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。

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
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 ,&nbsp;Menglin Guo ,&nbsp;Hong Wang ,&nbsp;Wenhui Gu ,&nbsp;Xiujun Xie ,&nbsp;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 ,&nbsp;Menglin Guo ,&nbsp;Hong Wang ,&nbsp;Wenhui Gu ,&nbsp;Xiujun Xie ,&nbsp;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}
引用次数: 0

摘要

叶藻(Pyropia yezoensis)是一种重要的潮间带大型经济藻类,它周期性地受到各种胁迫的影响,如无机碳(Ci)缺乏的限制。在这种环境下,yezoensis细胞内氧化还原稳态受到严重影响,激活活性氧(reactive oxygen species, ROS)信号转导系统调节光合活性。因此,叶藻如何管理活性氧以维持有效的光合固碳引起了人们的极大兴趣。在这里,我们在细胞生理学、生物化学和转录组学水平上描述了过度表达呼吸爆发氧化酶同源基因(Rboh)的转化子,Rboh是一种可以积极产生ROS的重要基因。我们的数据显示,Rboh过表达菌株Rboh的表达显著增加,α -型碳酸酐酶3 (αCA3)的表达显著上调,胞外碳酸酐酶活性增加。有趣的是,与野生型相比,转基因菌株在低Ci、高光条件下的光合活性显著提高,这表明在Ci源有限的情况下,Rboh过表达引发的ROS信号参与了调控紫杉对Ci的吸收和利用。综上所述,本研究为叶藻在逆境环境下ROS生成与Ci利用之间的相关性提供了证据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信