Long-term experimental evolution in Escherichia coli. IV. Targets of selection and the specificity of adaptation.

This study investigates the physiological manifestation of adaptive evolutionary change in 12 replicate populations of Escherichia coli that were propagated for 2000 generations in a glucose-limited environment. Representative genotypes from each population were assayed for fitness relative to their common ancestor in the experimental glucose environment and in 11 novel single-nutrient environments. After 2000 generations, the 12 derived genotypes had diverged into at least six distinct phenotypic classes. The nutrients were classified into four groups based upon their uptake physiology. All 12 derived genotypes improved in fitness by similar amounts in the glucose environment, and this pattern of parallel fitness gains was also seen in those novel environments where the limiting nutrient shared uptake mechanisms with glucose. Fitness showed little or no consistent improvement, but much greater genetic variation, in novel environments where the limiting nutrient differed from glucose in its uptake mechanisms. This pattern of fitness variation in the novel nutrient environments suggests that the independently derived genotypes adapted to the glucose environment by similar, but not identical, changes in the physiological mechanisms for moving glucose across both the inner and outer membranes.

[1]  A. F. Bennett,et al.  EVOLUTIONARY ADAPTATION TO TEMPERATURE. IV. ADAPTATION OF ESCHERICHIA COLI AT A NICHE BOUNDARY , 1996, Evolution; international journal of organic evolution.

[2]  R. Lenski,et al.  LONG‐TERM EXPERIMENTAL EVOLUTION IN ESCHERICHIA COLI. III. VARIATION AMONG REPLICATE POPULATIONS IN CORRELATED RESPONSES TO NOVEL ENVIRONMENTS , 1995, Evolution; international journal of organic evolution.

[3]  A. F. Bennett,et al.  Experimental tests of the roles of adaptation, chance, and history in evolution. , 1995, Science.

[4]  Richard E. Lenski,et al.  Long-Term Experimental Evolution in Escherichia coli. II. Changes in Life-History Traits During Adaptation to a Seasonal Environment , 1994, The American Naturalist.

[5]  S. Roseman,et al.  Sugar transport by the bacterial phosphotransferase system. Characterization of the Escherichia coli enzyme I monomer/dimer transition kinetics by fluorescence anisotropy. , 1994, The Journal of biological chemistry.

[6]  R. Lenski,et al.  Dynamics of adaptation and diversification: a 10,000-generation experiment with bacterial populations. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[7]  P. Postma,et al.  Quantification of the regulation of glycerol and maltose metabolism by IIAGlc of the phosphoenolpyruvate-dependent glucose phosphotransferase system in Salmonella typhimurium , 1994, Journal of bacteriology.

[8]  R. Lenski,et al.  Epistatic effects of promoter and repressor functions of the Tn10 tetracycline‐resistance operon on the fitness of Escherichia coli , 1994, Molecular ecology.

[9]  M. Saier,et al.  The mannitol repressor (MtlR) of Escherichia coli , 1994, Journal of bacteriology.

[10]  M H Saier,et al.  In vitro binding of the pleiotropic transcriptional regulatory protein, FruR, to the fru, pps, ace, pts and icd operons of Escherichia coli and Salmonella typhimurium. , 1993, Journal of molecular biology.

[11]  W. Boos,et al.  Induction of the lambda receptor is essential for effective uptake of trehalose in Escherichia coli , 1993, Journal of bacteriology.

[12]  G. Rummel,et al.  Crystal structures explain functional properties of two E. coli porins , 1992, Nature.

[13]  J. Bull,et al.  MOLECULAR GENETICS OF ADAPTATION IN AN EXPERIMENTAL MODEL OF COOPERATION , 1992, Evolution; international journal of organic evolution.

[14]  M. Saier,et al.  Proposed uniform nomenclature for the proteins and protein domains of the bacterial phosphoenolpyruvate: sugar phosphotransferase system , 1992, Journal of bacteriology.

[15]  John E Mittler,et al.  EVOLUTIONARY ADAPTATION TO TEMPERATURE. I. FITNESS RESPONSES OF ESCHERICHIA COLI TO CHANGES IN ITS THERMAL ENVIRONMENT , 1992, Evolution; international journal of organic evolution.

[16]  John Maddox,et al.  Is molecular biology yet a science? , 1992, Nature.

[17]  R. Lenski,et al.  Long-Term Experimental Evolution in Escherichia coli. I. Adaptation and Divergence During 2,000 Generations , 1991, The American Naturalist.

[18]  S. Roseman,et al.  Sugar transport by the bacterial phosphotransferase system. Structural and thermodynamic domains of enzyme I of Salmonella typhimurium. , 1991, The Journal of biological chemistry.

[19]  J. Drake A constant rate of spontaneous mutation in DNA-based microbes. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[20]  A. Kolb,et al.  CAP and Nag repressor binding to the regulatory regions of the nagE-B and manX genes of Escherichia coli. , 1991, Journal of molecular biology.

[21]  A. Danchin,et al.  Positive regulation of the pts operon of Escherichia coli: genetic evidence for a signal transduction mechanism , 1991, Journal of Bacteriology.

