• We are sorry, but NCBI web applications do not support your browser and may not function properly. More information
Logo of bmcsysbioBioMed Centralsearchsubmit a manuscriptregisterthis articleBMC Systems Biology
BMC Syst Biol. 2011; 5(Suppl 1): S12.
Published online Jun 20, 2011. doi:  10.1186/1752-0509-5-S1-S12
PMCID: PMC3121112

An improved kinetic model for the acetone-butanol-ethanol pathway of Clostridium acetobutylicum and model-based perturbation analysis



Comprehensive kinetic models of microbial metabolism can enhance the understanding of system dynamics and regulatory mechanisms, which is helpful in optimizing microbial production of industrial chemicals. Clostridium acetobutylicum produces solvents (acetone-butanol–ethanol, ABE) through the ABE pathway. To systematically assess the potential of increased production of solvents, kinetic modeling has been applied to analyze the dynamics of this pathway and make predictive simulations. Up to date, only one kinetic model for C. acetobutylicum supported by experiment has been reported as far as we know. But this model did not integrate the metabolic regulatory effects of transcriptional control and other complex factors. It also left out the information of some key intermediates (e.g. butyryl-phosphate).


We have developed an improved kinetic model featured with the incorporation of butyryl-phosphate, inclusion of net effects of complex metabolic regulations, and quantification of endogenous enzyme activity variations caused by these regulations. The simulation results of our model are more consistent with published experimental data than the previous model, especially in terms of reflecting the kinetics of butyryl-phosphate and butyrate. Through parameter perturbation analysis, it was found that butyrate kinase has large and positive influence on butanol production while CoA transferase has negative effect on butanol production, suggesting that butyrate kinase has more efficiency in converting butyrate to butanol than CoA transferase.


Our improved kinetic model of the ABE process has more capacity in approaching real circumstances, providing much more insight in the regulatory mechanisms and potential key points for optimization of solvent productions. Moreover, the modeling strategy can be extended to other biological processes.


System modeling for metabolism of industrial microorganisms is important in metabolic engineering, as a comprehensive model can reveal relevant factors related to high yield of target products. Based on such analyses, system modeling can further enhance developing operation strategies, or help optimizing cultivation processes [1-4]. C. acetobutylicum is an extensively studied organism used for industrial-scale production of important solvents acetone and butanol, through the acetone-butanol-ethanol (ABE) pathway (Figure (Figure1)1) [5,6]. The ABE pathway of C. acetobutylicum comprises two distinct branches: acidogenesis and solventogenesis. During acidogenesis, cells grow exponentially, acetate and butyrate are vigorously produced and the solvents (butanol, acetone and ethanol) are not obviously generated. While shifting to solventogenesis, the cells arrest their growth at stationary phase, solvents are produced and acids are reassimilated [5].

Figure 1
The acetone-butanol-ethanol (ABE) pathway of C. acetobutylicum. Reactions are represented by bold arrows and denoted by symbols from R1 to R21. The acidogenic reactions are R9 and R18 (catalyzed by PTA-AK and PTB-BK, respectively), generating acetate ...

So far, multiple models have been established to simulate the ABE pathway, which mostly apply the metabolic flux analysis (MFA) and flux-balance analysis (FBA) approaches [5,7-10]. Although stoichiometric models can simulate the overall flux distributions based on limited kinetic data by using physicochemical constraints, they cannot appropriately reflect the dynamics in real-time scale. In contrast, kinetics models integrated with biochemical information are more efficient in reflecting system dynamics. By perturbing a kinetic model, system states that deviate from the normal state can be simulated and it is possible to reveal which reactions have potential impacts on target products’ productions. To date, many experiments have explored the kinetic features of the ABE process of C. acetobutylicum[11-13] and a kinetic model was recently developed by Shinto et al. [14]. However, as most current models did, this model did not integrate the metabolic regulatory effects of transcriptional control and other complex factors [15-17]. Moreover, Shinto’s model did not include the information of some key metabolites, e.g. butyryl-phoshate (BuP), which has proved to be important in solventogensis [16-19].

To overcome the drawbacks of Shinto’s model, we developed an improved kinetic model for C. acetobutylicum ABE process. The simulation results based on our model were consistent with published experimental observations and more comprehensive than those of Shinto’s model. Furthermore, a series of perturbed circumstances were simulated as well, getting results which might provide insights for metabolic engineering aiming at increasing solvent productivity.


All the following results were based on our new model (Equation (1), section “Methods”), and they were compared with an experimental study (Zhao et al., 2005) that was independent of Shinto’s model or our work. The new model was established by integrating experimental information and knowledge not included in Shinto’s model (section “Methods”), and we applied some optimization methods to fix the unknown parameters introduced by integrating these information and knowledge. The parameter fitting was done only under the conditions described in Shinto’s work, only with respect to the metabolites contained in Shinto’s model, and we didn’t use any information related to BuP or the experimental study for comparison (Zhao et al., 2005). After these parameter values were derived, we first implemented dynamic simulation with respect to the conditions in Zhao et al.’s work and compared the results with experimental observations. We then carried out perturbation analysis to detect which reactions had large impacts on the overall butanol production in the system.

