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JBC, Vol. 254, Issue 19, 9640-9650, Oct, 1979
V. Massey, S. Ghisla and E. G. Moore
Representative examples of the various classes of flavoproteins have been
converted to their apoprotein forms and the native flavin replaced by
8-mercapto-FMN or 8-mercapto-FAD. The spectral and catalytic properties of
the modified enzymes are characteristically different from one group to
another; the results suggest that flavin interactions at positions N(1) or
N(5) of the flavin chromophore have profound influences on the properties
of the flavoprotein. 1. The 8-thiolate anion form of 8-mercaptoflavin has
an absorption maximum in the region 520 to 550 nm epsilon approximately 30
mM-1 cm-1). This form is retained on binding to flavoproteins whose
physiological reactions involve obligatory one-electron transfers (e.g.
flavodoxin, NADPH-cytochrome P-450 reductase). In the native form these
enzymes stabilize the blue neutral radical of the flavin. A radical form of
8-mercaptoflavin is also stabilized by these proteins. 2. The p-quinoid
form of 8-mercaptoflavin has an absorption maximum in the range 560 to 600
nm (epsilon approximately 30 mM-1 cm-1). This form is stabilized on binding
to flavoproteins of the dehydrogenase-oxidase class (e.g. glucose oxidase,
D-amino acid oxidase, lactate oxidase, Old Yellow Enzyme). These same
enzymes in their native flavin form stabilize the red semiquinone, and have
a pronounced reactivity with sulfite to form flavin N(5)-sulfite adducts.
These properties of the native enzyme, including the ability to react with
nitroalkane carbanions, are not exhibited by the 8-mercaptoflavoproteins.
3. A group of flavoenzymes fails to conform strictly to the above
classification, exhibiting some properties of both classes. These include
the examples of flavoprotein hydroxylases and transhydrogenases studied. 4.
The riboflavin-binding protein of hen egg whites binds 8-mercaptoriboflavin
preferentially in the unionized state, resulting in a shift in pK from 3.8
with free 8-mercaptoriboflavin to greater than or equal to 9.0 with the
protein-bound form.
8-Mercaptoflavins as active site probes of flavoenzymes
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