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艾晓寒, 夏亦雪, 许萍萍, 涂晓杰, 毕永红. 雪衣藻叶绿素荧光特性及抗氧化系统对汞胁迫的响应[J]. 水生生物学报, 2024, 48(5): 753-761. DOI: 10.7541/2024.2023.0290
引用本文: 艾晓寒, 夏亦雪, 许萍萍, 涂晓杰, 毕永红. 雪衣藻叶绿素荧光特性及抗氧化系统对汞胁迫的响应[J]. 水生生物学报, 2024, 48(5): 753-761. DOI: 10.7541/2024.2023.0290
AI Xiao-Han, XIA Yi-Xue, XU Ping-Ping, TU Xiao-Jie, BI Yong-Hong. RESPONSE OF CHLOROPHYLL FLUORESCENCE CHARACTERISTICS AND ANTIOXIDANT SYSTEMS OF CHLAMYDOMONAS NIVALIS UNDER MERCURY STRESS[J]. ACTA HYDROBIOLOGICA SINICA, 2024, 48(5): 753-761. DOI: 10.7541/2024.2023.0290
Citation: AI Xiao-Han, XIA Yi-Xue, XU Ping-Ping, TU Xiao-Jie, BI Yong-Hong. RESPONSE OF CHLOROPHYLL FLUORESCENCE CHARACTERISTICS AND ANTIOXIDANT SYSTEMS OF CHLAMYDOMONAS NIVALIS UNDER MERCURY STRESS[J]. ACTA HYDROBIOLOGICA SINICA, 2024, 48(5): 753-761. DOI: 10.7541/2024.2023.0290

雪衣藻叶绿素荧光特性及抗氧化系统对汞胁迫的响应

RESPONSE OF CHLOROPHYLL FLUORESCENCE CHARACTERISTICS AND ANTIOXIDANT SYSTEMS OF CHLAMYDOMONAS NIVALIS UNDER MERCURY STRESS

  • 摘要: 文章选用对汞(Hg)具有较强耐受性的雪衣藻(Chlamydomonas nivalis)为对象, 探究藻细胞对汞胁迫的响应及其耐受机制。结果表明, Hg2+对藻细胞的胁迫具有明显的时间依赖的量效关系, 48h半数效应浓度EC50为1.44 mg/L。与对照组相比, 1.0和1.5 mg/L Hg2+ 处理组能维持生长和光合活性; 2.0 mg/L Hg2+处理组生物量和色素含量在胁迫6h时无显著变化(P>0.05), 48h时均显著降低(P<0.05)。随着Hg2+浓度和暴露时间的增加, 藻细胞最大光化学量子产率(Fv/Fm)、最大电子传递速率(ETRmax)、半饱和光强(Ik)及光能利用效率(α)均降低, OJIP快速荧光诱导动力学曲线和\rmQ^-_\rmA再氧化变化明显, 光合电子传递受阻。Hg2+胁迫导致能量流的变化, 藻细胞部分反应中心失活, 显著增加用于热耗散的能量, 并提高有活性的反应中心的光合作用效率, 从而维持能量平衡和生命代谢活动。光合损伤也造成细胞活性氧(ROS)含量上升, 总可溶性蛋白含量降低, 超氧化物歧化酶(SOD)活性显著升高、还原型谷胱甘肽(GSH)含量降低, 以缓解细胞损伤。研究确认雪衣藻具有较强的Hg2+耐受性, 光系统Ⅱ是Hg2+的作用靶标; 光合能量分配及抗氧化系统是细胞对抗Hg2+胁迫的重要解毒机制。

     

    Abstract: Mercury (Hg) pollution is a global environmental problem and a major hazard to human health. Investigating the interactions between algae and Hg can provide a scientific basis for the assessment of Hg toxicity and ecological risk in aquatic ecosystems, as well as the bioremediation of Hg pollution. In this study, we selected Chlamydomonas nivalis as the object due to its strong adaptive ability to Hg, aiming to understand how algal cells respond to mercury stress and its tolerance mechanism. The results showed a time-dependent quantitative relationship between Hg2+ stress and algal cells, with a 48h half-effect concentration of 1.44 mg/L. Compared with the control group, algal cells subjected to low concentrations of Hg2+(≤1.5 mg/L) maintained growth and photosynthetic activity. The biomass and pigment content of the 2.0 mg/L Hg2+ treated group did not change significantly (P>0.05) at 6h of stress, but both decreased significantly (P<0.05) at 48h. As Hg2+ concentration and exposure time increased, the maximal photochemical efficiency, the maximum electron transfer reaction, half-saturation light intensity, and light use efficiency were reduced. Algal cells experienced inhibited photosynthetic electron transfer, as evidenced by notable alterations in rapid fluorescence-induced kinetic curve and \rmQ^-_\rmA reoxidation. Hg2+ stress disrupted energy flow, inactivated reaction centers in algal cells, led to a significant increase in energy dissipation, and elevated the photosynthetic efficiency of active reaction centers, maintaining energy balance and metabolic activity. The damage to the photosynthetic system led to an increase in the cellular reactive oxygen species content, a decrease in the total soluble protein content, a significant increase in superoxide dismutase activity and a decrease in the reduced glutathione content. In this study, we confirmed that Hg2+ tolerance was strong in Chlamydomonas nivalis, and photosystem Ⅱ was the target of Hg2+; the photosynthetic energy allocation strategy and antioxidant system were the important detoxification mechanisms of cells against Hg2+ stress.

     

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