Network analysis of the transcriptional pattern of young and old cells of Escherichia coli during lag phase
© Pin et al; licensee BioMed Central Ltd. 2009
Received: 15 May 2009
Accepted: 16 November 2009
Published: 16 November 2009
The aging process of bacteria in stationary phase is halted if cells are subcultured and enter lag phase and it is then followed by cellular division. Network science has been applied to analyse the transcriptional response, during lag phase, of bacterial cells starved previously in stationary phase for 1 day (young cells) and 16 days (old cells).
A genome scale network was constructed for E. coli K-12 by connecting genes with operons, transcription and sigma factors, metabolic pathways and cell functional categories. Most of the transcriptional changes were detected immediately upon entering lag phase and were maintained throughout this period. The lag period was longer for older cells and the analysis of the transcriptome revealed different intracellular activity in young and old cells. The number of genes differentially expressed was smaller in old cells (186) than in young cells (467). Relatively, few genes (62) were up- or down-regulated in both cultures. Transcription of genes related to osmotolerance, acid resistance, oxidative stress and adaptation to other stresses was down-regulated in both young and old cells. Regarding carbohydrate metabolism, genes related to the citrate cycle were up-regulated in young cells while old cells up-regulated the Entner Doudoroff and gluconate pathways and down-regulated the pentose phosphate pathway. In both old and young cells, anaerobic respiration and fermentation pathways were down-regulated, but only young cells up-regulated aerobic respiration while there was no evidence of aerobic respiration in old cells.
Numerous genes related to DNA maintenance and replication, translation, ribosomal biosynthesis and RNA processing as well as biosynthesis of the cell envelope and flagellum and several components of the chemotaxis signal transduction complex were up-regulated only in young cells. The genes for several transport proteins for iron compounds were up-regulated in both young and old cells. Numerous genes encoding transporters for carbohydrates and organic alcohols and acids were down-regulated in old cells only.
Network analysis revealed very different transcriptional activities during the lag period in old and young cells. Rejuvenation seems to take place during exponential growth by replicative dilution of old cellular components.
In a laboratory environment, bacteria inoculated in batch culture grow until a maximum density is reached, after which they stop growing and start a cellular degenerative process that ultimately leads to death. The latter period is known as stationary phase and its duration depends on the environment. Cellular degeneration of bacteria in stationary phase has been found to reveal similarities with the aging process of higher organisms . Senescence during stationary phase is followed by loss of ability to grow at the end of the stationary phase, which has been described as the nearest bacteria come to a "natural" death that occurs among aging organisms . If stationary-phase bacteria are subcultured into fresh media, at a lower cell density, they will enter lag phase and halt the degenerative process, getting ready to start the division cycles again. The duration of the lag phase depends on the length of time the cells have spent in stationary phase before inoculation [2, 3]; thus cells starved in stationary phase need a longer time to prepare for the first division.
Exponential growth rate can be predicted with a high degree of accuracy as a function of the current growth environment. Conversely, the duration of lag phase can be highly variable and single-cell studies have shown that it is influenced not only by the current growth environment but also by the previous history of the cells . The molecular mechanisms underlying lag phase remain to be characterized. A major problem is that the low concentration of cells during lag phase makes it challenging to apply a number of analytical techniques. In yeast, a number of genes induced during lag phase are known to be involved in molecular biosynthesis and carbohydrate metabolism [5, 6]. A rapid change in gene expression has also been detected in yeast populations entering lag phase . These authors detected 2500 genes immediately up-regulated at the initiation of the lag phase and showed that this was because the RNA polymerase II was "poised" upstream of many inactive genes in stationary phase. In Listeria monocytogenes, experiments involving a few specific genes showed that the transcripts from a functional sigB gene were accumulated for an extended period during lag phase after an osmotic upshift  and, at low temperatures, lag phase was extended in the absence of a functional sigB gene . In E. coli, chromatographic/mass spectrometry measurements have been optimized for the analysis of intracellular metabolites  and combined transcriptome and proteome analysis  has been carried out at high bacterial density during late exponential and stationary phase; however, such studies during lag phase are lacking and there is no comprehensive picture of the biochemical and molecular genetic activity of bacteria during this important period.
In our work, we have adopted a network-science approach to identify and interpret the differences at the transcriptional level between populations of young and old cells undergoing lag phase. The study of networks has a long tradition in graph theory and discrete mathematics, sociology, communication research, bibliometrics/scientometrics, webometrics/cybermetrics, in physics and, recently, in biology . This approach has already been used to model the transcriptional regulatory network of E. coli , based on the publicly available network of E. coli MG1655, which contained originally 418 operons and 519 interactions. Protein-protein interactions in E. coli have also been identified and compiled in a large scale network [14, 15]. More generally, the construction of metabolic networks in bacteria has been shown to be a very valuable tool to elucidate the components and pathways of biological processes [16–19].
