- Research article
- Open Access
The evolution of metabolic networks of E. coli
BMC Systems Biology volume 5, Article number: 182 (2011)
Despite the availability of numerous complete genome sequences from E. coli strains, published genome-scale metabolic models exist only for two commensal E. coli strains. These models have proven useful for many applications, such as engineering strains for desired product formation, and we sought to explore how constructing and evaluating additional metabolic models for E. coli strains could enhance these efforts.
We used the genomic information from 16 E. coli strains to generate an E. coli pangenome metabolic network by evaluating their collective 76,990 ORFs. Each of these ORFs was assigned to one of 17,647 ortholog groups including ORFs associated with reactions in the most recent metabolic model for E. coli K-12. For orthologous groups that contain an ORF already represented in the MG1655 model, the gene to protein to reaction associations represented in this model could then be easily propagated to other E. coli strain models. All remaining orthologous groups were evaluated to see if new metabolic reactions could be added to generate a pangenome-scale metabolic model (iEco1712_pan). The pangenome model included reactions from a metabolic model update for E. coli K-12 MG1655 (iEco1339_MG1655) and enabled development of five additional strain-specific genome-scale metabolic models. These additional models include a second K-12 strain (iEco1335_W3110) and four pathogenic strains (two enterohemorrhagic E. coli O157:H7 and two uropathogens). When compared to the E. coli K-12 models, the metabolic models for the enterohemorrhagic (iEco1344_EDL933 and iEco1345_Sakai) and uropathogenic strains (iEco1288_CFT073 and iEco1301_UTI89) contained numerous lineage-specific gene and reaction differences. All six E. coli models were evaluated by comparing model predictions to carbon source utilization measurements under aerobic and anaerobic conditions, and to batch growth profiles in minimal media with 0.2% (w/v) glucose. An ancestral genome-scale metabolic model based on conserved ortholog groups in all 16 E. coli genomes was also constructed, reflecting the conserved ancestral core of E. coli metabolism (iEco1053_core). Comparative analysis of all six strain-specific E. coli models revealed that some of the pathogenic E. coli strains possess reactions in their metabolic networks enabling higher biomass yields on glucose. Finally the lineage-specific metabolic traits were compared to the ancestral core model predictions to derive new insight into the evolution of metabolism within this species.
Our findings demonstrate that a pangenome-scale metabolic model can be used to rapidly construct additional E. coli strain-specific models, and that quantitative models of different strains of E. coli can accurately predict strain-specific phenotypes. Such pangenome and strain-specific models can be further used to engineer metabolic phenotypes of interest, such as designing new industrial E. coli strains.
The gram-negative bacterium E. coli is one of the best-studied microorganisms. This bacterial species includes pathogenic strains that cause disease in various tissues in mammalian and other vertebrate hosts. Some of the more common diseases associated with pathogenic E. coli strains are caused by bacteria found in the gastrointestinal tract or urinary tract, and is a major cause of human morbidity and mortality worldwide. E. coli infections cost the healthcare industry over a billion dollars annually with the enterohemorrhagic (EHEC) and uropathogenic (UPEC) E. coli strains alone responsible for more than 73,000 and 7,000,000 illnesses annually in the United States, respectively [1–3]. A number of genome sequences for these pathovars exist, and comparative analysis between commensal and pathogenic strains has revealed different virulence strategies [4–10]. However, the metabolic properties that differentiate these strains have not been thoroughly investigated. The metabolic content of the genomes of these strains is complex with each strain predicted to contain over 1,000 genes encoding metabolic enzymes and transporters . One method to investigate the complexity of genome-scale metabolic networks is through the construction of computational models.
Computational modeling of bacterial metabolism offers a promising approach to predict strain-to-strain variation in metabolic capabilities and microbial strategies used during host association. The number of available genome-scale metabolic models (GEMs) has grown recently, and they capture the metabolic capabilities of numerous microbial taxa important to human health, biotechnology and bioengineering [12, 13]. Systems biology combines computational and experimental approaches to study the complexity of biological networks at a systems level, where the cellular components and their interactions lead to complex cellular behaviors. Genome-scale biological networks have proven useful for interpreting high-throughput data and generating computational models. Mathematical models are constructed from network reconstructions, and they include variables, parameters, and equations to describe the potential behavior of these networks. Numerous types of genome-scale biological networks have been constructed including metabolic, regulatory, and transcriptional and translational machinery for E. coli K-12 [14–17].
To date, GEMs have been constructed for only two commensal strains of E. coli, E. coli K-12 (strain MG1655) and E. coli W [15, 18]. The E. coli K-12 GEM has been used to engineer strains to increase valuable product formation [19–23], facilitate enzyme function discoveries , provide insight into the genome evolution of other enterobacteria [25, 26], and improve the understanding of the connectivity of metabolic reactions within the cell . Furthermore, computational metabolic models can be validated and refined by comparing in silico predictions with experimental data, where the discovery of disagreements or incorrect in silico predictions can lead to improvements and/or hypotheses about component interactions and unknown network components. An iterative process thus develops where the models are used to analyze experimental data and discrepancies lead to improved models and additional biological discovery. Such approaches have proven successful for updates to the E. coli models for regulation and metabolism [14, 24, 28, 29].
Currently the construction of metabolic networks relies primarily on information derived from genome annotations, enzymatic/pathway databases, and published literature. By combining these resources, the elementally- and charged-balanced reactions catalyzed by enzymes associated with a given gene can be identified [30, 31]. These reactions incorporate pertinent information such co-factors, substrates, products, reversibility, stoichiometry, and subcellular location. A genome-scale metabolic network contains a list of reactions, as well as the gene to protein to reaction (GPR) associations, and is used to formulate constraint-based GEMs. By comparing GEMs for pathogenic and non-pathogenic E. coli strains, metabolic differences can be identified that may lead to the development of new control strategies for E. coli associated disease.
Here we describe the construction of a detailed GEM for the pangenome of the species E. coli, and the use of this GEM to rapidly generate six strain-specific GEMs to compare genome-scale metabolism between four strains from two pathogenic lineages with two commensal K-12 strains. In addition, an ancestral E. coli core GEM was constructed consisting of only those metabolic reactions associated with genes that are conserved across 16 E. coli genomes. The metabolic potential of this ancestral core was also examined. Experiments were performed to iteratively refine and validate the six strain-specific GEMs under aerobic and anaerobic conditions. Once strain-specific GEMs were validated, the properties and metabolic differences distinguishing these pathogenic and commensal E. coli strains were computationally investigated, revealing that some pathogenic E. coli strains are more metabolically efficient than other strains in some environmental conditions. The E. coli GEMs generated in this work provide new tools for investigating the evolutionary and metabolic differences of these strains in conditions reflecting those environments encountered in human hosts. This is the first study to examine the metabolic properties of numerous strains of such a phylogenetically related group of microorganisms, and provides insight into the evolution of metabolism for the species E. coli.
Bacterial strains and growth conditions
Six E. coli strains and one Salmonella strain were used in this study (listed in Table 1). Frozen cultures were streaked onto Luria Bertani (LB) agar plates and grown overnight at 37°C. Isolated colonies were then used to inoculate MOPS (morpholinepropanesulfonic acid) minimal media (TekNova, Hollister, CA) and incubated overnight with shaking (220 rpm) at 37°C, and then overnight cultures were used to inoculate batch cultures grown with continuous sparging aerobically (70% N2, 25% O2, and 5% CO2) or anaerobically (95% N2 and 5% CO2) as previously described . For carbon plate utilization assays, isolated colonies were used to inoculate Sheep Blood Agar plates (Biolog, Hayward, CA) and incubated at 37°C overnight aerobically or anaerobically in sealed Whirl-Pak® Long-Term Sample Retention Bags (Nasco, Fort Atkinson, Wisconsin) saturated with an anaerobic gas mixture (95% N2 and 5% CO2) as described [33, 34]. Anaerobic conditions were confirmed using an obligate aerobic bacterium that exhibited no growth and no respiration in any of the anaerobic conditions examined. Cells were collected and used to inoculate Biolog PM1 plates following the manufacturers recommendations with a minor modification of adding a top layer of mineral oil to each well for anaerobic culture conditions.
Updates to the E. coli K-12 MG1655 metabolic network
Prior to generating a pangenome GEM, additional genes in the genome of E. coli K-12 MG1655 were evaluated as possible updates to the most recent E. coli GEM (iAF1260). The annotations for E. coli K-12 MG1655 were obtained and examined from the ASAP, EcoGene, KEGG, and EcoCyc databases [35–38]. ORFs encoding enzymes that were not included in iAF1260 were further investigated to develop elementally and charge-balanced reactions and to assign the reaction to a subcellular location based on pSORT predictions . In some instances new ORFs were added as isozymes to existing reactions and the gene-to-protein-to-reaction associations updated. This resulted in the addition of 79 new ORFs to the iAF1260 GEM to create iEco1339_MG1655 (Additional file 1). Of the new 79 ORFs (Additional file 2), 62% were based on experimental data from the literature for E. coli strains [40–68] and the rest were based on sequence homology to enzymes already existing in E. coli metabolic networks or to experimentally characterized enzymes from other enterobacteria. These gene additions resulted in 42 new reactions, 32 new isozymes, and 30 new metabolites to the in silico model for E. coli K-12 MG1655.
