对Raphidiopsis raciborskii对冷/光胁迫响应机制的认识。

IF 2.8 3区 生物学 Q1 MARINE & FRESHWATER BIOLOGY
Nada Tokodi, Ewa Latkowska, Barbara Klimczak, Kinga Kłodawska, Przemysław Malec, Anusuya Willis, Mikołaj Kokociński, Adam Antosiak, Dariusz Dziga
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引用次数: 0

摘要

蓝藻,特别是Raphidiopsis raciborskii,以其有害的繁殖而闻名,对水生生态系统构成了重大的生态和经济挑战。本文研究了5株raciborskii菌株CS-505、CS-506、UAM/DH-KmRr、UAM/DH-BiRr和UAM/DH-MRr在低温高光胁迫下的生长、色素组成、光合活性、基因表达和毒素产生等方面的适应机制。结果显示,所有菌株的生长速率在胁迫下均显著降低,其中波兰菌株UAM/DH-MRr表现出最高的恢复力。胁迫条件导致叶绿素a水平降低,类胡萝卜素/Chl a比值升高,提示光保护适应性。光合量子效率(Fv/Fm)在冷/光胁迫下下降,胁迫后恢复,而电子传递速率(rETR)变化不显著。在CS-506和UAM/DH-MRr中,呼吸作用增强,光合出氧能力增强。主成分分析(PCA)强调色素含量和光合电子传递相关参数是影响响应的关键因素;关于广泛的参数范围,在菌株之间没有观察到变量特异性分组。基因表达分析显示,参与光合作用和柱状精子蛋白(CYN)生物合成的基因转录调控存在差异,有毒的CS-505在胁迫下上调cyr基因,而CS-506则下调CYN基因。应激下细胞内CYN水平下降,而CS-505细胞配额增加,这值得进一步研究。我们的研究结果表明菌株对冷/光胁迫的特异性反应的复杂性,并强调了了解生理机制对预测和管理不同气候条件下蓝藻华的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Toward understanding the mechanisms of Raphidiopsis raciborskii response to chill/light stress

Cyanobacteria, particularly Raphidiopsis raciborskii, are known for their harmful blooms, posing significant ecological and economic challenges in aquatic ecosystems. This study investigates the strain-specific adaptive mechanisms of five R. raciborskii strains (CS-505, CS-506, UAM/DH-KmRr, UAM/DH-BiRr, and UAM/DH-MRr) under chill/light stress (low temperature and high light intensity), focusing on growth, pigment composition, photosynthetic activity, gene expression, and toxin production. Results revealed that growth rates were significantly reduced under stress for all strains, with the Polish strain UAM/DH-MRr showing the highest resilience. Stress conditions caused a reduced chlorophyll a level and increased carotenoid/Chl a ratio, suggesting photoprotective adaptations. Photosynthetic quantum efficiency (Fv/Fm) declined during chill/light but was recovered post-stress, while electron transport rates (rETR) were not significantly altered. Enhanced respiration and increased photosynthetic oxygen evolution were observed, particularly in CS-506 and UAM/DH-MRr. Principal component analysis (PCA) highlighted pigment content and parameters related to photosynthetic electron transport as key factors influencing response; no variable-specific groupings were observed among strains regarding the broad range of parameters. Gene expression analyses revealed divergent transcriptional regulation of genes involved in photosynthesis and cylindrospermopsin (CYN) biosynthesis, with toxic CS-505 upregulating cyr genes under stress, while CS-506 down-regulated them. Intracellular CYN levels decreased under stress, yet cell quotas increased in CS-505, which warrants further investigation. Our results indicate the complexity of strain-specific responses to chill/light stress and highlight the importance of understanding physiological mechanisms for predicting and managing cyanobacterial blooms in diverse climates.

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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.
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