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- v.6; 2010
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# Emergent cooperation in microbial metabolism

^{1}Department of Systems Biology, Harvard Medical School, Boston, MA, USA

^{a}Department of Systems Biology, Harvard Medical School, 200 Longwood Avenue, WAB 536, Boston, MA 02115, USA. Tel.: + 1 617 432 6401; Fax: + 1 617 432 5012; Email: ude.dravrah.smh@revlis_alemap

## Abstract

Mixed microbial communities exhibit emergent biochemical properties not found in clonal monocultures. We report a new type of synthetic genetic interaction, synthetic mutualism in trans (SMIT), in which certain pairs of auxotrophic *Escherichia coli* mutants complement one another's growth by cross-feeding essential metabolites. We find significant metabolic synergy in 17% of 1035 such pairs tested, with SMIT partners identified throughout the metabolic network. Cooperative phenotypes show more growth on average by aiding the proliferation of their conjugate partner, thereby expanding the source of their own essential metabolites. We construct a quantitative, predictive, framework for describing SMIT interactions as governed by stoichiometric models of the metabolic networks of the interacting strains.

**Keywords:**cooperation, co-culture, flux balance analysis, metabolism, mutualism

## Introduction

Microbes in nature usually do not exist in isolation. The mixed microbial concourse is rich with opportunities for interaction. Metabolic interactions in particular can radically alter the biochemical phenotypes of the participating strains. Microbial communities differ from monocultures in terms of the toxins they degrade (Pelz et al, 1999), the natural products they produce (Pettit, 2009), and even their capacity to grow at all in certain environments (Schink, 2006). A complete understanding of microbial metabolism must extend from the properties of individual strains in pure culture to the combinatorial interactions supported by complex communities.

Recent studies have characterized the behavior of microbes in co-culture. Such strains may exhibit naturally complementary metabolism (Kim et al, 2008; Rozen et al, 2009; Hillesland and Stahl, 2010), or may be genetically engineered to interact (Shou et al, 2007; Balagaddé et al, 2008; Gore et al, 2009). Interacting partners share metabolites, such as hydrogen (Hillesland and Stahl, 2010), acetate (Rozen et al, 2009), amino acids (Shou et al, 2007), fixed nitrogen (Kim et al, 2008) or glucose (Kim et al, 2008; Gore et al, 2009). In each case, it has been possible to extrapolate interactive dynamics from the individual characteristics of the participating strains.

A general model of metabolic interaction would account for the variety of metabolites that can be exchanged and the genotypic diversity of the strains that exchange them. Ideally, such a model would not require detailed biochemical characterization of each individual participant to be predictive. Optimization-based techniques of flux balance analysis have been successful in describing metabolic systems (Feist et al, 2007). These approaches draw on the well-characterized biochemical reaction network of organisms such as *Escherichia coli* (Kanehisa and Goto, 2000), and can be easily generalized to more exotic species (Feist et al, 2009).

Using a model set of *E. coli* auxotrophs, we extend these approaches to the higher-order system of two strains in concourse. We find that certain pairs of auxotrophs will complement one-another's growth in minimal media by cross-feeding essential metabolites, a relationship we refer to as synthetic mutualism in trans (SMIT). The SMIT interactions constitute a class of synthetic genetic interactions because, similar to other synthetic interactions, they reflect and elucidate the genetic and metabolic network from which they derive. We develop a quantitative and predictive theoretical model that reveals the extent to which complex metabolic interactions emerge from the relatively simple topology of the biochemical reaction network.

## Results and discussion

We selected 46 conditionally lethal auxotrophic *E. coli* from the Keio collection (Baba et al, 2006). Each deletion blocks the biosynthesis of an essential metabolite, imparting a strict dependency on an external supply of that metabolite for growth. The selected mutations cover a significant portion of metabolic diversity and include genes required for the biosynthesis of amino acids, nucleotides, and cofactors, as well as genes involved in glycolysis and respiration. Each deletion strain exhibits robust growth in rich (LB) medium but no measurable growth in minimal (M9) medium. Strains were labeled individually with plasmids expressing either Venus or mCherry fluorescent proteins and co-cultured in minimal media in all pairwise combinations (Box 1). Growth was measured each day over 4 days by optical density. Flow cytometry allowed determination of the relative abundance of each strain in each pairing. Theoretical and empirical precedents have established that metabolic cooperation is enhanced at intermediate cell densities when the concentration of cross-fed metabolites is sufficiently high to improve cooperative fitness (Shou et al, 2007; Bull and Harcombe, 2009). Strains were therefore each inoculated at 10^{7} cells per ml, roughly 1/200th saturation density, and fold growth is reported relative to this initial inoculation level.

