Probing the role of protein conformational changes in the mechanism of prenylated-FMN-dependent phenazine-1-carboxylic acid decarboxylase

探究蛋白质构象变化在异戊二烯化FMN依赖性吩嗪-1-羧酸脱羧酶机制中的作用

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Abstract

Phenazine-1-carboxylic acid decarboxylase (PhdA) is a prenylated-FMN-dependent (prFMN) enzyme belonging to the UbiD family of decarboxylases. Many UbiD-like enzymes catalyze (de)carboxylation reactions on aromatic rings and conjugated double bonds and are potentially valuable industrial catalysts. We have investigated the mechanism of PhdA using a slow turnover substrate, 2,3-dimethylquinoxaline-5-carboxylic acid (DQCA). Detailed analysis of the pH dependence and solvent deuterium isotope effects associated with the reaction uncovered unusual kinetic behavior. At low substrate concentrations, a substantial inverse solvent isotope effect (SIE) is observed on V(max)/K(M) of ∼ 0.5 when reaction rates of DQCA in H(2)O and D(2)O are compared. Under the same conditions, a normal SIE of 4.15 is measured by internal competition for proton transfer to the product. These apparently contradictory results indicate that the SIE values report on different steps in the mechanism. A proton inventory analysis of the reaction under V(max)/K(M) and V(max) conditions points to a "medium effect" as the source of the inverse SIE. Molecular dynamics simulations of the effect of D(2)O on PhdA structure support that D(2)O reduces the conformational lability of the enzyme and results in a more compact structure, akin to the active, "closed" conformer observed in crystal structures of some UbiD-like enzymes. Consistent with the simulations, PhdA was found to be more stable in D(2)O and to bind DQCA more tightly, leading to the observed rate enhancement under V(max)/K(M) conditions.

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