Degradation of pesticides diazinon and diazoxon by phosphotriesterase

Enzymatic hydrolysis by phosphotriesterase (PTE) is one of the most effective ways of degrading organophosphorus pesticides, but the catalytic efficiency depends on the structural features of substrates. Here the enzymatic degradation of Diazinon (DIN) and diazoxon (DON), characterized by P[double bond, length as m-dash]S and P[double bond, length as m-dash]O, respectively, have been investigated by QM/MM calculations and MM MD simulations.

Our calculations demonstrate that the hydrolysis of DON (with P[double bond, length as m-dash]O) is inevitably initiated by the nucleophilic attack of the bridging-OH− on the phosphorus center, while for DIN (with P[double bond, length as m-dash]S), we proposed a new degradation mechanism, initiated by the nucleophilic attack of the Znα-bound water molecule, for its low-energy pathway.

For both DIN and DON, the hydrolytic reaction is predicted to be the rate-limiting step, with energy barriers of 18.5 and 17.7 kcal mol−1, respectively. The transportation of substrates to the active site, the release of the leaving group and the degraded product are generally verified to be favorable by MD simulations via umbrella sampling, both thermodynamically and dynamically. The side-chain residues Phe132, Leu271 and Tyr309 play the gate-switching role to manipulate substrate delivery and product release.

In comparison with the DON-enzyme system, the degraded product of DIN is more easily released from the active site. These new findings will contribute to the comprehensive understanding of the enzymatic degradation of toxic organophosphorus compounds by PTE.