COMPARISON OF VIBRATIONAL FREQUENCIES OF CRITICAL BONDS IN GROUND-STATE COMPLEXES AND IN A VANADATE-BASED TRANSITION-STATE ANALOG COMPLEX OF MUSCLE PHOSPHOGLUCOMUTASE - MECHANISTIC IMPLICATIONS

The Symmetric stretching frequency of the P-O bonds of the enzymic pho sphate group in muscle phosphoglucomutase was measured via O-16/O-18 R aman difference spectroscopy. This frequency, and its shift on isotopi c substitution, is characteristic of a dianionic phosphate ester. The P-O stretching frequency is not detectably altered by the binding of t he metal ion activators Mg2+, Zn2+, or Cd2+ nor by the subsequent bind ing of glucose phosphate. Hence, a binding-induced distortion/polariza tion of the enzymic phosphate group in the ground state, or enzyme-sub strate complex, cannot serve as a rationale for the large value of k(c at) in the phosphoglucomutase reaction. By contrast, the stretching fr equency of the V-O bonds within a vanadate group bound at the same sit e in the transition-state analog complex involving glucose 1-phosphate 6-vanadate is much lower than for a normal dianionic vanadate. This l ow V-O stretching frequency is best rationalized in terms of the exten sive polarization of all three nonbridging oxygens of the vanadate est er dianion plus the formation of a weak, fifth bond to the vanadium at om. This distortion/polarization of the VO32- group depends on the met al ion activator, since it is largely abolished, and the involvement o f the fifth ligand eliminated, by substitution of Li+ for Mg2+ at the metal activation site. To the extent that the vanadate-inhibitor compl ex mimics the transition state for the normal phosphoglucomutase react ion, as has been suggested [Ray, W. J., Jr., & Puvathingal, J. M. (199 0) Biochemistry 29, 2790], the normal PO3- transfer is best described as a process with S(N)2-like or associative character and thus is quit e different from the process by which model phosphate ester dianions n ormally react in aqueous solution.