We selected 46 conditionally lethal metabolic mutants from the Keio collection and labeled them with plasmids expressing Venus or mCherry fluorescent protein. Strains were co-cultured in all pairwise combinations in minimal medium in which no strain could grow independently.

A subset of mixed pairs showed improved growth relative to either corresponding monoculture (Figure 1). In control cultures of self-same pairs, no strain was observed to grow more than eight-fold. However, 17% of dissimilar pairings showed greater than 50-fold growth, indicating metabolic synergy. Growth phenotypes were variable, with alternately one strain, both, or neither benefiting from the interaction. For each strain, we were able to identify at least one partner with which synergistic growth was evident. Conversely, no strain exhibited a universally cooperative phenotype, either in the role of nutrient donor or recipient.

*Escherichia coli*metabolic mutants. Red and blue heat map intensity represents the fold growth of strain A and B, respectively, in each co-culture. Fold growth is expressed relative to the initial inoculation density. Self-same pairings,

**...**

We first explored how the growth of a given strain relates to its level of cooperation, as inferred from the growth of its partner strain. Cooperating strains in this system may show enhanced proliferation through the mechanism of *invested benefits* (Connor, 1995; West *et al*, 2007). Cooperation on the part of strain A will augment A's growth only if B cooperates in turn. By increasing B's abundance, A then cultivates the source of A's own metabolites and therefore A's own growth. Given the relatively low growth rates of the co-cultured strains and the excess availability of nutrients, we do not expect a significant metabolic burden to be associated with the production of shared metabolites. However, we do expect a limit to the invested benefits of cooperative growth. Specifically, this should arise when oversharing on the part of A results in B monopolizing the batch culture and therefore necessarily limiting A.

The data reflect a significant growth benefit for cooperating strains. We record an overall positive correlation between the growth of strains A and B (Spearman's ρ=0.2, *P*-value: <10^{−10}). This correlation was highest when the total growth of A and B was low to moderate. We could also observe a characteristic anti-correlation between the growth of A and B in cultures that approach saturation, when more growth of one strain tended to impede the other (Figure 2A).

**A**) The mean growth of strain B is presented for sets of co-cultures binned by the measured growth of strain A. The growth of strain B initially increases with that of A as B reaps

**...**

A simple dynamic model captures the essential features of this relationship.

A and B above represent the strain abundances. We assign cooperation levels, *C*_{A} and *C*_{B}, to quantify cooperation on the part of strain A and B, respectively. *K* is the logistic carrying capacity of the batch culture. Growth was allowed to proceed for a fixed and finite amount of time, so our system does not necessarily approach a steady state.

Although analytical solutions to (1) are not available, numerically solving the system of two equations for the two variables *C*_{A} and *C*_{B} transforms the growth data into biologically relevant parameters that reflect the level of cooperation evidenced by each strain. The measured growth of A increases monotonically with respect to the derived value of *C*_{B}, indicating that it is always beneficial to be partnered with a cooperating strain. A characteristically also increases with *C*_{A} for low *C*_{A}, as strain A reaps the invested benefits of cultivating strain B. However, A declines for high *C*_{A}, when excess cooperation allows B to dominate the available carrying capacity (Figure 2B).

We sought to relate the various observed cooperation phenotypes to the properties of individual mutations in the global context of *E. coli* metabolism. Synthetic genetic interactions, the synergistic growth effects of multiple gene deletions, are known to identify epistatic or modular relationships among genes (Segrè et al, 2005; Ooi et al, 2006; Motter et al, 2008). Previous studies emphasize the phenotypic consequences of multiple genetic deletions within the genome of a single strain. We define a new synthetic relationship, the synergistic growth between two otherwise lethal mutants, as SMIT.

Similar to other synthetic interactions, SMIT interactions can be applied to infer properties of the *E. coli* metabolic network. Pairings of strains with metabolic blocks in the same biosynthetic pathway grew less than pairings of strains blocked in distinct pathways. Approximately 3.6% of pathway-matched pairs showed growth above 50-fold against 18% of pathway-distinct pairs (*n*=55, *n*=980, respectively, *P*-value: 2 × 10^{−6}). However, mutants sharing pathways showed consistency in their set of cooperating partners (Supplementary Figure 1). We constructed for each strain a cooperation profile vector consisting of the measured growth of that strain and that of its partner strain in each of the 46 co-cultures. Correlations of the cooperation profiles therefore indicate the overall similarity of the cooperative behavior between two strains.

