Zhizhuo Shao , Menglin Guo , Hong Wang , Wenhui Gu , Xiujun Xie , Guangce Wang
{"title":"Rboh的过表达通过与碳酸酐酶的协同作用,促进了yezoensis对无机碳的获取。","authors":"Zhizhuo Shao , Menglin Guo , Hong Wang , Wenhui Gu , Xiujun Xie , Guangce Wang","doi":"10.1016/j.plantsci.2025.112497","DOIUrl":null,"url":null,"abstract":"<div><div><em>Pyropia yezoensis</em> is an important intertidal economic macroalgae, which is periodically affected by various stresses, such as the limitation of inorganic carbon (C<sub>i</sub>) deficiency. Under such environment, the redox homeostasis within the cells of <em>P. yezoensis</em> is seriously affected, and the reactive oxygen species (ROS) signal transduction system would be activated to regulate the photosynthetic activity. Therefore, how <em>P. yezoensis</em> manage ROS to maintain effective photosynthetic carbon fixation has aroused great interest. Here, we characterize transformants overexpressing respiratory burst oxidase homolog (<em>Rboh</em>), an important gene that can actively produce ROS, at the levels of cellular physiology, biochemistry, and transcriptomics. Our data indicated the expression of <em>Rboh</em> significantly increased, accompanied by a significant upregulated expression of alpha-type carbonic anhydrase 3 (α<em>CA3</em>) and increased extracellular carbonic anhydrase activity in the <em>Rboh</em> overexpressing strains. Interestingly, compared with the wild type, the photosynthetic activity of transgenic strains was significantly higher under the low C<sub>i</sub> and high light condition, implying that the ROS signal triggered by overexpression of <em>Rboh</em> was involved in regulating the C<sub>i</sub> absorption and utilization in <em>P. yezoensis</em> when the C<sub>i</sub> source was limited. In summary, this study provided evidence supporting the correlation between the ROS production and the Ci utilization under stress environments in <em>P. yezoensis</em>.</div></div>","PeriodicalId":20273,"journal":{"name":"Plant Science","volume":"356 ","pages":"Article 112497"},"PeriodicalIF":4.2000,"publicationDate":"2025-04-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Overexpression of Rboh enhances inorganic carbon acquisition through coordinating with carbonic anhydrase in Pyropia yezoensis\",\"authors\":\"Zhizhuo Shao , Menglin Guo , Hong Wang , Wenhui Gu , Xiujun Xie , Guangce Wang\",\"doi\":\"10.1016/j.plantsci.2025.112497\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div><em>Pyropia yezoensis</em> is an important intertidal economic macroalgae, which is periodically affected by various stresses, such as the limitation of inorganic carbon (C<sub>i</sub>) deficiency. Under such environment, the redox homeostasis within the cells of <em>P. yezoensis</em> is seriously affected, and the reactive oxygen species (ROS) signal transduction system would be activated to regulate the photosynthetic activity. Therefore, how <em>P. yezoensis</em> manage ROS to maintain effective photosynthetic carbon fixation has aroused great interest. Here, we characterize transformants overexpressing respiratory burst oxidase homolog (<em>Rboh</em>), an important gene that can actively produce ROS, at the levels of cellular physiology, biochemistry, and transcriptomics. Our data indicated the expression of <em>Rboh</em> significantly increased, accompanied by a significant upregulated expression of alpha-type carbonic anhydrase 3 (α<em>CA3</em>) and increased extracellular carbonic anhydrase activity in the <em>Rboh</em> overexpressing strains. Interestingly, compared with the wild type, the photosynthetic activity of transgenic strains was significantly higher under the low C<sub>i</sub> and high light condition, implying that the ROS signal triggered by overexpression of <em>Rboh</em> was involved in regulating the C<sub>i</sub> absorption and utilization in <em>P. yezoensis</em> when the C<sub>i</sub> source was limited. In summary, this study provided evidence supporting the correlation between the ROS production and the Ci utilization under stress environments in <em>P. yezoensis</em>.</div></div>\",\"PeriodicalId\":20273,\"journal\":{\"name\":\"Plant Science\",\"volume\":\"356 \",\"pages\":\"Article 112497\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-04-05\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Science\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0168945225001153\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Science","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168945225001153","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Overexpression of Rboh enhances inorganic carbon acquisition through coordinating with carbonic anhydrase in Pyropia yezoensis
Pyropia yezoensis is an important intertidal economic macroalgae, which is periodically affected by various stresses, such as the limitation of inorganic carbon (Ci) deficiency. Under such environment, the redox homeostasis within the cells of P. yezoensis is seriously affected, and the reactive oxygen species (ROS) signal transduction system would be activated to regulate the photosynthetic activity. Therefore, how P. yezoensis manage ROS to maintain effective photosynthetic carbon fixation has aroused great interest. Here, we characterize transformants overexpressing respiratory burst oxidase homolog (Rboh), an important gene that can actively produce ROS, at the levels of cellular physiology, biochemistry, and transcriptomics. Our data indicated the expression of Rboh significantly increased, accompanied by a significant upregulated expression of alpha-type carbonic anhydrase 3 (αCA3) and increased extracellular carbonic anhydrase activity in the Rboh overexpressing strains. Interestingly, compared with the wild type, the photosynthetic activity of transgenic strains was significantly higher under the low Ci and high light condition, implying that the ROS signal triggered by overexpression of Rboh was involved in regulating the Ci absorption and utilization in P. yezoensis when the Ci source was limited. In summary, this study provided evidence supporting the correlation between the ROS production and the Ci utilization under stress environments in P. yezoensis.
期刊介绍:
Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment.
Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.