This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Farrell, M. J.
Right arrow Articles by Finkel, S. E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Farrell, M. J.
Right arrow Articles by Finkel, S. E.

 Previous Article  |  Next Article 

Journal of Bacteriology, December 2003, p. 7044-7052, Vol. 185, No. 24
0021-9193/03/$08.00+0     DOI: 10.1128/JB.185.24.7044-7052.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

The Growth Advantage in Stationary-Phase Phenotype Conferred by rpoS Mutations Is Dependent on the pH and Nutrient Environment

Michael J. Farrell and Steven E. Finkel*

Molecular and Computation Biology Program, Department of Biological Sciences, University of Southern California, Los Angeles, California 90089-1340

Received 19 June 2003/ Accepted 15 September 2003

Escherichia coli cells that are aged in batch culture display an increased fitness referred to as the growth advantage in stationary phase, or GASP, phenotype. A common early adaptation to this culture environment is a mutant rpoS allele, such as rpoS819, that results in attenuated RpoS activity. However, it is important to note that during long-term batch culture, environmental conditions are in flux. To date, most studies of the GASP phenotype have focused on identifying alleles that render an advantage in a specific environment, Luria-Bertani broth (LB) batch culture. To determine what role environmental conditions play in rendering relative fitness advantages to E. coli cells carrying either the wild-type or rpoS819 alleles, we performed competitions under a variety of culture conditions in which either the available nutrients, the pH, or both were manipulated. In LB medium, we found that while the rpoS819 allele confers a strong competitive fitness advantage at basic pH, it confers a reduced advantage under neutral conditions, and it is disadvantageous under acidic conditions. Similar results were found using other media. rpoS819 conferred its greatest advantage in basic minimal medium in which either glucose or Casamino Acids were the sole source of carbon and energy. In acidic medium supplemented with either Casamino Acids or glucose, the wild-type allele conferred a slight advantage. In addition, populations were dynamic under all pH conditions tested, with neither the wild-type nor mutant rpoS alleles sweeping a culture. We also found that the strength of the fitness advantage gained during a 10-day incubation is pH dependent.


* Corresponding author. Mailing address: Molecular and Computational Biology Program, SHS 172, University of Southern California, Los Angeles, CA 90089-1340. Phone (213) 821-1498. Fax: (213) 740-8631. E-mail: sfinkel{at}usc.edu.


