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Jonas Cremer

Jonas Cremer

· Professor of Cell Bio Physics

Stanford University · Biology

Active 1991–2024

h-index24
Citations1.7k
Papers5421 last 5y
Funding
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About

We combine experimentation, data analysis, and mathematical modeling to unravel the eco-physiology of microbes — from individual cells to the gut microbiome and its impact on the human host.

Research topics

  • Computer Science
  • Biology
  • Computational biology
  • Engineering
  • Chemistry
  • Economics
  • Biophysics
  • Environmental resource management
  • Cell biology
  • Biotechnology
  • Biochemical engineering
  • Biological system
  • Genetics

Selected publications

  • An optimal regulation of fluxes dictates microbial growth in and out of steady state

    eLife · 2023 · 53 citations

    Senior authorCorresponding
    • Cell biology
    • Biology
    • Biochemical engineering

    establishes this regulatory mechanism's biological veracity and demonstrates that a remarkably wide range of growth phenomena in and out of steady state can be predicted with quantitative accuracy. This predictive power, achieved with only a few biological parameters, cements the preeminent importance of optimal flux regulation across conditions and establishes low-dimensional allocation models as an ideal physiological framework to interrogate the dynamics of growth, competition, and adaptation in complex and ever-changing environments.

  • Suboptimal resource allocation in changing environments constrains response and growth in bacteria

    Molecular Systems Biology · 2021 · 77 citations

    Senior authorCorresponding
    • Computer Science
    • Biology
    • Computational biology

    To respond to fluctuating conditions, microbes typically need to synthesize novel proteins. As this synthesis relies on sufficient biosynthetic precursors, microbes must devise effective response strategies to manage depleting precursors. To better understand these strategies, we investigate the active response of Escherichia coli to changes in nutrient conditions, connecting transient gene expression to growth phenotypes. By synthetically modifying gene expression during changing conditions, we show how the competition by genes for the limited protein synthesis capacity constrains cellular response. Despite this constraint cells substantially express genes that are not required, trapping them in states where precursor levels are low and the genes needed to replenish the precursors are outcompeted. Contrary to common modeling assumptions, our findings highlight that cells do not optimize growth under changing environments but rather exhibit hardwired response strategies that may have evolved to promote fitness in their native environment. The constraint and the suboptimality of the cellular response uncovered provide a conceptual framework relevant for many research applications, from the prediction of evolution to the improvement of gene circuits in biotechnology.

Frequent coauthors

  • Erwin Frey

    34 shared
  • Anna Melbinger

    Center for NanoScience

    22 shared
  • Terence Hwa

    18 shared
  • Tomoya Honda

    Lawrence Berkeley National Laboratory

    9 shared
  • Tobias Reichenbach

    Friedrich-Alexander-Universität Erlangen-Nürnberg

    9 shared
  • Anatolij Gelimson

    University of Oxford

    9 shared
  • Markus Arnoldini

    ETH Zurich

    9 shared
  • Leonardo Mancini

    University of Cambridge

    8 shared

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