Biochem Biophys Res Commun 2001, 284:57–64 PubMedCrossRef 37 Gao

Biochem Biophys Res Commun 2001, 284:57–64.PubMedCrossRef 37. Gao H, Wang Y, Liu X, Yan T, Wu L, Alm E, Arkin A, Thompson DK, Zhou J: Global transcriptome analysis of the heat shock response

of Shewanella oneidensis . J Bacteriol 2004,186(22):7796–7803.PubMedCrossRef 38. Ingram VM: Gene evolution and the haemoglobins. Nature 1961,4(189):704–708.CrossRef 39. Protein Tyrosine Kinase inhibitor Graf PCF, Jakob U: Redox-regulated molecular chaperones. Cell Mol Life Sci 2002, 59:1624–1631.PubMedCrossRef 40. Gustavsson N, Kokke BP, Anzeilius AB, Boelens WC, Sundby C: Substitution of conserved methionines by leucines in chloroplast small heat shock protein results in loss of redox-response but retained chaperone-like BIRB 796 order activity. Protein Sci 2001, 10:1785–1793.PubMedCrossRef 41. Fu X, Zhang H, Zhang X, Cao Y, Jião W, Liu C, Song Y, Abulimiti A, Chang Z: A dual role for the N-terminal region of Mycobacterium tuberculosis Hsp 16.3 in self-oligomerization and binding denaturing substrate proteins. J Biol Chem 2005, 280:6337–6384.PubMedCrossRef 42. Usui K, Hatipoglu OF, Ishii N, Yohda M: Role of the N-terminal

region of the crenarchaeal sHSP, Sthsp14.0, in thermal-induced disassembly of the complex and molecular chaperone activity. Biochem Biophys Res Commun 2004, 315:113–118.PubMedCrossRef 43. Goldenberg O, Erez E, Nimrod G, Ben-Tal N: The ConSurf-DB: pre-calculated evolutionary conservation profiles of protein structures. Nucleic Acids Res 2009, 37:D323-D327.PubMedCrossRef Ureohydrolase Authors’ contributions All authors have read and approved the final manuscript. DAR and LMMO SGC-CBP30 conceived the idea and designed the experiments. DAR and LFCF executed the RTq-PCR experiments. DAR wrote the manuscript. RV performed the bioinformatics analysis; LEVDB, the phylogenetic analysis; and MTM, the molecular modeling.”
“Background Bacteria, especially pathogenic bacteria, must deal with a very hostile environment on a nearly continuous basis. How pathogenic bacteria first respond to this environment

and lethal environmental stressors is a key element in their survival. Based on their initial response, either the pathogen may succumb and die, or it can respond and live despite its hostile surroundings. Long-term adaptive bacterial responses to antimicrobials include well-characterized mechanisms of expressing an altered version of the antibiotic target, enzymes to degrade the antibiotic, and transporters to remove the antibiotic [1]. Here, we consider the time immediately after the first exposure to a threat and before activation of long-term adaptive resistance to stressors. Understanding how bacteria mount this initial defense against stresses is critical to understanding how bacteria respond to, and survive, hostile environments.

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