We applied an unsupervised hierarchical clustering algorithm to the set of cooperation profiles, using the Spearman rank correlation between vectors as a distance metric and a complete linkage function. Mutants in the biosynthetic pathways of tryptophan, guanine, histidine, purine, pyramidine, arginine, cysteine, leucine, and pantothenate were recovered as distinct branches in the resulting dendrogram. Analysis of SMIT interactions is therefore capable of identifying biosynthetic modules (Figure 3A).

**A**) A dendrogram depicts hierarchical clusters derived from measured cooperation profiles. Most of the major metabolic pathways are recovered as distinct branches, implying that functional

**...**

More distal correspondence in the metabolic network can also be detected in the analysis of SMIT interactions. For each pair of interacting mutants, we define a shortest path through the metabolic network connecting the two reactions. Reactions are considered connected if they share a common metabolite. The correlation between the cooperation profiles characterizing any two strains declines with the distance spanning their mutations (ρ=−0.34, *P*-value: <10^{−10}). This suggests that, to a significant extent, the complex emergent phenotype of SMIT growth is governed by the relatively simple stoichiometries of the metabolic reaction network (Figure 3B).

Metabolic network stoichiometries can be applied to infer biochemical reaction rates through the method of flux balance analysis (FBA; Palsson, 2006). We extend FBA modeling from a single *E. coli* to a system of two interacting strains. Beginning with the standard iAF1260 reconstruction (Feist et al, 2007), the stoichiometric matrices and flux bounds for the two strains are concatenated appropriately to produce the joint model, allowing the free exchange of metabolites between the two mutants (see Materials and methods).

We derived solutions to the joint model by applying the minimization of metabolic adjustment (MOMA) objective function (Segrè et al, 2002). The MOMA methods hypothesize that mutant systems will tend to approximate the wild-type flux distribution, even as mutation precludes an exact match. This objective function is conservative; it identifies solutions in the joint vector closest, in the Euclidean sense, to the wild-type fluxes.

Total growth of the co-cultures was correlated with predicted growth derived from the joint flux model. We calculated a rank correlation of 0.42 across predictions for all pairs (*P*-value: <10^{−10}). This model performed less well in comparisons of the subset of pairs with mutations in the nucleotide biosynthesis pathway (ρ=0.17, *P*-value: 0.13, *n*=78), and better when both mutants were involved in amino-acid production (ρ=0.4, *P*-value: <10^{−10}, *n*=378), or in neither of those classes (ρ=0.72, *P*-value: 0.02, *n*=10). The joint flux model was effective in reproducing our observation that mutants in shared pathways generally do not supplement one another's growth (Supplementary Figure 2).

In general, growth predictions from the joint flux model were higher than those measured. This might be explained by the relatively high levels of cooperation implicit in the objective function. In selecting an optimal joint flux vector, fluxes are weighted equally in their contribution to minimizing the metabolic adjustment of their own strain and of the partner strain. This is theoretically unlike the situation *in vivo*, in which any flux optimality is expected only within a given strain, and any benefits to the partner strain are only as a byproduct. Indeed, our system has no co-evolutionary history and has not been optimized by natural selection in any sense. We therefore sought a predictive framework independent of optimality assumptions.

We reasoned that the likelihood of a given metabolite being shared should depend on the growth value of that metabolite to both the donor and recipient strain. Metabolites less valuable to the donor might be more readily shared, and metabolites more valuable to the recipient should effect more growth. In an efficient cooperative interaction, each strain would exchange growth-cheap metabolites for growth-dear metabolites (Boucher, 1988).

We can derive explicit predictions for the value of each exchanged metabolite for each mutant strain in our system as shadow prices. A shadow price, in a linear programming model, is defined as the marginal change in the objective function associated with the strengthening or loosening of a particular model constraint. As in standard flux balance models, calculating shadow prices requires only the reaction network stoichiometries and the measured composition of biomass. We solved the iAF1260 model for shadow prices representing the fitness benefit, *b*^{A}, to each strain A in taking up a unit of its required metabolite. For example, a tryptophan auxotroph is associated with a high benefit term because a unit of the rare amino acid tryptophan is sufficient to produce a relatively high amount of biomass. Similarly, we derive a cost term, *p*^{B}, representing the loss in growth rate for each strain, B, in secreting a given metabolite.

