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Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging

Author

Listed:
  • A. E. Vasdekis

    (University of Idaho)

  • H. Alanazi

    (University of Idaho)

  • A. M. Silverman

    (Massachusetts Institute of Technology)

  • C. J. Williams

    (University of Idaho)

  • A. J. Canul

    (University of Idaho)

  • J. B. Cliff

    (Pacific Northwest National Laboratory)

  • A. C. Dohnalkova

    (Pacific Northwest National Laboratory)

  • G. Stephanopoulos

    (Massachusetts Institute of Technology)

Abstract

Optimal metabolic trade-offs between growth and productivity are key constraints in strain optimization by metabolic engineering; however, how cellular noise impacts these trade-offs and drives the emergence of subpopulations with distinct resource allocation strategies, remains largely unknown. Here, we introduce a single-cell strategy for quantifying the trade-offs between triacylglycerol production and growth in the oleaginous microorganism Yarrowia lipolytica. The strategy relies on high-throughput quantitative-phase imaging and, enabled by nanoscale secondary ion mass spectrometry analyses and dedicated image processing, allows us to image how resources are partitioned between growth and productivity. Enhanced precision over population-averaging biotechnologies and conventional microscopy demonstrates how cellular noise impacts growth and productivity differently. As such, subpopulations with distinct metabolic trade-offs emerge, with notable impacts on strain performance and robustness. By quantifying the self-degradation of cytosolic macromolecules under nutrient-limiting conditions, we discover the cell-to-cell heterogeneity in protein and fatty-acid recycling, unmasking a potential bet-hedging strategy under starvation.

Suggested Citation

  • A. E. Vasdekis & H. Alanazi & A. M. Silverman & C. J. Williams & A. J. Canul & J. B. Cliff & A. C. Dohnalkova & G. Stephanopoulos, 2019. "Eliciting the impacts of cellular noise on metabolic trade-offs by quantitative mass imaging," Nature Communications, Nature, vol. 10(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-08717-w
    DOI: 10.1038/s41467-019-08717-w
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    Cited by:

    1. Jessica A Lee & Siavash Riazi & Shahla Nemati & Jannell V Bazurto & Andreas E Vasdekis & Benjamin J Ridenhour & Christopher H Remien & Christopher J Marx, 2019. "Microbial phenotypic heterogeneity in response to a metabolic toxin: Continuous, dynamically shifting distribution of formaldehyde tolerance in Methylobacterium extorquens populations," PLOS Genetics, Public Library of Science, vol. 15(11), pages 1-38, November.

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