Estimation of the number of extreme pathways for metabolic networks
- Matthew Yeung^{1},
- Ines Thiele^{1, 2} and
- Bernard Ø Palsson^{1}Email author
https://doi.org/10.1186/1471-2105-8-363
© Yeung et al.; licensee BioMed Central Ltd. 2007
Received: 21 February 2007
Accepted: 27 September 2007
Published: 27 September 2007
Abstract
Background
The set of extreme pathways (ExPa), {p_{ i }}, defines the convex basis vectors used for the mathematical characterization of the null space of the stoichiometric matrix for biochemical reaction networks. ExPa analysis has been used for a number of studies to determine properties of metabolic networks as well as to obtain insight into their physiological and functional states in silico. However, the number of ExPas, p = |{p_{ i }}|, grows with the size and complexity of the network being studied, and this poses a computational challenge. For this study, we investigated the relationship between the number of extreme pathways and simple network properties.
Results
We established an estimating function for the number of ExPas using these easily obtainable network measurements. In particular, it was found that log [p] had an exponential relationship with $\mathrm{log}\left[{\displaystyle {\sum}_{i=1}^{R}{d}_{{-}_{i}}{d}_{{+}_{i}}{c}_{i}}\right]$, where R = |R_{ eff }| is the number of active reactions in a network, ${d}_{{-}_{i}}$ and ${d}_{{+}_{i}}$ the incoming and outgoing degrees of the reactions r_{ i }∈ R_{ eff }, and c_{ i }the clustering coefficient for each active reaction.
Conclusion
This relationship typically gave an estimate of the number of extreme pathways to within a factor of 10 of the true number. Such a function providing an estimate for the total number of ExPas for a given system will enable researchers to decide whether ExPas analysis is an appropriate investigative tool.
Keywords
Background
Extreme pathways (ExPas) of a metabolic network are the irreducible set of vectors that define the basis of the null-space of the network's stoichiometric matrix. Every allowable solution to the flux balance equations of a reaction network in steady state, S·ν = 0, can be represented as a non-negative linear combination of the extreme pathway vectors. ExPas are biochemically and thermodynamically feasible pathways that transform a selection of the given substrates to a selection of allowable products. ExPas have been extensively used for the analyses of metabolic networks (see, for example, [1–5]). Typically, such analyses used ExPas to define possible phenotypic states of metabolic networks under different simulation conditions, to identify network redundancy, and to reveal eigenpathways that effectively characterize all relevant physiological states of a metabolic network. Modified versions of ExPa analyses have also been applied to regulatory networks [6, 7] and signaling pathways [8]. Such applications are still in their infancy and are important research topics. However, as the size of a network increases, the redundancy of the network, that is, the number of different pathways that transform given substrate(s) to given product(s) [9, 10], becomes more apparent, and the number of ExPas increases rapidly. Redundancy also exists in small systems but this can be easily handled and even provide insights to legitimate alternative pathways. As the number of ExPas increases at a drastic rate, performing insightful analyses using ExPas become increasingly difficult.
The fact that the set of ExPas of a biochemical reaction network defines the boundaries of its convex steady-state solution space makes them a valuable tool for metabolic network analysis. Further, they emphasize alternative pathways that exist in a network, which may otherwise be overlooked, and that can enrich the understanding of its possible physiological states. However, the increasing details included in reconstructed metabolic networks lead to the combinatorial explosion of the number of ExPas and their computation time. A method providing a good estimate for the final number of ExPas for a given system will enable researchers to decide whether ExPas analysis is a appropriate tool for their objectives.
Another method often used for characterizing the steady-state solution space for a biochemical reaction network is known as Elementary Modes (EMs) [11]. Both ExPa and EM analyses require the resulting solution vectors to be non-decomposable and unique. In addition, ExPa vectors are required to be systemically independent [12]. As a result, ExPas for a system are a minimal set of EMs, and the number of ExPas is less than or equal to the number of EMs. Since both ExPas and EMs are biochemically and thermodynamically feasible pathways, the number of these pathways cannot be estimated using traditional graph theoretical algorithms, such as the Dijkstra's algorithm [13], for finding all shortest paths.
