Team:Valencia/Project/Modeling

Oxidative phosphorylation model coupled with thermogenine expression

Our project consists of implementing a controlled heating system inside Saccharomyces cerevisiae. In order to obtain this we are going to use a mitocondrial membrane protein known as thermogenin used by mamalians cells to increase their temperature.

The working principle of thermogenin is based on the respiratory chain. The way in which thermogenin increases the temperature of the system can be described approximately as follows: It produces a hole on the mitocondrial membrane which makes difficult the production of a proton gradient in the membrane. The release of the mitocondrial proton gradient increases the temperature.

In order to describe the system three complementary models have been developed :

• Black box model of the temperature increase by the thermogenin.
• Detailed model of the respiratory electron transport chain.
• Regulatory model of the thermogenin expresion.

Theoretical evaluation of the idea

To evaluate the reliability of the idea we are going to estimate the maximal attainable temperature (obviously, the minimal temperature value is the corresponding to the culture conditions). This means to estimate the maximum heat production. The maximal temperature can be determined by supposing that the proton motive force is used solely in heat production mediated by thermogenine. The following calculations were made taking into account this assumption.

To calculate the energy produced per proton dissipated through the thermogenine we used the published turnover number (the maximum number of molecules of substrate that an enzyme can convert to product per catalytic site per unit time ) of ATP synthase( Abrams et al 1974) for Geobacillus stearothermophilus an estimation of the Saccharomyces cerevisiae real value.

To calculate the energy produced per proton dissipated through the thermogenine we used the published rate of ATP flow as an estimation of the Saccharomyces cerevisiae real value.

If ATP synthase needs four protons to produce one molecule of ATP, then we can easily calculate the proton flow through complex V.

The free energy associated to a single proton being dissipated through the ATP synthase is 20 Kj/mol. Balancing the units we get the energy dissipated per proton:

The energy flow is calculated by multiplying both figures and adjusting the result to the proper units:

Black box model of temperature increase produced by thermogenin

The black box model simulates the temperature evolution of the system as a function of the grow rate, galactose concentration and thermogenin expresion. We assume that the system can be reproduced by the following system of equations:

where:

• first equation: growth of the culture
• second equation: Galactose evolution in time. Galactose is the metabolite which induces the thermogenin expresion.
• third equation: Thermogenin concentration level.
• Fourth equation: Temperature evolution. the first term of the equation represents the losses to the ambient of the calorimeter and the second one the temperature increase as a consequence of the thermogenin expresion. This second term depens on the number of cells and also on other parameters like the number of mitocondria per cell and the like.

Growth equation

To get the following data we grew all our strains inside the LCC at 270 r.p.m. We fitted the curves using the non-linear curve fitting tool from OriginPro program.

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The exponential fitting is statistically significative (0.05)....

Temperature equation

The temperature equation has a heat loss term which follows Newton’s law of cooling. We adjusted the results from the LCC characterization in order to get the parameters for the loss term of the temperature evolution equation. Environment temperature remained constant at 22ºC.

Modeling the oxidative phosphorylation pathway

The energy, in form of ATP, necessary for all the cellular processes, is acquired mainly by the oxidative phosphorylation pathway. This pathway is wide-spread through the tree of life because it is a highly efficient way of releasing energy, compared to alternative fermentation processes such as anaerobic glycolysis. In eukaryotic organisms, the reaction takes place in the mitochondria where the electron transport chain catalyzes the electron flow from NADH and FADH ₂ to oxygen (becoming reduced to water). This exergonic reaction is coupled with the proton pumping from the matrix through the inner mitochondrial membrane, which generates an electroosmotic gradient used for ATP synthesis. This mechanism is called chemiosmosis, proposed in 1961 by Peter Mitchell.

With this model we want to evaluate the effects of the UCP1 in the ATP synthesis. We will take into account general issues about the electron transport chain as well as the particularities of our yeast Saccharomyces cerevisiae. We will have to consider the fermentative pathways presents for further applicability of the model.

Complex I

The first step of the respiratory chain is the oxidation of NADH through complex I (also known as NADH dehydrogenase). This multimeric complex is constituted by 43 different proteins, including a flavoprotein and six iron-sulfur clusters as prosthetic groups. The reactions catalyzed by this complex are coupled, so the exergonic transfer of electrons to quinone promotes the endergonic proton pumping from the matrix to the intermembrane space.

Saccharomyces cerevisiae lacks complex I( Vries et al 1988), but oxidizes NADH with the help two NADH dehydrogenases structurally different from complex I. Complex I is unable to use the citosolic pool of NADH (as is faced to the matrix and NADH does not diffuse through the inner membrane), but NADH dehydrogenases from Saccharomyces cerevisiae use both pools. So there are two enzymes: ones uses the external NADH while the other the internal. Both enzymes presence depends on culture growth conditions and phase.

From a structural point of view, these enzymes are much simpler than complex I. This feature is related to the fact that these NADH dehydrogenases transfer electrons without any translocation of protons across the membrane. Because of this reason, we will have two pools of NADH in our model as well as two different equation for NADH dehydrogenation.

The internal NADH dehydrogenase is a single subunit enzyme coded by nuclear DNA. It has FAD as prosthetic group, but lacks iron-sulfur clusters. Unlike complex I, which is a one electron reacting enzyme, internal NADH dehydrogenase is a two electron reacting enzyme, preventing the formation of ROS.

The enzyme follows a bi bi ping pong mechanism.The kinetic data was obtained with the artificial acceptor DCPIP instead of quinone( Velázquez et al 2001), nevertheless we will take its Michaelis constant as a reference for quinone real value.

The diagram shows the reaction, where NADH binds to the enzyme and transfers two electrons to the prosthetic group FAD. After the reduction of the enzyme (F) NAD⁺ is released and F recovers its redox state by reducing quinone.

The rate equation for the internal NADH dehydrogenase:

The external NADH dehydrogenase must follow the same kinetic scheme. We could not find data for the Michaelis constant for Q as well as for V_max, so we used the internal dehydrogenase values as an estimation.

Modeling the control system

Our device is able to increase the environment temperature. We would like to control the effect of our system so as to keep the surroundings near a desired temperature. With these features the final biological construction would resemble a heating system with a thermostat. In order to achieve it we will need a way of sensing temperature. We have designed a system based on cold shock proteins. By modifying the strength of the promoter of our constructions we will tune the setpoint temperature to the desired value.

References

Abrams, A.; Smith, J.B. (1974); The Enzymes, 3rd Ed. (Boyer, P.D., ed.) Bacterial membrane ATPase 10, 395-429.

Velázquez I.; Pardo J.P. (2001); Kinetic Characterization of the Rotenon-Insensitive Internal NADH: Ubiquinone Oxidoreductase of Mitochondria from Saccharomyces cerevisiae.Archives of Biochemistry and Byophysics.Vol 389 pp 7-14

Vries S.; Grivell L.A: (1988) ; Purification and characterization of a rotenone-insensitive NADH:Q6 oxidoreductase from mitochondria of Saccharomyces cerevisiae.European Journal of Biochemistry. 176: 377-384.