Literature DB >> 17707145

Bacterial physiology, regulation and mutational adaptation in a chemostat environment.

Thomas Ferenci1.   

Abstract

The chemostat was devised over 50 years ago and rapidly adopted for studies of bacterial physiology and mutation. Despite the long history and earlier analyses, the complexity of events in continuous cultures is only now beginning to be resolved. The application of techniques for following regulatory and mutational changes and the identification of mutated genes in chemostat populations has provided new insights into bacterial behaviour. Inoculation of bacteria into a chemostat culture results in a population competing for a limiting amount of a particular resource. Any utilizable carbon source or ion can be a limiting nutrient and bacteria respond to limitation through a regulated nutrient-specific hunger response. In addition to transcriptional responses to nutrient limitation, a second regulatory influence in a chemostat culture is the reduced growth rate fixed by the dilution rate in individual experiments. Sub-maximal growth rates and hunger result in regulation involving sigma factors and alarmones like cAMP and ppGpp. Reduced growth rate also results in increased mutation frequencies. The combination of a strongly selective environment (where mutants able to compete for limiting nutrient have a major fitness advantage) and elevated mutation rates (both endogenous and through the secondary enrichment of mutators) results in a population that changes rapidly and persistently over many generations. Contrary to common belief, the chemostat environment is never in "steady state" with fixed bacterial characteristics usable for clean comparisons of physiological or regulatory states. Adding to the complexity, chemostat populations do not simply exhibit a succession of mutational sweeps leading to a dominant winner clone. Instead, within 100 generations large populations become heterogeneous and evolving bacteria adopt alternative, parallel fitness strategies. Transport physiology, metabolism and respiration, as well as growth yields, are highly diverse in chemostat-evolved bacteria. The rich assortment of changes in an evolving chemostat provides an excellent experimental system for understanding bacterial evolution. The adaptive radiation or divergence of populations into a collection of individuals with alternative solutions to the challenge of chemostat existence provides an ideal model system for testing evolutionary and ecological theories on adaptive radiations and the generation of bacterial diversity.

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Year:  2008        PMID: 17707145     DOI: 10.1016/S0065-2911(07)53003-1

Source DB:  PubMed          Journal:  Adv Microb Physiol        ISSN: 0065-2911            Impact factor:   3.517


  42 in total

Review 1.  New insights into bacterial adaptation through in vivo and in silico experimental evolution.

Authors:  Thomas Hindré; Carole Knibbe; Guillaume Beslon; Dominique Schneider
Journal:  Nat Rev Microbiol       Date:  2012-03-27       Impact factor: 60.633

2.  The renaissance of continuous culture in the post-genomics age.

Authors:  Alan T Bull
Journal:  J Ind Microbiol Biotechnol       Date:  2010-09-11       Impact factor: 3.346

3.  Switching and growth for microbial populations in catastrophic responsive environments.

Authors:  Paolo Visco; Rosalind J Allen; Satya N Majumdar; Martin R Evans
Journal:  Biophys J       Date:  2010-04-07       Impact factor: 4.033

4.  Genomic identification of a novel mutation in hfq that provides multiple benefits in evolving glucose-limited populations of Escherichia coli.

Authors:  Ram Maharjan; Zhemin Zhou; Yan Ren; Yang Li; Joël Gaffé; Dominique Schneider; Christopher McKenzie; Peter R Reeves; Thomas Ferenci; Lei Wang
Journal:  J Bacteriol       Date:  2010-06-11       Impact factor: 3.490

5.  Genomic sequencing reveals regulatory mutations and recombinational events in the widely used MC4100 lineage of Escherichia coli K-12.

Authors:  Thomas Ferenci; Zhemin Zhou; Thu Betteridge; Yan Ren; Yu Liu; Lu Feng; Peter R Reeves; Lei Wang
Journal:  J Bacteriol       Date:  2009-04-17       Impact factor: 3.490

6.  Metabolic flux analysis of Escherichia coli creB and arcA mutants reveals shared control of carbon catabolism under microaerobic growth conditions.

Authors:  Pablo I Nikel; Jiangfeng Zhu; Ka-Yiu San; Beatriz S Méndez; George N Bennett
Journal:  J Bacteriol       Date:  2009-06-26       Impact factor: 3.490

7.  Leading the dog of selection by its mutational nose.

Authors:  Daniel S Fisher
Journal:  Proc Natl Acad Sci U S A       Date:  2011-02-02       Impact factor: 11.205

8.  Metabolic Trade-Offs Promote Diversity in a Model Ecosystem.

Authors:  Anna Posfai; Thibaud Taillefumier; Ned S Wingreen
Journal:  Phys Rev Lett       Date:  2017-01-12       Impact factor: 9.161

Review 9.  The functional basis of adaptive evolution in chemostats.

Authors:  David Gresham; Jungeui Hong
Journal:  FEMS Microbiol Rev       Date:  2014-12-04       Impact factor: 16.408

10.  Divergence involving global regulatory gene mutations in an Escherichia coli population evolving under phosphate limitation.

Authors:  Lei Wang; Beny Spira; Zhemin Zhou; Lu Feng; Ram P Maharjan; Xiaomin Li; Fangfang Li; Christopher McKenzie; Peter R Reeves; Thomas Ferenci
Journal:  Genome Biol Evol       Date:  2010-07-16       Impact factor: 3.416

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