The calculated costs and benefits produced the expected correlation with measured growth. The benefit associated with a metabolite *b*^{A} was positively correlated with the growth of strain A (ρ=0.11, *P*-value: 10^{−3}), but showed no correlation with the growth of the partner strain. Conversely, the production cost of metabolites *p*^{B}, incurred by strain B, was negatively correlated with A's growth (ρ=−0.26, *P*-value:<10^{−10}) but was uncorrelated with B's growth. Thus, strains tended to show the most growth when predicted to require only small quantities of metabolites that were cheap for their partner to produce.

We define the predicted efficiency of cooperation, ^{B}, as the ratio *b*^{A}/*p*^{B}. We observed that ^{B} was more predictive than either *b*^{A} or *p*^{B} alone in determining the growth of strain A (ρ: 0.31, *P*-value: <10^{−10}). We also determined an overall positive correlation between the growth of strain A and ^{A}, the efficiency term as calculated for the partner strain, consistent with the invested benefits A receives from the growth of B (ρ: 0.14, *P*-value: 10^{−5}). Indeed, in the regime of low A growth, ^{A} was more strongly correlated with A's growth than ^{B}, emphasizing the strong fitness advantage for efficient cooperators.

The cooperation efficiency terms reproduce the characteristic pattern in their correlation with strain growth, predicted in our invested benefits model of cooperation (Figure 3C). The term ^{B} is positively correlated with A's growth across all growth levels, as it is always beneficial to be paired with an efficient cooperator. The ^{A} correlates positively to A's growth for low growth, then negatively as the strains approach saturation. Only in this narrow range would the less generous show more growth.

Cooperation efficiencies derive purely from stoichiometric information, and so can be calculated for strains without detailed biochemical characterization. They are independent of the specific physiological mechanisms that effect metabolite production, secretion, and exchange, which in the case of this system remain to be described.

Intracellular metabolites represent valuable resources, and should therefore be retained by cell membranes in the absence of a specific mechanism for secreting them. Such reasoning can explain the behavior of most co-cultures, in which essential metabolites are retained and no cross-feeding occurs. *E. coli* are known to secrete a number of amino acids, particularly when starved or otherwise stressed (Burkovski et al, 1995; Kaderbhai et al, 2003; Valle et al, 2008). Alternately, the intracellular metabolite pool also undergoes significant changes during starvation (Tweeddale et al, 1998). Cell lysis may then be required for accumulated metabolites to be released and scavenged.

The results presented here reflect only cooperation before co-evolution, and do not reveal the evolutionarily stable steady state that may arise for cross-feeding organisms. To persist in natural systems, cooperative behavior must be robust to variations of environment, and to the emergence of exploitative mutants. Many natural syntrophic systems seem to be cases of byproduct cooperation, in which one strain feeds on the waste products of another (Marx, 2009; Rozen et al, 2009). We find that the metabolites most readily exchanged are those of little value to the secreting strain. This is consistent with proposals that byproduct cooperation evolves more readily than other forms, because it requires no active investment of one partner in the other (Connor, 1995).

The fitness costs and benefits of biological interactions are often difficult or impossible to quantify (Boucher, 1988), but are required for the application of population dynamic models (Nowak, 2006). The *a priori* prediction of such parameters in an experimentally tractable model organism brings a new degree of quantitative resolution to theories of metabolic interaction.

## Materials and methods

### Co-culture experiments

Deletion strains from the Keio collection were grown to saturation in rich (LB) medium with appropriate antibiotics, washed twice in PBS, and re-suspended in M9 minimal medium at a 1:100 dilution (6.8 g/l Na_{2}HPO_{4}, 3 g/l KH_{2}PO_{4}, 0.5 g/l NaCl, 1 g/l NH_{4}Cl, 20 g/l glucose, 100 μM CaCl_{2}, 1 mM MgSO_{4}, 50 μg/l ampicillin, and 100 μg/l kanamycin). Strains were cultured overnight in minimal medium to allow depletion of residual nutrients, then re-diluted to the initial 1:100 level. Residual growth was generally less than 10%. Viable cell counts were determined by plating for all strains both before and after starvation, and were observed to be linear with OD and similar for all strains. This indicated that total cell density could be accurately measured by OD, despite the unique genetic background and metabolic conditions of each co-culture. Incubation was carried out in sealed microplates at 37°C under continuous shaking. Growth was measured by optical density at 600 nm using a Perkin Elmer EnVision plate reader. Ratios were assessed with a BD LSR-II flow cytometer. Cell density for a strain A was calculated as δ·(OD_{M}−OD_{BKG})·A_{frac}, where OD_{M} is the measured OD, OD_{BKG} was the background absorbance of blank medium, δ is the linear scaling factor from OD to cell density, calculated by plating standard curves, and A_{frac} is the proportion of strain A as measured by flow cytometry.

