The growth of wild-type S. oneidensis MR-1 with glucose as the sole carbon source, directly following extended diauxic growth (Fig. 1d), supports the concept of either ‘conditioning’ needed for timely glucose utilization or, more likely, that a GASP glucose-use mutation was acquired (Finkel & Kolter, 1999). To narrow these two possibilities down, S. oneidensis strains EH1, EH2, and EH3 passed four times through medium with lactate as the sole carbon source and then grown successfully with glucose as the sole carbon source (Fig. 1d) supports the concept of these being GASP mutants, as GASP Selisistat mutants maintain their ‘evolved’ phenotype after repeated passages

through log-phase growth (Zambrano et al., 1993). The results of this study indicate that given initial exposure to glucose in an environment where glucose use is not immediately necessary (LB broth amended with glucose or MM containing both lactate and glucose), S. oneidensis MR-1 will develop, with high frequency, a GASP glucose-use mutation and acquire the ability to use glucose

as a substrate. The time needed for this to occur appears to be 24 h with cultures from glucose-amended LB broth and over 8 days (Fig. 1b), but < 16 days (Fig. 1c) in MM (G/L). Most or all genetic elements needed for glucose use are present in the S. oneidensis MR-1 genome (data not shown and Rodionov et al., 2010); however, the exact genetic mechanism(s) by which strains EH1-3 selleck screening library are

able to use glucose and not wild-type remains elusive. Our studies indicate that two potential glucose transporters, glcP and ptsG, are not functional in glucose acquisition in strains EH1-3 (gene sequencing and mRNA transcription analyses, respectively; data not shown). Zinser and Kolter (2000) found that in Escherichia coli K-12, GASP mutations were in global regulators, indicating that the physiological changes may be more global in scope. Differential protein or mRNA transcription patterns and resequencing of the genomes of glucose-utilizing strains are areas where further research can clarify the genetic underpinning(s). While the high frequency at which S. oneidensis populations acquire glucose utilization function can be explained either by GASP mutation(s), it is also possible that S. oneidensis MR-1 maintains a certain level of mutator bacteria within the population to gain short-term ecological advantages (Chao & Cox, 1983; Giraud et al., 2001a, b). Mutator bacteria contain mutations that inactivate mutation-avoidance genes (Giraud et al., 2001a, b). These mutations allow for an accelerated speed of evolution within the bacterial population, which can have great benefits on a short-term time scale for survival of a population in new environments (Perfeito et al., 2007).