The multidomain metalloenzyme SznF can specifically catalyze the conversion of Nω-methyl-l-arginine (l-NMA) to Nδ-hydroxy-Nω-methyl-Nω-nitroso-l-citrulline (l-NHMA), which is the key step for the biosynthesis of the N-nitrosourea pharmacophore, a precursor to the pancreatic cancer drug streptozotocin (SZN). The central domain of SznF is responsible for mediating the two sequential hydroxylations of l-NMA at Nδ and Nω positions to first generate Nδ,Nω-dihydroxy-Nω-methyl-l-arginine (l-DHMA), and the cupin domain of SznF promotes the N-migration and oxidative rearrangement of l-DHMA. This structural rearrangement contains both the C═N bond cleavage and N-N bond formation, and it is very challenging for chemical synthesis. To illuminate the catalytic mechanism of the cupin domain of SznF, we constructed the reactant models and performed a series of QM/MM calculations. We first determined the protonated states of two hydroxyls and imino of l-DHMA by calculating their pKa values, which are considered to be a crucial factor for theoretically exploring the reaction rhythm. The estimated pKa values revealed that the two hydroxyls and imino of l-DHMA should be in protonated states, and the previously proposed reaction mechanism in which superoxo addition to the unsaturated carbon as the first step is unlikely. Instead, the FeII-O2•- unit should first abstract a hydrogen from the Nω-hydroxyl group to trigger the reaction, and then the generated FeIII-OOH attacks the unsaturated carbon to form the peroxide-bridged intermediate, followed by the concerted O-O and N-C bond cleavage leading to the formation of the Fe-coordinated NO radical, which is the precondition for N-migration. During the reaction, the iron ion plays important roles, not only as a central ion to coordinate with the substrate to mediate the H-abstraction, Fe-OOH attack as well as the bond cleavage and formation but also in stabilizing the NO radical and promoting the final N-N bond formation. These results may deepen the understanding of the catalysis of nonheme iron enzymes.
Li et al. (Wed,) studied this question.