Growth experiments were conducted in duplicate and with label-switched pairs, a total of four replicates for each of 1035 possible experimental pairs. Growth measurements were reproducible in both biological replicates (ρ=0.92) and label-switched replicates (ρ=0.9). Following data acquisition, a random sample of 50 growing mixed cultures were struck out on rich medium and minimal medium. In no case were single colonies observed to grow on minimal plates, indicating that observed growth was not due to the restoration of prototrophy in a single lineage from any genetic event.

### Data analysis

Calculations and simulations were performed in MATLAB. Convex programming was performed using MOSEK Optimization Software. Correlation coefficients are Spearman's rank correlation unless otherwise noted. Metabolic network distances were calculated excluding metabolites with very high connectivities (>20 reactions), because of their effect of radically shrinking the network radius.

### The joint stoichiometric model

A standard metabolic optimization problem with a MOMA-type objective function identifies a flux vector **J** in the mutant flux space, which minimizes the Euclidean distance to the wild-type flux vector. Thus, it satisfies the following:

where **J**^{WT} denotes a wild-type flux vector, derived from a standard FBA formulation (Segrè et al, 2002). Upper and lower bounds on the internal fluxes are set to **τ**_{L} and **τ**_{U}. Bounds on the exchange fluxes, corresponding to the media conditions, are set to **τ**_{U} and **τ**_{L}. **S** represents the internal reaction stoichiometries and **X** the exchange stoichiometries. Finally, **J**_{S} and **J**_{X} are the subsets of internal and exchange fluxes of **J**.

For the joint problem, we concatenate the flux vectors, bounds, and stoichiometric matrices appropriately to define a joint flux space, thus solving:

Superscripts A and B denote fluxes, matrices and bounds associated with strain A or B. The exchange matrix, **X**, is identical for all mutants. The third row of the joint stoichiometric matrix allows the exchange of metabolites between strains. The upper bounds of the exchange reactions, **β**′_{U}, are modified to allow the uptake of all shared metabolites. The term 2**X****β**′_{U} transposes the unmodified bounds from the individual fluxes on problem 2 to apply to the sum of the joint fluxes, maintaining conservation of mass between the two strains.

### Mean marginal cost and benefit

The mean marginal production cost of a metabolite m, *p*_{m}, we define as the reciprocal of the solution to a linear programming problem:

This represents the minimum flux value, that is, the maximum secretion level, which can be attained consistent with a growth rate of at least 90% wild type. The reciprocal of this solution, 1/**J**_{m}, is proportional to the mean shadow price associated with the bound on the exchange flux of metabolite m, **J**_{m}, taken over the interval 100–90% of wild-type growth rate. We allow *p*_{m} to take the value of infinity for those cases when **J**_{m}=0, meaning a given metabolite is stoichiometrically blocked from being secreted and is therefore not available at any cost.

The mean marginal benefit, *b*_{m}^{σ}, which a given strain, σ, receives from a metabolite, m, is the reciprocal of the solution to a similar problem:

Note that although secretion costs are calculated with respect to the wild-type strain background, uptake benefits are defined with respect to a specific mutant strain that can not grow without supplemented metabolites. Problem 4 identifies the minimum supplemental flux consistent with growth of at least 10% of the wild-type level. Most metabolites are not capable of rescuing growth of most mutant strains, therefore the solution to problem 4 is undefined and we allow *b*_{m}^{σ}=0. Otherwise . As above, the benefit is proportional to the mean shadow price for the uptake bound on metabolite m over the interval 0–10% of wild-type growth rate.

In cases, in which *p*_{m}^{B} and *b*_{m}^{A} are defined for more than one m, because strain A can be rescued by more than one metabolite, we take the values *p*^{B} and *b*^{A} to be the mean values over all m for which they are defined.

The efficiency of cooperation for a strain B, ^{B}, for a strain B as the ratio *b*^{A}/*p*^{B}. In cases, in which A can be rescued by more than one metabolite, we take ^{B} to be the mean ratio for all such metabolites.

## Acknowledgments

We thank Roy Kishony for insight and discussions. Stewart Rudnicki, Caroline Shamu and the ICCB-Longwood Screening Facility provided advice and experimental assistance. Devin Burrill, Tami Lieberman, Patrick Boyle and Christina Agapakis contributed to revisions. EW was supported through the NSF Graduate Research Fellowship Program.

## Footnotes

The authors declare that they have no conflict of interest.

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