Cell-to-cell variation and specialization in sugar metabolism in clonal bacterial populations

PLoS Genet. 2017 Dec 18;13(12):e1007122. doi: 10.1371/journal.pgen.1007122. eCollection 2017 Dec.

Abstract

While we have good understanding of bacterial metabolism at the population level, we know little about the metabolic behavior of individual cells: do single cells in clonal populations sometimes specialize on different metabolic pathways? Such metabolic specialization could be driven by stochastic gene expression and could provide individual cells with growth benefits of specialization. We measured the degree of phenotypic specialization in two parallel metabolic pathways, the assimilation of glucose and arabinose. We grew Escherichia coli in chemostats, and used isotope-labeled sugars in combination with nanometer-scale secondary ion mass spectrometry and mathematical modeling to quantify sugar assimilation at the single-cell level. We found large variation in metabolic activities between single cells, both in absolute assimilation and in the degree to which individual cells specialize in the assimilation of different sugars. Analysis of transcriptional reporters indicated that this variation was at least partially based on cell-to-cell variation in gene expression. Metabolic differences between cells in clonal populations could potentially reduce metabolic incompatibilities between different pathways, and increase the rate at which parallel reactions can be performed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptation, Physiological
  • Arabinose / metabolism
  • Carbohydrate Metabolism*
  • Escherichia coli / growth & development
  • Escherichia coli / metabolism*
  • Gene Expression
  • Genes, Bacterial
  • Glucose / metabolism
  • Metabolic Networks and Pathways
  • Phenotype
  • Single-Cell Analysis

Substances

  • Arabinose
  • Glucose

Grants and funding

NN and TB were supported by the Swiss National Science Foundation grant 31003A_130735 to MA. NN was supported by the FEMS Research Grant for visits to the MPI for Marine Microbiology in Bremen, Germany. NN is currently supported by the ISTFELLOW program of the IST Austria and the European Commission. FS was supported by a Leopoldina postdoctoral fellowship (LPDS 2009-42), a Marie-Curie-Intra-European fellowship for career development (FP7-MC-IEF; 271929; Phenofix), a Synthesis Grant of the ETH Zurich Center for Adaptation to a Changing Environment (ACE), and by Eawag. DJK was supported by the ETH Fellowship program. ADC and DJK were supported by the Swiss National Science Foundation grant 31003A_149267 to MA. SL and MMMK were supported by the Max Planck Society. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.