A QM/MM investigation of the catalytic mechanism of acetylene hydratase: insights into engineering a more effective enzyme

In the present investigation, a QM/MM approach was used to better understand the effect of the second environmental shell of the active site on the catalytic conversion of acetylene to acetaldehyde by acetylene hydratase (AH). In addition, the effect of substituting W-coordinating sulfur atoms with selenium atoms was done to provide insight into the influence of the W-coordinating atoms on the catalytic reaction. From the results, it found that the presence of the second shell environment had a significant effect on the reaction. Specifically, in the absence of the MM second shell environment (i.e., QM-cluster model), the rate-determining step is defined by the first proton transfer step. In contrast, for the QM/MM model, the rate-determining step is defined by the water attacking step. Moreover, with the presence of the MM second shell environment, a key intermediate found in the DFT-cluster investigation does not exist in the QM/MM investigation. Rather, what was a two-step process in the DFT-cluster study was calculated to occur in a single step for the QM/MM study. Regarding the sulfur to selenium substitutions, it was found that Gibbs energy for the acetylene binding phase was significantly affected. Notably, the trans-position selenium made the binding of acetylene 65.6 kJ mol(-1) less endergonic. Moreover, the overall reaction became 38.2 kJ mol(-1) less endergonic compared with the wild type (WT) Ali model. Thus, the substitution of key W-coordinating sulfur atoms with selenium atoms may offer a means to enhance the catalytic mechanism of AH considerably.

Automated summary

In this study, the QM/MM approach was used to investigate the impact of the second environmental shell of the active site on the catalytic conversion of acetylene to acetaldehyde by acetylene hydratase (AH). Results indicated that the presence of the second shell environment significantly affected the reaction, and substitutions of sulfur atoms with selenium atoms had a notable impact on the Gibbs energy for acetylene binding. The study suggested that substituting key W-coordinating sulfur atoms with selenium atoms may enhance the catalytic mechanism of AH.