Cell physiology and metabolic flux response of Klebsiella pneumoniae to aerobic conditions

2009 ◽  
Vol 44 (8) ◽  
pp. 862-868 ◽  
Author(s):  
Zhen Chen ◽  
Hong-Juan Liu ◽  
Jian-An Zhang ◽  
De-Hua Liu
2007 ◽  
Vol 35 (2) ◽  
pp. 336-339 ◽  
Author(s):  
F.G. Berger ◽  
D.L. Kramer ◽  
C.W. Porter

While polyamine homoeostasis is clearly important in maintenance of normal cell function, the roles of these cations, as well as the enzymes that regulate their metabolism, in the neoplastic process are not clear. In particular, the polyamine catabolic enzyme SSAT (spermidine/spermine N1-acetyltransferase) seems to have different roles in tumorigenesis, depending upon the particular system being analysed. In attempts to clarify the function of SSAT in tumour development, we have utilized the ApcMin/+ mouse, which carries a mutant allele of the Apc (adenomatous polyposis coli) gene, rendering it susceptible to the formation of multiple adenomas in the small intestine and colon. Using genetically engineered animals (i.e. transgenic and knockout mice), we have shown that SSAT acts as a tumour promoter in the ApcMin/+ model. Modulation of tumorigenesis is not associated with changes in tissue levels of either spermidine or spermine. These findings, along with those made in other animal models of cancer, have prompted us to propose that metabolic flux through the polyamine biosynthetic and catabolic pathways, and the consequent changes in levels of various metabolites within the cell (i.e. the metabolome), is critical to tumour development. The metabolic flux model represents a novel way of thinking about the role of polyamines in cell physiology and the neoplastic process.


Author(s):  
Pierre Millard ◽  
Julien Pérochon ◽  
Fabien Letisse

L-rhamnose and L-fucose are the two main 6-deoxyhexoses Escherichia coli can use as carbon and energy sources. Deoxyhexose metabolism leads to the formation of lactaldehyde whose fate depends on oxygen availability. Under anaerobic conditions, lactaldehyde is reduced to 1,2-propanediol whereas under aerobic condition, it should be oxidised into lactate and then channelled into the central metabolism. However, although this all-or-nothing view is accepted in the literature, it seems overly simplistic since propanediol is also reported to be present in the culture medium during aerobic growth on L-fucose. To clarify the functioning of 6-deoxyhexose sugar metabolism, a quantitative metabolic analysis was performed to determine extra- and intracellular fluxes in E. coli K-12 MG1655 (a laboratory strain) and in E. coli Nissle 1917 (a human commensal strain) during anaerobic and aerobic growth on L-rhamnose and L-fucose. As expected, lactaldehyde is fully reduced to 1,2-propanediol in anoxic conditions allowing complete reoxidation of the NADH produced by glyceraldehyde-3-phosphate-dehydrogenase. We also found that net ATP synthesis is ensured by acetate production. More surprisingly, lactaldehyde is also primarily reduced into 1,2-propanediol under aerobic conditions. For growth on L-fucose, 13 C-metabolic flux analysis revealed a large excess of available energy, highlighting the need to better characterize ATP utilization processes. The probiotic E. coli Nissle 1917 strain exhibits similar metabolic traits, indicating that they are not the result of the K-12 strain’s prolonged laboratory use. IMPORTANCE E. coli ’s ability to survive, grow and colonize the gastrointestinal tract stems from its use of partially digested food and hydrolysed glycosylated proteins (mucins) from the intestinal mucus layer as substrates. These include L-fucose and L-rhamnose, two 6-deoxyhexose sugars, whose catabolic pathways have been established by genetic and biochemical studies. However, the functioning of these pathways has only partially been elucidated. Our quantitative metabolic analysis provides a comprehensive picture of 6-deoxyhexose sugar metabolism in E. coli under anaerobic and aerobic conditions. We found that 1,2-propanediol is a major by-product under both conditions, revealing the key role of fermentative pathways in 6-deoxyhexose sugar metabolism. This metabolic trait is shared by both E. coli strains studied here, a laboratory strain and a probiotic strain. Our findings add to our understanding of E. coli ’s metabolism and of its functioning in the bacterium’s natural environment.


2007 ◽  
Vol 29 (8) ◽  
pp. 1281-1285 ◽  
Author(s):  
Hai-Jun Liu ◽  
Dai-Jia Zhang ◽  
You-Hai Xu ◽  
Ying Mu ◽  
Ya-Qin Sun ◽  
...  

2016 ◽  
Vol 21 (2) ◽  
pp. 250-260 ◽  
Author(s):  
Changman Kim ◽  
Satish Kumar Ainala ◽  
You-Kwan Oh ◽  
Byong-Hun Jeon ◽  
Sunghoon Park ◽  
...  

2007 ◽  
Vol 31 (2) ◽  
pp. 127-135 ◽  
Author(s):  
Qingrui Zhang ◽  
Hu Teng ◽  
Yaqin Sun ◽  
Zhilong Xiu ◽  
Anping Zeng

2003 ◽  
Vol 63 (2) ◽  
pp. 143-146 ◽  
Author(s):  
X. Chen ◽  
D.-J. Zhang ◽  
W.-T. Qi ◽  
S.-J. Gao ◽  
Z.-L. Xiu ◽  
...  

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