Generation of an E. coli pangenome metabolic network
Draft and complete enterobacterial genomes in the ASAP database have been continually updated using new publicly accessible genomes since the database's inception . There are more than 150 genomes of enterobacteria in the ASAP database (along with predicted orthologs), 39 of which are E. coli genomes. Of these E. coli genomes, 16 are completely finished, and we have used the information from these genomes and that of Salmonella typhimurium LT2 (Table 2) to generate an E. coli pangenome metabolic network based on metabolic enzymes present in the union of 76,990 ORFs. Each ORF was assigned in the ASAP database to an ortholog cluster group (OCG), and the 76,990 ORFs map to 17,647 OCGs. This reduced the number of genes that had to be evaluated for inclusion in the metabolic network and allowed generation of strain-specific GPRs to rapidly be formulated (Additional file 3). Not all of these OCGs play a metabolic role and/or have sufficient experimentally determined details for metabolic network inclusion. For example only 32.3% of ORFs in the total genome (1,339/4,141) are accounted for in the updated GEM for E. coli K-12 MG1655 (iEco1339_MG1655). All of the gene to protein to reaction association information from the E. coli K-12 MG1655 (iEco1339_MG1655) and the Salmonella LT2 (iRR1083) GEMs were mapped to the OCGs that contained the respective ORFs. The annotations for the genes composing the remaining OCGs were analyzed for additional new metabolic reactions and isozyme additions (Additional file 4) leading to the generation of an E. coli pan-GEM named iEco1712_pan (Additional file 5). All eight SBML files generated in this work were checked for syntax and internal consistency using the validation tool (http://sbml.org/validator/validate.php) and found to conform to all specifications of SBML through Level 3 Version 1 Core (Release 1).
Flux Balance Analysis
Fluxes through metabolic network reactions can be predicted using flux balance analysis (FBA) . In FBA, fluxes are constrained by steady-state mass balances, enzyme capacities and reaction directionality. These constraints yield a solution space of possible flux values, and FBA uses an objective function to identify flux distributions that maximize (or minimize) the physiologically relevant predicted solution. Cellular growth rate (or biomass production) is often used as an objective function for FBA , and was used for FBA analyses performed in this study. The same biomass equation, growth (GAM) and non-growth (NGAM) associated ATP requirement values, and PO (number of ATP molecules produced per pair of electrons donated to the electron transport system) ratio were used for all E. coli developed models, and were the same as that in iAF1260. For FBA and dynamic simulations the reported  wildtype biomass was used and for determination of essential reactions the core biomass was used. Using FBA, in silico predictions of growth yield, growth rate, and carbon source utilization were compared to experimentally determined values for all six E. coli strains and for Salmonella LT2 in both aerobic and anaerobic conditions (Additional files 6 and 7). For carbon source utilization and gene deletion simulations, a maximum uptake rate of 10 mmol per gram of dry weight per hour (mmol/gDW cell/h) was used. FBA was also used to predict essential reactions by constraining reactions to have zero flux and maximizing growth rate. If the resulting maximum predicted growth rate (using FBA) was zero then the reaction was considered to be essential. Reaction deletion simulations were evaluated under both aerobic and anaerobic conditions.
Batch Growth Experiments and Simulations
We performed dynamic FBA simulations of batch growth  and compared these results with experimental data (Additional file 6). In the laboratory, cells were grown overnight in MOPS minimal medium with the addition of glucose (11 mM) as the sole carbon source, and used to inoculate batch cultures to an optical density (OD600 nm) of ~0.02. Batch growth under aerobic and anaerobic conditions was conducted at 37°C and spectrophotometric measurements, viable cells/ml, and biomass (g dry cell weight) were determined at each time point. Samples were collected every hour and passed through a 0.2 μm syringe filter, and then frozen at -70°C for subsequent UPLC analysis. The filtered supernatants were then analyzed to determine glucose concentrations at each time point using a UPLC following manufacturers recommendations (Waters Co., Milford, MA). Growth rates, growth yields, and glucose specific uptake rates were determined from experimental data using the linear least squares estimate as described . Biomass to OD600 conversion values were also calculated for each strain (Table 3). These conversion values were used to estimate initial biomass (T0) values using the initial OD600 measurements (O.D.600 = ~0.02) for each experiment. The T0 values were used as parameters for dynamic FBA simulations of batch growth to determine the exponential growth rates (1/h), biomass yields (g biomass/1g glucose), and times (h) needed to reach stationary phase for the corresponding experimental conditions (aerobic or anaerobic growth in MOPS with 11 mM glucose). For each strain, experimental values from three biological replicates were then compared to those calculated from three computational simulations with matching starting biomass values under aerobic and anaerobic conditions.
Glucose analysis was conducted using an Acquity UPLC equipped with an Acquity BEH Glycan column (Waters). A mobile phase (75% [v/v] Acetonitrile/25% [v/v] H2O with 0.2% [v/v] Triethylamine; pH 9.1) was used at a flow rate of 0.1 ml/min to separate small molecules on a Waters Acquity UPLC equipped with an evaporative light scattering detector and photodiode array.
A maximum parsimony phylogenetic analyses of seven taxa were conducted in MEGA4  using a concatenated protein sequence data set of AcnA, GapA, IcdA, Mdh, MtlD, Pgi, and ProA with S. typhimurium LT2 used as the outgroup species. These genes were chosen since they have been successfully used for phylogenetic analyses of enterobacteria . The alignment for this data set and subsequent maximum likelihood phylogenetic analyses was performed in MEGA4 using default parameters.
The metabolic model for E. coli K-12 MG1655 was developed 20 years ago and has undergone numerous improvements and updates. It is now a sophisticated compartmentalized GEM containing over 1,200 genes and 2,000 reactions. It has been used extensively for biotechnology and discovery applications. Here we generated a GEM for the pangenome of E. coli, and used the information from this larger metabolic network to generate strain-specific E. coli GEMs for two pathogenic lineages and an ancestral core GEM containing reactions conserved across all E. coli strains. Using this new collection of GEMs we validated strain-specific models by comparing predictions to experimental data, conducted a comparison of strain-specific GEMs from three E. coli lineages (commensal, EHEC, and UPEC), and examined the metabolic networks of numerous E. coli strains in an evolutionary perspective based on phenotypic traits.
Updating the E. coliK-12 MG1655 metabolic model
The contents of the E. coli K-12 MG1655 genome were surveyed for new genes/reactions to add to the existing GEM (iAF1260). This effort added a total of 79 genes to iAF1260, of which 15 encoded proteins with significant similarity to proteins with characterized enzymatic activity, 15 were added based on orthology to genes found in the S. typhimurium LT2 GEM (iRR1083), and 49 were added based on experimental evidence from the scientific literature (Additional file 2). Three of the new genes were linked to metabolic reactions that were already included in iAF1260, but whose associated genes were previously unknown (i.e. orphan reactions). The 79 new genes added 42 new metabolic reactions and 30 new metabolites to the GEM. Exchange/transport reactions to permit cis-dihydrodiol-phenylacetyl-CoA utilization were also added resulting in an updated GEM for E. coli K-12 MG1655 designated as iEco1339_MG1655 composed of 1,339 genes, 1,069 metabolites, and 2,428 reactions (Additional file 1). This includes eight new reactions for phenylacetate metabolism that were added following our observation that E. coli K-12 MG1655 can grow in minimal media with phenylacetate as a sole carbon source (data not shown). The 42 new reactions in iEco1339_MG1655 were classified into 15 metabolic subsystems (Figure 1A). There were 24 genes added to the GEM that likely encode isozymes that participate in 32 existing reactions across 13 metabolic subsystems (Additional file 2). A total of 370 reactions in iEco1339_MG1655 contain multiple isozymes.
Generation of an E. colipangenome metabolic model
Understanding the evolution of metabolism for the species E. coli requires comparing genome-scale metabolic content among different strains of E. coli and its relatives. To faciltate these comparisons we mined the contents of 16 E. coli genomes to identify reactions that could be added to iEco1339_MG1655 to generate a pangenome metabolic network representing all metabolic reactions associated with genes present in any one of the E. coli genomes (Table 2). All genes from the sixteen E. coli and the S. typhimurium LT2 genomes (81,496 ORFs total) were classified into orthologous cluster groups (OCGs) based on ortholog relationships from the ASAP database . This analysis resulted in a total of 17,647 OCGs with 16,417 representing the E. coli pangenome and 1,230 OCGs unique to S. typhimurium LT2. Of the 16,417 E. coli pangenome OCGs, 2,894 are found in all sixteen E. coli genomes, 4,146 are shared by two or more E. coli strains, and 9,377 are unique to individual E. coli genomes. Each additional genome added on average 806 new genes; however this number decreased as more genomes were analyzed (Figure 2).
A GEM for the pangenome was then constructed. Existing gene to protein to reaction (GPR) associations from GEMs of iEco1339_MG1655 and S. typhimurium LT2 (iRR1083) were mapped to their corresponding OCGs. The remaining OCGs were analyzed to see if they could be added to the pangenome metabolic network by adding additional isozymes or new reactions. This led to the addition of 373 OCGs and 32 new reactions beyond those found in the updated E. coli K-12 MG1655 GEM (iEco1339_MG1655), resulting in a pan-GEM, iEco1712_pan (Additional file 5), consisting of 1,712 genes, 1093 metabolites, and 2,452 reactions (Additional file 4). Each additional E. coli genome added to the pangenome metabolic analysis resulted on average added 27 new metabolic genes, 20 isozymes, and approximately 2 new metabolic reactions to the pan-GEM (Figure 2). The 32 reactions added to iEco1712_pan fall into 11 metabolic subsystems (Figure 1B), with the majority being related to alternate carbon metabolism (56%, associated with 4-hydroxyphenylacetate and propanediol metabolism) and oxidative phosphorylation (9%). Other added OCGs resulted in addition of isozymes associated with 14 metabolic subsystems, with the most abundant being alternate carbon metabolism (18%), cell envelope biosynthesis (11%), oxidative phosphorylation (11%), nitrogen metabolism (8%), glutamate metabolism (6%), and the remaining 9 subsystems consisted of a single reaction addition (Additional file 4).