Dynamical simulation

The initial value of our model was set according to the conditions described in the experiment by Zhao et al. (2005) [16], and the simulation results of metabolites’ kinetic profiles were shown in Figure Figure2A2A and and2C.2C. Since our model parameters were fitted under Shinto’s experiment conditions, the metabolites’ kinetic profiles were naturally consistent with those in Shinto’s experiment when Shinto’s conditions were substituted in. So the comparison with Shinto’s experiment was not shown and we only focused on comparing with Zhao et al.’s experiment here. These simulation results were shown to be quite consistent with experimental observations (Figure (Figure2B2B and and2D).2D). The metric units in Figure Figure2A2A and and2B2B were different (Figure (Figure2A:2A: mM; Figure Figure2B:2B: pmol/gDW), since the measurement of BuP in Zhao et al’s experiment accepted the unit of pmol/gDW. It was impossible to exactly know the conversion between mM and pmol/gDW because there was no such relationship established in the SI metric unit system. But the quantity scale could be approximated given the size of an ordinary C. acetobutylicum cell, and this scale was consistent with that in our simulation results. Since bacteria cells might vary in their sizes, we could not give a general estimation that could represent all the others, so we just showed the original quantities on the vertical axis in Figure Figure2B2B.

Figure 2
Comparison of simulation results with the experimental observations of Zhao et al. A is the simulation results of BuP kinetics, in which data spots are concentrations and represented in blue. B is the experimental observation of BuP kinetics, in which ...

In our simulation results, the first peak of BuP was shown to coincide with the onset of solvent production (Figure 2A, 2C). This was a phenomenon that was reported in experimental literatures and had biological implications [16-19]. Besides BuP, we also demonstrated that we had a more precise simulation on butyrate, one crucial product in cell growth and solvent production [5] (Figure (Figure3).3). In Shinto’s model, when substituting in Zhao et al.’s conditions, the quantity scale of butyrate curve (Figure (Figure3B)3B) didn’t resemble precisely with the experimental curve in Zhao et al.’s experiment (Figure (Figure2D).2D). This further demonstrated that our model had more capability in approaching real biological events.

Figure 3
Comparison of simualtion results of butyrate kinetics with Shinto’s model under Zhao et al’s conditions A is the simulation results of butyrate kinetics based on our new model under Zhao et al.’s conditions. B is the simulation ...

Perturbation analysis

Among the solvents (ethanol, acetone, butanol) produced in the ABE fermentation, butanol was considered to be the more valuable product, since it had advantageous properties over acetone and ethanol (e.g. better value for the heat of combustion) [6]. So we implemented a series of perturbation analyses to assess which enzymes/reactions had relatively large impacts on butanol production. Here we used Rd values to measure the impacts (see section “Methods” for Rd’s definition). We carried out perturbation tests both on single parameters and double parameter pairs, the magnitude was 5% and shift directions (upward/downward) were considered. We traversed the entire parameter set. The result set of single parameter perturbations included An external file that holds a picture, illustration, etc.
Object name is 1752-0509-5-S1-S12-i1.gif entries (additional file 1 and 2). And the result set of double parameter perturbations included An external file that holds a picture, illustration, etc.
Object name is 1752-0509-5-S1-S12-i2.gif entries (additional file 3, 4, 5, 6). Here Table Table11 and and22 showed some results with respect to the enzymes located on or close to acidogenic/solventogenic reactions in single and double parameter perturbations, respectively.

Table 1
Part of the results of single parameter perturbation analysis.
Table 2
Part of the results of double parameter perturbation analysis

Among all results, there were several interesting ones that might provide some insights for understanding the ABE process. Before examining the results, we could intuitively hypothesize that BK might be relatively important in solventogensis since it connected two important metabolites butyrate and BuP. Based on the analyses, we indeed found that shifting BK’s Vmax alone or in combination with other enzyme parameters (e.g. the apparent Vmax parameter of BHBD – CRO – BCD) resulted in relatively large influences on butanol production (Table (Table1,1, ,2).2). Actually, BK activity had positive effect on butanol production and the change in butanol quantity caused by shifting BK’s Vmax ranked the 5th in the profile of single parameter shifts (see Table Table11 and additional file 1, 2). This suggested that BK, which coupled PTB to generate butyrate as well as catalyzing butyrate reassimilation, was important to butanol production as compared with other enzymes such as AAD (indexed as R11). Besides, AK also had positive effect on butanol production (but with a smaller Rd values than BK, see Table Table1),1), indicating acetate reassimilation had similar influence as butyrate reassimilation in solventogenesis, but with less magnitude.

