Frontiers of Chemical Science and Engineering >
The rpoS deficiency suppresses acetate accumulation in glucose-enriched culture of Escherichia coli under an aerobic condition
Received date: 16 Jun 2011
Accepted date: 26 Feb 2012
Published date: 05 Jun 2012
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The role of Escherichiacoli rpoS on the central carbon metabolism was investigated through analyzing the deficiency of this regulon gene under aerobic and glucose-enriched culture conditions. The experimental results showed that while the wild type cells exhibited an overflow metabolism effect, the rpoS-deleting mutation alleviated this effect with the significant suppression of acetate accumulation under a high glucose condition. This gene deletion also induced the twofold upregulation of gltA and one-tenth downregulation of poxB, respectively. The overflow metabolism effect was confirmed to be recovered by re-introducing rpoS gene into the mutant. These results demonstrated rpoS changed the central carbon metabolism toward acetate overflow through dehydrogenation of pyruvate and reduction of TCA cycle activity.
Prayoga SURYADARMA , Yoshihiro OJIMA , Yuto FUKUDA , Naohiro AKAMATSU , Masahito TAYA . The rpoS deficiency suppresses acetate accumulation in glucose-enriched culture of Escherichia coli under an aerobic condition[J]. Frontiers of Chemical Science and Engineering, 2012 , 6(2) : 152 -157 . DOI: 10.1007/s11705-012-1287-0
1 |
Hengge-Aronis R. Signal transduction and regulatory mechanisms involved in control of the σS (rpoS) subunit of RNA polymerase. Microbiology and Molecular Biology Reviews, 2002, 66(3): 373–395
|
2 |
Eisenstark A, Calcutt M J, Becker-Hapak M, Ivanova A. Role of Escherichia coli rpoS and associated genes in defense against oxidative damage. Free Radical Biology and Medicine, 1996, 21(7): 975–993
|
3 |
González-Flecha B, Demple B. Metabolic sources of hydrogen peroxide in aerobically growing Escherichia coli. Journal of Biological Chemistry, 1995, 270(23): 13681–13687
|
4 |
Imlay J A, Fridovich I. Assay of metabolic superoxide production in Escherichia coli. Journal of Biological Chemistry, 1991, 266(11): 6957–6965
|
5 |
Storz G, Imlay J A. Oxidative stress. Current Opinion in Microbiology, 1999, 2(2): 188–194
|
6 |
Chang Y Y, Wang A Y, Cronan J E Jr. Expression of Escherichia coli pyruvate oxidase (PoxB) depends on the sigma factor encoded by the rpoS(katF) gene. Molecular Microbiology, 1994, 11(6): 1019–1028
|
7 |
Patten C L, Kirchhof M G, Schertzberg M R, Morton R A, Schellhorn H E. Microarray analysis of rpoS-mediated gene expression in Escherichia coli K-12. Molecular Genetics and Genomics, 2004, 272(5): 580–591
|
8 |
Ueguchi C, Misonou N, Mizuno T. Negative control of rpoS expression by phosphoenolpyruvate: Carbohydrate phosphotransferase system in Escherichia coli. Journal of Bacteriology, 2001, 183(2): 520–527
|
9 |
Saka K, Tadenuma M, Nakade S, Tanaka N, Sugawara H, Nishikawa K, Ichiyoshi N, Kitagawa M, Mori H, Ogasawara N, Nishimura A. A complete set of Escherichia coli open reading frames in mobile plasmids facilitating genetic studies. DNA Research, 2005, 12(1): 63–68
|
10 |
Cooper C M, Fernstrom G A, Miller S A. Performance of agitated gas-liquid contactors. Industrial and Engineering Chemistry, 1944, 36(6): 504–509
|
11 |
Ojima Y, Kawase D, Nishioka M, Taya M. Functionally undefined gene, yggE, alleviates oxidative stress generated by monoamine oxidase in recombinant Escherichia coli. Biotechnology Letters, 2009, 31(1): 139–145
|
12 |
Andersen K B, von Meyenburg K. Are growth rates of Escherichia coli in batch cultures limited by respiration? Journal of Bacteriology, 1980, 144(1): 114–123
|
13 |
Phue J N, Shiloach J. Impact of dissolved oxygen concentration on acetate accumulation and physiology of E. coli BL21, evaluating transcription levels of key genes at different dissolved oxygen conditions. Metabolic Engineering, 2005, 7(5–6): 353–363
|
14 |
Iuchi S, Lin E C. arcA (dye), a global regulatory gene in Escherichia coli mediating repression of enzymes in aerobic pathways. Proceedings of the National Academy of Sciences of the United States of America, 1988, 85(6): 1888–1892
|
15 |
Majewski R A, Domach M M. Simple constrained-optimization view of acetate overflow in Escherichia coli. Biotechnology and Bioengineering, 1990, 7(7): 732–738
|
16 |
Britten R. Extracellular metabolic product of Escherichia coli during rapid growth. Science, 1954, 119: 578–578
|
17 |
Han K, Lim H C, Hong J. Acetic acid formation in Escherichia coli fermentation. Biotechnology and Bioengineering, 1992, 39(6): 663–671
|
18 |
Vemuri G N, Altman E, Sangurdekar D P, Khodursky A B, Eiteman M A. Overflow metabolism in Escherichia coli during steady-state growth: transcriptional regulation and effect of the redox ratio. Applied and Environmental Microbiology, 2006, 72(5): 3653–3661
|
19 |
Ingledew W J, Poole R K. The respiratory chains of Escherichia coli. Microbiological Reviews, 1984, 48(3): 222–271
|
20 |
Gray C T, Wimpenny J W, Mossman M R. Regulation of metabolism in facultative bacteria: II. Effects of aerobiosis, anaerbiosis and nutrition on the formation of Krebs cycle enzymes in Escherchia coli. Biochimica et Biophysica Acta. G, General Subjects, 1966, 1(1): 33–41
|
21 |
Amarasingham C R, Davis B D. Regulation of α-ketoglutarate dehydrogenase formation in Escherichia coli. Journal of Biological Chemistry, 1965, 240(9): 3664–3668
|
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