Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, United States; The BEACON Center for the Study of Evolution in Action, East Lansing, United States
Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, United States; The BEACON Center for the Study of Evolution in Action, East Lansing, United States
Sumaya T Ahmed
Department of Biology, Kenyon College, Gambier, United States
Tanush Jagdish
The BEACON Center for the Study of Evolution in Action, East Lansing, United States; Program for Systems, Synthetic, and Quantitative Biology, Harvard University, Cambridge, United States
Jessica A Baxter
Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, United States
Brooke A Sommerfeld
Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, United States
Alice Tillman
Department of Biology, Kenyon College, Gambier, United States
Jeremy Moore
Department of Biology, Kenyon College, Gambier, United States
The BEACON Center for the Study of Evolution in Action, East Lansing, United States; Department of Molecular Biosciences, The University of Texas, Austin, United States
Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, United States; The BEACON Center for the Study of Evolution in Action, East Lansing, United States
Evolutionary innovations allow populations to colonize new ecological niches. We previously reported that aerobic growth on citrate (Cit+) evolved in an Escherichia coli population during adaptation to a minimal glucose medium containing citrate (DM25). Cit+ variants can also grow in citrate-only medium (DM0), a novel environment for E. coli. To study adaptation to this niche, we founded two sets of Cit+ populations and evolved them for 2500 generations in DM0 or DM25. The evolved lineages acquired numerous parallel mutations, many mediated by transposable elements. Several also evolved amplifications of regions containing the maeA gene. Unexpectedly, some evolved populations and clones show apparent declines in fitness. We also found evidence of substantial cell death in Cit+ clones. Our results thus demonstrate rapid trait refinement and adaptation to the new citrate niche, while also suggesting a recalcitrant mismatch between E. coli physiology and growth on citrate.