Also, our computation results showed that CoAT, which also accepted butyrate as substrate, had a negative effect on butanol production as up-shifting its catalytic capacity (increasing Vmax or decreasing Km) diminished butanol quantity (Table (Table1,1, ,2).2). Because up-shifting the catalytic capacity of BK (increasing its Vmax or decreasing its Km) or down-shifting the catalytic capacity of CoAT (decreasing its Vmax or increasing its Km) would cause more butyrate molecules received by BK and the reverse operations would cause more butyrate received by CoAT, and given the fact that BK and CoAT both accepted butyrate as substrate, we could see that if more butyrate was received by BK, the butanol production would increase, i.e. more butyrate molecules were converted and acid reassimilation was more efficient; and if more butyrate was received by CoAT, the situation would be on the contrary (Figure (Figure4).4). Therefore we could conclude that BK had more efficiency than CoAT during acid reassimilation and solventogenesis.

Figure 4
Illustration of the influences on butanol production originated from BK, CoAT and AK. The influence originated from BK is positive effect on butanol production, as indicated by the green arrow in the same direction with that of butanol production. The ...

There were some places where our new model’s predictions differed from those of Shinto’s model. For instance, our model predicted that PTS had positive influence on butanol production, as increasing its Vmax (or decreasing its Km) resulted in amplified Rd value. While by Shinto’s model, PTS’s influence was negative. Given the fact that PTS acted in nutrient uptake and many processes relating to the ABE pathway were subjected to nutrient induction, our prediction might be more intuitively consistent with common sense [20].


Rational system modeling and comprehensive system analysis can serve as prior guidelines for understanding and deducing biological mechanisms. We can retrieve quantitative knowledge for assessing an organism’s metabolic capacity and use this knowledge for in-lab experiments to develop new strains with advantageous productivity [3,4], or optimizing the cultivation process of existing strains [2].

Model improvements

Since many studies related to C. acetobutylicum ABE pathway have been reported (including parameter values and the rate equation formulas [14,21]), kinetic modeling of the ABE pathway becomes feasible and enables us to simulate the system dynamics. Nevertheless, the previous kinetic model of C. acetobutylicum ABE process (Shinto et al, 2007) has several drawbacks as described in earlier context. To overcome these drawbacks, we have established a new model featured with three improvements over the previous one.

First, we have incorporated the key metabolite BuP, reflecting the relevant biological events that are specific to ABE kinetics [15-18]. The correspondence between BuP concentration climax and solventogenesis onset is not merely a natural consequence of the fact that BuP is the intermediate between butyryl-CoA and butyrate. There are implications on the genetic level as stated in Zhao et al’s study [16-19]. There are many important solventogenic genes, such as adhE1 (CAP0162), adhE2 (CAP0035 ), ctfA (CAP0163), ctfB (CAP0164), adc (CAP0165), bdhA (CAC3298), bdhB (CAC3299), etc., having expression profiles that show a strictly correlated pattern with the kinetics of BuP. Although the detailed mechanism of how BuP acts to regulate ABE process has not been very clear yet, its functional importance has been experimentally confirmed [16-19]. Our new model accounts for this knowledge and is successful in representing the phenomenon.

Second, we describe the regulatory effects of complex factors using a time division pattern. In Shinto’s model, the metabolic regulation beyond the level of substrate/product inhibition/activation is simply defined as the input of glucose. The shut-downs of several acidogenic/solventogenic enzymes (like PTB, BDH, etc) are solely due to the insufficiency of glucose. However, various evidences indicate that even with sufficient supply of glucose, the acidogenic enzymes are still shut down in the solventogenic phase, and the solventogenic enzymes are necessarily inactivated at the beginning of the acidogenic phase [15,22,23]. Therefore, the metabolic regulations are not of the simple pattern as Shinto suggested, but a significant 2-phase mode is shown (acids are generated during the earlier phase and solvents are generated during the latter one). In our work, this mode is approximated by considering endogenous enzyme activity variations, assuming enzymes are regulated by many factors (e.g. transcription control) to exhibit different activity levels to fulfill conditional system requirements of different periods. This assumption is equivalent to extending the application of biochemical system theory (BST). In BST, which is based on in vitro experiments, enzyme concentrations and endogenous enzyme activity levels are constant by default. Hence kinetic models based on BST are rigorously suitable for chemical simulations but may not entirely appropriate for in vivo conditions. Under in vivo conditions, the rate of a reaction does not solely depend on substrate/product concentrations, because the endogenous enzyme activity itself is regulated by many factors and its variation in turn affects the reaction rate [15-17]. Our model divides time into a set of periods according to the enzymes’ activity variations, allowing enzyme activities to vary throughout these periods.

Third, we introduce the “enzyme activity coefficient (EAC)” to quantify endogenous enzyme activity variations caused by metabolic regulations (see section “Methods” for EAC’s definition). For the quantification of enzyme activity curves, numerical interpolation (e.g. Lagrange, Legendre, etc.) should have been employed as to obtain fully continuous functions. But measurements in activity assays are usually not precise. If the errors are large, interpolation may result in huge errors or mistakes, causing the trouble of overfitting and distorting the original curve profile. On the contrary, the computation of EAC leaves the error just as the original error. Hence, using EAC will at least not amplify the error or distort the curve when the measurements are not precise. Moreover, our design of EAC is calculating a ratio instead of the particular value at each time instance, and this allows the error to be divided by a denominator, thus lowering the error level in computation.

