Phenotypic Patterning through Copy Number Adaptation to Environmental Gradients.
Paige L SteppeCamilo Rey-BedónShalni KumarEmerald ForrestNiklas Van Der WagtArnav TayalLev S TsimringJeff HastyPublished in: ACS synthetic biology (2024)
We recently described a paradigm for engineering bacterial adaptation using plasmids coupled to the same origin of replication. In this study, we use plasmid coupling to generate spatially separated and phenotypically distinct populations in response to heterogeneous environments. Using a custom microfluidic device, we continuously tracked engineered populations along induced gradients, enabling an in-depth analysis of the spatiotemporal dynamics of plasmid coupling. Our observations reveal a pronounced phenotypic separation within 4 h exposure to an opposing gradient of AHL and arabinose. Additionally, by modulating the burden strength balance between coupled plasmids, we demonstrate the inherent limitations and tunability of this system. Intriguingly, phenotypic separation persists for an extended time, hinting at a biophysical spatial retention mechanism reminiscent of natural speciation processes. Complementing our experimental data, mathematical models provide invaluable insights into the underlying mechanisms and guide optimization of plasmid coupling for prospective applications of environmental copy number adaptation engineering across separated domains.
Keyphrases
- copy number
- escherichia coli
- mitochondrial dna
- genome wide
- room temperature
- crispr cas
- dna methylation
- klebsiella pneumoniae
- single cell
- liquid chromatography
- human health
- high glucose
- signaling pathway
- diabetic rats
- high throughput
- genetic diversity
- gene expression
- optical coherence tomography
- mass spectrometry
- machine learning
- oxidative stress
- circulating tumor cells
- electronic health record
- risk assessment
- big data
- deep learning
- drug induced
- data analysis
- cell fate
- electron transfer