An unexpected turn. NikO, the putative enolpyruvyl transferase involved in the formation of the aminohexuronic acid moiety of nikkomycins catalyzes the formation of 3′‐enolpyruvyl‐UMP from UMP (see scheme). This finding contradicts the current model for the biosynthesis of aminohexuronic acid.
UDP-N-acetylglucosamine enolpyruvyl transferase (MurA), catalyzes the first step in the biosynthesis of peptidoglycan, involving the transfer of the intact enolpyruvyl moiety from phosphoenolpyruvate to the 3¢-hydroxyl group of UDP-Nacetylglucosamine (UDPNAG). The enzyme is irreversibly inhibited by the antibiotic fosfomycin. The inactivation is caused by alkylation of a highly conserved cysteine residue (C115) that participates in the binding of phosphoenolpyruvate. The three-dimensional structure of the enzyme suggests that two residues may play a decisive role in fosfomycin binding: K22 and R120. To investigate the role of these residues, we have generated the K22V, K22E, K22R and R120K single mutant proteins as well as the K22V/ R120K and K22V/R120V double mutant proteins. We demonstrated that the K22R mutant protein behaves similarly to wild-type enzyme, whereas the K22E mutant protein failed to form the covalent adduct. On the other hand, the K22V mutant protein requires the presence of UDPNAG for the formation of the adduct indicating that UDPNAG plays a crucial role in the organization of productive interactions in the active site. This model receives strong support from heat capacity changes observed for the K22V/R120K and R120K mutant proteins: in both mutant proteins, the heat capacity changes are markedly reduced indicating that their ability to form a closed protein conformation is impeded due to the R120K exchange.
Background: Nikkomycins are potent antibiotics. NikO is a key enzyme in their biosynthesis. Results: NikO is structurally closely related to other enolpyruvyl transferases and is inhibited by fosfomycin. Conclusion: Conservation of important active site residues indicates mechanistic similarities to MurA. Significance: The structure of NikO is the first of an enzyme participating in the formation of the aminohexuronic acid moiety in nikkomycin biosynthesis.
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