In this paper, we have compared the lag-phase transcription profile of cells originated from an early stationary phase culture (young cells) with that of cells originated from a culture starved in stationary phase for 16 days (old cells). A genome scale network was constructed according to the metabolic pathways, functional roles, transcriptional regulation and predicted operon composition of E. coli. Our aim was to quantify and compare the complexity of the intracellular events during the lag phase of cells of different ages.
Results and Discussion
Quantitative microarray results
Number of genes up and down-regulated during lag phase with respect to stationary phase
Sampling time during lag (min)
In all samples
Sampling time during lag (min)
In all samples
Number of genes in each category according to their expression: down- or up-regulated or not modified, NM, during the lag phase of young and old cells
Young cells inoculum
Old cells inoculum
Number of genes
Only three genes showed an opposite regulation response between old cells and young cells. The gene sdhA, a subunit of succinate dehydrogenase, was up-regulated in young cells and down-regulated in old cells. The genes sufA, whose product is involved in the biosynthesis of iron-sulfur clusters, and yhaH, a putative cytochrome, were down-regulated in young cells and up-regulated in old cells. Cluster analysis was carried out on the correlation matrix of the transcription profile of the genes up- and down-regulated during the lag phase (additional file 1: Fig S1). Expression patterns in time could not be identified. Some discontinuities in the expression patterns were assumed to be due to detection limits. There were no genes that were detected as both up- and down-regulated at different sampling times during lag, either in young cells or old cells.
Analysis of the genome scale network and the sub-netwroks of genes up- and down-regulated during the lag time of young and old cells
Description of the genome scale network for E. coli and of the sub-networks of the genes differentially expressed during the lag time of old and young cells
Young cells network
Old cells network
Connectivity, degree distribution, modularity and nestedness  were estimated on the genome scale network and compared with the sub-networks corresponding to genes differentially expressed in old and young cells. To assess the results, we analysed between 10 and 50 networks, with the same number of genes randomly selected.
The genome scale network had a giant connected component with 3645 nodes (63% of the total number of nodes) and 262 small disconnected components, each with a number of nodes between 2 and 11. The sub-network for young cells had a component connecting 43% of the nodes and numerous smaller components with less than 3% of nodes. The sub-network for old cells had two components connecting 20 and 8% of the vertices and smaller components with a percentage of nodes smaller than 5%. The random networks generated for young and old cells showed very similar connectivity patterns.
Modularity was estimated with the program implementing the fast modularity maximization algorithm . Networks have communities of highly interconnected nodes that are less connected in other modules and this organization in communities is quantified by the modularity value, Q. If the fraction of within-community edges is no different from what we would expect for a randomized network, then Q will be zero. Nonzero values represent deviations from randomness, and in practice it is found that a value above about 0.3 is a good indicator of significant community structure in a network . The value of Q was 0.6 for the genome scale network while the sub-networks of young and old cells showed a greater modularity, with values of 0.87 and 0.91, respectively. These modularity values were not different from those generated for the correspondent randomly generated networks. Fig 4b shows the distribution of nodes in modules. The genome scale network had 231 modules with more than 3 nodes each. From these, 10% of the modules included 80% of the nodes (Fig 4b). The networks for young and old cells showed a larger relative number of modules, 40% and 60%, respectively, containing 80% of the nodes. These distributions were not different from the correspondent randomly generated networks (Fig 4b) and therefore the greater level of modularity is due to the smaller numbers of nodes.
Nestedness (N) quantification for the genome scale network and for the sub-networks of differentially expressed genes during the lag phase of old and young cells
Young cells network
Old cells network
Therefore, the most relevant topological features of the genome scale network either remain constant in the sub-networks of the genes differentially expressed in old and young cells or, should they change, this change is also detected in the correspondent randomly generated network.
Comparing transcriptional activity during the lag phase of young and old cells
Changes in gene expression were difficult to differentiate from failure in detection for samples obtained at different time points during the lag period as seen by cluster analysis (additional file 1: Fig S1). Therefore, the transcriptional regulatory network and predicted operons, detected as up- and/or down-regulated in both young and old cells, were in general not affected by the sampling time during lag (additional file 2: Fig S2 and additional file 3: Fig S3). Neither the regulation of metabolic pathways and functional roles varied through the lag period. Most of the transcriptional changes were detected on entering lag phase and were maintained throughout this period. For this reason, the sampling time during the lag period was not taken into account for the analysis.
