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

Author:

Noonan Avery J C1,Qiu Yilin1,Ho Joe C H2,Ocampo Jewel2,Vreugdenhil K A1,Marr R Alexander1,Zhao Zhiying3,Yoshikuni Yasuo34567,Hallam Steven J128910

Affiliation:

1. Genome Science and Technology Program, University of British Columbia, 2329 West Mall, Vancouver, BC V6T 1Z4, Canada

2. Department of Microbiology & Immunology, University of British Columbia, Vancouver, BC, Canada, Canada V6T 1Z3

3. US Department of Energy Joint Genome Institute, Lawrence Berkeley National Laboratory, Berkeley, CA, USA

4. Environmental Genomics and Systems Biology Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA

5. Biological Systems and Engineering Division, Lawrence Berkeley National Laboratory, Berkeley, CA, USA

6. Center for Advanced Bioenergy and Bioproducts Innovation, Urbana, IL, USA

7. Global Institution for Collaborative Research and Education, Hokkaido University, Hokkaido, Japan

8. Graduate Program in Bioinformatics, University of British Columbia, Vancouver, BC, Canada, Canada V6T 1Z4

9. Biofactorial High-throughput Biology Facility, University of British Columbia, Vancouver, BC, Canada, Canada V6T 1Z3

10. Life Sciences Institute, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3

Abstract

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 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 PemrR-green fluorescent protein (GFP) monoaromatic reporter used in plate-based functional screening. CRAGE was used to construct E. coli EPI300 strains constitutively expressing red fluorescent protein (RFP) and the relationship between RFP expression and optical density (OD600) 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

Publisher

Oxford University Press (OUP)

Subject

Agricultural and Biological Sciences (miscellaneous),Biomedical Engineering,Biomaterials,Bioengineering,Biotechnology

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