Abstract

Bacteria are known to display extensive metabolic diversity and many studies have shown that they can use an extensive repertoire of small molecules as carbon‐ and energy sources. However, it is less clear to what extent a bacterium can expand its existing metabolic capabilities by acquiring mutations that, for example, rewire its metabolic pathways. To investigate this capability and potential for evolution of novel phenotypes, we sampled large populations of mutagenized Salmonella enterica to select very rare mutants that can grow on minimal media containing 124 low molecular weight compounds as sole carbon sources. We found mutants growing on 18 of these novel carbon sources, and identified the causal mutations that allowed growth for four of them. Mutations that relieve physiological constraints or increase expression of existing pathways were found to be important contributors to the novel phenotypes. For the remaining 14 novel phenotypes, whole genome sequencing of independent mutants and genetic analysis suggested that these novel metabolic phenotypes result from a combination of multiple mutations. This work, by virtue of identifying the genetic and mechanistic basis for new metabolic capabilities, sheds light on the properties of adaptive landscapes underlying the evolution of novel phenotypes.

Highlights

  • Evolution of novel phenotypes is one of the central questions in evolutionary biology, playing a key role in major evolutionary transitions (Wong 1991; Szathmary and Smith 1995)

  • We used an experimental design to comprehensively explore the evolutionary potential for novel metabolic capabilities in a model organism, Salmonella enterica serovar Typhimurium strain LT2

  • TYPHIMURIUM MUTANTS THAT CAN GROW ON NORMALLY NONUTILIZABLE CARBON SOURCES The potential carbon sources used for selection in our study were a subset of the list generated by Gutnik et al (1969)

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Summary

Introduction

Evolution of novel phenotypes is one of the central questions in evolutionary biology, playing a key role in major evolutionary transitions (Wong 1991; Szathmary and Smith 1995). An understanding of the mechanistic and genetic basis for the evolution of such novel functions, as well as of the associated trade-offs, would give insights about the characteristics of the adaptive landscapes for these major transitions. To address this question, we used an experimental design to comprehensively explore the evolutionary potential for novel metabolic capabilities in a model organism, Salmonella enterica serovar Typhimurium strain LT2 NOVEL METABOLIC CAPABILITIES colonize new niches within the human host (Sokurenko et al 1999; Eisenreich et al 2010; Bianconi et al 2011; Rohmer et al 2011; Fuchs et al 2012)

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