Generation of an E. colicore metabolic model
E. coli strains are thought to have diverged from a common ancestor ~10 million years ago (mya)  and it is of interest in understanding how strain-specific metabolism has evolved over time to have an estimate of the metabolic capabilities of an ancestral core for the species E. coli. We assume that genes conserved across the genomes of all strains represents a conservative estimate of the core genome of the ancestor of modern E. coli strains and used this collection of 2,894 conserved genes to construct an ancestral core GEM named iEco1053_core (Additional file 8). There are 1,053 of these genes in the E. coli K-12 MG1655 GEM (iEco1339_MG1655). The GEM for the E. coli ancestral core was made by removing OCGs and their associated reactions from the iEco1339_MG1655 GEM if one or more of the sixteen E. coli genomes did not have a gene assigned to the OCG (Additional file 3). If removing a reaction prevented biomass production for anaerobic growth on glucose (predicted using FBA) then the reaction was added back to the metabolic reconstruction without a gene associated with it and this occurred 24 times (Additional file 9). Using this approach 286 ORFS associated with 184 reactions and 177 isozymes were removed from iEco1339_MG1655 resulting in an E. coli ancestral core GEM (iEco1053_core) consisting of a total of 1,053 ORFs and 2,244 reactions (Table 4), and these 184 reactions we removed were classified based on metabolic subsystem (Figure 1C).
Characteristics of five new E. colistrain specific models
The pan-GEM was used to expedite the process of generating five new strain-specific E. coli GEMs, since the pangenome has reactions connected to cluster groups, a given strains genome contents were analyzed to identify what cluster groups its genes belong to and those associated reactions were included (Additional file 3). The E. coli strains we selected include an additional E. coli K-12 strain (W3110), two enterohemmoraghic E. coli O157:H7 strains (EDL933 and Sakai), and two uropathogenic strains (CFT073 and UTI89). Comparisons to iEco1339_MG1655, including the total number of strain-specific gene additions and deletions and the corresponding metabolic reactions are shown in Table 4. The two K-12 strains are laboratory strains derived from the same isolate and not surprisingly their GEMs, were very similar with the sole difference being removal of a few isozymes and a gene associated with galactitol transport from the W3110 GEM named iEco1335_W3110 (Additional file 10) due to a W3110-specific IS insertion in the gatA gene . We built the five new E. coli GEMs named iEco1335_W3110 (Additional file 10), iEco1344_EDL933 (Additional file 11), iEco1345_Sakai (Additional file 12), iEco1288_CFT073 (Additional file 13), and iEco1301_UTI89 (Additional file 14) by deleting genes and reactions from the pan-GEM when missing from the genome under consideration (Additional file 15). If removing a reaction prevented biomass production for anaerobic growth on glucose (predicted using FBA) then the reaction was added back to the metabolic reconstruction without a gene associated with it. The number of these reactions without associated genes varied from 5 to 10 for each of the pathogenic E. coli strains (Table 4). Five of these reactions without associated genes were required in all four pathogenic E. coli GEMs (Additional file 9). Of the remaining five reactions, two were required for strains EDL933 and Sakai, one was required for strains EDL933, Sakai, and UTI89, and the remaining three are specific to E. coli strain CFT073.
Even though the genomes of the four pathogenic E. coli strains contain between 700-1,000 genes not present in the genome of E. coli K-12 MG1655, relatively few pathogen-specific metabolic genes were added to each GEM (Table 4). Eight new reaction additions were unique to the GEMs of the EHEC strains (iEco1344_EDL933 and iEco1345_Sakai) and consisted of urease, UDP-N-acetylglucosamine 4-epimerase, salicylate hydroxylase, gentisate 1,2,-dioxygenase, sucrose transport, tellurite reduction, fucose synthetase, and perosamine synthetase reactions. The two UPEC strain GEMs (iEco1288_CFT073, and iEco1301_UTI89) shared only one lineage-specific reaction addition for propionate CoA-transferase and each has a single strain-specific reaction addition unique to each strain; galactose isomerase activity for iEco1288_CFT073 and hydroxypyruvate reductase activity for iEco1301_UTI89.
In contrast to the relatively small number of gene and reaction additions there were a large number of reaction deletions for the pathogenic strain GEMs compared to iEco1339_MG1655 (Figure 3, Additional file 15). For EHEC strain GEMs, iEco1344_EDL933 and iEco1345_Sakai, there were 52 genes found in the E. coli K-12 MG1655 GEM (iEco1339_MG1655) that had no orthologous gene in the genomes of the two EHEC strains. These missing genes resulted in 60 reaction deletions in both iEco1344_EDL933 and iEco1345_Sakai, and these were classified based on metabolic subsystem (Figure 1D). There was only one additional reaction deletion unique to iEco1345_Sakai for D-cysteine desulfhydrase, whereas the ORF encoding this enzyme was still intact in the EDL933 strain. For each of the two UPEC strains there were 55 reactions that were missing in both iEco1288_CFT073 and iEco1301_UTI89 compared to iEco1339_MG1655, and these were further classified into metabolic subsystems (Figure 1E). Each of the two UPEC strains also contained numerous reaction deletions unique to each strain (Additional file 5).
When GEMs for all four pathogens (iEco1344_EDL933, iEco1345_Sakai, iEco1288_CFT073, and iEco1301_UTI89) were compared to those of the two K-12 strains (iEco1339_MG1655 and iEco1335_W3110), 21 shared reaction deletions were common to all four pathogenic E. coli strains, and they were categorized into the metabolic subsystems of alternate carbon metabolism, cell envelope biosynthesis, inorganic ion transport and metabolism, lipopolysaccharide biosynthesis, methionine metabolism, nitrogen metabolism, inner membrane transport, and outer membrane transport (Figure 1F).
Assessment and validation of models for carbon source utilization
To evaluate the accuracy of the GEMs for all six E. coli strains, we examined each strain's ability to use different carbon sources under aerobic and anaerobic conditions using Biolog phenotypic arrays. There were numerous strain-specific differences in carbon source utilization in both aerobic (Figure 4A) and anaerobic conditions (Figure 4B). These experimental results were then compared to FBA predictions of growth using different carbon sources. For those compounds included in the Biolog plates that have transporters in the model, FBA was used to predict if they could be used for growth as sole carbon source. This included 76 potential carbon sources for the six E. coli strains and 54 potential carbon sources for Salmonella LT2. If FBA calculated a zero growth rate then the compound was predicted not to be usable as a sole carbon source, while positive calculated growth rates indicated that the model predicted the compound could be used as the sole carbon source. Of the 76 compounds, there were 59 (aerobic) and 56 (anaerobic) carbon sources where model predictions and experiments agreed for all six E. coli models (Additional file 7). The 16 and 19 carbon sources with discrepancies between in silico and experimental results in at least one model (shown in Figure 5) fall into two categories i) when strains did not grow and the model predicted growth (false positive), and ii) instances where strains grew and the model predicted no growth (false negative).
For aerobic carbon source utilization, the number of false positives varied from one to four, and the most accurate models (one false positive each) were for E. coli K-12 W3110 (iEco1335_W3110) and UTI89 (iEco1301_UTI89) (Figure 5). The number of aerobic false negatives was greater than false positives and ranged from three to seven with the least observed for iEco1339_MG1655 and the most observed for iEco1288_CFT073. Of these model-data discrepancies, there were some carbon sources that led to inaccurate predictions by all six E. coli strain specific models such as the utilization of D-aspartic acid (false positive) and M-inositol and tyramine (false negative). The two pathogenic lineages (EHEC or UPEC) exhibited some lineage-specific false negatives for alpha-keto-butyric acid and acetoacetic acid utilization (iEco1344_EDL933 and iEco1345_Sakai) or D-melibiose (iEco1288_CFT073 and iEco1301_UTI89). FBA predictions using a mixture of L- and R- isomers of 1,2 propanediol (a racemic mixture of 1,2 propanediol is used as the sole carbon source in Biolog PM1 plates) resolved aerobic false negative discrepancies for 1,2 propanediol for five E. coli strains, without introducing any new false positives (data not shown).
For anaerobic carbon source utilization, there were no false positives observed for three E. coli strains (iEco1335_W3110, iEco1288_CFT073, and iEco1301_UTI89) and either one or two false positives observed for carbon sources such as D-Threonine (iEco1339_MG1655), D-Aspartic acid (iEco1344_EDL933), and L-Lyxose (iEco1344_EDL933 and iEco1345_Sakai). In contrast to the aerobic results, there were generally more false negative than false positive predictions, with the number of false negatives ranging from 10 (for iEco1339_MG1655) to 14 (for iEco1288_CFT073) for the six E. coli strains (Figure 5). Of these compounds associated with anaerobic false negatives, there were 10 that led to inaccurate growth predictions for all six E. coli strains (succinic acid, formic acid, acetic acid, 1,2-propanediol, alpha-keto-butyric acid, M-inositol, propionic acid, glycolic acid, acetoacetic acid, and tyramine) (Figure 5).
The Biolog phenotype assay uses reduction of a colorimetric tetrazolium dye to measure microbial respiration. Our initial FBA predictions used an objective function that relates to the ability of the bacterium to convert a particular carbon source into biomass. There may be carbon compounds that the bacteria are able to metabolize but which do not result in measurable growth, thus leading to false negatives. To see if changing the objective function from biomass production to indicator dye reduction improves the FBA predictions under both aerobic and anaerobic conditions, two additional reactions were added to each of the models representing the movement of electrons from reduced quinones to the indicator dye used in Biolog plates (RESP1: mql8 => 2H+ + mqn8; and RESP2: q8h2 => 2H+ + q8). FBA was used again but a new objective function, equal to the sum of flux through these two new reactions, was maximized. If the maximum sum of fluxes was zero then the model predicted the carbon source could not be metabolized, while a positive sum of fluxes indicated a carbon source could be metabolized. These new FBA predictions (using respiration instead of growth as an objective) significantly reduced the number of anaerobic false negatives to between two (iEco1339_MG1655) and eight (iEco1288_CFT073) (Figure 5 and Table 5), while not affecting the number of false positives.
