A. Pacheco et al., MULTIFREQUENCY ESEEM SPECTROSCOPY OF SULFITE OXIDASE IN PHOSPHATE BUFFER - DIRECT EVIDENCE FOR COORDINATED PHOSPHATE, Inorganic chemistry, 35(24), 1996, pp. 7001-7008
The molybdenum(V) coordination environment of sulfite oxidase has been
investigated by multifrequency ESEEM spectroscopy in similar to 70 mM
phosphate buffer at pH = 6.5 in both H2O and D2O. The FT-ESEEM spect
ra in H2O typically consist of three lines. One of these lines is alwa
ys close to twice the Larmor frequency of the P atom (2 nu(P)) and is
assigned to one or more coordinated phosphates, providing the first di
rect unambiguous detection of such coordination. Extensive simulations
of this phosphate signal at the various operational frequencies indic
ated that the coordinated phosphate group(s) probably does (do) not ad
opt a fixed orientation, and as a result, a description of the Mo...P
hyperfine interaction required the introduction of a distribution of s
uch orientations, with Mo...P distance(s) of 3.2-3.3 Angstrom. The oth
er two lines in the FT-ESEEM spectra in H2O, located at nu(H) and 2v(H
), were assigned to matrix protons, In D2O buffer two additional lines
, assigned to matrix deuterons, were also seen.