The combinatorial complexity of Elementary Modes of a network was previously described by Klamt et al. [14] by providing an upper-bound for the number of EMs. In their work, the authors considered the following combinatoric problem: given a network with n reactions and m metabolites, the maximal number of independent pathways occurs when each possible subset of the reactions consisting of the m metabolites are independent. This maximal number was found to be $\left(\begin{array}{c}n\\ m+1\end{array}\right)$. They further improved the upper-bound by removing those reactions that were not utilized (redundant reactions) in the condition-specific models of the network. Klamt et al. generated 5 models of the E. coli reconstruction, which yielded 599 to 507632 elementary modes. The upper-bounds for these models ranged from 5.57 × 10^{17} to 4.39 × 10^{21}, which were subsequently reduced to 1.67 × 10^{11} to 4.85 × 10^{13} after removing redundant reactions identified using FluxAnalyzer. Despite an improvement of a factor of 6 to 8, when comparing the upper-bounds to the actual number of EMs calculated for the models, they typically overestimated by approximately 6 × 10^{9}% [14]. Although their work dealt with EMs, the problem was constructed as a purely combinatoric problem. Therefore the same reasoning can be directly applied to Extreme Pathways.
In this study, we investigated the relationship between the number of ExPas for a given network, p = |{p_{ i }}|, and its basic network measurements. Several network measurements are commonly used in describing the topological features of a network and include connectivity, clustering coefficient, network diameter, and degree distribution [15]. The number of ExPas for a network can vary dramatically under different simulation conditions, that is, different environmental constraints. Consequently, basic network information such as the numbers of reactions and metabolites of the network cannot be solely used to provide a meaningful estimate. Since ExPas are connected reactions, we hypothesized that the higher the reaction connections, the larger the number of ExPas. Based on this hypothesis, we demonstrated an exponential relationship between log [p] and $\mathrm{log}\left[{\displaystyle {\sum}_{i=1}^{R}{d}_{{-}_{i}}{d}_{{+}_{i}}{c}_{i}}\right]$, where R = |R_{ eff }| is the active (or effective) reactions in the network, ${d}_{{-}_{i}}$ and ${d}_{{+}_{i}}$ are the incoming and outgoing degrees of a reaction, and c_{ i }is the clustering coefficient for each active reaction. This relationship typically gave an estimate of the number of ExPas to within a factor of 10. Since these network measurements can be calculated quickly and easily for any sized network, an estimation of ExPa numbers can be readily obtained as this serves as an assessment of the feasibility of ExPas as an analysis tool.
Results
The number of extreme pathways (ExPa), p = |{p_{ i }}|, for a metabolic network increases drastically with the complexity and size of the network. An estimate for p for a given network can help one decide whether ExPa analysis is a feasible tool for one's research objective. In this study, we investigated the relationship between p and a number of factors, θ_{ i }, formed by simple network measurements such as the incoming and outgoing degree of reactions, d_{∓}(r_{ i }) = ${d}_{{\mp}_{i}}$, and clustering coefficient of each reaction, c(r_{ i }) = c_{ i }. These measurements were chosen as they could be calculated quickly and easily, and their definitions can be found in the sections titled 'Reaction Connectivity d_{±}(r_{ i }) = ${d}_{{\pm}_{i}}$' and 'Reaction Clustering Coefficient c_{ i }= c(r_{ i })', respectively. A total of 52 models, generated from 6 reconstructed metabolic networks by altering environmental conditions, were used to determine a relationship between p and θ_{ i }. The ExPas and corresponding network measurements for these models were calculated and used to identify possible estimating functions. Analyses on logged data (the logarithmic values of the data) revealed an exponential relationship between log [p] and log [θ_{ i }]. A total of 4 estimating functions using two factors were obtained, which were then tested for robustness using an additional 16 models. The numbers of ExPas for most of these models were successfully estimated to within a factor of 10. We concluded that it was possible to formulate an estimating function for the number of ExPas of a model, p', that typically falls within a factor of 10 of the actual number of ExPa.
