Mirams, Ruth ESmith, Sarah JHadler, Kieran SOllis, DavidSchenk, GerhardGahan, Lawrence2015-12-100949-8257http://hdl.handle.net/1885/52366The glycerophosphodiester-degrading enzyme GpdQ from Enterobacter aerogenes is a promising bioremediator owing to its ability to degrade some organophosphate pesticides and diester products originating from the hydrolysis of nerve agents such as VX. Here, the cadmium derivative of GpdQ was prepared by reconstituting the apoenzyme. Catalytic measurements with (Cd2+)2-GpdQ and the phosphodiester substrate bis(4-nitrophenyl)phosphate yield kcat = 15 s-1. The pKa of 9.4, determined from the pH dependence of the catalytic activity, implicates a hydroxide ligand as the catalytic nucleophile. Also prepared was the cadmium-containing biomimetic [Cd2((HP)2B)(OAc)2(OH2)](PF6) (where (HP)2B is [2,6-bis([(2-pyridylmethyl)(2-hydroxyethyl)amino]methyl)-4- methylphenol]), which mimics the asymmetry of the metal ion coordination in the active site of GpdQ. The phosphoesterase-like activity of [Cd2((HP)2B)(OAc)2(OH2)](PF6) was studied using the substrate bis(2,4-dinitrophenyl)phosphate, yielding a kinetically relevant pKa of 8.9, with kcat = 0.004 s-1. In summary, the model is both an adequate structural and a reasonable functional mimic of GpdQ.Keywords: [2,6 bis[[(2 pyridylmethyl)(2 hydroxyethyl)amino]methyl] 4 methylphenol]; apoenzyme; biomimetic material; bis(4 nitrophenyl) phosphate; cadmium; cadmium derivative; GpdQ enzyme; hydroxide; ligand; phosphodiesterase; unclassified drug; article; biomimetics Binuclear metallohydrolases; Biomimetics; Bioremediation; Cadmium complexes; Glycerophosphodiester-degrading enzyme200810.1007/s00775-008-0392-52015-12-09