Zhang Chengyu, Wang Danni, Wang Cong, Yu Huijuan, Zhong Peng, Dang Weifan, Yang Yufan, Wang Yuefei, Yan Xiaohui
State Key Laboratory of Chinese Medicine Modernization, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China; Haihe Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China.
State Key Laboratory of Chinese Medicine Modernization, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China; Haihe Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 301617, China.
J Hazard Mater. 2025 Mar 5;485:136829. doi: 10.1016/j.jhazmat.2024.136829. Epub 2024 Dec 9.
Aflatoxin B1 (AFB1) exposure often causes serious food safety problems and illnesses in humans and animals, even at extremely low content. Therefore, effective degradation of AFB1 is vitally significant. Biodegradation by enzymes is an effective method to eliminate hazardous toxins, but the degradation efficiency and cost of the enzyme limit its wide application. In this work, we found that CotA derived from Bacillus subtilis can rapidly degrade AFB1 into small molecules with low toxicity. Molecular docking analysis was used to evaluate the feasibility of rapid degradation of AFB1 by CotA, and the UPLC-Q-TOF-MS was used to deduce the degradation products and pathways. Two biotransformation pathways were proposed based on the structures of these degradation products. Inspired by commercial Ni-NTA purification media, Ni-grafted magnetic nanoparticles (PNMP) were designed to capture CotA from cell-lysis buffer onto the PNMP surface, enabling direct immobilization of CotA to form PNMP@CotA. The PNMP@CotA exhibits higher activity, good tolerance to temperature and pH than free CotA. Furthermore, in vitro and in vivo experiments revealed a significant reduction in the toxicity of AFB1 degradation products.
黄曲霉毒素B1(AFB1)即使含量极低,其暴露也常常会在人类和动物中引发严重的食品安全问题和疾病。因此,有效降解AFB1至关重要。酶促生物降解是消除有害毒素的一种有效方法,但酶的降解效率和成本限制了其广泛应用。在这项工作中,我们发现源自枯草芽孢杆菌的 CotA 能够迅速将AFB1降解为低毒的小分子。利用分子对接分析评估CotA快速降解AFB1的可行性,并使用超高效液相色谱-四极杆-飞行时间质谱(UPLC-Q-TOF-MS)推断降解产物和途径。基于这些降解产物的结构提出了两条生物转化途径。受商业镍-亚氨基二乙酸(Ni-NTA)纯化介质的启发,设计了镍接枝磁性纳米颗粒(PNMP),将CotA从细胞裂解缓冲液中捕获到PNMP表面,从而能够直接固定CotA以形成PNMP@CotA。PNMP@CotA 比游离CotA表现出更高的活性、对温度和pH的良好耐受性。此外,体外和体内实验表明AFB1降解产物的毒性显著降低。