Overall, once the FBA objective was changed from biomass to respiration, all E. coli models exhibited a statistically significant relationship between model predictions and experimental growth phenotypes (chi-squared test statistic yields p < 0.05) for both aerobic (>88% accurate) and anaerobic (>89% accurate) conditions (Table 5). The carbon sources M-Inositol and tyramine still led to false negative predictions for all E. coli models examined under both aerobic and anaerobic conditions, which may indicate that missing reactions or gaps may exist in pathways for utilization of these carbon compounds. When considering both the aerobic and anaerobic conditions the overall accuracy for individual strain-specific models was iEco1301_UTI89 (95.3%), iEco1335_W3110 (94.7%), iEco1339_MG1655 (93.4%), iEco1345_Sakai (91.4%), iEco1344_EDL933 (90.8%), and iEco1288_CFT073 (88.8%).
Batch growth predictions
To further evaluate model predictions, dynamic FBA was used to predict time-courses (for substrate, product and cell concentrations), exponential growth rates (1/hr) and biomass yields (gDW cells/g glucose) for aerobic and anaerobic batch cultures in MOPS minimal media with the addition of glucose as the sole carbon and energy source. Batch culture experiments were conducted for each strain, and conversion factors for optical density to biomass, optical density to viable cell concentration, and biomass per viable cell values (Table 3) were determined for each strain in both anaerobic and aerobic conditions. These conversion values were then used to approximate starting biomass values used in the dynamic FBA simulations. For each E. coli strain, the maximum glucose uptake rates used for dynamic FBA were those reported for E. coli K-12 strain W3110  (10 and 18.5 mmol glucose/gDW/h for aerobic and anaerobic conditions, respectively). The predicted growth rates and biomass yields from the model were then compared to experimental results of batch culture of each strain under anaerobic or aerobic conditions. For both aerobic or anaerobic growth conditions, the calculated growth rate (1/hr) for each E. coli strain was compared to the experimentally determined values (Table 6) and the agreement between in silico and experimental values was strong and significant (Pearson correlation test statistic yields p < 0.0002 for both aerobic and anaerobic conditions), yet when viewed separately for aerobic or anaerobic conditions, the correlation was not as strong and was not significant (Pearson correlation test statistic yields p < 0.37 for aerobic, and p < 0.45 for anaerobic conditions). In addition, the growth yields were calculated under aerobic or anaerobic growth conditions in MOPS minimal media for both aerobic and anaerobic growth conditions, and the in silico growth yields for each strain were compared to those determined experimentally (Figure 6) and the agreement between in silico and experimental values was strong and significant (Pearson correlation test statistic yields p < 0.0001 for both aerobic and anaerobic conditions).
The maximum glucose uptake rate from one E. coli strain from each lineage K-12 (MG1655), EHEC (EDL933), UPEC (UTI89) was determined from experimental data for both aerobic and anaerobic conditions. These results revealed that the uptake rates for E. coli K-12 MG1655 were not similar to previously published values for E. coli K-12 W3110 (Table 6). When compared to the two pathogenic lineages, the two E. coli K-12 strains appear to have significantly higher glucose uptake rates in aerobic conditions but significantly lower glucose uptake rates in anaerobic conditions. The dynamic FBA simulations were repeated using the measured lineage-specific glucose uptake rates as parameters. The recalculated growth rates (Table 6), still showed a moderately strong correlation overall between in silico and experimental values (p < 0.0006), yet when viewed separately, resulted in a decreased correlation for aerobic conditions, and a increased correlation between in silico and experimental values for anaerobic conditions (Pearson correlation test statistic yields p < 0.00003). Figure 7 shows a phylogenetic tree of the strain relationships plotted along with the growth rate data, displaying the aerobic and anaerobic growth rates calculated without the uptake rate correction. Additionally we determined the amount of time needed to reach stationary phase experimentally and computationally using dynamic FBA for each strain in each condition. Evaluation of these results reveal that some of the pathogenic lineages attain final biomass in less time compared to the E. coli K-12 strains (Table 7).
Analysis of reaction essentiality
To further explore the metabolic differences and similarities between all six E. coli strain-specific GEMs, we compared reaction essentiality predictions for in silico conditions simulating aerobic and anaerobic growth in glucose minimal media. The number of predicted essential reactions shared in common for all six E. coli strains and also the E. coli ancestral core in both aerobic and anaerobic growth conditions was determined (n = 280) (additional file 16), and their corresponding reactions were further classified by metabolic subsystem (Table 8). Additionally for all six E. coli strains and the E. coli ancestral core, there were 15 additional conserved essential reactions predicted to be required under anaerobic conditions and these involve reactions assigned to subsystems for anaplerotic reactions (1), citric acid cycle (1), cofactor and prosthetic group biosynthesis (5), glycolysis/gluconeogenesis (2), purine and pyrimidine biosynthesis (1), inner membrane transport (2), and outer membrane transport (1). In addition to the shared predicted essential reactions for all E. coli strains examined, there were two lineage-specific reactions predicted as essential under both aerobic and anaerobic conditions for both EHEC strains (iEco1344_EDL933, iEco1345_Sakai), and the corresponding reactions were for fumarate reductase and glycolate oxidase. For the E. coli ancestral core (iEco1053_core), there were five additional reactions predicted as essential that were not predicted for any of the six E. coli strains (additional file 16), and these involve reactions assigned to subsystems for alanine and aspartate metabolism, glutamate metabolism, inner membrane transport, glycolate exchange, and outer membrane porin transport.
This study describes the generation of GEMs representing the union (pangenome) and also the intersection (core) of all identifiable metabolic reactions contained in sixteen genomes of E. coli. We used the E. coli pan-GEM to rapidly construct six E. coli strain-specific GEMs. A comparison between model growth predictions and Biolog phenotypes measured in the laboratory demonstrated an accuracy of more than 88%, including those under anaerobic conditions Additional quantitative data was generated for each strain and used to validate the correlation between model predictions and experimental physiology of the strains in the laboratory. These new E. coli GEMs serve as a framework to examine genome-scale metabolic similarities and differences between strains in an evolutionary context with respect to the commensal, EHEC, and UPEC lineages.
The two E. coli K-12 strains (MG1655 and W3110) are widely used laboratory strains that are believed to have diverged from the same parental strain (strain EMG2 or WG1) approximately 50 years ago . The sole identified metabolic differences between the two E. coli K-12 strains based on genome comparison include the gatA gene that is involved in galactitol transport, dcuA and dcuC involved in C4-dicarboxylate transport metabolism, and also tnaB thought to be involved in the utilization of tryptophan as a carbon and/or nitrogen source . Of these four metabolic gene differences, only inactivation of gatA leads to a loss of a reaction in iEco1335_W3110, compared to iEco1339_MG1655 since dcuA, dcuC and tnaB have other isozymes. The gatA gene contains an insertion sequence (IS) element in E. coli W3110, which suggests a phenotypic loss for galactitol utilization as a carbon source, yet experimental data (Figure 5) reveals that the strain can still use this substrate as sole carbon source, indicating that other transporters may permit galactitol transport for E. coli W3110. Although the two E. coli K-12 strains (MG1655 and W3110) exhibited no differences in their GEMs, quantitative and strain-specific differences were observed during batch growth in minimal media with glucose as the sole carbon source. While in silico predictions for growth yield were similar for iEco1339_MG1655 and iEco1335_W3110, experimental data reveal that in both aerobic and anaerobic conditions, strain MG1655 had higher growth yields, higher growth rate, and attained the final biomass value in less time than strain W3110 (Figure 7). Therefore, although the in silico models for these two strains are nearly indistinguishable, strain specific differences in complex traits such as biomass composition , ATP requirements, PO ratios, and glucose uptake rates may account for these experimental differences. Previous studies have shown that despite their nearly identical genomes and very similar growth patterns in a bioreactor, W3110 and MG1655 have many significant differences in their transcriptomes and proteomes. These include differential expression of pathways affecting central metabolism and the generation of precursor metabolites and energy  suggesting that future models for even these very similar strains will need to account for subtle genetic differences between strains to accurately predict phenotypic traits in simulated culture conditions.
Previous analyses of the E. coli pangenome estimated that on average each new E. coli genome sequence added about 176 unique genes to the pangenome [8, 9], and among these unique genes, we found each additional E. coli genome resulted in 27 metabolic gene additions corresponding to about 2 new metabolic reactions and 20 isozymes suitable for inclusion in the pan-GEM (Figure 2). Clearly some of the metabolic differences between E. coli strains are due to the addition of genes with new metabolic activity. However, our ability to add new reactions to the metabolic reconstructions is severely limited by the paucity of experimental characterization of the metabolic genes, proteins, and reactions unique to pathogenic strains. Since the strain-specific portions of the genomes remain largely uncharacterized, our current understanding of the metabolic functions they encode is dominated by the presence and absence of genes encoding functions represented in the iEco1339_MG1655 GEM. Many of the genes included in this model are not universally conserved among the genomes we examined; resulting in strain-specific GEMs with an average of 70 fewer genes than iEco1339_MG1655 (Table 9). This observation is also consistent with draft GEMs generated using the Model SEED  where the GEM for E. coli MG1655 contained more genes (>60) and reactions (>460) than the draft GEMs for all four pathogenic E. coli strains examined in this work (data not shown).
