1016/j.bbamem.2012.09.017 16. Wolfe AJ: The acetate switch. Microbiol Mol Biol Rev 2005,69(1):12–50.PubMedCrossRef Selleckchem BMN673 17. LCZ696 cell line Gimenez R,
Nunez MF, Badia J, Aguilar J, Baldoma L: The gene yjcG, cotranscribed with the gene acs, encodes an acetate permease in Escherichia coli. J Bacteriol 2003,185(21):6448–6455.PubMedCrossRef 18. Jolkver E, Emer D, Ballan S, Krämer R, Eikmanns BJ, Marin K: Identification and characterization of a bacterial transport system for the uptake of pyruvate, propionate, and acetate in Corynebacterium glutamicum. J Bacteriol 2009,191(3):940–948.PubMedCrossRef 19. Kasianowicz J, Benz R, McLaughlin S: The kinetic mechanism by which CCCP (carbonyl cyanide m-chlorophenylhydrazone) transports protons across membranes. J Membr Biol 1984,82(2):179–190.PubMedCrossRef 20. Hosie AHF, Allaway D, Poole PS: A monocarboxylate permease
of Rhizobium leguminosarum is the first member of a new subfamily of transporters. J Bacteriol 2002,184(19):5436–5448.PubMedCrossRef 21. Oehmen A, Yuan Z, Blackall LL, Keller J: Comparison of acetate and propionate uptake by polyphosphate accumulating organisms and glycogen accumulating organisms. Biotechnol see more Bioeng 2005,91(2):162–168.PubMedCrossRef 22. Borghese R, Cicerano S, Zannoni D: Fructose increases the resistance of Rhodobacter capsulatus to the toxic oxyanion tellurite through repression of acetate permease (ActP). Antonie Van Leeuwenhoek 2011,100(4):655–658.PubMedCrossRef Oxalosuccinic acid 23. Burow LC, Mabbett AN, McEwan AG, Bond PL, Blackall LL: Bioenergetic models for acetate and phosphate transport in bacteria important in enhanced biological phosphorus removal. Environ Microbiol 2008,10(1):87–98.PubMed Competing interests The authors declare that they have no competing interests. Authors contributions XS and KFK designed and carried out the studies and drafted the manuscript. JSHT conceived of the study, participated in the design and coordination of the study and drafted the manuscript.
All authors read and approved the final manuscript.”
“Background Bacteriophages have critically important roles in genome diversification and the evolution of virulence and host adaptation of enteric bacteria. Genes encoding Shiga toxins (Stx) 1 and 2 are found on lambdoid phages in Shiga-toxigenic Escherichia coli, while similar Gifsy and Fels phages encode a number of virulence factors in Salmonella enterica serovar Typhimurium. In addition to carrying genes encoding virulence factors, integrated prophage can affect gene expression of the host bacterium. The recent demonstration of three distinct bacteriophages integrated into the genome of Campylobacter jejuni chicken isolate RM1221 suggested that such phages may be common and important for the biology of C. jejuni[1]. At least one of these three C. jejuni integrated elements (CJIEs) [2] was a Mu-like phage inducible with mitomycin C designated CJIE1 (or Campylobacter Mu-like phage 1, CMLP1).