The mechanisms of osmotolerance are not fully understood. Bacteria utilize intracellular compatible osmolytes such as glutamate, betaine, proline, and trehalose to adapt to osmotic stress arising from extracellular solutes [24, 25]. Upon entering lag phase, both young and old cells up-regulated several elements of the glycine-betaine osmoprotective system (Fig 5, 5B). The betA, betB and betT genes and the BetI TF, which regulates the transcription of the system, were all up-regulated in young cells (Fig 2 and additional file 4, 4D) and two of them, the betT gene and BetI TF, were up-regulated also in old cells (Fig 3, 1A). In addition, genes from the proVWX operon for the transport of glycine-betaine were up-regulated in both cultures (Fig 5, 6E). Regarding the metabolism of proline, the genes encoding the PutP transport protein for proline uptake and the PutA TF that represses proline catabolism genes  were up-regulated in young cells only (Fig 2 and additional file 4, E3, 1F). These changes are perhaps surprising given that the inoculation of stationary phase cells into fresh medium did not impose an osmotic stress. It is likely that the change in the medium afforded cells the opportunity to modify the mechanism to contend with the osmotic potential of the medium. E. coli is able to synthesize glutamate, betaine, proline, and trehalose during oxidative metabolism provided that choline is available, but biosynthesis is limited to glutamate and trehalose in anaerobic conditions such as stationary phase [24, 25]. In young cells, but not in old cells, glutamate metabolism and transport (Fig 2 and additional file 4, 2E), as well as the signal transduction complex to sense extracellular osmotic stress and synthesize large amounts of trehalose (Fig 2 and additional file 4, 4E), were active during stationary phase and were down-regulated when cells were inoculated in fresh medium at a lower cell concentration. The same pattern was observed with TreR, the TF that regulates the latter system. High cell density in a batch culture in stationary phase causes an anaerobiosis situation that reverts when cells are inoculated at lower cell concentration into fresh medium.
Three known systems have evolved for stationary-phase acid resistance in E. coli . The acid resistance system 1 requires the sigmaS subunit of the RNA polymerase, RpoS, which is the master regulator of the general stress response . This sigma factor was not differentially transcribed upon entrance into lag phase either in old or young cells. The acid resistance system 2 was down-regulated in both young and old cells. This system is glutamate-dependent and it couples the transport activity of the GadC protein with a glutamate decarboxylase, GadA/GadB. The genes encoding these proteins are part of the operons gadAXW and gadBC and were down-regulated during the lag phase of both young and old cells. The GadW TF that represses the expression of this system was also down-regulated in both cultures. The last system is arginine-dependent and is based on the arginine decarboxylase and the AdiC antiporter to exchange extracellular arginine with agmatine, which is the product of arginine decarboxylation. The genes encoding the AdiC antiporter and the ArtJ and ArtP proteins for arginine uptake, together with the argF, argG, and argI genes associated with arginine biosynthesis from glutamate, were all down-regulated in young cells only. However, the gene for the adiY TF that controls the arginine decarboxylase system under anaerobic conditions  was down-regulated in both young and old cells. The observed pH values were of ca. 6 and ca. 7 after 1 day (young cells) and 16 days (old cells) in stationary phase, respectively. Although these pH values do not imply acid stress, several responses to acid stress were activated during the stationary phase. It has been already shown that defence systems against acid stress respond positively to stationary phase, and its induction does not require external acid pH [30, 31]
Three distinct superoxide dismutases (SOD) have been described in E. coli: the manganese-SOD, encoded by the sodA gene, detected in aerobiosis and mainly responsible for preventing damage to DNA, the iron-SOD encoded by the sodB gene, detected in both anaerobiosis and aerobiosis and mainly responsible for protecting cytoplasmic enzymes  and a copper-zinc-SOD found in a mutant unable to produce any of the previous two enzymes . Upon entering lag, both old and young cells down-regulated the gene encoding iron-SOD (Fig 5, 5C). The gene for manganese-SOD was up-regulated only in young cells, while the gene for the Rob TF that activates its transcription was down-regulated (Fig 2 and additional file 4, 4D). These changes could be a consequence of anaerobiosis associated with high cell density in stationary phase. On the other hand, the katG gene encoding hydroperoxidase I, which functions as both a catalase and a broad spectrum peroxidase , was up-regulated in both young and old cells in lag phase (Fig 5, 5C). Therefore, the strategy to contend with the redox potential of the medium changed when cells entered lag period.
Oxidative damage has been associated with cellular senescence in E. coli in stationary phase . Heat shock proteins have been linked to a possible role in counteracting protein oxidation in E. coli cells in stationary-phase cells . These proteins have been shown to mitigate starvation-induced protein carbonylation, which is an irreversible modification associated with senescence . The heat shock response in E. coli is controlled by two distinct RNA polymerase species in E. coli: the sigma E or 24 and sigma H or 32 factors [36, 37]. In young cells, the genes encoding both these factors, as well as several genes whose transcription is regulated by them, were down-regulated (Fig 2 and additional file 4, 4B, 5B). The sigma E factor is regulated by a multistep protease system that senses protein disruption . Its transcriptional initiation targets include the UspA and UspD proteins and the Sigma 32 factor, all of them detected as down-regulated in young cells (Fig 2 and additional file 4, 4B, 5B). The UspA and UspD proteins are universal stress response regulators recently linked to oxidative stress defence and important in delaying cell senescence [1, 39]. The Sigma 32 factor regulates the DnaK/DnaJ/GrpE, IbpA/IbpB and GroEL/GroES chaperone systems, which were all down-regulated in young cells (Fig 2 and additional file 4, 4B, 5B). These systems assist protein folding and stabilization and prevent aggregation of misfolded proteins . The DnaK/DnaJ and GroEL/GroES systems are strongly involved in defence against oxidative stress . Therefore, this defence mechanism against oxidative damage to proteins was down-regulated in young cells but not in old cells. It would appear that old cells keep this system active even after encountering an optimum environment or may deactivate this mechanism after some time in stationary phase. The wrbA gene, encoding a quinone oxidoreductase involved in resistance to oxidative stress , was down-regulated in both cultures (Fig 5, 6C).