Dynamical simulation and perturbation analysis

After the addition of BuP, 5 unknown parameters are introduced into the system. We have used Genetic Algorithm to estimate their values. In the process of parameter estimation, we used Shinto’s experimental observations of 16 metabolites to formulate the fitness function, but we didn’t employ any information about BuP. And in order to avoid the mistake of reasoning in a circle, we compare our results with observations of another experiment (Zhao et al.’s). It turns out that our results are significantly consistent with the observations and have shown some superiority over Shinto’s model in reflecting the kinetics of BuP and butyrate. This indicates that Shinto’s model is well fitted for its own condition but may not be suited well for other conditions. In contrast, our model has more capacity in approaching real cases because of the improvements we have made.

Simulations based on kinetic models can help develop in-lab strategies, thus increasing the success rate of metabolic engineering. In our work, we have simulated thousands of perturbed conditions to detect and assess potential spots that have large influences on butanol production. The magnitude of in silico perturbations should not be too large because the system may exhibit alternative activations for other pathways when undergoing substantial fluctuations [24,25]. When the system is encountering slight perturbations, its overall properties will not change substantially due to biological robustness [25-27]. So it would be fairly assumed that when the perturbation magnitude on enzymatic parameters is 5%, the system will still survive and its functional normality is not interrupted or diverted. In the computation, we have identified an interesting phenomenon that BK’s catalytic capacity exhibits positive influence on butanol production while CoAT has negative influences, as elevating BK activity results in increased Rd value and uplifting CoAT activity diminishes the value. And more convincingly, Rd decreases when increasing the Vmax values of BK and CoAT at the same time, which means the negative effect of CoAT can balance the positive effect of BK, confirming that CoAT has large effect in impairing butanol production. Based on this discovery, we propose a possible scenario that if more metabolites are received by BK as substrates, the overall acid (butyrate) reassimilation efficiency will be benefited and butanol production is enhanced. And if more metabolites are received by CoAT as substrates, the situation will be on the contrary. It may not seem economical for the bacteria to use the BK-PTB path (see Figure Figure1)1) to reassimilate butyrate since running through this path consumes ATP. Nonetheless, based on our computation results and biochemical knowledge, we raise a predictive explanation for the underlying mechanism: in acidogenic phase, the metabolic flux actually runs in the direction of PTB-BK (confirmed by both our computation of kinetic profiles and experimental literature [5,16,21]), thus this path generates ATP for the growth of the bacteria; when the bacteria enters solventogenic phase, it doesn’t need to grow and ATP has surplus, these surplus ATPs are utilized to proceed butyrate reassimilation. It’s noteworthy that acids are severely poisonous to bacteria cells and it is a priority for the bacteria to convert acids to other forms (e.g. alcohol). In addition, enhanced butanol production means more acids are converted. Hence, although reactions through BK cost ATP, but so far as BK’s efficiency is concerned, BK is still the preferred enzyme through which the bacteria reassimilates butyrate during solventogenesis. Therefore, the reason why the ATP-costing path BK-PTB is more efficient over the path catalyzed by CoAT (not ATP-costing) in reassimilating butyrate is probably because of responding to severe poison stress, and the energetic basis for this process is the ATP surplus generated during acidogenic phase. Our prediction is equivalent to considering the bacterial cellular behaviour to be related with biological robustness, as supposing that the bacteria is not seeking for its optimality when undergoing stress response, but seeking for sub-optimality. In such case, certain costs or sacrifices are tolerated as long as it can survive (or maintain minimal fluctuation from normality) [24,26].

In double parameter perturbation tests, we noticed that the net effect of combinatorial perturbation was equal to the sum of effects of individual perturbations, indicating that no crossover or nonlinear amplification originated from perturbations with mild magnitudes. This is probably because when the system is undergoing mild perturbation, it tries to maintain the normal status with minor alterations by means of system robustness. To demonstrate the hypothesis further, we implemented some three-parameter combinatorial perturbation tests. We randomly chose a number of three-parameter triplets and randomly decided their shift directions. For example, if we increased three parameters Vmax14, Vmax19, Vmax17 by 5% each and re-computed our model (Equation (1)), we obtained Rd=2.14%, which exactly equalled the sum of individual effects of these perturbations. Again, if we increased Km15b and Vmax19 by 5% and decreased Vmax18 by 5%, we obtained Rd=2.09%, still equalled to the sum of individual effects. Hence, we raise a hypothetic measure for increased butanol production: By slightly perturbing parameters in suitable directions and with appropriately mild magnitudes, we possibly can obtain a metabolic phenotype that can have amplified butanol production, and the strain can steadily and safely survive as well. The amplification magnitudes of multiple parameter perturbations can be much greater than those in single parameter perturbations, if adequately many parameters are manipulated appropriately. Meanwhile, from an engineering point of view, multiple spot modifications can make the risks of system fluctuations or external impulsions more distributive than in the case that all alterations are concentrated on a single spot. Hence, this strategy provides a way that can make a more stable high-production system. But this strategy requires high-precision genetic manipulation.