Identification of Significant Contributing Factors
We aimed to identify factors that can be used for establishing appropriate estimating functions. Desirable factors must be i) easily obtained and ii) specific for a given model. For example, network measurements such as the incoming and outgoing degrees of each reaction, d_{∓}(r_{ i }) = ${d}_{{\mp}_{i}}$, their clustering coefficients, c(r_{ i }) = c_{ i }, as well as the number of external metabolites and their degrees can be obtained quickly. In addition, we required factors to be highly correlated to the number of ExPas and, furthermore, increased in values consistently with p to avoid misrepresentation due to incomparable ranges. The network measurements used in this study are detailed in the 'Network Measurements' section.
Identification of Potential Contributing Factors
R | * ∑(d_{+}d_{-}) | ∑c | * ∑(d_{+}d_{-}c) | $\frac{{\displaystyle \sum ({d}_{+}{d}_{-})}}{R}$ | $\frac{{\displaystyle \sum {c}_{i}}}{R}$ | $\frac{{\displaystyle \sum ({d}_{+}{d}_{-}c)}}{R}$ | $\sum}_{\mathcal{I}}{d}_{i$ | ${\sum}_{\mathcal{O}}d$ | $\left({\displaystyle {\sum}_{\mathcal{I}}d}\right)\left({\displaystyle {\sum}_{\mathcal{O}}d}\right)$ | ||
---|---|---|---|---|---|---|---|---|---|---|---|
r Pre-log | 0.459 | 0.656 | 0.509 | 0.666 | 0.6 | 0.0178 | 0.62 | 0.135 | 0.604 | 0.408 | |
r Post-log | 0.827 | 0.875 | 0.764 | 0.870 | 0.860 | 0.343 | 0.856 | 0.426 | 0.561 | 0.623 | |
ρ | 0.841 | 0.876 | 0.943 | 0.876 | 0.855 | -0.059 | 0.845 | 0.478 | 0.496 | 0.603 | |
Range | Min | 8 | 15 | 5 | 2 | 1.67 | 0.09 | 0.06 | 2 | 2 | 6 |
Max | 174 | 89132 | 35.08 | 5781.73 | 665.38 | 0.9 | 47.78 | 25 | 47 | 414 |
Single Factor Estimate
where ${\widehat{p}}_{k}$ is the estimated number of ExPas for a given model k, θ_{j, k}are the values of the factors θ_{ j }, j = 1, 2 for the k^{th} model, and R_{ k }is the number of active reactions in model k. The estimating functions were formulated using the factors θ_{ j }solely (case i = 1) and by scaling these factors with ${R}_{k}^{\omega}$ (case i = 2). For the former, the parameter ω_{1} had the value 0. For the latter case, ω_{2} was the optimal value for which the highest Pearson's correlation between log [p] and log [${\widehat{p}}_{k}$] could be obtained using the two different factors. This number was found to be the same for both factors and had the value ω_{2} = 2.124857. The parameters α_{i, j}, β_{i, j}, and γ_{i, j}take on different values for the four estimating functions f_{ i }(θ_{ j }), which are detailed in the following subsections 'Estimation Using θ_{1}' and 'Estimation Using θ_{2}'.
Estimation Using θ_{1}
Fit of Training Data to Estimating Functions
Fit of Factors | Over-Estimation | Under-Estimation | |||||
---|---|---|---|---|---|---|---|
Factor | Correlation r | m.a.e. | r.m.s. | Max. Value | Members>1 | Min. Value | Members<1 |
θ_{1} = ∑d_{+}d_{-}c | 0.883439 | 0.407565 | 0.539834 | 1.512650 | 5 | -1.138180 | 1 |
θ_{1} = ∑d_{+}d_{-} | ^{†}0.887057 | 0.406882 | 0.544633 | 1.585230 | 3 | -1.071100 | 1 |
R ^{ ω } θ _{1} | ^{‡}0.900704 | 0.383868 | 0.512515 | 1.629060 | 3 | -0.918259 | 0 |
R ^{ ω } θ _{1} | 0.898332 | 0.381380 | 0.518272 | 1.674300 | 3 | -0.963172 | 0 |
Estimation Using θ_{2}
The relationships between log [p] and Equations (4) and (5) are displayed in Figure 2. In this case, the Pearson's correlation before the inclusion of R^{ ω }was 0.887057, and was improved to 0.898332 after scaling.
