bioRxiv Science⌕ Search

bioRxiv · 10.1101/575068

Engineered phenotype patterns in microbial populations

Abstract

Rapid advances in cellular engineering1,2 have positioned synthetic biology to address therapeutic3,4 and industrial5 problems, but a significant obstacle is the myriad of unanticipated cellular responses in heterogeneous environments such as the gut6,7, solid tumors8,9, bioreactors10 or soil11. Complex interactions between the environment and cells often arise through non-uniform nutrient availability, which can generate bidirectional coupling as cells both adjust to and modify their local environment through different growth phenotypes across a colony.12,13 While spatial sensing14 and gene expression patterns15-17 have been explored under homogeneous conditions, the mutual interaction between gene circuits, growth phenotype, and the environment remains a challenge for synthetic biology. Here, we design gene circuits which sense and control spatiotemporal phenotype patterns in a model system of heterogeneous microcolonies containing both growing and dormant bacteria. We implement pattern control by coupling different downstream modules to a tunable sensor module that leverages E. colis stress response and is activated upon growth arrest. One is an actuator module that slows growth and thereby creates an environmental negative feedback via nutrient diffusion. We build a computational model of this system to understand the interplay between gene regulation, population dynamics, and chemical transport, which predicts oscillations in both growth and gene expression. Experimentally, this circuit indeed generates robust cycling between growth and dormancy in the interior of the colony. We also use the stress sensor to drive an inducible gating module that enables selective gene expression in non-dividing cells. The stress-gated lysis circuit derived from this module radically alters the growth pattern through elimination of the dormant phenotype upon a chemical cue. Our results establish a strategy to leverage and control the presence of distinct microbial growth phenotypes for synthetic biology applications in complex environments.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bittihn, P., Didovyk, A., Tsimring, L. S., Hasty, J.. 2019-03-13. Engineered phenotype patterns in microbial populations. https://doi.org/10.1101/575068

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Associative Learning and Memory Erasure in a Synthetic Multicellular System

Learning is a basic form of adaptation that organisms display from neural systems to single cells. In associative learning, the pairing of two stimuli lets one of them evoke the response to the other. Engineering this behavior in a living cell is difficult, because coincidence detection, memory, and conditional readout must be wired into a single regulatory network. Here we build a consortium of five E. coli strains that distributes the operations of associative learning and communicates through one diffusible quorum-sensing signal. The same signal acts as the memory trace. One strain detects the coincidence of the two inputs, a second maintains the memory through positive feedback in the shared medium, a third reads it out on the conditioned stimulus, a fourth reports the unconditioned response, and a fifth erases the memory on command. We show experimentally that the assembled consortium learns the association, since a stimulus that is silent before training evokes a strong response after pairing. Memory is retained through a medium exchange in which both stimuli are removed, and then the conditioned stimulus alone evokes the response. The reporter is not produced without its input. An erase command returns the response to the background. A population model of the consortium accounts for the sequence of responses and gives design rules for writing, retention, and erasure, and a trade-off in storing memory in a shared extracellular signal. Distributing the operations over strains makes each of them separately tunable and testable and provides a route to microbial communities that learn from their history.

synthetic biology↗

Self-organized criticality in a mammalian RNA-interference circuit

Living systems have been argued to operate near critical points, but their relevance at the cellular level is poorly understood. Critical states allow for a high sensitivity to external inputs and maximal information transfer and display fluctuations at all scales. Critical points are very special, and require the fine tuning of a control parameter, which is hard to reconcile with the robustness of living cells. Self-organized criticality (SOC) proposes that feedback, rather than tuning, brings a system to its critical point. Here we show that RNA interference, in which messenger RNAs compete for shared silencing machinery and so queue for service, together with negative feedback gives rise to SOC in mammalian cells. In a synthetic circuit, a protein repressor whose mRNA competes with the mRNA of a fluorescent reporter that it represses senses the congestion of the queue, closing the feedback loop. Theory and stochastic simulations show that the loop holds the queue near its critical point despite changes in its parameters, and that expression becomes intermittent, with scale-free bursts. Measurements in human cell lines show the predicted power-law distributions of single-cell fluorescence. RNA interference could thus support engineered SOC in animal cells and may also contribute to SOC in natural systems.

synthetic biology↗

An anaerobic cell-free protein synthesis formulation for the in vitro study of oxygen sensitive proteins

Anaerobic microbes harbor unique enzymes and metabolic pathways with potential biotechnological applications, yet these microbes remain difficult to study and engineer. Research is limited by the labor-intensive workflows required to maintain anoxic environments and the lack of genetic tools available for non-model anaerobes. Here, we present an anaerobic cell-free protein synthesis (CFPS) platform for the in vitro study of oxygen-sensitive enzymes. This study establishes two methods for conducting anaerobic CFPS, achieving an anoxic environment by (1) sparging with inert gas or (2) lyophilizing to remove oxygenated water. We show the functionality of our anaerobic CFPS formulation by producing oxygen-independent fluorescent protein reporters and a [4Fe-4S] cluster pyruvate:ferredoxin oxidoreductase (PFOR) with a specific activity of 5.2 {+/-} 0.3 x 10-4 U/{micro}L cell-free extract. This highly modular platform will allow study of diverse oxygen-sensitive proteins and requires only minor modifications to commonly used CFPS workflows.

synthetic biology↗