Other environmental stresses
Several genes induced by the Sigma E factor and involved in adaptation to and/or defence against stress conditions were also down-regulated in young cells (Fig 2 and additional file 4, 4B). These included the gene for the CspD protein that inhibits chromosome replication in stationary phase and the lpxP gene demonstrated to respond to cold shock conditions. A number of genes for membrane transporter systems with detoxification activities were down-regulated in young cells only. These were the EvgA TF (Fig 2 and additional file 4, 3E), associated with acid and multidrug resistance, and components of the MdtEF-TolC multidrug efflux transport system (Fig 2 and additional file 4, 3E) and of some transporters from the Rhs family (Fig 2 and additional file 4, 2F) reported to prevent toxicity in stationary phase . Some genes related to stress response were also down-regulated in old cells after inoculation in fresh medium. The slp-dctR operon that encodes starvation lipoproteins was down-regulated in both young and old cells (Fig 3, 6F).
Therefore, responses to several stresses were down-regulated upon transfer to improved growth conditions. The number of genes related to stress response in stationary phase and down-regulated in young cells was larger than in old cells. This could indicate that the stress response is activated at the beginning of the stationary phase and partially deactivated later.
Carbohydrate catabolism and energy generation
E. coli is capable of three alternative modes of energy generation: aerobic respiration, anaerobic respiration and fermentation . During lag phase, young cells appeared to begin aerobic respiration, whereas in old cells there was no evidence of aerobic respiration. In both old and young cells, anaerobic respiration and fermentation pathways were down-regulated after inoculation into fresh medium.
Practically all genes of the main operons encoding the enzymatic complexes involved in aerobic oxidative phosphorylation were up-regulated in young cells but not in old cells. These operons were those encoding NADH dehydrogenase and its transcription regulator, Fis protein (Fig 2 and additional file 4, 1C), fumarate reductase/succinate dehydrogenase (Fig 2 and additional file 4, 3CD), cytochrome oxidase (Fig 2 and additional file 4, 2C) and ATP synthase (Fig 2 and additional file 4, 1D). However, in old cells, the sdhA gene that encodes a component of one of these enzymes, succinate dehydrogenase (SdhCDAB), associated with aerobic respiration, was down-regulated (Fig 3, 3E). In young cells, although genes encoding the SoxR and Rob TFs that activate the transcription of the aerobic fumarase C were down-regulated, the gene, fumC, encoding that enzyme was nevertheless up-regulated (Fig 2 and additional file 4, 4D). Other TCA cycle genes up-regulated in young cells were those of the sdhCDAB-sucABCD operon, encoding the already-mentioned succinate dehydrogenase and the succinyl-CoA synthetase, and the icd encoding for the isocitrate dehydrogenase (Fig 2 and additional file 4, 3C). Also in young cells only, the gene encoding the UhpA TF, promoting the uptake of exogenous hexose phosphates , was up-regulated (Fig 2 and additional file 4, 3F).
Two genes, cydA and cydB, expressing the subunits of the cytochrome bd-I terminal oxidase, were down-regulated in old cells (Fig 3, 3F) and one of them, the cydA gene, was also down-regulated in young cells (Fig 2 and additional file 4, 2D). This enzymatic complex has been associated with aerobic respiration under microaerobiosis , which would explained its role during stationary phase, followed by down-regulation when cells encounter aerobic conditions after inoculation in fresh medium at lower cellular concentration. Regarding anaerobic metabolism, the expression of the hya operon and its transcription regulator, AppY, were down-regulated in young cells (Fig 2 and additional file 4, 3B). This operon encodes the hydrogenase 1 and it is induced under anaerobic conditions and by the presence of formate . The frdA gene from the fumarate reductase complex (FrdABCD), which acts most effectively under anaerobic conditions  and the genes encoding the anaerobic dehydrogenase protein complex, GlpABC, were down-regulated in old cells (Fig 3, 2DE). Upon entering lag phase, young cells repressed the transcription of the enzymatic complex FadI/FadJ that catalyzes the beta oxidation of fatty acids and allows E. coli to use this compounds as carbon and energy source under anaerobic conditions , as well as of the CaiF TF that activates the transcription of enzymes involved in the metabolism of carnitine, which is essential for fatty acid metabolism and transport  (Fig 2 and additional file 4, 1F). In old cells, the genes glpB, glpA, glpQ and glpT, encoding enzymes for the anaerobic metabolism of glycerol and glycerophospholipids, were down-regulated (Fig 3, 2D).
