Nonlinear control techniques by means of a software sensor that are commonly
used in chemical engineering could be also applied to genetic regulation
processes. We provide here a realistic formulation of this procedure by
introducing an additive white Gaussian noise, which is usually found in
experimental data. Besides, we include model errors, meaning that we assume we
do not know the nonlinear regulation function of the process. In order to
illustrate this procedure, we employ the Goodwin dynamics of the concentrations
[B.C. Goodwin, Temporal Oscillations in Cells, (Academic Press, New York,
1963)] in the simple form recently applied to single gene systems and some
operon cases [H. De Jong, J. Comp. Biol. 9, 67 (2002)], which involves the
dynamics of the mRNA, given protein, and metabolite concentrations. Further, we
present results for a three gene case in co-regulated sets of transcription
units as they occur in prokaryotes. However, instead of considering their full
dynamics, we use only the data of the metabolites and a designed software
sensor. We also show, more generally, that it is possible to rebuild the
complete set of nonmeasured concentrations despite the uncertainties in the
regulation function or, even more, in the case of not knowing the mRNA
dynamics. In addition, the rebuilding of concentrations is not affected by the
perturbation due to the additive white Gaussian noise and also we managed to
filter the noisy output of the biological systemComment: 21 pages, 7 figures; also selected in vjbio of August 2005; this
version corrects a misorder in the last three references of the published
versio