Abstract

BackgroundMicrobial co-cultures and consortia are of interest in cell-based molecular production and even as “smart” therapeutics in that one can take advantage of division of labor and specialization to expand both the range of available functions and mechanisms for control. The development of tools that enable coordination and modulation of consortia will be crucial for future application of multi-population cultures. In particular, these systems would benefit from an expanded toolset that enables orthogonal inter-strain communication.ResultsWe created a co-culture for the synthesis of a redox-active phenazine signaling molecule, pyocyanin (PYO), by dividing its synthesis into the generation of its intermediate, phenazine carboxylic acid (PCA) from the first strain, followed by consumption of PCA and generation of PYO in a second strain. Interestingly, both PCA and PYO can be used to actuate gene expression in cells engineered with the soxRS oxidative stress regulon, although importantly this signaling activity was found to depend on growth media. That is, like other signaling motifs in bacterial systems, the signaling activity is context dependent. We then used this co-culture’s phenazine signals in a tri-culture to modulate gene expression and production of three model products: quorum sensing molecule autoinducer-1 and two fluorescent marker proteins, eGFP and DsRed. We also showed how these redox-based signals could be intermingled with other quorum-sensing (QS) signals which are more commonly used in synthetic biology, to control complex behaviors. To provide control over product synthesis in the tri-cultures, we also showed how a QS-induced growth control module could guide metabolic flux in one population and at the same time guide overall tri-culture function. Specifically, we showed that phenazine signal recognition, enabled through the oxidative stress response regulon soxRS, was dependent on media composition such that signal propagation within our parsed synthetic system could guide different desired outcomes based on the prevailing environment. In doing so, we expanded the range of signaling molecules available for coordination and the modes by which they can be utilized to influence overall function of a multi-population culture.ConclusionsOur results show that redox-based signaling can be intermingled with other quorum sensing signaling in ways that enable user-defined control of microbial consortia yielding various outcomes defined by culture medium. Further, we demonstrated the utility of our previously designed growth control module in influencing signal propagation and metabolic activity is unimpeded by orthogonal redox-based signaling. By exploring novel multi-modal strategies for guiding communication and consortia outcome, the concepts introduced here may prove to be useful for coordination of multiple populations within complex microbial systems.

Highlights

  • Microbial co-cultures and consortia are of interest in cell-based molecular production and even as “smart” therapeutics in that one can take advantage of division of labor and specialization to expand both the range of available functions and mechanisms for control

  • The authors showed that the co-culture synthesized pyocyanin, but they did not investigate the effect of culture composition on pyocyanin synthesis

  • Several host strains were transformed with high copy number plasmid pZE-phzMS containing phzMS under a LacO-1 promoter. 30 μM phenazine carboxylic acid (PCA) was added to cultures grown in M9 media and, after overnight growth, cell-free conditioned media (CM) samples were collected (Fig. 2a)

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Summary

Introduction

Microbial co-cultures and consortia are of interest in cell-based molecular production and even as “smart” therapeutics in that one can take advantage of division of labor and specialization to expand both the range of available functions and mechanisms for control. One strategy that continues to gain traction is the use of microbial co-cultures or consortia, where the tasks required to produce a molecular product are divided amongst multiple populations, rather than being carried out by a single population [2, 3] Implementation of this strategy allows for division of labor between populations and modularity, where host strains can be optimized for specific tasks [4]. Partitioning a product pathway among different populations enables culture composition as a control parameter beyond traditional targeting of transcription or translation To utilize this advantage, development of new methods that allow for robust regulation and coordination of subpopulations for functional control of the whole consortia is necessary. While there are many examples of co-cultures being used to synthesize products [9,10,11,12,13,14], there are few examples with modulated coordination of culture composition and activity

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