Similar to the case for θ_{1}, the errors were reduced after scaling (Table 2). The unscaled estimating function, Equation (4), again, described most of the models (48 out of 52) to within a a factor of 10 with respect to the actual ExPa numbers (Table 2). The inclusion of the scaling factor resulted in less outliers, a better correlation and reduced errors (Table 2).
Performance of Estimations Functions
Fit of Test Data to Estimating Functions
Fit of Factors | Over-Estimation | Under-Estimation | |||||
---|---|---|---|---|---|---|---|
Factor | Correlation r | m.a.e. | r.m.s. | Max. Value | Members>1 | Min. Value | Members<1 |
f_{1} (θ_{1}) | 0.893058 | 0.956777 | 1.042668 | 1.513670 | 7 | -0.785898 | 0 |
f_{2} (θ_{1}) | *0.894445 | 0.806018 | 0.919502 | 1.353102 | 7 | -0.765522 | 0 |
f_{1} (θ_{2}) | 0.864965 | 0.891715 | 1.004652 | 1.501480 | 7 | -0.851316 | 0 |
f_{2} (θ_{2}) | 0.876409 | 0.777881 | 0.897856 | 1.401680 | 7 | -0.808617 | 0 |
Consideration of Other Network Measurements
During the development of these estimating functions, other factors such as the degrees of exchange metabolites were considered. In the case of exchange metabolites, the correlation of the sum of the degrees of all input metabolites, ${D}_{in}={\displaystyle {\sum}_{i=1}^{\left|{M}^{-}\right|}d({m}_{i}^{-})}$ was found to have a low correlation (< 0.5) to the number of extreme pathways, both before and after the data was logged. The correlation for output metabolites, ${D}_{out}={\displaystyle {\sum}_{i=1}^{\left|{M}^{+}\right|}d({m}_{i}^{+})}$, however, was found to have a high correlation (> 0.5) to p. Their product, D_{ in }·D_{ out }, had correlations of 0.408543 and 0.638261 before and after the data was logged. A similar situation existed for the number of effective reactions R, which had a low and high correlation before and after the data was logged. By inspection, a relationship in the bform of Equation (1) could have been established for R. However, the range of R did not grow as consistently as θ_{1} and θ_{2}. As an example, for one H. pylori model, 174 effective reactions resulted in 204,412 extreme pathways, whereas for the Mitochondria model with the reaction SUCD3-u10 m removed, 174 effective reactions only produced 4209 ExPas. This then led to the conclusion that R alone was not an appropriate factor of estimation. The fact that the factor θ_{1} grows consistently with p may have over-shadowed the importance of these factors.
Discussion
The goal for this study was to produce an estimating function using basic network measurements. Specifically, we aimed to obtain a function such that only a single factor is used for estimation. In principle, it was possible to use a multivariate (polynomial) regression method using a number of the factors described in the section 'Identification of Significant Contributing Factors'. However, the independence assumption upon which this method is based was not applicable as the factors themselves tend to be highly correlated. Furthermore, it would have been difficult to interpret which factors were truly responsible for the increase in p, and would probably lead to inaccurate estimations in test models. Here, the most descriptive factor was θ_{1}, which includes the clustering coefficients. The interpretation of the clustering coefficient used in this study is also often used in sociology and biochemical networks (see, for example, [15, 17]). There are other interpretations of the clustering coefficient, such as that described by Soffer et al. [18]. Their definition eliminates degree-correlation biases, thus, quantifying the connectivity amongst the neighbors of a vertex independent to its degree and the degree of its neighbors. It would be interesting to use a similar definition for directed graphs and investigate its effects on ExPa estimation. Additionally, it is possible that other factors may provide a more accurate estimation for the number of ExPas. However, these factors may only be found by detailed analyses of network structures.
The estimating function given by Equation (3) typically estimated the number of ExPas of the test models to within a factor of 10. In cases where it failed, it did not under-estimate the number of ExPas. The version of the E. coli reconstructed network used by Klamt et al. [14] was not elementally- and charge-balanced and has since been replaced by updated versions [19, 20]. We used a revised version iJE660a, which was found to be the closest to what they used, and is publicly available [19, 21], to compare our method with Klamt's. When the estimating function was applied to this version, assuming that all reactions were active concurrently, 7 × 10^{12} ExPas were estimated with our method, whereas Klamt's method yielded an upper-bound of 5 × 10^{13} after disregarding inactive reactions in the unbalanced and smaller model. Given that iJE660a has 41 more reactions and all the reactions are elementally- and charge-balanced, we are confident that our estimating function can also serve as a conservative upper-bound of the number of ExPas after some adjustments. For larger networks such as the latest published reconstruction of E. coli consisting of 904 cited reactions [20], we estimate 3 × 10^{18} ExPas, The Human reconstructed network with 3311 reactions [22] is predicted to have 10^{29} ExPas when all reactions were active concurrently.