Although carbon source utilization has become a standard method to assess the validity of computational metabolic model predictions, this study was the first to examine this procedure under anaerobic conditions. Initially, the accuracy of predictions for carbon source utilization during anaerobic conditions was less than those determined during aerobic conditions. We account this difference to comparisons between Biolog carbon source assays, which examine the ability of a microbial strain to generate energy from each sole carbon source, to in silico analysis that determines growth as a positive flux value for the biomass reaction. One possible explanation for experimental and in silico data discrepancies may be that a microbial strain may be able to generate energy from a given carbon source, but that the carbon source is not suitable to sustain growth (i.e. generate a positive biomass value). Therefore, rather than maximize the objective value for the biomass equation, we added two reactions to monitor the ability to generate energy through electron transfer to quinones, and in many cases this analysis resolved discrepancies between in silico predictions and experimental data, especially for anaerobic conditions. Although this methodology of examining carbon source utilization seems trivial, validation for accurate carbon source utilization is important for modeling complex environments such as those encountered in a host, as 31 of the 76 carbon sources tested here were used to simulate the conditions reflecting invasion of a human cell to study S. typhimurium LT2 infection . Therefore, the validation of these strain-specific metabolic models for carbon source utilization will prove useful for future computational modeling of pathogenic E. coli strains in conditions encountered in the gastrointestinal tract or in other locations such as the urinary tract in mammalian hosts.
With the generation of the first GEMs for pathogenic E. coli strains, two EHEC strains and two UPEC strains, properties of these genome-scale metabolic networks were investigated to identify differences that may play a role in human disease. We analyzed two E. coli O157:H7 strains associated with foodborne outbreaks, strain EDL933 isolated from ground beef in the U.S in 1982 and strain Sakai isolated from contaminated radish sprouts that sickened thousands in Japan in 1996. Strains CFT073 and UTI89, which cause human disease outside of the intestine, were isolated from patients with acute urinary tract infections. A comparison of reaction deletions between the EHEC and UPEC metabolic networks reveals that the EHEC strains have more missing genes corresponding to reactions for inner membrane transport in comparison to the UPEC strains. In addition, the reaction deletions that occur in both pathogenic lineages relative to E. coli K-12 strains are mainly associated with genes involved in lipopolysaccharide biosynthesis/recycling and alternate carbon utilization. It seems likely that some of these missing reactions are the result of acquisition of genes during the evolution of the K-12 lineage. Perhaps some of the reactions missing from both pathogen lineages arise from parallel deletions arising from selective pressures common to both pathogens.
Batch growth experiments were conducted to compare growth yields, growth rates, and the amount of time to attain final biomass among strains. We were surprised that EDL933, Sakai and CFT073 have significantly higher growth rates than MG1655 during aerobic growth conditions yet the in silico predictions reveal little to no differences. We sought to determine if strain-specific glucose uptake rates may improve in silico growth rate predictions. Experimentally determined glucose uptake rates were actually lower for EDL933 and CFT073 than for MG1655, and did not improve in silico predictions. The growth yield values we measured in the laboratory also showed significantly (student's t-test statistic yields p < 0.05) higher yields for EDL933 and CFT073 than the two K-12 strains, but in silico predictions showed only minor strain-to-strain variations. Dynamic FBA using the strain specific E. coli GEMs predicts a similar growth rate from all models including the model for the ancestral core of E. coli. Yet the actual growth rates determined experimentally vary significantly between strains suggesting that our models are not accounting for some strain-specific factors such as oxygen uptake rates, biomass composition, ATP requirement parameters, or additional uncharacterized reactions. The length of time required to attain final biomass was significantly (student's t-test statistic yields p < 0.05) shorter for the four pathogens suggesting that they may be more efficient at biomass production during glucose catabolism, and dynamic FBA analysis accurately predicted this phenotypic difference among the strains.
In anaerobic batch growth conditions there were also differences between strains. All pathogenic strains have higher growth rates than the K-12 strains. The FBA predictions for EHEC strains both reflect this phenotype, but the in silico growth rate predictions for the UPEC strains did not reflect this trend. The experimentally determined glucose uptake rates are higher for both pathogenic lineages than K-12, and these organism-specific parameters improved the FBA predictions. The growth yields determined experimentally are significantly (student's t-test statistic yields p < 0.005) higher for the four pathogens than the K-12 strains. The length of time required to attain final biomass predicted by FBA and determined experimentally was significantly (student's t-test statistic yields p < 0.05) shorter for the EHEC strains than the K-12 strains. Overall, for anaerobic glucose catabolism, all four pathogens appear to grow better than both E. coli K-12 strains.
Even though the metabolic networks of each E. coli strain differ, there were relatively few strain-to-strain differences in reactions predicted as essential for the two growth conditions examined. While there were some identified for all strains that were unique for anaerobic growth in comparison to aerobic, there were relatively few differences between all strains. The two reactions (fumarate reductase and glycolate oxidase) predicted as essential for the E. coli O157:H7 strains, play essential metabolic roles for glycolate recycling and the reoxidation of menaquinol, and represent new targets for control strategies that may help to prevent and treat human EHEC illness.
The comparison of the pan- and core-GEMs reveals that a substantial fraction of the reactions in our current pan-GEM are also in the ancestral core-GEM (92%). However, our knowledge of the detailed biochemistry of the pangenome is likely incomplete since many of the genes in other E. coli strains have unknown functions. One reason why the number of reactions in the core- and pan-GEMs are so similar is because the genes that have been well-characterized biochemically in E. coli tend to be the genes that are conserved and likely ancestral. While the pathogenic E. coli strains are of great interest medically, they are not typically the focus of intense biochemical study to uncover the functions of their novel metabolic genes.
Overall, when data for aerobic conditions is viewed phylogenetically (Figure 7A), there is no clear trend specific to the two pathogenic lineages, yet it appears that E. coli CFT073 has evolved with a similar growth rate in comparison to the E. coli ancestral core predictions, where as all other strains have evolved with higher growth rates and yields (Figure 7A).
In contrast, in anaerobic conditions (Figure 7B), higher growth yields and faster batch growth performance were observed for both EHEC E. coli strains (EDL933 and Sakai), and the insight derived from E. coli ancestral core in silico predictions suggest that the UPEC and K-12 lineages have evolved with less efficient anaerobic glucose catabolism then the EHEC lineage. One possible explanation for this behavior may be that the K-12 and UPEC strains do not routinely encounter the selective pressure from anaerobic conditions, whereas the EHEC strains may have evolved for improved growth in anaerobic conditions enabling their growth in both bovine and mammalian GI tracts, thus suggesting that many EHEC strains may have a better-suited anaerobic metabolism for glucose utilization. These findings suggest that E. coli K-12 strains could be engineered to be more efficient for anaerobic batch growth and that other E. coli strains not examined in this work may yield similar results, yet additional studies are warranted to examine more E. coli strain-specific GEMs, quantitative parameters, and catabolism of additional substrates other than glucose.
Here we have presented an update to the E. coli K-12 MG1655 GEM and an extensive new collection of GEMs for five E. coli strains including the first for two pathogenic lineages. These models have been validated through experimental data for aerobic and anaerobic conditions. This work demonstrated a new approach for validation of carbon source utilization, yielding accuracies of >88% for aerobic and anaerobic conditions for all six E. coli strains examined. In addition new lineage-specific quantitative data were generated and led to validation of the correlation between in silico predictions and experimental batch culture data for glucose catabolism during aerobic and anaerobic growth conditions. Thus, the iEco1339_MG1655, iEco1335_W3110, iEco1344_EDL933, iEco1345_Sakai, iEco1288_CFT073, and iEco1301_UTI89 GEMs provide new suitable platforms for computing cellular phenotypes in conditions reflecting those encountered in mammalian hosts such as the intestine or urinary tracts and for further integration of high throughput data generated from these bacterial strains during the course of infection in animal models.
Distinctive lineage-specific differences in the GEMs were identified and reveal that the main delineating metabolic factors between pathogenic and commensal E. coli strains are due to numerous gene/reaction deletions and not additions, and this observation was consistent with the number of genes and reactions contained in draft GEMs for all six E. coli strains generated using Model SEED. Historically many researchers have noticed that some pathogenic E. coli strains grow faster in comparison to commensal strains such as K-12, yet this phenotype has remained unexplained. These strain-specific models offer new tools for further investigation to determine precisely what combination of gene/reaction deletions account for the faster and more efficient biomass production observed experimentally for some of the pathogenic strains, thus providing new insight for bioengineering of industrial E. coli strains.
The generation of an E. coli pan-GEM (iEco1712_pan) consisting of all metabolic genes and reactions from 16 E. coli genomes, represents a new framework to rapidly generate additional E. coli strain/lineage-specific GEMs consisting of > 1,200 genes and >2,000 metabolic reactions. Finally, this study is the first to use a "paleo systems biology" approach to generate a GEM for an ancestral core of E. coli (iEco1053_core) providing the first insight to metabolic traits of an E. coli relative that may have existed ~10 mya, and demonstrated the use of an ancestral model to examine a closely related phylogenetic group of E. coli strains in the context of evolution.
Foxman B: Epidemiology of urinary tract infections: incidence, morbidity, and economic costs. Am J Med. 2002, 113 (Suppl 1A): 5S-13S.
Rangel JM, Sparling PH, Crowe C, Griffin PM, Swerdlow DL: Epidemiology of Escherichia coli O157:H7 outbreaks, United States, 1982-2002. Emerg Infect Dis. 2005, 11 (4): 603-609.
Russo TA, Johnson JR: Medical and economic impact of extraintestinal infections due to Escherichia coli: focus on an increasingly important endemic problem. Microbes Infect. 2003, 5 (5): 449-456. 10.1016/S1286-4579(03)00049-2.
Blattner FR, Plunkett G, Bloch CA, Perna NT, Burland V, Riley M, Collado-Vides J, Glasner JD, Rode CK, Mayhew GF, Gregor J, Davis NW, Kirkpatrick HA, Goeden MA, Rose DJ, Mau B, Shao Y: The complete genome sequence of Escherichia coli K-12. Science. 1997, 277 (5331): 1453-1462. 10.1126/science.277.5331.1453.
