Biophys J, March 1998, p. 1229-1240, Vol. 74, No. 3

Bistability in the Isocitrate Dehydrogenase Reaction: An Experimentally Based Theoretical Study

 ^*Faculté des Sciences, Université Libre de Bruxelles, B-1050 Brussels, Belgium, and  ^#CNRS, Laboratoire d'Enzymologie, F-91198 Gif-Sur-Yvette, France

The enzyme isocitrate dehydrogenase (IDH, EC 1.1.1.42) can exhibit activation by one of its products, NADPH. This activation is competitively inhibited by the substrate NADP⁺, whereas NADPH competes with NADP⁺ for the catalytic site. Experimental observations briefly presented here have shown that if IDH is coupled to another enzyme, diaphorase (EC 1.8.1.4), which transforms NADPH into NADP⁺, the system can attain either one of two stable states, corresponding to a low and a high NADPH concentration. The evolution toward either one of these stable states depends on the time of addition of diaphorase to the medium containing IDH and its substrate NADP⁺. We present a theoretical and numerical analysis of a model for the IDH-diaphorase bienzymatic system, based on the regulatory properties of IDH. The results confirm the occurrence of bistability for parameter values derived from the experiments. Depending on the total concentration of NADP⁺ plus NADPH and the concentration of IDH, the system can either admit a single steady state or display bistability. We obtain an expression for the critical time t*, before which diaphorase addition leads to the lower steady state and after which addition of the enzyme leads to the upper steady state of NADPH. The analysis is extended to the case where the second substrate of IDH, isocitrate, is consumed in the course of the reaction without being regenerated. Bistability occurs only as a transient phenomenon in these conditions.

Biophys J, March 1998, p. 1229-1240, Vol. 74, No. 3
© 1998 by the Biophysical Society   0006-3495/98/03/1229/12  $2.00