Turkey Tail, Yun Zhi · 2024 · Research Support, Non U.S. Gov'T
High relevanceMechanism of non-phenolic substrate oxidation by the fungal laccase Type 1 copper site from Trametes versicolor: the case of benzo[a]pyrene and anthracene.
Trametes versicolor
Key points
- Laccases (EC 1.10.3.2) are multicopper oxidases with the capability to oxidize diverse phenolic and non-phenolic substrates
- While the molecular mechanism of their activity towards phenolic substrates is well-established, their reactivity towards non-phenolic substrates, such as polycyclic aromatic hydrocarbons (PAHs), remains unclear
- To elucidate the oxidation mechanism of PAHs, particularly the activation mechanism of the sp 2 aromatic C-H bond, we conducted a density functional theory investigation on the oxidation of two PAHs (anthracene and benzo[ a ]pyrene) using an extensive model of the T1 copper catalytic site of the fungal laccase from Trametes versicolor
Metadata-grounded summary
Citation abstract
Laccases (EC 1.10.3.2) are multicopper oxidases with the capability to oxidize diverse phenolic and non-phenolic substrates. While the molecular mechanism of their activity towards phenolic substrates is well-established, their reactivity towards non-phenolic substrates, such as polycyclic aromatic hydrocarbons (PAHs), remains unclear. To elucidate the oxidation mechanism of PAHs, particularly the activation mechanism of the sp 2 aromatic C-H bond, we conducted a density functional theory investigation on the oxidation of two PAHs (anthracene and benzo[ a ]pyrene) using an extensive model of the T1 copper catalytic site of the fungal laccase from Trametes versicolor.
Citation
Orlando C, Rizzo IC, Arrigoni F, Zampolli J, Mangiagalli M, Di Gennaro P, et al. (2024). Mechanism of non-phenolic substrate oxidation by the fungal laccase Type 1 copper site from Trametes versicolor: the case of benzo[a]pyrene and anthracene. Dalton transactions (Cambridge, England: 2003) https://doi.org/10.1039/d4dt01377h PMID: 38989958
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