Chen SL, Hung CS, Xu J, Reigstad CS, Magrini V, Sabo A, Blasiar D, Bieri T, Meyer RR, Ozersky P, Armstrong JR, Fulton RS, Latreille JP, Spieth J, Hooton TM, Mardis ER, Hultgren SJ, Gordon JI: Identification of genes subject to positive selection in uropathogenic strains of Escherichia coli: a comparative genomics approach. Proc Natl Acad Sci USA. 2006, 103 (15): 5977-5982. 10.1073/pnas.0600938103.
Hayashi T, Makino K, Ohnishi M, Kurokawa K, Ishii K, Yokoyama K, Han CG, Ohtsubo E, Nakayama K, Murata T, Tanaka M, Tobe T, Iida T, Takami H, Honda T, Sasakawa C, Ogasawara N, Yasunaga T, Kuhara S, Shiba T, Hattori M, Shinagawa H: Complete genome sequence of enterohemorrhagic Escherichia coli O157:H7 and genomic comparison with a laboratory strain K-12. DNA Res. 2001, 8 (1): 11-22. 10.1093/dnares/8.1.11.
Perna NT, Plunkett G, Burland V, Mau B, Glasner JD, Rose DJ, Mayhew GF, Evans PS, Gregor J, Kirkpatrick HA, Posfai G, Hackett J, Klink S, Boutin A, Shao Y, Miller L, Grotbeck EJ, Davis NW, Lim A, Dimalanta ET, Potamousis KD, Apodaca J, Anantharaman TS, Lin J, Yen G, Schwartz DC, Welch RA, Blattner FR: Genome sequence of enterohaemorrhagic Escherichia coli O157:H7. Nature. 2001, 409 (6819): 529-533. 10.1038/35054089.
Rasko DA, Rosovitz MJ, Myers GS, Mongodin EF, Fricke WF, Gajer P, Crabtree J, Sebaihia M, Thomson NR, Chaudhuri R, Henderson IR, Sperandio V, Ravel J: The pangenome structure of Escherichia coli: comparative genomic analysis of E. coli commensal and pathogenic isolates. J Bacteriol. 2008, 190 (20): 6881-6893. 10.1128/JB.00619-08.
Touchon M, Hoede C, Tenaillon O, Barbe V, Baeriswyl S, Bidet P, Bingen E, Bonacorsi S, Bouchier C, Bouvet O, et al, et al.: Organised genome dynamics in the Escherichia coli species results in highly diverse adaptive paths. PLoS Genet. 2009, 5 (1): e1000344-10.1371/journal.pgen.1000344.
Welch RA, Burland V, Plunkett G, Redford P, Roesch P, Rasko D, Buckles EL, Liou SR, Boutin A, Hackett J, Stroud D, Mayhew GF, Rose DJ, Zhou S, Schwartz DC, Perna NT, Mobley HL, Donnenberg MS, Blattner FR: Extensive mosaic structure revealed by the complete genome sequence of uropathogenic Escherichia coli. Proc Natl Acad Sci USA. 2002, 99 (26): 17020-17024. 10.1073/pnas.252529799.
Vieira G, Sabarly V, Bourguignon PY, Durot M, Le Fevre F, Mornico D, Vallenet D, Bouvet O, Denamur E, Schachter V, Medigue C: Core and panmetabolism in Escherichia coli. J Bacteriol. 2011, 193 (6): 1461-1472. 10.1128/JB.01192-10.
Feist AM, Herrgard MJ, Thiele I, Reed JL, Palsson BO: Reconstruction of biochemical networks in microorganisms. Nat Rev Microbiol. 2009, 7 (2): 129-143.
Oberhardt MA, Palsson BO, Papin JA: Applications of genome-scale metabolic reconstructions. Mol Syst Biol. 2009, 5: 320-
Covert MW, Knight EM, Reed JL, Herrgard MJ, Palsson BO: Integrating high-throughput and computational data elucidates bacterial networks. Nature. 2004, 429 (6987): 92-96. 10.1038/nature02456.
Feist AM, Henry CS, Reed JL, Krummenacker M, Joyce AR, Karp PD, Broadbelt LJ, Hatzimanikatis V, Palsson BO: A genome-scale metabolic reconstruction for Escherichia coli K-12 MG1655 that accounts for 1260 ORFs and thermodynamic information. Mol Syst Biol. 2007, 3: 121-
Reed JL, Vo TD, Schilling CH, Palsson BO: An expanded genome-scale model of Escherichia coli K-12 (iJR904 GSM/GPR). Genome Biol. 2003, 4 (9): R54-10.1186/gb-2003-4-9-r54.
Thiele I, Jamshidi N, Fleming RM, Palsson BO: Genome-scale reconstruction of Escherichia coli's transcriptional and translational machinery: a knowledge base, its mathematical formulation, and its functional characterization. PLoS Comput Biol. 2009, 5 (3): e1000312-10.1371/journal.pcbi.1000312.
Archer CT, Kim JF, Jeong H, Park JH, Vickers CE, Lee SY, Nielsen LK: The genome sequence of E. coli W (ATCC 9637): comparative genome analysis and an improved genome-scale reconstruction of E. coli. BMC Genomics. 2011, 12: 9-10.1186/1471-2164-12-9.
Alper H, Jin YS, Moxley JF, Stephanopoulos G: Identifying gene targets for the metabolic engineering of lycopene biosynthesis in Escherichia coli. Metab Eng. 2005, 7 (3): 155-164. 10.1016/j.ymben.2004.12.003.
Fong SS, Burgard AP, Herring CD, Knight EM, Blattner FR, Maranas CD, Palsson BO: In silico design and adaptive evolution of Escherichia coli for production of lactic acid. Biotechnol Bioeng. 2005, 91 (5): 643-648. 10.1002/bit.20542.
Lee KH, Park JH, Kim TY, Kim HU, Lee SY: Systems metabolic engineering of Escherichia coli for L-threonine production. Mol Syst Biol. 2007, 3: 149-
Lee SJ, Lee DY, Kim TY, Kim BH, Lee J, Lee SY: Metabolic engineering of Escherichia coli for enhanced production of succinic acid, based on genome comparison and in silico gene knockout simulation. Appl Environ Microbiol. 2005, 71 (12): 7880-7887. 10.1128/AEM.71.12.7880-7887.2005.
Park JH, Lee KH, Kim TY, Lee SY: Metabolic engineering of Escherichia coli for the production of L-valine based on transcriptome analysis and in silico gene knockout simulation. Proc Natl Acad Sci USA. 2007, 104 (19): 7797-7802. 10.1073/pnas.0702609104.
Reed JL, Patel TR, Chen KH, Joyce AR, Applebee MK, Herring CD, Bui OT, Knight EM, Fong SS, Palsson BO: Systems approach to refining genome annotation. Proc Natl Acad Sci USA. 2006, 103 (46): 17480-17484. 10.1073/pnas.0603364103.
Feist AM, Palsson BO: The growing scope of applications of genome-scale metabolic reconstructions using Escherichia coli. Nat Biotechnol. 2008, 26 (6): 659-667. 10.1038/nbt1401.
Yizhak K, Tuller T, Papp B, Ruppin E: Metabolic modeling of endosymbiont genome reduction on a temporal scale. Mol Syst Biol. 2011, 7: 479-
Burgard AP, Nikolaev EV, Schilling CH, Maranas CD: Flux coupling analysis of genome-scale metabolic network reconstructions. Genome Res. 2004, 14 (2): 301-312. 10.1101/gr.1926504.
Barua D, Kim J, Reed JL: An automated phenotype-driven approach (GeneForce) for refining metabolic and regulatory models. PLoS Comput Biol. 2010, 6 (10): e1000970-10.1371/journal.pcbi.1000970.
Kumar VS, Maranas CD: GrowMatch: an automated method for reconciling in silico/in vivo growth predictions. PLoS Comput Biol. 2009, 5 (3): e1000308-10.1371/journal.pcbi.1000308.
Reed JL, Famili I, Thiele I, Palsson BO: Towards multidimensional genome annotation. Nat Rev Genet. 2006, 7 (2): 130-141. 10.1038/nrg1769.
Thiele I, Palsson BO: A protocol for generating a high-quality genome-scale metabolic reconstruction. Nat Protoc. 2010, 5 (1): 93-121. 10.1038/nprot.2009.203.
Sutton VR, Kiley PJ: Techniques for studying the oxygen-sensitive transcription factor FNR from Escherichia coli. Methods Enzymol. 2003, 370: 300-312.
Bochner BR: Global phenotypic characterization of bacteria. FEMS Microbiol Rev. 2009, 33 (1): 191-205. 10.1111/j.1574-6976.2008.00149.x.
Borglin S, Joyner D, Jacobsen J, Mukhopadhyay A, Hazen TC: Overcoming the anaerobic hurdle in phenotypic microarrays: generation and visualization of growth curve data for Desulfovibrio vulgaris Hildenborough. J Microbiol Methods. 2009, 76 (2): 159-168. 10.1016/j.mimet.2008.10.003.
Glasner JD, Rusch M, Liss P, Plunkett G, Cabot EL, Darling A, Anderson BD, Infield-Harm P, Gilson MC, Perna NT: ASAP: a resource for annotating, curating, comparing, and disseminating genomic data. Nucleic Acids Res. 2006, D41-45. 34 Database
Kanehisa M, Goto S: KEGG: kyoto encyclopedia of genes and genomes. Nucleic Acids Res. 2000, 28 (1): 27-30. 10.1093/nar/28.1.27.
Keseler IM, Bonavides-Martinez C, Collado-Vides J, Gama-Castro S, Gunsalus RP, Johnson DA, Krummenacker M, Nolan LM, Paley S, Paulsen IT, Peralta-Gil M, Santos-Zavaleta A, Shearer AG, Karp PD: EcoCyc: a comprehensive view of Escherichia coli biology. Nucleic Acids Res. 2009, D464-470. 37 Database
Rudd KE: EcoGene: a genome sequence database for Escherichia coli K-12. Nucleic Acids Res. 2000, 28 (1): 60-64. 10.1093/nar/28.1.60.