Traditional kinetic models cannot accommodate complex metabolic regulation effects (e.g. gene transcriptional control). Hence previous integrative modeling approaches for metabolic system are mainly based on the FBA method, in which the gene transcription regulations are described by Boolean logic and the metabolic level is expressed by flux balance equations. Since FBA based methods and Boolean logic cannot adequately reflect system dynamics, we have developed a new model as an attempt towards solving the problem. Actually, our modeling strategy is equivalent to extending the traditional BST, degenerating complex metabolic regulation effects to a form that is compatible with kinetic models. This strategy provides a way for integrating complex factors and knowledge from multiple levels into the framework of kinetic models. Moreover, our approach of describing metabolic regulation effects with a time division pattern and EAC is extendable. For instance, we can relate the enzyme activities to gene transcriptional level, build a formulism between them, and include the effects of other factors such as impulse and stochasticity. Our modeling method can be generalized and extended to the modeling of other bio-processes.

In this post-genomic era, massive information and experimental data have been accumulated. Therefore, it is important to develop methods or tools that are able to make use of existed information/data and capable of organizing, manipulating and interpreting them more comprehensively [28,29]. Our work just attempts to serve that goal by integrating existed information from multiple aspects and describing them mathematically. Nevertheless, the usage of “net effects of regulatory factors” in our modeling doesn’t seem to build direct links between the genetic level and metabolic level. But if adequately more information about the regulatory factors on the genetic level is revealed, better formulism can be built to link the two levels and further studies on the control of bacteria cellular systems can be conducted.


We have developed a new kinetic model featured with major improvements over the previous one (Shinto’s model), with the information of BuP incorporated and the effects of complex metabolic regulatory factors included. The simulation results based on our model are highly consistent with published experimental data and have more superiority in precision and subtlety than the previous model. We have successfully simulated the right profile of BuP kinetics, which is not included in the previous model. And we can make more precise prediction on the kinetics of butyrate, another important intermediate in the ABE process. Through perturbation analysis, we predict that the path catalyzed by BK is more efficient over the one catalyzed by CoAT in converting butyrate to butanol during solventogenesis, although ATPs are consumed.


We made improvements to Shinto’s model with respect to three points: (i) incorporating key compound butyryl-phosphate (BuP); (ii) describing the net effects of complex ABE metabolic regulations with a time division pattern according to endogenous enzyme activity variations, and (iii) introducing the “enzyme activity coefficient” to quantify endogenous enzyme activity variations. After the model framework was established, parameter estimation was followed to obtain unknown parameter values. We then implemented perturbation analysis to detect sensitivities of reactions/enzymes.

Incorporating BuP

BuP was key intermediate in conversions between butyrate (But) and butyryl-CoA (BCoA). It was reported that BuP played a crucial role in solventogenesis, as the initial peak of its concentration marked the onset of solvent production [16]. Adding in BuP meant splitting the originally lumped reactions between But and BCoA (as in Shinto’s model) so as to represent their intermediate BuP as a system component. Here we added two new reactions to denote the conversions from BuP to But and BCoA respectively. Hence, the butyrate formation/reassimilation branch was restructured and BuP appeared as another system component. Mathematically, we created rate equations for the new reactions and re-formulated the mass balance equations relating to But, BCoA and BuP. For details, see additional file 8.

Time division pattern

We assumed endogenous enzyme activity variations were net effects of transcriptional control and other complex factors. As experimental studies suggested enzyme activities varied with time [15,21-23,30], we developed a time division pattern to reflect the regulatory effects. We divided time into several intervals according to the enzymes’ activity variation profiles [22,23]. Here we only considered a subset of enzymes, which were either located on acid/solvent production reactions or directly associated to them. We adopted activity variations of the enzymes in consideration and regarded others’ as constants. All enzyme activity profiles were collected from published experimental studies [22,23] and the experiments were done under the identical culture conditions as our simulation [14,16]. For details of constructing the time division pattern, see additional file 8.

Enzyme activity coefficient

We introduced EAC to quantify endogenous enzyme activity variations. EACs were formulated as time-dependent functions. At each time instance, the EAC value was the ratio of the current enzyme activity to its maximum activity. Here we employed the divided intervals in the time division pattern (see the previous paragraph) as markers of time. And for computation simplicity, we approximated EAC with a set of 0th splines with respect to these markers. In other word, the EAC value remained constant within a divided interval and changed to another constant when stepping into another interval. The constant was the ratio of the average activity level in the interval to the maximum activity. We calculated all EACs of the considered enzymes and multiplied them to their corresponding rate equations to reflect endogenous activity variations. All enzyme activities data were collected from literatures [22,23]. For details of computing EAC, see additional file 8.

New Model

The new model contained 21 rate equations and 17 differential equations, involving 50 kinetic parameters. The model was built by integrating ABE kinetic features identified so far. Except for those included in Shinto’s model [11-14], EACs were multiplied to rate equations. The model was expressed in the form of ordinary differential equation (ODE) system as in Equation (1):

equation image

where Y was the vector of metabolites’ concentrations; A was the stoichiometric matrix of mass balance equations; E=diag{EAC1,…,EAC21} and EACs corresponding to enzymes with constant activities were set to 1; An external file that holds a picture, illustration, etc.
Object name is 1752-0509-5-S1-S12-i4.gif was the vector of rate equations without EACs; and P was the entire set of parameters. For details of the equations, symbols and abbreviations in the model, see additional file 8.