Journal of Bacteriology, December 2003, p. 7044-7052, Vol. 185, No. 24
0021-9193/03/$08.00+0     DOI: 10.1128/JB.185.24.7044-7052.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Welander, P. V., Hunter, R. C., Zhang, L., Sessions, A. L., Summons, R. E., Newman, D. K. (2009). Hopanoids Play a Role in Membrane Integrity and pH Homeostasis in Rhodopseudomonas palustris TIE-1. J. Bacteriol. 191: 6145-6156 [Abstract] [Full Text]  
  • Palchevskiy, V., Finkel, S. E. (2009). A Role for Single-Stranded Exonucleases in the Use of DNA as a Nutrient. J. Bacteriol. 191: 3712-3716 [Abstract] [Full Text]  
  • Lemonnier, M., Levin, B. R, Romeo, T., Garner, K., Baquero, M.-R., Mercante, J., Lemichez, E., Baquero, F., Blazquez, J. (2008). The evolution of contact-dependent inhibition in non-growing populations of Escherichia coli. Proc R Soc B 275: 3-10 [Abstract] [Full Text]  
  • Stevens, M. H. H., Sanchez, M., Lee, J., Finkel, S. E. (2007). Diversification Rates Increase With Population Size and Resource Concentration in an Unstructured Habitat. Genetics 177: 2243-2250 [Abstract] [Full Text]  
  • Swartz, T. H., Ito, M., Ohira, T., Natsui, S., Hicks, D. B., Krulwich, T. A. (2007). Catalytic Properties of Staphylococcus aureus and Bacillus Members of the Secondary Cation/Proton Antiporter-3 (Mrp) Family Are Revealed by an Optimized Assay in an Escherichia coli Host. J. Bacteriol. 189: 3081-3090 [Abstract] [Full Text]  
  • Bodini, S., Nunziangeli, L., Santori, F. (2007). Influence of Amino Acids on Low-Density Escherichia coli Responses to Nutrient Downshifts. J. Bacteriol. 189: 3099-3105 [Abstract] [Full Text]  
  • Bacher, J. M., Metzgar, D., de Crecy-Lagard, V. (2006). Rapid Evolution of Diminished Transformability in Acinetobacter baylyi. J. Bacteriol. 188: 8534-8542 [Abstract] [Full Text]  
  • Bhagwat, A. A., Tan, J., Sharma, M., Kothary, M., Low, S., Tall, B. D., Bhagwat, M. (2006). Functional Heterogeneity of RpoS in Stress Tolerance of Enterohemorrhagic Escherichia coli Strains.. Appl. Environ. Microbiol. 72: 4978-4986 [Abstract] [Full Text]  
  • Franchini, A. G., Egli, T. (2006). Global gene expression in Escherichia coli K-12 during short-term and long-term adaptation to glucose-limited continuous culture conditions. Microbiology 152: 2111-2127 [Abstract] [Full Text]  
  • Palchevskiy, V., Finkel, S. E. (2006). Escherichia coli Competence Gene Homologs Are Essential for Competitive Fitness and the Use of DNA as a Nutrient. J. Bacteriol. 188: 3902-3910 [Abstract] [Full Text]  
  • King, T., Seeto, S., Ferenci, T. (2006). Genotype-by-Environment Interactions Influencing the Emergence of rpoS Mutations in Escherichia coli Populations. Genetics 172: 2071-2079 [Abstract] [Full Text]  
  • Liu, J., Xue, Y., Wang, Q., Wei, Y., Swartz, T. H., Hicks, D. B., Ito, M., Ma, Y., Krulwich, T. A. (2005). The Activity Profile of the NhaD-Type Na+(Li+)/H+ Antiporter from the Soda Lake Haloalkaliphile Alkalimonas amylolytica Is Adaptive for the Extreme Environment. J. Bacteriol. 187: 7589-7595 [Abstract] [Full Text]  
  • Bhagwat, A. A., Chan, L., Han, R., Tan, J., Kothary, M., Jean-Gilles, J., Tall, B. D. (2005). Characterization of Enterohemorrhagic Escherichia coli Strains Based on Acid Resistance Phenotypes. Infect. Immun. 73: 4993-5003 [Abstract] [Full Text]  
  • Heurlier, K., Denervaud, V., Haenni, M., Guy, L., Krishnapillai, V., Haas, D. (2005). Quorum-Sensing-Negative (lasR) Mutants of Pseudomonas aeruginosa Avoid Cell Lysis and Death. J. Bacteriol. 187: 4875-4883 [Abstract] [Full Text]  
  • Hicks, W. M., Kotlajich, M. V., Visick, J. E. (2005). Recovery from long-term stationary phase and stress survival in Escherichia coli require the L-isoaspartyl protein carboxyl methyltransferase at alkaline pH. Microbiology 151: 2151-2158 [Abstract] [Full Text]  
  • Mandel, M. J., Silhavy, T. J. (2005). Starvation for Different Nutrients in Escherichia coli Results in Differential Modulation of RpoS Levels and Stability. J. Bacteriol. 187: 434-442 [Abstract] [Full Text]  
  • Saint-Ruf, C., Taddei, F., Matic, I. (2004). Stress and Survival of Aging Escherichia coli rpoS Colonies. Genetics 168: 541-546 [Abstract] [Full Text]  
  • Trotochaud, A. E., Wassarman, K. M. (2004). 6S RNA Function Enhances Long-Term Cell Survival. J. Bacteriol. 186: 4978-4985 [Abstract] [Full Text]