Formylglycinamide Ribonucleotide Synthetase from Escherichia coli: Cloning, Sequencing, Overproduction, Isolation, and Characterization

The purL gene of Escherichia coli encoding the enzyme formylglycinamidine ribonucleotide (FGAM) synthetase which catalyzes the conversion of formylglycinamide ribonucleotide (FGAR), glutamine, and MgATP to FGAM, glutamate, ADP, and P_i has been cloned and sequenced. The mature protein, as deduced by the structural gene sequence, contains 1628 amino acids and has a calculated M_r of 141 418. Comparison of the purL control region to other pur loci control regions reveals a common region of dyad symmetry which may be the binding site for the “putative” repressor protein. Construction of an overproducing strain permitted purification of the protein to homogeneity. N-Terminal sequence analysis and comparison of glutamine binding domain sequences (Ebbole & Zalkin, 1987) confirm the amino acid sequence deduced from the gene sequence. The purified protein exhibits glutaminase activity of 0.02% the normal turnover, and NH₃ can replace glutamine as a nitrogen donor with a K_m=1 M and a turnover of 3 min⁻¹(2% glutamine turnover). The enzyme forms an isolable (1:1) complex with glutamine: t_1/2 is 22 min at 4°C. This isolated complex is not chemically competent to complete turnover when FGAR and ATP are added, demonstrating that ammonia and glutamine are not covalently bound as a thiohemiaminal available to complete the chemical conversion to FGAM. Hydroxylamine trapping experiments indicate that glutamine is bound covalently to the enzyme as a thiol ester. Initial velocity and dead-end inhibition kinetic studies on FGAM synthetase are most consistent with a sequential mechanism in which glutamine binds followed by rapid equilibrium binding of MgATP and then FGAR. Incubation of [¹⁸O]FGAR with enzyme, ATP, and glutamine results in quantitative transfer of the ¹⁸O to P_i.