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Bacterial Energy Taxis: a Global Strategy?

Overview
Journal Arch Microbiol
Specialty Microbiology
Date 2010 Apr 23
PMID 20411245
Citations 42
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Abstract

A functional energy metabolism is one of the most important requirements for survival of all kinds of organisms including bacteria. Therefore, many bacteria actively seek conditions of optimal metabolic activity, a behaviour which can be termed "energy taxis". Motility, combined with the sensory perception of the internal energetic conditions, is prerequisite for tactic responses to different energy levels and metabolic yields. Diverse mechanisms of energy sensing and tactic response have evolved among various bacteria. Many of the known energy taxis sensors group among the methyl-accepting chemotaxis protein (MCP)-like sensors. This review summarizes recent advances in the field of energy taxis and explores the current concept that energy taxis is an important part of the bacterial behavioural repertoire in order to navigate towards more favourable metabolic niches and to survive in a specific habitat.

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References
1.
Taylor B, Zhulin I, Johnson M . Aerotaxis and other energy-sensing behavior in bacteria. Annu Rev Microbiol. 1999; 53:103-28. DOI: 10.1146/annurev.micro.53.1.103. View

2.
Wadhams G, Armitage J . Making sense of it all: bacterial chemotaxis. Nat Rev Mol Cell Biol. 2004; 5(12):1024-37. DOI: 10.1038/nrm1524. View

3.
Stingl K, Uhlemann E, Schmid R, Altendorf K, Bakker E . Energetics of Helicobacter pylori and its implications for the mechanism of urease-dependent acid tolerance at pH 1. J Bacteriol. 2002; 184(11):3053-60. PMC: 135060. DOI: 10.1128/JB.184.11.3053-3060.2002. View

4.
Bren A, Eisenbach M . How signals are heard during bacterial chemotaxis: protein-protein interactions in sensory signal propagation. J Bacteriol. 2000; 182(24):6865-73. PMC: 94809. DOI: 10.1128/JB.182.24.6865-6873.2000. View

5.
Genin S, Boucher C . Lessons learned from the genome analysis of ralstonia solanacearum. Annu Rev Phytopathol. 2004; 42:107-34. DOI: 10.1146/annurev.phyto.42.011204.104301. View