During fermentative growth, glycolytic carbon sources are converted to pyruvate, and thence to acetyl-CoA and formate by the activity of the pyruvate formate-lyase, PflA, enzyme . Upon entering lag phase, young and old cells down-regulated this enzyme (Fig 5, 3C). The resulting formate may then be either excreted, by the FocA formate transporter, or further metabolized by the formate hydrogenlyase, Fhl-1, system. The genes required for the synthesis of Fhl-1 system form the formate regulon, which includes three transcriptional units, namely, the hycABCDEFGHI and hyp-fhlA operons and the fdhF gene . The gene encoding the FocA transporter (Fig 2 and additional file 4, 3E) and the three transcriptional units of the formate regulon (Fig 2 and additional file 4, 3B) were all down-regulated in young cells.
Changes in carbohydrate metabolism in old cells were related to the Entner Doudoroff and gluconate pathways. The Entner Doudoroff pathway involves gluconate and its degradation . The edd gene from the Entner Doudoroff pathway, together with genes for the GntU gluconate transporter and for the gluconate kinase enzyme, encoded by the gntK gene and involved in gluconate degradation, were up-regulated in old cells (Fig 3, 3E). In young cells, the edd gene from the Entner Doudoroff pathway was also up-regulated, but genes related to gluconate degradation were not detected and furthermore the genes for the gluconate transporter, GntT, and for the transcription regulator of this system, the GntR TF, were down-regulated (Fig 2 and additional file 4, 3F). Intracellular gluconate can also be obtained via the pentose phosphate pathway. In old cells, genes encoding enzymes of the pentose phosphate pathway were down-regulated (Fig 3, 4D). In addition, the L-ascorbate degradation pathway was also down-regulated (Fig 3, 5A); this pathway results in products that can enter the non-oxidative branch of the pentose phosphate pathway . Therefore, the pentose phosphate pathway seems to be active in old cells in stationary phase but it is deactivated upon entering lag phase. Similarly, galactitol metabolism was down-regulated in old cells, because the gene for galactitol permease, together with several genes related to its degradation and also the GatR TF which regulates transcription of the system, were all down-regulated (Fig 3, 3B).
Fig 6 shows that a number of genes associated with salvage pathways, as well as with pathways for the de novo biosynthesis of pyrimidine and purine nucleotides, were up-regulated during the lag phase of young cells only (Fig 2 and additional file 4, 2D, 3D), together with genes encoding several proteins related to DNA metabolism. These were the bacterial histone-like HU protein involved in DNA compaction, the XthA protein, related to the organization and maintenance of nucleotide structure, the PriB protein, involved in replication, and the Fis protein (Fig 2 and additional file 4, 1B, 1C). The primary role of Fis is to maintain the structure of the genome. Fis also regulates the transcription of a large number of genes involved in a variety of functional roles . Several genes regulated by Fis and related mainly to aerobic respiration were also up-regulated only in young cells, as already mentioned. The regulation of genes encoding proteins associated with genomic DNA methylation essential for cell division  was variable; whilst the gene encoding the YhdJ protein was up-regulated (Fig 2 and additional file 4, 1B), those encoding the MetJ TF and MetK protein were down-regulated (Fig 2 and additional file 4, 2C, 3C) in young cells.
Translation and protein biosynthetic activities were only up-regulated in young cells. Thus, genes upregulated included those encoding several proteins involved in the biosynthesis of both the large and the small ribosomal subunits (Fig 2 and additional file 4, 2B); the valS, glyQ and tgt genes, encoding products for the aminoacylation (Fig 2 and additional file 4, 5D) of tRNA, and genes encoding ribonucleases for processing of tRNA, rRNA and mRNA (Fig 2 and additional file 4, 3B).
Transcription of genes encoding transport proteins for amino acids, peptides and amines was variable in young cells, while in old cells this function was not significantly affected. The PotABCD transport system for polyamines, putrescine and spermidine was up-regulated in young cells (Fig 2 and additional file 4, 1E). Lack of polyamines is associated with abnormal growth and oxidative stress-induced damage . As mentioned above, genes for the transporters for glycine-betaine, ProXVW, and proline, PutP, were up-regulated, while the transcription of the gene for the AdiC antiporter for arginine, together with transcription of the genes for other transport proteins associated with acid and osmotic stress, was down-regulated in young cells (Fig 2 and additional file 4, 1E).
