The photosynthetic performance and photoprotective role of carotenoids response to light stress in intertidal red algae Neoporphyra haitanensis

IF 2.8 3区 生物学 Q1 MARINE & FRESHWATER BIOLOGY
Yongbo Huang, Ziyu Weng, Shuang Li, Shuyu Zhang, Haimin Chen, Qijun Luo, Rui Yang, Tao Liu, Tiegan Wang, Peng Zhang, Juanjuan Chen
{"title":"The photosynthetic performance and photoprotective role of carotenoids response to light stress in intertidal red algae Neoporphyra haitanensis","authors":"Yongbo Huang,&nbsp;Ziyu Weng,&nbsp;Shuang Li,&nbsp;Shuyu Zhang,&nbsp;Haimin Chen,&nbsp;Qijun Luo,&nbsp;Rui Yang,&nbsp;Tao Liu,&nbsp;Tiegan Wang,&nbsp;Peng Zhang,&nbsp;Juanjuan Chen","doi":"10.1111/jpy.13480","DOIUrl":null,"url":null,"abstract":"<p><i>Neoporphyra haitanensis</i>, a red alga harvested for food, thrives in the intertidal zone amid dynamic and harsh environments. High irradiance represents a major stressor in this habitat, posing a threat to the alga's photosynthetic apparatus. Interestingly, <i>N. haitanensis</i> has adapted to excessive light despite the absence of a crucial xanthophyll cycle-dependent photoprotection pathway. Thus, it is valuable to investigate the mechanisms by which <i>N. haitanensis</i> copes with excessive light and to understand the photoprotective roles of carotenoids. Under high light intensities and prolonged irradiation time, <i>N. haitanensis</i> displayed reduction in photosynthetic efficiency and phycobiliproteins levels, as well as different responses in carotenoids. The decreased carotene contents suggested their involvement in the synthesis of xanthophylls, as evidenced by the up-regulation of lycopene-β-cyclase (<i>lcyb</i>) and zeaxanthin epoxidase (<i>zep</i>) genes. Downstream xanthophylls such as lutein, zeaxanthin, and antheraxanthin increased proportionally to light stress, potentially participating in scavenging reactive oxygen species (ROS). When accompanied by the enhanced activity of ascorbate peroxidase (APX), these factors resulted in a reduction in ROS production. The responses of intermediates α-cryptoxanthin and β-cryptoxanthin were felt somewhere between carotenes and zeaxanthin/lutein. Furthermore, these changes were ameliorated when the organism was placed in darkness. In summary, down-regulation of the organism's photosynthetic capacity, coupled with heightened xanthophylls and APX activity, activates photoinhibition quenching (qI) and antioxidant activity, helping <i>N. haitanensis</i> to protect the organism from the damaging effects of excessive light exposure. These findings provide insights into how red algae adapt to intertidal lifestyles.</p>","PeriodicalId":16831,"journal":{"name":"Journal of Phycology","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Phycology","FirstCategoryId":"99","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jpy.13480","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MARINE & FRESHWATER BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Neoporphyra haitanensis, a red alga harvested for food, thrives in the intertidal zone amid dynamic and harsh environments. High irradiance represents a major stressor in this habitat, posing a threat to the alga's photosynthetic apparatus. Interestingly, N. haitanensis has adapted to excessive light despite the absence of a crucial xanthophyll cycle-dependent photoprotection pathway. Thus, it is valuable to investigate the mechanisms by which N. haitanensis copes with excessive light and to understand the photoprotective roles of carotenoids. Under high light intensities and prolonged irradiation time, N. haitanensis displayed reduction in photosynthetic efficiency and phycobiliproteins levels, as well as different responses in carotenoids. The decreased carotene contents suggested their involvement in the synthesis of xanthophylls, as evidenced by the up-regulation of lycopene-β-cyclase (lcyb) and zeaxanthin epoxidase (zep) genes. Downstream xanthophylls such as lutein, zeaxanthin, and antheraxanthin increased proportionally to light stress, potentially participating in scavenging reactive oxygen species (ROS). When accompanied by the enhanced activity of ascorbate peroxidase (APX), these factors resulted in a reduction in ROS production. The responses of intermediates α-cryptoxanthin and β-cryptoxanthin were felt somewhere between carotenes and zeaxanthin/lutein. Furthermore, these changes were ameliorated when the organism was placed in darkness. In summary, down-regulation of the organism's photosynthetic capacity, coupled with heightened xanthophylls and APX activity, activates photoinhibition quenching (qI) and antioxidant activity, helping N. haitanensis to protect the organism from the damaging effects of excessive light exposure. These findings provide insights into how red algae adapt to intertidal lifestyles.

潮间带红藻 Neoporphyra haitanensis 的光合性能和类胡萝卜素对光胁迫的光保护作用。
新海藻(Neoporphyra haitanensis)是一种用作食物的红色藻类,在潮间带的动态和恶劣环境中茁壮成长。高辐照度是这种栖息地的主要压力源,对藻类的光合装置构成威胁。有趣的是,尽管缺乏依赖于黄绿素循环的重要光保护途径,但海坛藻仍能适应过强的光照。因此,研究海坛藻应对过度光照的机制以及了解类胡萝卜素的光保护作用非常有价值。在高光照强度和长时间照射下,海坛藻的光合效率和藻体蛋白水平降低,类胡萝卜素的反应也不同。胡萝卜素含量的减少表明它们参与了黄绿素的合成,这从番茄红素-β-环化酶(lcyb)和玉米黄素环氧化酶(zep)基因的上调可以得到证明。叶黄素、玉米黄质和花叶黄质等下游黄体素随光胁迫成比例增加,可能参与清除活性氧(ROS)。当抗坏血酸过氧化物酶(APX)的活性增强时,这些因子会减少 ROS 的产生。中间体α-隐黄素和β-隐黄素的反应介于胡萝卜素和玉米黄质/叶黄素之间。此外,将生物体置于黑暗环境中时,这些变化会得到改善。总之,生物体光合作用能力的下调,加上黄体素和 APX 活性的提高,激活了光抑制淬灭(qI)和抗氧化活性,从而帮助海红藻保护生物体免受过度光照的损害。这些发现为红藻如何适应潮间带生活方式提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Phycology
Journal of Phycology 生物-海洋与淡水生物学
CiteScore
6.50
自引率
3.40%
发文量
69
审稿时长
2 months
期刊介绍: The Journal of Phycology was founded in 1965 by the Phycological Society of America. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, taxonomist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems. All aspects of basic and applied research on algae are included to provide a common medium for the ecologist, physiologist, cell biologist, molecular biologist, morphologist, oceanographer, acquaculturist, systematist, geneticist, and biochemist. The Journal also welcomes research that emphasizes algal interactions with other organisms and the roles of algae as components of natural ecosystems.
×
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:481959085
Book学术官方微信