Enzyme Kinetics

Discussion of [S] Values


The question now arises, "Does the Michaelis-Menten Equation fit?" At low [S] , when [S] < 0.1 Km, it can be shown that

v=(Vm/Km)[S] = k[S]

i.e., the Michaelis-Menten Equation would predict that v = k[S]; that is, the rate is directly proportional to the concentration of one of the reactants (the substrate), so this is a first order reaction. This can be explained by saying that the enzyme is not saturated with substrate and therefore, as we add more substrate we get more ES formed, and more ES breaking down to give P.

At high [S], when [S] > 10 Km

v=Vm=k

i.e., the Michaelis-Menten Equation would predict that v = k. This means that the rate is independent of the concentration of the substrate. This is a zero order reaction and can be explained by saying that the enzyme is saturated with substrate. Even when more substrate is added to the solution we cannot get any more ES formed and, therefore, the rate does not change. So the Michaelis-Menten Equation does fit the empirical curve at both high and low [S].

Note that when there is more enzyme present the rate is always higher for a given [S]. This means that the Vm will also be higher.


[Start Over] [Index] [Previous Page] [Next Page]
Maintained by AISR Education Services (EdServices@jeffline.tju.edu)
Copyright © Thomas Jefferson University. All Rights Reserved.

The Thomas Jefferson University web site, its contents and programs, is provided for informational and educational purposes only and is not intended as medical advice nor is it intended to create any physician-patient relationship. Please remember that this information should not substitute for a visit or a consultation with a health care provider. The views or opinions expressed in the resources provided do not necessarily reflect those of Thomas Jefferson University, Thomas Jefferson University Hospital, or the Jefferson Health System or staff.

Return to Thomas Jefferson University Home Page