Unknown parameter estimation

We applied Genetic Algorithm (GA) to de novo estimate unknown parameters introduced by new reactions (previous subsection “Incorporating BuP”). We considered the experimental observations of 16 metabolites in Shinto’s work to be valid, and assumed that the correct value assignment of the unknown parameters definitely reproduced these valid observations under Shinto’s conditions. Therefore the fitness function in optimization was formed by forcing the 16 metabolites’ concentrations Y(1:16) to match Shinto’s observations Y0(1:16). We computed parameter values that minimized the fitness function and accepted them as numerical solutions. In addition, we didn’t employ any qualitative or quantitative information of BuP or Zhao et al.’s experiment in this process. For parameter values, see additional file 7. And for details of parameter estimation, see additional file 8.

Perturbation analysis

We performed perturbation analysis to assess enzymes/reactions’ impacts on butanol production. By consecutively shifting the enzymes’ Vmax and Km values and using the normal state as control, relative changes of in silico butanol production were computed. We defined the relative change in butanol production as Rd (a ratio expressed in Formula (2)):

equation image

where yp was the instantaneous butanol concentration in perturbed state, and yc was that in normal state. For approximation, we discretized the integrals in Formula (2) with the trapezoid method. The results of perturbation analysis were in additional files 1, 2, 3, 4, 5, 6, and for details of computation, see additional file 8.

List of abbreviations

PTS: phosphotransferase system; AK: acetate kinase; PTA: phosphotransacetylase; CoAT: CoA transferase; AAD: alcohol/ aldehyde dehydrogenase; BHBD: β-hydroxybutyryl-CoA dehydrogenase; CRO: crotonase; BK: butyrate kinase; PTB: phosphotransbutyrylase; BDH: butanol dehydrogenase; BCD: butyryl-CoA dehydrogenase; AADC: acetoacetate decarboxylase; THL: thiolase

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

Building the kinetic model: RDL and CR. Designing and performing numerical experiments: RDL and LYL. Data acquisition and analysis: RDL. Conceiving and designing the research: YYL, LL, YXL. Drafting the manuscript: RDL, YYL, LL.

Supplementary Material

Additional file 1:

Results of single parameter perturbation tests with magnitude +5%. The data entries included are numerical results obtained by increasing the value of every kinetic parameter by 5%. All parameters are traversed. There are 50 entries and the dataset is organized as a table in the format of *.xls (Excel worksheet). The first column is the index of the parameter perturbed, the second column is the parameter perturbed, and the third column is the Rd value that is used to evaluate how much impact the perturbation causes to butanol production.

Additional file 2:

Results of single parameter perturbation tests with magnitude -5%. The data entries included are numerical results obtained by decreasing the value of every kinetic parameter by 5%. All parameters are traversed. There are 50 entries and the dataset is organized as a table in the format of *.xls (Excel worksheet). The first column is the index, the second column is the parameter perturbed, and the third column is the Rd value that is used to evaluate how much impact the perturbation causes to butanol production.

Additional file 3:

Results of double parameter perturbation tests with respective magnitudes +5% and +5%. The data entries included are numerical results obtained by increasing the values of every pair of kinetic parameters by 5% each. All 2-parameter combinations are traversed. There are 1225 entries and the dataset is organized as a table in the format of *.xls (Excel worksheet). The first column is the pair of indexes of the parameters perturbed, the second and third columns are the parameters perturbed, respectively, and the fourth column is the Rd value that is used to evaluate how much impact the perturbation causes to butanol production.

Additional file 4:

Results of double parameter perturbation tests with respective magnitudes +5% and -5%. The data entries included are numerical results obtained by altering the values of every pair of kinetic parameters, increasing the first parameter by 5% and decreasing the other one by 5%. All 2-parameter combinations are traversed. There are 1225 entries and the dataset is organized as a table in the format of *.xls (Excel worksheet). The first column is the pair of indexes of the parameters perturbed, the second and third columns are the parameters perturbed, respectively, and the fourth column is the Rd value that is used to evaluate how much impact the perturbation causes to butanol production.

Additional file 5:

Results of double parameter perturbation tests with respective magnitudes -5% and +5%. The data entries included are numerical results obtained by altering the values of every pair of kinetic parameters, decreasing the first parameter by 5% and increasing the other one by 5%. All 2-parameter combinations are traversed. There are 1225 entries and the dataset is organized as a table in the format of *.xls (Excel worksheet). The first column is the pair of indexes of the parameters perturbed, the second and third columns are the parameters perturbed, respectively, and the fourth column is the Rd value that is used to evaluate how much impact the perturbation causes to butanol production.