Conclusion
In this study, we investigated the possibility of estimating with confidence the number of extreme pathways (ExPa), p, for metabolic networks. Our effort concentrated on the use of simple network measurements, namely the incoming and outgoing degrees, ${d}_{{\mp}_{i}}$ and the clustering coefficients, c_{ i }, for each of the active reactions, r_{ i }∈ R_{ eff }. In particular, it was found that log [p] was correlated to the factors ${\theta}_{1}={\displaystyle {\sum}_{i=1}^{R}{d}_{{-}_{i}}{d}_{{+}_{i}}{c}_{i}}$ and ${\theta}_{2}={\displaystyle {\sum}_{i=1}^{R}{d}_{{-}_{i}}{d}_{{+}_{i}}}$ with an exponential relationship. These factors can be calculated quickly and easily, and were found to increase in values consistently with p. The resulting estimating functions, in particular that given by Equation (3), typically estimated the number of ExPas to within a factor of 10. Therefore we are confident that these estimating functions are scalable and can be reliably applied to larger networks. These estimating functions will therefore enable researchers to decide whether ExPa analysis is an appropriate investigative tool for their objectives.
The set of extreme pathways is the convex basis used for biochemical characterization of the null-space of the stoichiometric matrix for a biochemical reaction network. ExPa analyses have typically been used to characterize phenotypic states of metabolic networks and identify network redundancy. Beyond these uses, the singular value decomposition of the extreme pathway matrix has been used to identify eigenpathways that are capable of characterizing phenotypic states of a system [23, 24]. Nevertheless, applications such as these require ExPas to be calculated prior to any analysis. The number of ExPas is set to increase dramatically with network size and complexity. In particular, with the increase in details of metabolic network reconstructions and the emergence of reconstruction of global transcription/translation networks, new techniques for calculating and analyzing ExPas are much needed. Since the goal of systems biology is to study an organism as a whole, different types of biochemical networks will eventually be combined so that the system can be studied in its entirety. To over-come future computational challenges as well as being equipped with the necessary analytical techniques should become our immediate goal.
Methods
Basic Concepts and Notations
Hypergraph
We introduce some basic concepts and notations that will assist us in describing the measurements needed. We first note that a metabolic network can be described as a directed-hypergraph, where a node represents a metabolite and an edge a reaction. The stoichiometric matrix, S, can thus be seen as a node-edge incidence matrix. A directed-hypergraph $\mathscr{H}$(V, E) consists of nodes (vertices) v ∈ V and edges e ∈ E. Let the matrix S be the node-edge incident matrix such that s_{i, j}< 0 if node v_{ i }is at the tail of edge e_{ j }, s_{i, j}> 0 if v_{ i }is at the head of e_{ j }, and s_{i, j}= 0 if e_{ j }does not contain v_{ i }. We define the set of nodes v that are tails (heads) of edge r to be T(e) (H(e)). It can easily be seen that T(e) ∩ H(e) = ∅.
Reaction Adjacency and Neighbourhood Matrices Â, $\widehat{\Delta}$
The elements of the adjacency matrix ${\widehat{a}}_{i,j}$ = 1 if and only if there exists an metabolite m_{ k }such that s_{k, i}> 0 and s_{k, j}< 0; i.e. reaction r_{ i }'goes into' reaction r_{ j }. In terms of the matrix Â, two reactions r_{ i }and r_{ j }are adjacent if either ${\widehat{a}}_{i,j}$ or ${\widehat{a}}_{j,i}$ is non-zero, which is in agreement with the above definition.
where ${\widehat{s}}_{i,j}=1$ if s_{i, j}is non-zero and 0 otherwise, and ${\widehat{\delta}}_{i,j}=1$ iff r_{ i }and r_{ j }are connected.
