Li Dandan, Wang Xiaoyu, Xie Chen, Fan Ziwu, Ding Rui, Liu Songqi, Chen Yu, Yu Kai
Nanjing Hydraulic Research Institute, Nanjing 210029, China; Key Laboratory of Taihu Basin Water Resources Management, Ministry of Water Resources, Wuxi 214131, China.
Nanjing Hydraulic Research Institute, Nanjing 210029, China; Key Laboratory of Taihu Basin Water Resources Management, Ministry of Water Resources, Wuxi 214131, China.
J Hazard Mater. 2025 Aug 15;494:138752. doi: 10.1016/j.jhazmat.2025.138752. Epub 2025 May 27.
The widespread co-existence of triphenyl phosphate (TPhP) and heavy metals in sediments raises significant concerns. However, uncertainty still exists regarding the degradation characteristics of TPhP in the presence of cadmium (Cd). Therefore, this research was conducted to elucidate the impacts of Cd on TPhP degradation in sediments. Results showed that the biodegradation efficiency of TPhP in sediments exceeded 90 %. The identified degradation products of TPhP indicated that the degradation pathway primarily involved oxidative cleavage, hydroxylation, and methylation, which was further supported by condensed dual descriptors (CDD). However, the presence of Cd significantly inhibited TPhP degradation, with greater inhibition at higher concentrations of both TPhP and Cd. Transcriptomic analysis revealed that xenobiotic metabolism was significantly suppressed. Furthermore, pathways associated with cell motility, membrane transport, and energy metabolism were impaired. These disruptions likely contributed to the decreased degradation efficiency and prolonged half-life of TPhP. Interestingly, biomarkers in Firmicutes were enriched in the high-concentration TPhP + Cd treatment and strongly correlated with degradation-related gene expression, suggesting their significance in TPhP degradation under heavy metal stress. Overall, this research provides insights into the inhibitory effects of Cd on TPhP degradation and offers theoretical support for the bioremediation of TPhP-contaminated sediments with heavy metals.
沉积物中磷酸三苯酯(TPhP)与重金属的广泛共存引发了人们的重大担忧。然而,在镉(Cd)存在的情况下,TPhP的降解特性仍存在不确定性。因此,开展本研究以阐明Cd对沉积物中TPhP降解的影响。结果表明,沉积物中TPhP的生物降解效率超过90%。鉴定出的TPhP降解产物表明,降解途径主要涉及氧化裂解、羟基化和甲基化,凝聚双描述符(CDD)进一步支持了这一点。然而,Cd的存在显著抑制了TPhP的降解,在TPhP和Cd浓度较高时抑制作用更强。转录组分析表明,异源生物代谢受到显著抑制。此外,与细胞运动、膜转运和能量代谢相关的途径也受到损害。这些干扰可能导致TPhP降解效率降低和半衰期延长。有趣的是,厚壁菌门中的生物标志物在高浓度TPhP + Cd处理中富集,且与降解相关基因表达密切相关,表明它们在重金属胁迫下TPhP降解中具有重要意义。总体而言,本研究深入了解了Cd对TPhP降解的抑制作用,并为生物修复受重金属污染的含TPhP沉积物提供了理论支持。