Rey S, Acab M, Gardy JL, Laird MR, deFays K, Lambert C, Brinkman FS: PSORTdb: a protein subcellular localization database for bacteria. Nucleic Acids Res. 2005, D164-168. 33 Database
Boyd LA, Adam L, Pelcher LE, McHughen A, Hirji R, Selvaraj G: Characterization of an Escherichia coli gene encoding betaine aldehyde dehydrogenase (BADH): structural similarity to mammalian ALDHs and a plant BADH. Gene. 1991, 103 (1): 45-52. 10.1016/0378-1119(91)90389-S.
Brinkkotter A, Kloss H, Alpert C, Lengeler JW: Pathways for the utilization of N-acetyl-galactosamine and galactosamine in Escherichia coli. Mol Microbiol. 2000, 37 (1): 125-135. 10.1046/j.1365-2958.2000.01969.x.
Condemine G, Robert-Baudouy J: Analysis of an Erwinia chrysanthemi gene cluster involved in pectin degradation. Mol Microbiol. 1991, 5 (9): 2191-2202. 10.1111/j.1365-2958.1991.tb02149.x.
Ferrandez A, Garcia JL, Diaz E: Transcriptional regulation of the divergent paa catabolic operons for phenylacetic acid degradation in Escherichia coli. J Biol Chem. 2000, 275 (16): 12214-12222. 10.1074/jbc.275.16.12214.
Fuhrer T, Chen L, Sauer U, Vitkup D: Computational prediction and experimental verification of the gene encoding the NAD+/NADP+-dependent succinate semialdehyde dehydrogenase in Escherichia coli. J Bacteriol. 2007, 189 (22): 8073-8078. 10.1128/JB.01027-07.
Heurgue-Hamard V, Champ S, Engstrom A, Ehrenberg M, Buckingham RH: The hemK gene in Escherichia coli encodes the N(5)-glutamine methyltransferase that modifies peptide release factors. EMBO J. 2002, 21 (4): 769-778. 10.1093/emboj/21.4.769.
Ismail W, El-Said Mohamed M, Wanner BL, Datsenko KA, Eisenreich W, Rohdich F, Bacher A, Fuchs G: Functional genomics by NMR spectroscopy. Phenylacetate catabolism in Escherichia coli. Eur J Biochem. 2003, 270 (14): 3047-3054. 10.1046/j.1432-1033.2003.03683.x.
Itoh T, Mikami B, Hashimoto W, Murata K: Crystal structure of YihS in complex with D-mannose: structural annotation of Escherichia coli and Salmonella enterica yihS-encoded proteins to an aldose-ketose isomerase. J Mol Biol. 2008, 377 (5): 1443-1459. 10.1016/j.jmb.2008.01.090.
Jiang M, Cao Y, Guo ZF, Chen M, Chen X, Guo Z: Menaquinone biosynthesis in Escherichia coli: identification of 2-succinyl-5-enolpyruvyl-6-hydroxy-3-cyclohexene-1-carboxylate as a novel intermediate and re-evaluation of MenD activity. Biochemistry. 2007, 46 (38): 10979-10989. 10.1021/bi700810x.
Jiang M, Chen X, Guo ZF, Cao Y, Chen M, Guo Z: Identification and characterization of (1R,6R)-2-succinyl-6-hydroxy-2,4-cyclohexadiene-1-carboxylate synthase in the menaquinone biosynthesis of Escherichia coli. Biochemistry. 2008, 47 (11): 3426-3434. 10.1021/bi7023755.
Kammler M, Schon C, Hantke K: Characterization of the ferrous iron uptake system of Escherichia coli. J Bacteriol. 1993, 175 (19): 6212-6219.
Kuznetsova E, Proudfoot M, Gonzalez CF, Brown G, Omelchenko MV, Borozan I, Carmel L, Wolf YI, Mori H, Savchenko AV, et al, et al.: Genome-wide analysis of substrate specificities of the Escherichia coli haloacid dehalogenase-like phosphatase family. J Biol Chem. 2006, 281 (47): 36149-36161. 10.1074/jbc.M605449200.
Kuznetsova E, Proudfoot M, Sanders SA, Reinking J, Savchenko A, Arrowsmith CH, Edwards AM, Yakunin AF: Enzyme genomics: Application of general enzymatic screens to discover new enzymes. FEMS Microbiol Rev. 2005, 29 (2): 263-279.
Lamark T, Kaasen I, Eshoo MW, Falkenberg P, McDougall J, Strom AR: DNA sequence and analysis of the bet genes encoding the osmoregulatory choline-glycine betaine pathway of Escherichia coli. Mol Microbiol. 1991, 5 (5): 1049-1064. 10.1111/j.1365-2958.1991.tb01877.x.
Liang X, Thorpe C, Schulz H: 2,4-Dienoyl-CoA reductase from Escherichia coli is a novel iron-sulfur flavoprotein that functions in fatty acid beta-oxidation. Arch Biochem Biophys. 2000, 380 (2): 373-379. 10.1006/abbi.2000.1941.
Loh KD, Gyaneshwar P, Markenscoff Papadimitriou E, Fong R, Kim KS, Parales R, Zhou Z, Inwood W, Kustu S: A previously undescribed pathway for pyrimidine catabolism. Proc Natl Acad Sci USA. 2006, 103 (13): 5114-5119. 10.1073/pnas.0600521103.
Moreno-Bruna B, Baroja-Fernandez E, Munoz FJ, Bastarrica-Berasategui A, Zandueta-Criado A, Rodriguez-Lopez M, Lasa I, Akazawa T, Pozueta-Romero J: Adenosine diphosphate sugar pyrophosphatase prevents glycogen biosynthesis in Escherichia coli. Proc Natl Acad Sci USA. 2001, 98 (14): 8128-8132. 10.1073/pnas.131214098.
Nishida M, Kong KH, Inoue H, Takahashi K: Molecular cloning and site-directed mutagenesis of glutathione S-transferase from Escherichia coli. The conserved tyrosyl residue near the N terminus is not essential for catalysis. J Biol Chem. 1994, 269 (51): 32536-32541.
Nogales J, Macchi R, Franchi F, Barzaghi D, Fernandez C, Garcia JL, Bertoni G, Diaz E: Characterization of the last step of the aerobic phenylacetic acid degradation pathway. Microbiology. 2007, 153 (Pt 2): 357-365.
Okuyama M, Mori H, Chiba S, Kimura A: Overexpression and characterization of two unknown proteins, YicI and YihQ, originated from Escherichia coli. Protein Expr Purif. 2004, 37 (1): 170-179. 10.1016/j.pep.2004.05.008.
Preusser A, Wagner U, Elssner T, Kleber HP: Crotonobetaine reductase from Escherichia coli consists of two proteins. Biochim Biophys Acta. 1999, 1431 (1): 166-178. 10.1016/S0167-4838(99)00032-1.
Rakus JF, Fedorov AA, Fedorov EV, Glasner ME, Hubbard BK, Delli JD, Babbitt PC, Almo SC, Gerlt JA: Evolution of enzymatic activities in the enolase superfamily: L-rhamnonate dehydratase. Biochemistry. 2008, 47 (38): 9944-9954. 10.1021/bi800914r.
Rea D, Hovington R, Rakus JF, Gerlt JA, Fulop V, Bugg TD, Roper DI: Crystal structure and functional assignment of YfaU, a metal ion dependent class II aldolase from Escherichia coli K12. Biochemistry. 2008, 47 (38): 9955-9965. 10.1021/bi800943g.
Rohankhedkar MS, Mulrooney SB, Wedemeyer WJ, Hausinger RP: The AidB component of the Escherichia coli adaptive response to alkylating agents is a flavin-containing, DNA-binding protein. J Bacteriol. 2006, 188 (1): 223-230. 10.1128/JB.188.1.223-230.2006.
Stojiljkovic I, Baumler AJ, Heffron F: Ethanolamine utilization in Salmonella typhimurium: nucleotide sequence, protein expression, and mutational analysis of the cchA cchB eutE eutJ eutG eutH gene cluster. J Bacteriol. 1995, 177 (5): 1357-1366.
Toyota CG, Berthold CL, Gruez A, Jonsson S, Lindqvist Y, Cambillau C, Richards NG: Differential substrate specificity and kinetic behavior of Escherichia coli YfdW and Oxalobacter formigenes formyl coenzyme A transferase. J Bacteriol. 2008, 190 (7): 2556-2564. 10.1128/JB.01823-07.
Uehara T, Park JT: An anhydro-N-acetylmuramyl-L-alanine amidase with broad specificity tethered to the outer membrane of Escherichia coli. J Bacteriol. 2007, 189 (15): 5634-5641. 10.1128/JB.00446-07.
Woo HJ, Hwang YK, Kim YJ, Kang JY, Choi YK, Kim CG, Park YS: Escherichia coli 6-pyruvoyltetrahydropterin synthase ortholog encoded by ygcM has a new catalytic activity for conversion of sepiapterin to 7,8-dihydropterin. FEBS Lett. 2002, 523 (1-3): 234-238. 10.1016/S0014-5793(02)02997-6.
Yoshimoto T, Higashi H, Kanatani A, Lin XS, Nagai H, Oyama H, Kurazono K, Tsuru D: Cloning and sequencing of the 7 alpha-hydroxysteroid dehydrogenase gene from Escherichia coli HB101 and characterization of the expressed enzyme. J Bacteriol. 1991, 173 (7): 2173-2179.
Raghunathan A, Reed J, Shin S, Palsson B, Daefler S: Constraint-based analysis of metabolic capacity of Salmonella typhimurium during host-pathogen interaction. BMC Syst Biol. 2009, 3: 38-10.1186/1752-0509-3-38.