The genes encoding several transport proteins for cations and iron compounds were up-regulated in both young and old cells, such as the entCEBA operon involved in the biosynthesis of the enterobactin siderophore from chorismate (Fig 5, 1E). The aroA and aroD genes involved in chorismate biosynthesis were up-regulated in old cells only (Fig 3, 4E). Chorismate is also an intermediate metabolite required for the biosynthesis of the aromatic amino acids, phenylalanine, tyrosine and tryptophan. The gene encoding the outer membrane receptor for iron transport, Fiu, and the fecABCDE and fepA-entD operons related to iron transport and metabolism were up-regulated in both young and old cells (Fig 5, 4D). However, on entering lag phase, young cells down-regulated the bfr gene encoding the iron-storage protein, bacterioferritin, and the gene encoding the FeaA iron transport protein (Fig 2 and additional file 4, 5C).
The genes encoding numerous transporters for carbohydrates and organic acids and alcohols were down-regulated in old cells, whereas in young cells a smaller number of transport systems were affected. Systems down-regulated in old cells included those encoding for galactitol, GatABC, and mannose, ManXYZ, permeases, as already mentioned, and the rbsDACBKR operon encoding the ribose transporter. Also down-regulated in old cells were the genes encoding the DctA protein required for dicarboxylate transport, the LamB for diffusion of maltodextrins, components of the MalKFGE maltose transport system, the MglB component of the galactose transporter and the LsrA uncharacterized sugar transporter  (Fig 3, 3C). In young cells, the transport systems down-regulated included the genes for the already-mentioned gluconate and formate transporters, GntT and FocA, and trehalose permease, TreB. The genes encoding the long-chain fatty acid transporter, FadL, and the UhpA TF for the uptake of hexoses phosphates, as explained above, were up-regulated (Fig 2 and additional file 4, 3E). Both in old and young cells, the gene encoding the TsgA protein, a member of the major facilitator superfamily of transporters of metabolites, was up-regulated (Fig 5, 1C).
Genes related to the biosynthesis of cell envelope components were up-regulated in young cells only. These included the mraY, mrdB and dacB genes involved in peptidoglycan biosynthesis and the accD gene, encoding a sub-unit of acetyl-CoA carboxylase, which catalyzes an initial step in the biosynthesis of phospholipid components of the cell membrane (Fig 2 and additional file 4, 3E). However, the murI gene that encodes the glutamate racemase involved in peptidoglycan biosynthesis was down-regulated (Fig 2 and additional file 4, 3E). Similarly, the tar-tap-cheRBYZ, motAB-cheAW operons and flgK and fliD were up-regulated only in young cells (Fig 2 and additional file 4, 5E). These genes encode structural components of the flagellum and several components of the chemotaxis signal transduction complex involved in the transmission of sensory signals to the flagellar motors that affect swimming behaviour (Fig 2 and additional file 4, 4E) .
The 'general secretory pathway', GSP, and its associated secreton complex, Sec, is used by most proteins that are completely translocated across the inner membrane and end up in the periplasm or outer membrane . The genes encoding the SecD and SecF elements of the secretion complex were up-regulated in young cells. Conversely, the gspM and gspC genes that are similar to those coding for the main terminal branch of the general secretory pathway in Klebsiella oxytoca , together with those encoding other putative transporters, were down-regulated in young cells (Fig 2 and additional file 4, 5E).
Upon entering lag phase, the gene encoding the BolA TF, associated with the maintenance of cell morphology in stationary phase, was down-regulated in both old and young cells. Numerous other TFs were down-regulated in both old and young cells. Thus, the genes for seven out of a total of nine TFs that were differentially expressed in old cells were down-regulated and, similarly, 16 out of a total of 21 were down-regulated in young cells (Fig 5, 5B). Some genes regulated by these TFs were differentially expressed but their expression did not always agree with the expected regulation. As an example, from the 173 genes regulated by Fis, 10 and 2 genes were, as expected, up- and down-regulated, respectively; whereas the dusB and hupB genes that were expected to be down-regulated by Fis were up-regulated and the mazG and deoC genes theoretically up-regulated by Fis were down-regulated (additional file 2: Fig S2). This is to be expected since static views provide poor quality maps of the transcriptional network, which is the result of precise expression timing and subsequent refinements. Apart from the already-mentioned TFs, the genes encoding the CueR TF, related to copper homeostasis, and the MtlR TF, for mannitol utilization, were only down-regulated in young cells. Conversely, the genes encoding the LsrR TF, involved in quorum sensing, the TdcA TF, for transport and metabolism of threonine and serine during anaerobic growth  and the AtoC TF, related to short-chain fatty acid metabolism, were all down-regulated only in old cells. The gene encoding the RcnR protein that regulates nickel, cobalt and iron homeostasis  was up-regulated during the lag of old cells only.