Additional file 6:

Results of double parameter perturbation tests with respective magnitudes -5% and -5%. The data entries included are numerical results obtained by decreasing the values of every pair of kinetic parameters by 5% each. All 2-parameter combinations are traversed. There are 1225 entries and the dataset is organized as a table in the format of *.xls (Excel worksheet). The first column is the pair of indexes of the parameters perturbed, the second and third columns are the parameters perturbed, respectively, and the fourth column is the Rd value that is used to evaluate how much impact the perturbation causes to butanol production.

Additional file 7:

The values of kinetic parameters There are 50 parameters in our kinetic model. The dataset is organized as a table in the format of *.xls (Excel worksheet). The first column contains the indexes of reactions, the second column contains the parameters involved in each reaction, and the third column contains the parameter values.

Additional file 8:

Description of the modeling method This is the detailed description of the method of modeling, including the incorporation of BuP, the construction of time division pattern, the computation of EACs, parameter estimation procedure, and the computation of perturbation analysis. This file is in the format of * (Word document). This file contains 4 supplementary figures (Figure S1 - S4) and a supplementary table (Table S1).


This work was supported by National High-Tech R&D Program (863) (2007AA02Z330, 2007AA02Z331, 2007AA02Z332), National Basic Research Program of China (973) (2006CB0D1203, 2007CB707803), National Natural Science Foundation of China (30770497) and the Shanghai Commission of Science and Technology (08JC1416600, 08ZR1415800).

This article has been published as part of BMC Systems Biology Volume 5 Supplement 1, 2011: Selected articles from the 4th International Conference on Computational Systems Biology (ISB 2010). The full contents of the supplement are available online at http://www.biomedcentral.com/1752-0509/5?issue=S1.