Network Measurements
Effective Number of Reactions R= |R_{ eff }|
For any models of a reconstructed network, redundancy in terms of reactions that are not utilized is often expected. This is due to the fact that, for any specific model, there is a set of reactions that is not used under the specific simulation conditions, and therefore can be removed from the network without affecting the model's function. Extreme pathways are classified into 3 types, with Type-I being those that have exchange fluxes across the system boundaries that correspond to non-currency metabolites [25]. Here, we denote the set of reactions that are present in at least one Type-I ExPas by R = |R_{ eff }|. This number can be obtained by optimization techniques such as Flux-Balance Analysis [26] using tools such as SimPheny by Genomatica or FluxAnalyzer [27].
Reaction Connectivity d_{±}(r_{ i }) = ${d}_{{\pm}_{i}}$
Having identified the set of reactions from a reconstruction that are active in a model, the stoichiometric matrix S can then be reduced by removing inactive reactions and metabolites. The connectivity (degree) of each active reaction can then be calculated. Since S can be considered the node-edge incidence matrix for a directed-hypergraph, it is more appropriate to consider the incoming and outgoing metabolites separately. The adjacency and connectivity between each pair of reactions can then be described in terms of the definition given in the section titled 'Reaction Adjacency and Neighbourhood Matrices Â, $\widehat{\Delta}$'. The number of reactions that produce at least one product which is consumed by reaction r_{ i }gives rise to the quantity ${d}_{{-}_{i}}$ = d_{ i }(r_{ i }), and the number of reactions that consume one or more of the products of r_{ i }is defined by the quantity ${d}_{{+}_{i}}$ = d_{+}(r_{ i }).
Reaction Clustering Coefficient c_{ i }= c(r_{ i })
Reconstructed Networks and Simulation Conditions
Basic Information of Models Used
Network | # Rxns | Reversible | # Mets | Models Used | Source |
---|---|---|---|---|---|
H.pylori | 479 | 166 | 485 | 13 | [3] |
Mitochondria | 200 | 92 | 238 | 16 | [4] |
Core E.coli | 62 | 35 | 63 | 9 | [28] |
Central E.coli | 56 | 19 | 62 | 2 | [30] |
Toy E.coli | 50 | 37 | 53 | 4 | [31] |
Red Blood Cell | 32 | 17 | 39 | 8 | [5] |
Environmental Conditions of Models. Table detailing the models used for estimation formulation, along with their environmental conditions.
Core Metabolites | Core Metabolites | Specification | |||||
---|---|---|---|---|---|---|---|
Organisms | Name | Type | Inputs | Outputs | Free | ||
H. pylori | co2 | Free | Ac | ac | mal-L | Single Input along with core metabolite, allowing all outputs (unless specified as input only) | |
fe2 | Free | acac | akg | orn | |||
fe3 | Free | ad | asp-L | phe-L | |||
h2o | Free | ade | acald | pro-L | |||
h | Free | akg | etoh | pyr | |||
nh4 | Free | etoh | fum | ser-L | |||
pi | Free | fum | glu-L | succ | |||
so4 | Free | gsn | gsn | thr-L | |||
o2 | Free | lac | gua | trp-L | |||
mal | h2co3 | tyr-L | |||||
pyr | hxan | urea | |||||
succ | lac-L | ||||||
urea | lys-L | ||||||
Mitochondria | co2 | Free | arachd | atp | glu-L | Single Input along with core metabolite, allowing all outputs (unless specified as input only) | |
h | Free | bhb | pheme | gly | |||
h2o | Free | crvnc | phs-L | glyc | |||
fe2 | Input | glc-D | 12dgr_m | glyc3p | |||
o2 | Input | glu-L | acac | hdca | |||
pi | Input | hdca | arachd | lac-L | |||
urea | Output | lac-L | bhb | ocdca | |||
ocdc All | coa | ocdcea | |||||
