MULTIFREQUENCY ESEEM SPECTROSCOPY OF SULFITE OXIDASE IN PHOSPHATE BUFFER - DIRECT EVIDENCE FOR COORDINATED PHOSPHATE

Citation
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
Citations number
36
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
00201669
Volume
35
Issue
24
Year of publication
1996
Pages
7001 - 7008
Database
ISI
SICI code
0020-1669(1996)35:24<7001:MESOSO>2.0.ZU;2-Q
Abstract
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.