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CRAGE-mediated insertion of fluorescent chromosomal markers for accurate and scalable measurement of co-culture dynamics in Escherichia coli .

Authors :
Noonan AJC
Qiu Y
Ho JCH
Ocampo J
Vreugdenhil KA
Marr RA
Zhao Z
Yoshikuni Y
Hallam SJ
Source :
Synthetic biology (Oxford, England) [Synth Biol (Oxf)] 2020 Sep 03; Vol. 5 (1), pp. ysaa015. Date of Electronic Publication: 2020 Sep 03 (Print Publication: 2020).
Publication Year :
2020

Abstract

Monitoring population dynamics in co-culture is necessary in engineering microbial consortia involved in distributed metabolic processes or biosensing applications. However, it remains difficult to measure strain-specific growth dynamics in high-throughput formats. This is especially vexing in plate-based functional screens leveraging whole-cell biosensors to detect specific metabolic signals. Here, we develop an experimental high-throughput co-culture system to measure and model the relationship between fluorescence and cell abundance, combining chassis-independent recombinase-assisted genome engineering (CRAGE) and whole-cell biosensing with a P <subscript>emrR</subscript> -green fluorescent protein (GFP) monoaromatic reporter used in plate-based functional screening. CRAGE was used to construct Escherichia coli EPI300 strains constitutively expressing red fluorescent protein (RFP) and the relationship between RFP expression and optical density (OD <subscript>600</subscript> ) was determined throughout the EPI300 growth cycle. A linear equation describing the increase of normalized RFP fluorescence during deceleration phase was derived and used to predict biosensor strain dynamics in co-culture. Measured and predicted values were compared using flow cytometric detection methods. Induction of the biosensor lead to increased GFP fluorescence normalized to biosensor cell abundance, as expected, but a significant decrease in relative abundance of the biosensor strain in co-culture and a decrease in bulk GFP fluorescence. Taken together, these results highlight sensitivity of population dynamics to variations in metabolic activity in co-culture and the potential effect of these dynamics on the performance of functional screens in plate-based formats. The engineered strains and model used to evaluate these dynamics provide a framework for optimizing growth of synthetic co-cultures used in screening, testing and pathway engineering applications.<br /> (© The Author(s) 2020. Published by Oxford University Press.)

Details

Language :
English
ISSN :
2397-7000
Volume :
5
Issue :
1
Database :
MEDLINE
Journal :
Synthetic biology (Oxford, England)
Publication Type :
Academic Journal
Accession number :
33381654
Full Text :
https://doi.org/10.1093/synbio/ysaa015