The genome scale network built for E. coli provided an insight into the molecular responses occurring during lag phase, in relation to the duration of the immediately-preceding stationary phase. Information related to component systems, signalling, metabolic pathways, transcriptional control and specific cellular activities was integrated in a genome-scale partially directed network. This network met the important goal of handling different layers of information at the genome scale that otherwise would have required a great human and computing effort.
Stationary phase is a reversible process, such that if the growth-limiting factor is removed (i.e. the overpopulation condition and the chemical environmental changes associated with it), stationary phase cells are able to resume growth. Thus, stationary phase cells responded quickly to the new growth conditions by adjusting their transcriptional activity immediately after inoculation in fresh medium. Fig 2 and additional file 4 show how the network of genes differentially transcribed in young cells had a larger number of nodes and connections than the network for old cells. A greater transcriptional activity might be anticipated in old cells as a mechanism to counteract senescence during stationary phase. In addition, similar intracellular activities might be envisaged by the end of the lag period in both old and young cells. However, lag time does not seem to be the period in which senescence is wholly reversed; rather, during lag phase, cells prepare to start the division cycle by adopting different metabolic strategies according to their initial condition. In old cells, this process is longer and less efficient than in young cells, as shown by the lack of up-regulation of aerobic respiration, possibly because of the damage associated with aging. Rejuvenation may, effectively, take place later, during the exponential growth phase. Replicative rejuvenation during exponential phase is the converse of the process described as replicative senescence. Bacterial cells have been shown to exhibit signs of replicative aging, or loss of fitness, in a sibling-specific manner during exponential growth; i.e., a cumulative loss of fitness in sibling lineages that inherit old cellular poles . However, and conversely, the same mechanism may in fact be contemplated equally as a replicative cellular rejuvenation process. A population starting from one single cell after m successive generations will include 2m-1cells (half the population) with structures formed during the last, m, and last but one, m-1, division cycles. Less than 1/4 cells of the population will have structures formed in division cycles previous to the m-2th division. In fact, only two cells will have the poles of the original single cell. Therefore, the findings described previously  can be read as conferring a growth advantage on cells with newly-formed poles; and furthermore, such cells represent the vast majority of the population. During exponential growth phase, the successive division cycles will have a dilution effect on the old and/or damaged cellular structures previously accumulated during senescence and will hence ensure the rejuvenation of the population.
Bacterial strain and growth conditions
E. coli K-12 substrain MG1655 was grown at 25°C for 48 hours (young culture) and 17 days (old culture) in Luria-Bertani broth (10 g/l Tryptone, 5 g/l yeast extract and 10 g/l NaCl; pH 7.2) with 0.2% glucose. Cultures were grown statically and reached stationary phase after ca. 24 h; therefore the time spent in stationary phase was ca. 1 and 16 days, for young and old cells, respectively. The time in stationary phase is considered as the age of the population, as it approximates the time elapsed from the last division for most of the cells in the population. These cultures were used to inoculate aliquots of 750 ml of fresh medium to give an initial concentration of 105-106 cells/ml. The lag phases were ca. 1.5-1.8 and 4.7-5.1 hours for cultures inoculated with young and old cells, respectively. Samples were obtained for gene expression analysis at 0, 0.25, 0.5, 0.75 and 1 hours, and at 0, 1.25, 2.5, 3.75 and 5 hours after inoculation of the young and old culture, respectively. At each sampling time, the 750 ml culture was harvested by adding 1/5 volume of 5% phenol 95% ethanol (v/v) and placing the flask on ice for 30 minutes . The cellular material was then pelleted by centrifugation at 6000 × g at 4°C for 15 minutes, with the pellet stored at -80°C until RNA isolation was carried out. Cell concentration was monitored by viable counts on Tryptone soy agar. The whole experiment was repeated twice.
Construction of DNA microarrays
The E. coli K-12 MG1655 DNA microarrays used in this work were produced as described previously , with additional features added. Each microarray included approximately 100 features of serially diluted chromosomal DNA (15-20 replicates of each dilution) isolated from the same strain used for the microarray design (MG1655). These features are referred as genomic controls and used in data analysis.
RNA and DNA purification and microarray hybridizations
RNA was purified from E. coli as described previously . RNA quality and quantity was checked using the Agilent 2100 Bioanalyzer (Agilent Technologies). Genomic DNA was isolated using the QIAgen DNeasy™ method (QIAgen) following the manufacturer's instructions. Genomic DNA was labelled with Cy3-dCTP (Amersham) using a protocol based on the BioPrime labelling kit (Invitrogen), whilst RNA was labelled with Cy5-dCTP (Amersham) using Stratascript Reverse Transcriptase (Stratagene). The labelled cDNA and DNA were mixed together and competitively hybridized on a microarray slide overnight at 62°C. Following hybridization, microarray slides were washed and scanned using an Axon GenePix 4000A Microarray scanner (Axon Instruments, CA) and the feature intensities were quantified using GenePix Pro software (Molecular Devices). Full labelling, hybridisation and washing protocols are available on the IFR Microarrays web-site.
