Biochemistry 1999,38(2):643–650 PubMedCrossRef 15

Bandow

Biochemistry 1999,38(2):643–650.PubMedCrossRef 15.

Bandow JE, Becher D, Buttner selleck chemical K, Hochgrafe F, Freiberg C, Brotz H, Hecker M: The role of peptide deformylase in protein biosynthesis: a proteomic study. Proteomics 2003,3(3):299–306.PubMedCrossRef 16. Guillon JM, Mechulam Y, Schmitter JM, Blanquet S, Fayat G: Disruption of the gene for Met-tRNA(fMet) formyltransferase severely impairs growth of Escherichia coli. J Bacteriol 1992, 174:4294–4301.PubMed 17. Somerville GA, Said-Salim B, Wickman JM, Raffel SJ, Kreiswirth BN, Musser JM: Correlation of acetate catabolism and growth yield in Staphylococcus aureus: implications for host-pathogen interactions. InfectImmun 2003,71(8):4724–4732. 18. Pagels M, Fuchs S, Pane-Farre J, Kohler C, Menschner L, Hecker M, McNamarra PJ, Bauer MC, von Wachenfeldt C, Liebeke M, et al.: Redox sensing by a Rex-family repressor is involved in the regulation of anaerobic gene expression in Staphylococcus aureus. Mol Microbiol 2010,76(5):1142–1161.PubMedCrossRef 19. Galkin A, Kulakova L, Sarikaya E, Lim K, Howard A, Herzberg O: Structural

insight into arginine degradation Adriamycin mw by arginine deiminase, an antibacterial and parasite drug target. J Biol Chem 2004,279(14):14001–14008.PubMedCrossRef 20. Hitchings GH: Mechanism of action of trimethoprim-sulfamethoxazole. I. J Infect Dis Selleckchem Baf-A1 1973,128(Suppl):433–436.PubMedCrossRef

21. Birkenstock T, Liebeke M, Winstel V, Krismer B, Gekeler C, Niemiec MJ, Bisswanger H, Lalk M, Peschel A: Exometabolome analysis identifies pyruvate dehydrogenase as a target for the antibiotic triphenylbismuthdichloride in multiresistant bacterial pathogens. J Biol Chem 2012,287(4):2887–2895.PubMedCrossRef 22. Liebeke M, Brozel VS, Hecker M, Lalk M: Chemical characterization of soil extract as growth media for the ecophysiological study of bacteria. Appl Microbiol Biotechnol 2009,83(1):161–173.PubMedCrossRef Competing interests The authors declare to have no competing interests. Authors’ contributions DM, MLi, VW, KM, ML performed the experiments; FG, MLa, AP conceived the study; AP wrote the manuscript. All authors read and approved the final manuscript.”
“In 1861, Louis Pasteur observed that yeast cultivated under aerobic growth conditions had an increased biomass relative to yeast grown under anaerobic conditions, and that this increase in biomass correlated with a decrease in fermentative metabolism [1]. This observation would become known as the Pasteur Effect; however, it would take nearly a century to provide the metabolic explanations for this observation (e.g., NAD+-dependent activation of isocitrate dehydrogenase and feedback inhibition of phosphofructokinase; [2]).

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