Key Laboratory of Coastal Zone Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, PR China; Shandong Marine Resource and Environment Research Institute, Yantai 264006, PR China.
Key Laboratory of Coastal Zone Environmental Processes and Ecological Remediation, Yantai Institute of Coastal Zone Research, Chinese Academy of Sciences, Yantai 264003, PR China; Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266237, PR China.
Aquat Toxicol. 2018 Nov;204:9-18. doi: 10.1016/j.aquatox.2018.08.016. Epub 2018 Aug 23.
The major hazard of arsenic in living organisms is increasingly being recognized. Marine mollusks are apt to accumulate high levels of arsenic, but knowledge related to arsenic detoxification in marine mollusks is still less than sufficient. In this study, arsenic bioaccumulation as well as the role of glutathione S-transferase omega (GSTΩ) in the process of detoxification were investigated in the Ruditapes philippinarum clam after waterborne exposure to As(III) or As(V) for 30 days. The results showed that the gills accumulated significantly higher arsenic levels than the digestive glands. Arsenobetaine (AsB) and dimethylarsenate (DMA) accounted for most of the arsenic found, and monomethylarsonate (MMA) can be quickly metabolized. A subcellular distribution analysis showed that most arsenic was in biologically detoxified metal fractions (including metal-rich granules and metallothionein-like proteins), indicating their important roles in protecting cells from arsenic toxicity. The relative mRNA expressions of two genes encoding GSTΩ were up-regulated after arsenic exposure, and the transcriptional responses were more sensitive to As(III) than As(V). The recombinant GSTΩs exhibited high activities at optimal conditions, especially at 37 °C and pH 4-5, with an As(V) concentration of 60 mM. Furthermore, the genes encoding GSTΩ significantly enhance the arsenite tolerance but not the arsenate tolerance of E. coli AW3110 (DE3) (ΔarsRBC). It can be deduced from these results that GSTΩs play an important role in arsenic detoxification in R. philippinarum.
生物体中砷的主要危害正日益受到重视。海洋贝类容易积累高水平的砷,但有关海洋贝类砷解毒的知识仍然不足。在这项研究中,研究了菲律宾蛤仔在暴露于砷(III)或砷(V) 30 天后,通过水相摄入砷时砷的生物累积以及谷胱甘肽 S-转移酶 ω(GSTΩ)在解毒过程中的作用。结果表明,鳃比消化腺积累了明显更高水平的砷。砷甜菜碱(AsB)和二甲基砷酸(DMA)占发现砷的大部分,而一甲基砷酸(MMA)可以迅速代谢。亚细胞分布分析表明,大部分砷位于具有生物解毒功能的金属部分(包括富含金属的颗粒和金属硫蛋白样蛋白)中,这表明它们在保护细胞免受砷毒性方面发挥着重要作用。砷暴露后,编码 GSTΩ 的两个基因的相对 mRNA 表达上调,且对 As(III)的转录响应比 As(V)更敏感。重组 GSTΩs 在最佳条件下表现出高活性,尤其是在 37°C 和 pH4-5 时,其砷(V)浓度为 60mM。此外,编码 GSTΩs 的基因显著增强了大肠杆菌 AW3110(DE3)(ΔarsRBC)的亚砷酸盐耐受性,但不能增强砷酸盐耐受性。由此可以推断,GSTΩs 在菲律宾蛤仔的砷解毒中发挥着重要作用。