Abstract
A mathematical model for recombinant bacteria which includes foreign protein production is developed. The experimental system consists of an Escherichia Coli strain and plasmid pIT34 containing genes for bioluminescence and production of a protein, β-galactosidase. This recombinant strain is constructed to facilitate on-line estimation and control in a complex bioprocess. Several batch experiments are designed and performed to validate the developed model. The design of a model structure, the identification of the model parameters and the estimation problem are three parts of a joint design problem. A nonlinear observer is designed and an experimental evaluation is performed on a batch fermentation process to estimate the substrate consumption.
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Abbreviations
- X :
-
Biomass concentration (g/l)
- S :
-
Substrate concentration (g/l)
- P :
-
Protein concentration in the reactor (g/l)
- P c :
-
Protein concentration in the cell (g/cell)
- L :
-
Light intensity (V)
- I :
-
Inducer concentration (g/l)
- Oo :
-
Oxygen concentration (g/l)
- μ:
-
Specific growth reaction rate (1/h)
- ν:
-
Biosynthesis reaction rate (1/h)
- y i :
-
Yield coefficient (g/g)
- M c :
-
Cell mass in moles (g/mole)
- φ1 :
-
Death kinetics (l/h)
- φ2 :
-
Inducer effect
- φ3 :
-
Oxygen limitation
- α:
-
Inducer degradation effect (1/h)
- k m :
-
Maintenance constant associate to the substrate (1/h)
- m o :
-
Maintenance constant associated to the oxygen (1/h)
- k s :
-
Saturation constant associated to the oxygen (g/l)
- k o :
-
Saturation constant associated to the substrate (g/l)
- K l a :
-
Oxygen saturation constant (1/h)
- S in :
-
Substrate concentration in the input stream (g/l)
- D :
-
Dilution rate (1/h)
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Appendix 1
Appendix 1
We will show that the estimation error \(e(t)=\hat{x}(t)-x(t)\) exponentially converges to zero. Using (13), we obtain:
We will use the following decomposition:
From the mean value theorem we get:
where \( A(\hat x,\,x) = \left[ {\begin{array}{*{20}c} 0 & {\frac{{\partial F_1 }} {{\partial x_2 }}(x_1 ,\,\hat x_2 + \tau e_2 ,\,u)} \\ 0 & 0 \\ \end{array} } \right], \) and τ∈[0, 1] is a number which may depend on \((u,\hat x,x).\) Similarly, from the mean value theorem we have:
where τ i ∈[0, 1], 1,2. Combining (18) and (19), we deduce:
Now setting \( \bar e =\Delta_\theta ^{-1}e,\) then, it suffices to show that \(\|\bar e(t)\|\) exponentially converges to 0 as t→ +∞. To do so, we can easily check that:
Now, consider the following positive definite quadratic function: \(V=\bar{e}^TR\bar{e}.\) We only need to show that \(\dot{V}\leq -\gamma V\) for some constant γ >0.
Using (21) we obtain:
Since A(t) is of the form \( {\left[ {\begin{array}{*{20}l} {0 \hfill} & {{a(t)} \hfill} \\ {0 \hfill} & {0 \hfill} \\ \end{array} } \right]}, \) where \(\alpha_1\leq a(t)={\partial F_1}/ {\partial x_2}(x_1,\hat x_2+\tau e_2,u) \leq \alpha_2,\) and α1, α2 are fixed constants given by (H2).
Obviously R is an SPD matrix. Indeed, let x∈IR n, x≠ 0, then
Now let us set P=A T R+RA−ρ C T C.
Using a similar argument as above, we obtain:
From inequalities (14), we deduce \(1-\alpha_2 R_{11}/{\sqrt{2\rho \alpha_1|R_{12}|}}>0.\) Hence,
From (23), we get:
Now, using the triangular structure of \(B(\hat x,x,u)\) and the fact that F is a global Lipschitz function (assumption (H1)), we can easily see that for every θ ≥ 1 we have: \(\|\Delta_\theta^{-1} B(\hat x,x) \bar e\| \leq \sqrt{2}c \|\bar e\|,\) where c is the Lipschitz constant given by (H1). Hence,
where λmin(R) denotes the smallest eigenvalue of R. To end the proof, it suffices to chose θ such that \(\theta\geq \theta_0={2\sqrt{2}c\|R\|}/ {\eta}.\)
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Nadri, M., Trezzani, I., Hammouri, H. et al. Modeling and observer design for recombinant Escherichia coli strain. Bioprocess Biosyst Eng 28, 217–225 (2006). https://doi.org/10.1007/s00449-005-0008-1
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DOI: https://doi.org/10.1007/s00449-005-0008-1