ocdca | crvnc | ocdcya | |||||
ocdcea | cys-L | pheme | |||||
ocdcya | glc-D | ps_m | |||||
Mitochondria | co2, h, h20 fe2, fe3, o2 urea | Free | acac | atp | 12dgr_m | (1) Single K/O of: CYOOm3, SUCD3-u10m | |
Input | arachd | lac-L | coa | ||||
Output | Bhb | pheme | cys-L | ||||
crvnc | phs-L | glu-L | (2) Individual Request for: atp, phs-L, pheme | ||||
glc-D | gly | ||||||
glyc | ps_m | ||||||
glyc3p | |||||||
hdca | |||||||
ocdca | |||||||
ocdcea | |||||||
ocdcya | |||||||
E. coli Core | co2 | Free | ac | ac | Single Input along with core metabolite, allowing all outputs (unless specified as input only) | ||
h | Free | akg | akg | ||||
h2o | Free | etoh | etoh | ||||
o2 | Input | for | for | ||||
pi | Input | fum | fum | ||||
glc-D | lac-D | ||||||
lac-D | pyr | ||||||
pyr | succ | ||||||
succ | |||||||
RBC | adp, atp, co2, h, h2o, nad, nadh nadp, nadph, nh3, pi | Free | ade | 23dpg | ino | (1) Single Input along with core metabolite, allowing all outputs (unless specified as input only) | |
Free | ado | ade | lac | ||||
Free | glc | ado | pyr | ||||
hx | glc | ||||||
ino | hx | ||||||
lac | |||||||
pyr | |||||||
glc | 23dpg | ade | (2) Multiple Inputs | ||||
hx | ado | ||||||
ino | |||||||
pyr | |||||||
ino | |||||||
Central E. coli | adp, atp, coa, co2, h, h2o, nad, nadh, nadp, nadph, pi, ppi | Free | glycogen | 2dmmql8 | mqn8 | (1) Glycogen as Primary Input | |
Free | 2dmmq8 | mql8 | |||||
Free | 3pg | oaa | |||||
akg | pep | ||||||
amp | pyr | ||||||
e4p | q8 | ||||||
fad | q8h2 | ||||||
fadh2 | r5p | ||||||
fad | 2dmmq8 | pyr | (2) A different set of Primary Input | ||||
q8 | fadh2 | pep | |||||
2dmmql8 | q8h2 | e4p | |||||
amp | r5p | ||||||
oaa | 3pg | ||||||
akg |
External Metabolites Abbreviation
Exchange Metabolite Abbreviation | |||
---|---|---|---|
12dgr_m | 1,2-Diacylglycerol | hx | Hypoxanthine |
23dpg | 2,3-Phospho-D-glyceroyl phosphate | hxan | Hypoxanthine |
2dmmq8 | 2-Demethylmenaquinone 8 | ile-L | L-Isoleucine |
2dmmql8 | 2-Demethylmenaquinol 8 | ino | Inosine |
3pg | 3-Phospho-D-glycerate | lac | Lactate |
ac | Acetate | lac-L | L-Lactate |
acac | Acetoacetate | leu-L | L-Leucine |
acald | Acetaldehyde | lys-L | L-Lysine |
ad | Acetamide | mal | Malate |
ade | Adenine | mal-L | L-Malate |
ado | Adenosine | meoh | Methanol |
adp | ADP | mql8 | Menaquinol 8 |
akg | 2-Oxoglutarate | mqn8 | Menaquinone 8 |
ala-L | L-Alanine | nad | Nicotinamide adenine dinucleotide |
ala-S | S-Alanine | nadh | Nicotinamide adenine dinucleotide – reduced |
amp | AMP | nadp | Nicotinamide adenine dinucleotide phosphate |
arachd | Arachidonic Acid (C20:4) | nadph | Nicotinamide adenine dinucleotide phosphate – reduced |
asp-L | L-Asparagine | nh3 | Ammonium |
atp | ATP | nh4 | Ammonium Ion |
bhb | (2)-3-Hydroxybuanoate | o2 | O2 |
ch4 | Methan | oaa | Oxaloacetate |
co2 | CO2 | ocdc All | octadecanoate, octadecenoate, octadecynoate |
coa | Coenzyme A | ocdca | octadecanoate |
crvnc | Cervonic Acid (C22:6, n-3) | ocdcea | octadecenoate |
cys-L | L-Cysteine | ocdcya | octadecynoate |
e4p | D-Erythrose 4-phosphate | orn | Ornithine |
etoh | Ethanol | pep | Phosphoenolpyruvate |
fad | Flavin adenine dinucleotide | phe-L | L-Phenylalanine |
fadh2 | Flavin adenine dinucleotide (reduced form) | pheme | Protoheme |
fe2 | Iron (II) | phs-L | Phospholipid |
fe3 | Iron (III) | pi | Phosphate |
for | Formate | ppi | Diphosphate |
fum | Fumarate | pro-L | L-Proline |
glc | Glucose | ps_m | Phosphatidylserine |
glc-D | D-Glucose | pyr | Pyruvate |
glu-L | L-Glutamate | q8 | Ubiquinone-8 |