[22]  H. Kornberg,et al.  Sequence similarities between the gene specifying 1-phosphofructokinase (fruK), genes specifying other kinases in Escherichia coli K12, and lacC of Staphylococcus aureus , 1990, Proceedings of the Royal Society of London. Series B: Biological Sciences.

[23]  D. Dykhuizen,et al.  Enzyme activity and fitness: Evolution in solution. , 1990, Trends in ecology & evolution.

[24]  S. Busby,et al.  The Escherichia coli melR gene encodes a DNA-binding protein with affinity for specific sequences located in the melibiose-operon regulatory region. , 1989, Gene.

[25]  T. Mizuno,et al.  Nucleotide sequence of the region encompassing the glpKF operon and its upstream region containing a bent DNA sequence of Escherichia coli. , 1989, Nucleic acids research.

[26]  M. Saier Protein phosphorylation and allosteric control of inducer exclusion and catabolite repression by the bacterial phosphoenolpyruvate: sugar phosphotransferase system. , 1989, Microbiological reviews.

[27]  W. Rice ANALYZING TABLES OF STATISTICAL TESTS , 1989, Evolution; international journal of organic evolution.

[28]  M. Saier,et al.  Positive and negative regulators for glucitol (gut) operon expression in Escherichia coli. , 1988, Journal of molecular biology.

[29]  A Danchin,et al.  The ptsH, ptsI, and crr genes of the Escherichia coli phosphoenolpyruvate-dependent phosphotransferase system: a complex operon with several modes of transcription , 1988, Journal of bacteriology.

[30]  T. Larson,et al.  Structures of the promoter and operator of the glpD gene encoding aerobic sn-glycerol-3-phosphate dehydrogenase of Escherichia coli K-12 , 1988, Journal of bacteriology.

[31]  L. Mueller,et al.  Evolution of competitive ability in Drosophila by density-dependent natural selection. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[32]  R. Lenski EXPERIMENTAL STUDIES OF PLEIOTROPY AND EPISTASIS IN ESCHERICHIA COLI. I. VARIATION IN COMPETITIVE FITNESS AMONG MUTANTS RESISTANT TO VIRUS T4 , 1988, Evolution; international journal of organic evolution.

[33]  M. Saier,et al.  Nucleotide sequence of the mannitol (mtl) operon in Escherichia coli , 1988, Molecular microbiology.

[34]  M. Saier,et al.  Glucitol-specific enzymes of the phosphotransferase system in Escherichia coli. Nucleotide sequence of the gut operon. , 1987, The Journal of biological chemistry.

[35]  Michael R Rose,et al.  LABORATORY EVOLUTION OF POSTPONED SENESCENCE IN DROSOPHILA MELANOGASTER , 1984, Evolution; international journal of organic evolution.

[36]  T. Tsuchiya,et al.  Nucleotide sequence of the melB gene and characteristics of deduced amino acid sequence of the melibiose carrier in Escherichia coli. , 1984, The Journal of biological chemistry.

[37]  S. Roseman,et al.  Sugar transport by the bacterial phosphotransferase system. Studies on the molecular weight and association of enzyme I. , 1982, The Journal of biological chemistry.

[38]  Dm Jones,et al.  Fundamentals of Oncology , 1981 .

[39]  T. Ferenci,et al.  Lambda Receptor in the Outer Membrane of Escherichia coli as a Binding Protein for Maltodextrins and Starch Polysaccharides , 1980, Journal of bacteriology.

[40]  B. Müller-Hill,et al.  Sequence of the lactose permease gene , 1980, Nature.

[41]  S. Gould,et al.  The spandrels of San Marco and the Panglossian paradigm: a critique of the adaptationist programme , 1979, Proceedings of the Royal Society of London. Series B. Biological Sciences.

[42]  J. Rosenbusch,et al.  Matrix protein from Escherichia coli outer membranes forms voltage-controlled channels in lipid bilayers. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[43]  F. M. Stewart,et al.  Resource-Limited Growth, Competition, and Predation: A Model and Experimental Studies with Bacteria and Bacteriophage , 1977, The American Naturalist.

[44]  S. Roseman,et al.  The physiological behavior of enzyme I and heat-stable protein mutants of a bacterial phosphotransferase system. , 1970, The Journal of biological chemistry.

[45]  Charles W. Dunnett,et al.  New tables for multiple comparisons with a control. , 1964 .

[46]  S. Roseman,et al.  Sugar transport by the bacterial phosphotransferase system. Characterization of the Escherichia coli enzyme I monomer/dimer equilibrium by fluorescence anisotropy. , 1994, The Journal of biological chemistry.

[47]  G R Jacobson,et al.  Phosphoenolpyruvate:carbohydrate phosphotransferase systems of bacteria. , 1993, Microbiological reviews.

[48]  H. Goldie,et al.  Cloning and characterization of the N-acetylglucosamine operon of Escherichia coli. , 1990, Biochemistry and cell biology = Biochimie et biologie cellulaire.

[49]  E. Waygood,et al.  Sequence of cloned enzyme IIN-acetylglucosamine of the phosphoenolpyruvate:N-acetylglucosamine phosphotransferase system of Escherichia coli. , 1988, Biochemistry.

[50]  M. R. Rose,et al.  Three Approaches to Trade-Offs in Life-History Evolution , 1987 .