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Biophys J, March 2000, p. 1087-1093, Vol. 78, No. 3
and
*Section of Plastic and Reconstructive Surgery, Dept. of Surgery MC
6035, University of Chicago, Chicago, Illinois 60637 USA; and
Department of Molecular Cell Physiology, Faculty of
Biology, Free University, 1081 HV Amsterdam, the Netherlands
Of all the lifeforms that obtain their energy from
glycolysis, yeast cells are among the most basic. Under certain
conditions the concentrations of the glycolytic intermediates in yeast
cells can oscillate. Individual yeast cells in a suspension can
synchronize their oscillations to get in phase with each other.
Although the glycolytic oscillations originate in the upper part of the
glycolytic chain, the signaling agent in this synchronization appears
to be acetaldehyde, a membrane-permeating metabolite at the bottom of
the anaerobic part of the glycolytic chain. Here we address the issue
of how a metabolite remote from the pacemaking origin of the
oscillation may nevertheless control the synchronization. We present a
quantitative model for glycolytic oscillations and their
synchronization in terms of chemical kinetics. We show that, in
essence, the common acetaldehyde concentration can be modeled as a
small perturbation on the "pacemaker" whose effect on the period of
the oscillations of cells in the same suspension is indeed such that a
synchronization develops.
Biophys J, March 2000, p. 1087-1093, Vol. 78, No. 3
© 2000 by the Biophysical Society 0006-3495/00/03/1087/07 $2.00
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