光合作用
金鱼藻
水生植物
光合效率
生物化学
塑料醌
光合反应中心
生物
化学
生物物理学
叶绿体
生态学
水生植物
类囊体
基因
作者
Xiang Li,Weitao Liu,Ruiying Shi,Yichen Ge,Qi Wang,Chuan Yin,Jinzheng Liu,Xinwei Shi,Fan Mo,Cuihong Chen,Jing An
标识
DOI:10.1021/acs.est.5c03958
摘要
Emerging evidence indicates that N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine (6PPD) and its derivative 6PPD-quinone (6PPD-Q) exert photosynthetic toxicity on aquatic macrophytes. However, their precise inhibitory mechanisms and toxic targets within the photosynthetic pathways remain poorly understood. Through a combination of physio-biochemical indicators, multiomics analysis, and molecular docking simulation, this study systematically explored the photosynthetic toxic effects of 6PPD and 6PPD-Q on Ceratophyllum demersum L. (C. demersum). Transcriptomic data identified photosynthetic antenna proteins as primary molecular targets, with both contaminants perturbing the transcriptional regulation of genes and impairing the structural plasticity of associated proteins. These molecular perturbations consequently disrupted the photosynthetic electron transport efficiency. Metabolomic evidence revealed subsequent carbohydrate metabolism imbalances, suggesting compromised carbon fixation capacity of C. demersum. Additionally, molecular docking simulations demonstrated superior binding affinities for both compounds with antenna proteins, particularly emphasizing the enhanced interactions mediated by 6PPD-Q's quinone structure. Comparative analysis indicated that 6PPD-Q's structural modifications may confer greater photosynthetic toxicity compared to the parent compound 6PPD. This multiomics investigation reveals the mechanistic basis of 6PPD and 6PPD-Q-driven photosynthetic toxicity and underscores their potential to destabilize aquatic ecosystems by disrupting primary productivity.
科研通智能强力驱动
Strongly Powered by AbleSci AI