工作流程
机器学习
人工智能
计算机科学
概化理论
转化(遗传学)
生化工程
光催化
工作(物理)
污染物
抗生素
环境科学
吉布斯自由能
抗生素耐药性
产量(工程)
抗性(生态学)
数量结构-活动关系
可扩展性
降级(电信)
密度泛函理论
生物圈
系统工程
人类健康
风险分析(工程)
作者
Chen‐Chen Zhao,Sihan Xing,Cheng Fu,Lifeng Zheng,Huaizhu Wang,Zhong Jin,Shuhua Li,Shujuan Zhang,J. Ma
标识
DOI:10.1002/anie.202520124
摘要
The photocatalytic degradation of antibiotics is effective but may yield transformation products (TPs) that sustain or amplify ecological risks, including antibiotic resistance gene (ARG) induction. This study developed a predictive framework that couples photocatalytic experiments, high-resolution mass spectrometry, density functional theory (DFT) calculations and machine learning (ML) to assess risks of TPs. Using tetracycline as a model compound, we constructed a reaction network over 120 steps and 9 533 reactions, and trained an ML model to rapidly predict Gibbs free energy changes with DFT accuracy. Automatic transition-state searches were integrated to evaluate kinetic accessibility within the network. The generalizability of this approach was validated with pathways of five different antibiotics involving 545 reactions. Furthermore, a multi-dimensional scoring system was developed that integrates diversity, ecotoxicity, biodegradability, and feasibility (DEBF) to prioritize pathways by both reactivity and sustainability. Several hydroxylated, aminated, and amide-ketone TPs were identified as high-risk species with enhanced ARG-binding potential. By bridging molecular energetics with ecological outcomes, this work offers a generalizable, mechanism-anchored, and risk-aware approach for analyzing photocatalytic transformations and deriving design principles for pollutant degradation that balance efficiency with ecological safety.
科研通智能强力驱动
Strongly Powered by AbleSci AI