Orth JD, Thiele I, Palsson BO: What is flux balance analysis?. Nat Biotechnol. 2010, 28 (3): 245-248. 10.1038/nbt.1614.
Feist AM, Palsson BO: The biomass objective function. Curr Opin Microbiol. 2010, 13 (3): 344-349. 10.1016/j.mib.2010.03.003.
Becker SA, Feist AM, Mo ML, Hannum G, Palsson BO, Herrgard MJ: Quantitative prediction of cellular metabolism with constraint-based models: the COBRA Toolbox. Nat Protoc. 2007, 2 (3): 727-738. 10.1038/nprot.2007.99.
Varma A, Palsson BO: Stoichiometric flux balance models quantitatively predict growth and metabolic by-product secretion in wild-type Escherichia coli W3110. Appl Environ Microbiol. 1994, 60 (10): 3724-3731.
Tamura K, Dudley J, Nei M, Kumar S: MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) software version 4.0. Mol Biol Evol. 2007, 24 (8): 1596-1599. 10.1093/molbev/msm092.
Ma B, Hibbing ME, Kim HS, Reedy RM, Yedidia I, Breuer J, Glasner JD, Perna NT, Kelman A, Charkowski AO: Host range and molecular phylogenies of the soft rot enterobacterial genera pectobacterium and dickeya. Phytopathology. 2007, 97 (9): 1150-1163. 10.1094/PHYTO-97-9-1150.
Reid SD, Herbelin CJ, Bumbaugh AC, Selander RK, Whittam TS: Parallel evolution of virulence in pathogenic Escherichia coli. Nature. 2000, 406 (6791): 64-67. 10.1038/35017546.
Hayashi K, Morooka N, Yamamoto Y, Fujita K, Isono K, Choi S, Ohtsubo E, Baba T, Wanner BL, Mori H, Horiuchi T: Highly accurate genome sequences of Escherichia coli K-12 strains MG1655 and W3110. Mol Syst Biol. 2006, 2: 2006 0007-
Senger RS: Biofuel production improvement with genome-scale models: The role of cell composition. Biotechnol J. 2010, 5 (7): 671-685. 10.1002/biot.201000007.
Vijayendran C, Polen T, Wendisch VF, Friehs K, Niehaus K, Flaschel E: The plasticity of global proteome and genome expression analyzed in closely related W3110 and MG1655 strains of a well-studied model organism, Escherichia coli-K12. J Biotechnol. 2007, 128 (4): 747-761. 10.1016/j.jbiotec.2006.12.026.
Henry CS, DeJongh M, Best AA, Frybarger PM, Linsay B, Stevens RL: High-throughput generation, optimization and analysis of genome-scale metabolic models. Nat Biotechnol. 2010, 28 (9): 977-982. 10.1038/nbt.1672.
Kang Y, Weber KD, Qiu Y, Kiley PJ, Blattner FR: Genome-wide expression analysis indicates that FNR of Escherichia coli K-12 regulates a large number of genes of unknown function. J Bacteriol. 2005, 187 (3): 1135-1160. 10.1128/JB.187.3.1135-1160.2005.
Boyd JM, Lewis JA, Escalante-Semerena JC, Downs DM: Salmonella enterica requires ApbC function for growth on tricarballylate: evidence of functional redundancy between ApbC and IscU. J Bacteriol. 2008, 190 (13): 4596-4602. 10.1128/JB.00262-08.
Acknowledgements and Funding
We are grateful and would like to acknowledge the following for provision of bacterial strains used in this study: Prof. Scott Hultgren (Dept of Molecular Microbiology, Washington University School of Medicine, St. Louis) for provision of E. coli strain UTI89, Prof. Patricia Kiley (Dept. of Medical Microbiology, University of Wisconsin-Madison) for provision of E. coli K-12 strain MG1655, and Prof. Diana Downs (Dept. of Microbiology, University of Wisconsin-Madison) for provision of Salmonella LT2. We would also like to thank the Great Lakes Bioenergy Research Center for use of the UPLC instrument for analysis. This work was funded by the US Department of Energy Genomics:GTL and SciDAC Programs (DE-FG02-04ER25627) for the BACTER Institute Post-Doctoral Fellowship (D.J.B) and also the National Library of Medicine, National Institutes of Health, Grant No. 5T15LM007359 to the Computation and Informatics in Biology and Medicine Training Program for a Post-Doctoral Traineeship (D.J.B) and in part by NIH grant #NIH/GNM GM62994-02. Finally, we would like to thank Dr. Eric Cabot and Christopher Tervo for assistance in generation of the SBML model files.
DB constructed the pangenome, core, and the six strain-specific GEMs and performed all in silico analyses. DB and RP obtained all of the experimental data. DB, JG, and NP designed the study. DB and JR analyzed and interpreted the data and performed the statistical analysis. DB, JG, JR, and NP wrote the manuscript. DB generated all eight SBML model files. All authors approve the content of this manuscript.
Electronic supplementary material
Additional file 1: Genome-scale metabolic model for E. coliK-12 strain MG1655. SBML format of iEco1339_MG1655 for distribution and use in other modeling environments. (XML 3 MB)
Additional file 2: Gene to protein to reaction (GPR) updates for E. coli K-12 MG1655 in the final version of the reconstruction. This file contains two tables, the first contains all new GPR information added to the previous E. coli K-12 MG1655 GEM (iAF1260), and the second contains the final GPR information for iEco1339_MG1655. (XLS 536 KB)
Additional file 3: Orthologous gene cluster groupings for all ORFs in 16 E. coli genomes and one Salmonella genome. This file contains the mapping of orthologous cluster group identifiers to each ASAP feature identifier and locus tag for all ORFs contained in the genomes of 16 strains of E. coli and one Salmonella genome. (XLS 6 MB)
Additional file 4: E. coli pangenome orthologous cluster group identifier (OCG) to protein to reaction information for the E. coli pan-GEM. This file contains four tables, the first contains all gene additions, the second contains all metabolite additions, and the third contains all reaction additions to iEco1339_MG1655 to construct the E. coli pan-GEM (Eco1712_pan). The fourth table contains the final OCG to protein to reaction information for Eco1712_pan. (XLS 702 KB)
Additional file 5: Pangenome-scale metabolic model representing the E. colipangenome. SBML format of iEco1712_pan for distribution and use in other modeling environments. (XML 3 MB)
Additional file 6: Quantitative experimental batch growth data for six E. coli and one Salmonella strain for aerobic and anaerobic conditions. This file contains 3 tables, the first contains the biomass data (g/L), the second contains glucose data (g/L), and the third contains the optical density data (600 nm and 1 cm cuvette path length) for experimental batch growth of six E. coli and one Salmonella strain for aerobic or anaerobic conditions. Values highlighted in yellow reflect the timepoints used to determine lineage-specific glucose uptake rates and strain-specific growth rates. (XLS 56 KB)
Additional file 7: Experimental and in silico carbon source utilization data. This file contains two tables, the first contains experimental and in silico carbon source utilization data during aerobic conditions, and the second contains experimental and in silico carbon source utilization data during anaerobic conditions for six E. coli and a Salmonella strain. Values highlighted in blue represent false negatives and those highlighted in magenta represent false positives. (XLS 58 KB)
Additional file 8: Genome-scale metabolic model representing the ancestral core of E. coli. SBML format of iEco1053_core for distribution and use in other modeling environments. (XML 3 MB)
Additional file 9: Necessary orphan reactions required for biomass production. List of metabolic reactions without corresponding genes necessary for each E. coli strain-specific GEM for biomass production in minimal media with glucose added as the sole carbon source. (XLS 18 KB)
Additional file 10: Genome-scale metabolic model for E. coliK-12 strain W3110. SBML format of iEco1335_W3110 for distribution and use in other modeling environments. (XML 3 MB)
Additional file 11: Genome-scale metabolic model for enterohemorrhagic E. coliO157:H7 strain EDL933. SBML format of iEco1344_EDL933 for distribution and use in other modeling environments. (XML 3 MB)
Additional file 12: Genome-scale metabolic model for enterohemorrhagic E. coliO157:H7 strain Sakai. SBML format of iEco1345_Sakai for distribution and use in other modeling environments. (XML 3 MB)
Additional file 13: Genome-scale metabolic model for uropathogenic E. colistrain CFT073. SBML format of iEco1288_CFT073 for distribution and use in other modeling environments. (XML 3 MB)
Additional file 14: Genome-scale metabolic model for uropathogenic E. colistrain UTI89. SBML format of iEco1301_UTI89 for distribution and use in other modeling environments. (XML 3 MB)
Additional file 15: Deleted reactions for strain-specific E. coli GEMs and the E. coli ancestral core GEM. This file contains three tables; the first contains all gene and corresponding reactions deleted for five E. coli strains in comparison to Eco1339_MG1655, the second contains all deleted genes corresponding to isozymes for five E. coli strains in comparison to Eco1339_MG1655, the third contains all reactions deleted from Eco1339_MG1655 to generate the E. coli ancestral core GEM (iEco1053_core). (XLS 38 KB)
Additional file 16: Reactions corresponding to essential gene predictions for all six strain-specific E. coli GEMs and for the E. coli ancestral core GEM. This file contains three tables, the first contains all predicted essential reactions during both aerobic and anaerobic conditions, the second contains all anaerobic-specific predicted essential reactions, the third contains predicted strain- or core-specific essential reactions for all six strain-specific E. coli GEMs and for the E. coli ancestral core E. coli GEM. (XLS 78 KB)
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Baumler, D.J., Peplinski, R.G., Reed, J.L. et al. The evolution of metabolic networks of E. coli. BMC Syst Biol 5, 182 (2011). https://doi.org/10.1186/1752-0509-5-182
- Metabolic Network
- Metabolic Model
- Flux Balance Analysis
- Carbon Source Utilization
- Glucose Uptake Rate