  • Granström T, Aristidou AA, Leisola M. Metabolic flux analysis of Candida tropicalis growing on xylose in an oxygen-limited chemostat. Metab Eng. 2002;4:248–256. doi: 10.1006/mben.2002.0230. [PubMed] [Cross Ref]
  • Shimizu H, Takiguchi N, Tanaka H, Shioya S. A maximum production strategy of lysine based on a simplified model derived from a metabolic reaction network. Metab Eng. 1999;1:299–308. doi: 10.1006/mben.1999.0127. [PubMed] [Cross Ref]
  • Stephanopoulos G, Vallino JJ. Network rigidity and metabolic engineering in metabolite overproduction. Science. 1991;252:1675–1681. doi: 10.1126/science.1904627. [PubMed] [Cross Ref]
  • Bailey JE. Toward a science of metabolic engineering. Science. 1991;252:1668–1675. doi: 10.1126/science.2047876. [PubMed] [Cross Ref]
  • Desai RP, Harris LM, Welker NE, Papoutsakis ET. Metabolic flux analysis elucidates the importance of the acid-formation pathways in regulating solvent production by Clostridium acetobutylicum. Metab Eng. 1999;1:206–213. doi: 10.1006/mben.1999.0118. [PubMed] [Cross Ref]
  • Gapes JR. The economics of acetone-butanol fermentation: Theoretical and market considerations. J Mol Microbiol Biotechnol. 2000;2:27–32. [PubMed]
  • Senger RS, Papoutsakis ET. Genome-scale model for Clostridium acetobutylicum: Part I. Metabolic network resolution and analysis. Biotechnol Bioeng. 2008;101:1036–1052. doi: 10.1002/bit.22010. [PMC free article] [PubMed] [Cross Ref]
  • Desai RP, Nielsen LK, Papoutsakis ET. Stoichiometric modeling of Clostridium acetobutylicum fermentations with non-linear constraints. J Biotechnol. 1999;71:191–205. doi: 10.1016/S0168-1656(99)00022-X. [PubMed] [Cross Ref]
  • Senger RS, Papoutsakis ET. Genome-scale model for Clostridium acetobutylicum: Part II. Development of specific proton flux states and numerically determined sub-systems. Biotechnol Bioeng. 2008;101:1053–1071. doi: 10.1002/bit.22009. [PMC free article] [PubMed] [Cross Ref]
  • Lee J, Yun H, Feist AM, Palsson BO. Genome-scale reconstruction and in silico analysis of the Clostridium acetobutylicum ATCC 824 metabolic network. Appl Microbiol Biotechnol. 2008;80:849–862. doi: 10.1007/s00253-008-1654-4. [PubMed] [Cross Ref]
  • Jones DT, Woods DR. Acetone-butanol fermentation revisited. Microbiol Rev. 1986;50:484–524. [PMC free article] [PubMed]
  • Tashiro Y, Takeda K, Kobayashi G, Sonomoto K, Ishizaki A. et al. High butanol production by Clostridium saccharoperbutylacetonicum N1-4 in fed-batch culture with pH-stat continuous butyric acid and glucose feeding method. J Biosci Bioeng. 2004;98:263–268. [PubMed]
  • Soni BK, Das K, Ghose TK. Inhibitory factors involved in acetone-butanol fermentation by Clostridium saccharoperbutylacetonicum. Curr Microbiol. 1987;16:61–67. doi: 10.1007/BF01588173. [Cross Ref]
  • Shinto H, Tashiro Y, Yamashita M, Kobayashi G, Sekiguchi T. et al. Kinetic modeling and sensitivity analysis of acetone-butanol-ethanol production. J Biotechnol. 2007;131:45–56. doi: 10.1016/j.jbiotec.2007.05.005. [PubMed] [Cross Ref]
  • Alsaker KV, Papoutsakis ET. Transcriptional program of early sporulation and stationary-phase events in Clostridium acetobutylicum. J Bacteriol. 2005;187:7103–7118. doi: 10.1128/JB.187.20.7103-7118.2005. [PMC free article] [PubMed] [Cross Ref]
  • Zhao Y, Tomas CA, Rudolph FB, Papoutsakis ET, Bennett GN. Intracellular butyryl phosphate and acetyl phosphate concentrations in Clostridium acetobutylicum and their implications for solvent formation. Appl Environ Microbiol. 2005;71:530–537. doi: 10.1128/AEM.71.1.530-537.2005. [PMC free article] [PubMed] [Cross Ref]
  • Thormann K, Feustel L, Lorenz K, Nakotte S, Durre P. Control of butanol formation in Clostridium acetobutylicum by transcriptional activation. J Bacteriol. 2002;184:1966–1973. doi: 10.1128/JB.184.7.1966-1973.2002. [PMC free article] [PubMed] [Cross Ref]
  • Green EM, Boynton ZL, Harris LM, Rudolph FB, Papoutsakis ET. et al. Genetic manipulation of acid formation pathways by gene inactivation in Clostridium acetobutylicum ATCC 824. Microbiology. 1996;142:2079–2086. doi: 10.1099/13500872-142-8-2079. [PubMed] [Cross Ref]
  • Harris LM, Welker NE, Papoutsakis ET. Northern, morphological, and fermentation analysis of spo0A inactivation and overexpression in Clostridium acetobutylicum ATCC 824. J Bacteriol. 2002;184:3586–3597. doi: 10.1128/JB.184.13.3586-3597.2002. [PMC free article] [PubMed] [Cross Ref]
  • Monot F, Martin J, Petitdemange H, Gay R. Acetone and butanol production by Clostridium acetobutylicum in a synthetic medium. Appl Environ Microbiol. 1982;44:1318–1324. [PMC free article] [PubMed]
  • Gheshlaghi R, Scharer JM, Moo-Young M, Chou CP. Metabolic pathways of clostridia for producing butanol. Biotechnol Adv. 2009;27:764–781. doi: 10.1016/j.biotechadv.2009.06.002. [PubMed] [Cross Ref]
  • Hartmanis MGN, Gatenbeck S. Intermediary metabolism in Clostridium acetobutylicum: Levels of enzymes involved in the formation of acetate and butyrate. Appl Environ Microbiol. 1984;47:1277–1283. [PMC free article] [PubMed]
  • Tummala SB, Welker NE, Papoutsakis ET. Development and characterization of a gene expression reporter system for Clostridium acetobutylicum ATCC 824. Appl Environ Microbiol. 1999;65:3793–3799. [PMC free article] [PubMed]
  • Segrè D, Vitkup D, Church GM. Analysis of optimality in natural and perturbed metabolic networks. Proc Natl Acad Sci U S A. 2002;99:15112–15117. doi: 10.1073/pnas.232349399. [PMC free article] [PubMed] [Cross Ref]
  • Shlomi T, Berkman O, Ruppin E. Regulatory on/ off minimization of metabolic flux changes after genetic perturbations. Proc Natl Acad Sci U S A. 2005;102:7695–7700. doi: 10.1073/pnas.0406346102. [PMC free article] [PubMed] [Cross Ref]
  • Kitano H. Biological robustness. Nat Rev Genet. 2004;5:826–837. doi: 10.1038/nrg1471. [PubMed] [Cross Ref]
  • Bloom JD, Lu Z, Chen D, Raval A, Venturelli OS. et al. Evolution favors protein mutational robustness in sufficiently large population. BMC Biol. 2007;5:29. doi: 10.1186/1741-7007-5-29. [PMC free article] [PubMed] [Cross Ref]
  • Ideker T, Galitski T, Hood L. A new approach to decoding life: Systems biology. Annu Rev Genom Human Genet. 2001;2:343–372. doi: 10.1146/annurev.genom.2.1.343. [PubMed] [Cross Ref]
  • Hood L. Systems biology: integrating technology, biology and computation. Mech Ageing Dev. 2003;124:9–16. doi: 10.1016/S0047-6374(02)00164-1. [PubMed] [Cross Ref]
  • Tomas CA, Beamish J, Papoutsakis ET. Transcriptional analysis of butanol stress and tolerance in Clostridium acetobutylicum. J Bacteriol. 2004;186:2006–2018. doi: 10.1128/JB.186.7.2006-2018.2004. [PMC free article] [PubMed] [Cross Ref]

Articles from BMC Systems Biology are provided here courtesy of BioMed Central


Related citations in PubMed

See reviews...See all...

Cited by other articles in PMC


Recent Activity

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...