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JBC, Vol. 251, Issue 10, 2916-2921, May, 1976
L. A. Bentle and H. A. Lardy
The catalytic activity of phosphoenolpyruvate carboxykinase in rat liver
cytosol is stimulated by incubating with Fe2+, Mn2+, Co2+, and Cd2+. When
purified, the enzyme no longer responds to Fe2+, Co2+, or Cd2+ but retains
a response to Mn2+. Low concentrations of SO4(2-) in the incubation medium
with enzyme and divalent transition metal allow stimulation by Fe2+ and
Co2+ and enhance the response to Mn2+. Under identical conditions,
orthophosphate with Fe2+ is a potent inhibitor of the enzyme (half-maximal
inhibition at 50 muM). A thiol is required in the incubation medium for the
effects of Fe2+ plus sulfate or orthophosphate to be expressed. The
magnitude of these effects depends on the thiol concentration.
Dithiothreitol is more effective than GSH and activation by sulfate plus
Fe2+ appears to require the reduced form of dithiothreitol. Sulfate ion is
not considered to be the physiological Fe2+-activator of P-enolpyruvate
carboxykinase in rat liver cytosol, as this function is fulfilled by a
newly discovered liver protein. Knowledge concerning the interaction of
Fe2+ and sulfate with the enzyme may be useful in examining their
interaction between the enzyme, ferrous ion, and this activator protein.
Interaction of anions and divalent metal ions with phosphoenolpyruvate carboxykinase
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