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Biology subjects

Csicsery, N.

Publications and source records attributed to Csicsery, N..

2 recordsLinked to original sources

Evolved microbial diversity enables combinatoric biosensing in complex environments

Whole-cell biosensors (WCBs) offer rapid, cost-effective monitoring of environmental contamination and human disease. Current WCB efforts to optimize detection of single target analytes under laboratory conditions have achieved vastly improved performance, setting the stage for WCB deployment in complex environments. We propose a framework that leverages the cross-specificity of single-target WCBs to quantify multiple targets using supervised machine learning. Specifically, we engineer six sensors for heavy metal contaminants in laboratory E. coli. We then evolve the strain to generate five chassis with improved growth in seawater conditions. We transform the chassis with the sensors, creating a set of 30 variants. The variant dynamic responses are characterized with microfluidics, revealing significant diversity. Leveraging this diversity, we construct a consortium to combinatorically quantify multiple analytes with machine learning, outperforming single-target biosensors in over 90% of our test samples. These results form a generalizable framework that facilitates WCB translation toward settings beyond the laboratory.

bioengineering↗

Multiplexed Screening of Population-level Synthetic Gene Oscillator Libraries

Directed evolution has become an invaluable tool in protein engineering and has also greatly influenced the construction of synthetic gene circuits. The ability to generate diversity at precise targets for directed evolution approaches has improved vastly, allowing researchers to create large, specific mutant libraries with relative ease. Screening approaches for large mutant libraries have similarly come a long way, especially when the desired behavior can easily be tested for with static, single time-point assays. For more complex gene circuits with dynamic phenotypes that change over time, directed evolution approaches to controlling and tuning circuit behavior have been hindered by the lack of sufficiently high-throughput screening methods to isolate variants with desired characteristics. Here we utilize directed mutagenesis and multiplexed microfluidics to develop a workflow for creating, screening and tuning dynamic gene circuits that operate at the population level. Specifically, we create a mutant library of an existing oscillator, the synchronized lysis circuit, and tune its dynamics while uncovering principles regarding its behavior. Lastly, we utilize this directed evolution workflow to construct a new synchronized genetic oscillator that exhibits robust dynamics over long time scales.

synthetic biology↗