gly | Glycine | q8h2 | Ubiquinol-8 |
glyc | Glycerol | r5p | alpha-D-Ribose 5-phosphate |
glyc3p | Glycerol 3-phosphate | ser-L | L-Serine |
gsn | Guanosine | so4 | Sulfate |
gua | Guanine | succ | Succinate |
h | H+ | thr-L | L-Threonine |
h2 | H2 | trp-L | L-Tryptophan |
h2co3 | carbonic acid | tyr-L | L-Tyrosine |
h2o | H2O | urea | Urea |
hdca | Hexadecanoate (n-C16:0) | val-L | L-Valine |
A total of 16 functional models from 3 different organisms were used to test the validity of estimations formulated in the section 'Single Factor Estimate'. The networks used were 2 reduced versions of H. pylori, one consisting of 168 reactions and 170 metabolites, the other with 48 reactions and 65 metabolites. Reduced versions of the networks of M. barkeri [16] and H. influenzae [1] were also used. These consisted of 84 and 61 reactions and 121 and 83 metabolites, respectively. These networks are similar to the core E. coli model, with each reaction being mass- and charge-balanced. They were also tested for the production of biomass using SimPheny and hence are functional systems.
The number of data points may seem unorthodox. Although in theory it was possible to automatically generate networks of different input/output combinations, leading to a larger number of training and validation data points, in practice, only a few of such combinations would have resulted in models that produce non-Type-III extreme pathways as well as biomass constituents. For the validation stage, models producing biomass constituents as well as non-Type-III pathways that could be calculated quickly were desired. By drastically reducing networks, it was difficult to construct models that maintained biomass production.
Environmental Conditions of Test Models
Organism | #Rxn | #Met | External Metabolites |
---|---|---|---|
M. barkeri | 84 | 121 | ac, ala-L, alac-S, ch4, co2, cys-L, gly, h, h2 h2o, ile-L, leu-L, meoh, pi, pyr, val-L |
H. influenzae | 61 | 83 | ac, akg, co2, for, fum, glc-D, h, hxan nh4, mal-L, pi, pyr |
H. pylori | 48 | 65 | acald, akg, co2, etoh, for, fum, glc-D, h h2co3, lac-L, mal-L, o2, pi |
H. pylori | 168 | 170 | ac, acald, akg, asp-L, co2, etoh, fum, glc-D, glu-L, h, h2co3, h2o, lac-L, lys-L, mal-L, nh4, o2, phe-L, pi, pyr, ser-L, succ, thr-L, trp-L, tyr-L, urea |
Calculation of Extreme Pathways and Network Measurements
The extreme pathways of all models were computed using an implementation of the algorithm given in [29]. This implementation includes the C++ STL and the number theory library NTL. Algorithms for calculating the greatest common factor of a set of integers of arbitrary size and for sparse-matrix operations were also implemented. Network properties, including incoming and outgoing degrees and clustering coefficients of reactions, were calculated using a C++ implementation of the methods described in 'Basic Concepts and Notations' and 'Network Measurements' using sparse-matrix algorithms and bitwise operations.
Correlation Coeffcients
where D_{ i }is the difference in the ranks of the corresponding values of the n pairs (x_{ i }, y_{ i }). This was used to decide whether a factor increased monotonically with the number of ExPas p.
Declarations
Acknowledgements
This work was funded by National Institute of General Medical Sciences (NIGMS, grant number GM68837). BØP serves on the Scientific Advisory Board of Genomatica Inc. The authors would like to thank Marc Abrams for critical reading of this manuscript.
Authors’ Affiliations
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