reduction, along with a decrease in callose, cellulose, and phenolic acid content, likely accelerated cell growth by reducing cell wall crosslinking and stiffness. The content of reactive oxygen/nitrogen species i.e., hydrogen peroxide (H<sub>2</sub>O<sub>2</sub>), hydroxyl radical (<sup>.</sup>OH), and nitric oxide (NO) radicals significantly decreased in response to clinorotation compared with 1g-grown cells. Hierarchical cluster analysis revealed a strong negative correlation between NO and catalase (CAT) activity. The observed decrease in these oxidants can be attributed, at least in part, to the increased content of soluble sugars through the oxidative pentose-phosphate pathway or tricarboxylic acid cycle (TCA), and more significantly, to the enhancement of catalase activity and flavonoid content.</div></div>","PeriodicalId":16808,"journal":{"name":"Journal of plant physiology","volume":"308 ","pages":"Article 154489"},"PeriodicalIF":4.0000,"publicationDate":"2025-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of plant physiology","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0176161725000719","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0
Abstract
In addition to their nutritional role, carbohydrates play essential roles in metabolism, growth, development, and response to the environment. In the present study, the effects of clinorotation on structural and soluble sugar metabolism and the redox system were investigated in cultured Malva neglecta cells. A rapidly growing cell line was established from leaf explants of M. neglecta on a solidified LS medium, and the cells were exposed to 2D-clinostat for 7 days. Clinorotation significantly increased monosaccharide content, including glucose, fructose, rhamnose, mannose, and xylose, while reducing sucrose levels compared to control groups. The activities of pectin methylesterase (PME) and β-1, 3-glucanase increased, whereas those of covalently wall-bound peroxidase (CPO) and polyphenol oxidase (PPO) decreased. This reduction, along with a decrease in callose, cellulose, and phenolic acid content, likely accelerated cell growth by reducing cell wall crosslinking and stiffness. The content of reactive oxygen/nitrogen species i.e., hydrogen peroxide (H2O2), hydroxyl radical (.OH), and nitric oxide (NO) radicals significantly decreased in response to clinorotation compared with 1g-grown cells. Hierarchical cluster analysis revealed a strong negative correlation between NO and catalase (CAT) activity. The observed decrease in these oxidants can be attributed, at least in part, to the increased content of soluble sugars through the oxidative pentose-phosphate pathway or tricarboxylic acid cycle (TCA), and more significantly, to the enhancement of catalase activity and flavonoid content.
期刊介绍:
The Journal of Plant Physiology is a broad-spectrum journal that welcomes high-quality submissions in all major areas of plant physiology, including plant biochemistry, functional biotechnology, computational and synthetic plant biology, growth and development, photosynthesis and respiration, transport and translocation, plant-microbe interactions, biotic and abiotic stress. Studies are welcome at all levels of integration ranging from molecules and cells to organisms and their environments and are expected to use state-of-the-art methodologies. Pure gene expression studies are not within the focus of our journal. To be considered for publication, papers must significantly contribute to the mechanistic understanding of physiological processes, and not be merely descriptive, or confirmatory of previous results. We encourage the submission of papers that explore the physiology of non-model as well as accepted model species and those that bridge basic and applied research. For instance, studies on agricultural plants that show new physiological mechanisms to improve agricultural efficiency are welcome. Studies performed under uncontrolled situations (e.g. field conditions) not providing mechanistic insight will not be considered for publication.
The Journal of Plant Physiology publishes several types of articles: Original Research Articles, Reviews, Perspectives Articles, and Short Communications. Reviews and Perspectives will be solicited by the Editors; unsolicited reviews are also welcome but only from authors with a strong track record in the field of the review. Original research papers comprise the majority of published contributions.