Computational insight into biotransformation of halophenols by cytochrome P450: Mechanism and reactivity for epoxidation. (January 2022)

• Record Type: Journal Article
• Authors: Han, Cenyang; Zhu, Wenyou; Ma, Guangcai; Chen, Yewen; Li, Xinqi; Wei, Xiaoxuan; Yu, Haiying
• Is Part Of: Chemosphere. Volume 286:Part 2(2022)
• Publication Date: 2022-01
• Subjects: Halophenol -- Epoxidation -- Cytochrome P450 -- Quantum chemical calculation; Pollution -- Periodicals; Pollution -- Physiological effect -- Periodicals; Environmental sciences -- Periodicals; Atmospheric chemistry -- Periodicals; 551.511
• DOI: 10.1016/j.chemosphere.2021.131708
• Languages: English
• ISSNs: 0045-6535

Abstract

Abstract: Halophenols (XPs) have aroused great interests due to their high toxicity and low biodegradability. Previous experimental studies have shown that XPs can be catalytically transformed into epoxides and haloquinones by cytochrome P450 enzymes (CYPs). However, these metabolites have never been detected directly. Moreover, the effects of the reaction site and the type and number of halogen substituents on the biotransformation reactivity of halophenols still remain unknown. In this work, we performed density functional theory (DFT) calculations to simulate the CYP-mediated biotransformation of 36 XPs with mono-, di-, and tri-halogen (F, Cl, and Br) substitutions to unravel the mechanism and relevant kinetics of XPs epoxidation. The whole epoxidation process consists of initial rate-determining O-addition and subsequent ring-closure steps. The simulation results show that the epoxidation in low-spin (LS) state is kinetically preferred over that in high-spin (HS) state, and the formation of epoxide metabolite is strongly exothermic. For all XPs, the epoxidation reactivity follows the order of ortho/para O-addition > meta O-addition. Moreover, the O-addition with higher energy barriers roughly corresponds to chlorophenols and fluorophenols with more halogen atoms. Compared with dichlorophenols, the additional ortho-Cl substitution on trichlorophenols can slightly increase the energy barriers of meta O-addition. By contrast, the additional inclusion of an ortho-Cl to monochlorophenols enhances the meta O-addition reactivity of dichlorophenols. Overall, the present work clarifies the biotransformation routes of XPs to produce epoxides, and identifies the key factors affecting the epoxidation reactivity, which are beneficial in understanding comprehensively the metabolic fate and toxicity of XPs. Highlights: Epoxidation pathway contains initial rate-determining O-addition and subsequent ring-closure steps. O-addition reactivity follows the order of ortho/para > meta site. More F/Cl substituents result in higher energy barrier for O-addition. Additional inclusion of ortho-Cl atom to dichlorophenol slightly reduces the meta O-addition reactivity.