Microarray data analysis
Data normalization and analysis was carried out using the program ArrayLeaRNA, which implements a Bayesian inference method based on genomic controls and operon transcription pattern . Fluorescence intensities detected in the samples during lag were compared with the intensities of the sample obtained in stationary phase used as the inoculum (time 0). Only genes detected as up- (down-) regulated at least once in each replicated experiment carried out either with young or old cells were considered as differentially expressed. Three genes that were detected as both up- and down-regulated during the lag of young cells were deleted from the analysis.
Genome scale network construction
A bi-partite network was constructed for the genome of E. coli K-12 as follows. Edges/arcs connected two sets of nodes. Genes constituted one of these sets of nodes. The genome composition was obtained from the EcoCyc database . The other set of nodes included 5 categories: transcription factors; sigma factors and operons, as denoted in the RegulonDB v 6.0 database ; metabolic pathways, according to the KEGG database ; and functional role categories, as described in the CMR-TIGR database . The information was completed and revised according to the Ecocyc database .
For network representation and topological quantification we used the programs PAJEK  and Cytoscape . Networks modularity was estimated with the program implementing the fast modularity maximization algorithm . The level of nestedness organization of the networks was estimated with the nestedness calculator program .
Statistical test on the significance of the changes on expression of metabolic pathways, cell functional categories and operons
For an observed sample, the statistical evaluation of the up(down)-regulation of a particular metabolic pathway, functional category or operon was carried out as follows:
T = total number of genes in the genome;
M = number of genes in the total genome known to belong to that metabolic pathways, cell functional category or operon;
n = total number of up(down)-regulated genes in the sample.
When the p-value was smaller than 0.05, the X = k event being unlikely to have happened purely by chance, we considered that the metabolic pathway, cell functional category or operon was significantly differentially expressed.
Microarray data have been deposited with Array Express [Array Express:E-MEXP-2379]
We gratefully acknowledge the support from the BBSRC core strategic grants 42266A and 42230A
- Fredriksson A, Nystrom T: Conditional and replicative senescence in Escherichia coli. Curr Opin Microbiol. 2006, 9 (6): 612-618.View ArticlePubMedGoogle Scholar
- Weichart DH, Kell DB: Characterization of an autostimulatory substance produced by Escherichia coli. Microbiology. 2001, 147 (Pt 7): 1875-1885.View ArticlePubMedGoogle Scholar
- Pin C, Baranyi J: Single-cell and population lag times as a function of cell age. Appl Environ Microbiol. 2008, 74 (8): 2534-2536.PubMed CentralView ArticlePubMedGoogle Scholar
- D'Arrigo M, Garcia de Fernando GD, Velasco de Diego R, Ordonez JA, George SM, Pin C: Indirect measurement of the lag time distribution of single cells of Listeria innocua in food. Appl Environ Microbiol. 2006, 72 (4): 2533-2538.PubMed CentralView ArticlePubMedGoogle Scholar
- Brejning J, Arneborg N, Jespersen L: Identification of genes and proteins induced during the lag and early exponential phase of lager brewing yeasts. J Appl Microbiol. 2005, 98 (2): 261-271.View ArticlePubMedGoogle Scholar
- Brejning J, Jespersen L: Protein expression during lag phase and growth initiation in Saccharomyces cerevisiae. Int J Food Microbiol. 2002, 75 (1-2): 27-38.View ArticlePubMedGoogle Scholar
- Radonjic M, Andrau JC, Lijnzaad P, Kemmeren P, Kockelkorn TT, van Leenen D, van Berkum NL, Holstege FC: Genome-wide analyses reveal RNA polymerase II located upstream of genes poised for rapid response upon S. cerevisiae stationary phase exit. Mol Cell. 2005, 18 (2): 171-183.View ArticlePubMedGoogle Scholar
- Cetin MS, Zhang C, Hutkins RW, Benson AK: Regulation of transcription of compatible solute transporters by the general stress sigma factor, sigmaB, in Listeria monocytogenes. J Bacteriol. 2004, 186 (3): 794-802.PubMed CentralView ArticlePubMedGoogle Scholar
- Moorhead SM, Dykes GA: Influence of the sigB gene on the cold stress survival and subsequent recovery of two Listeria monocytogenes serotypes. Int J Food Microbiol. 2004, 91 (1): 63-72.View ArticlePubMedGoogle Scholar
- Winder CL, Dunn WB, Schuler S, Broadhurst D, Jarvis R, Stephens GM, Goodacre R: Global metabolic profiling of Escherichia coli cultures: an evaluation of methods for quenching and extraction of intracellular metabolites. Anal Chem. 2008, 80 (8): 2939-2948.View ArticlePubMedGoogle Scholar
- Corbin RW, Paliy O, Yang F, Shabanowitz J, Platt M, Lyons CE, Root K, McAuliffe J, Jordan MI, Kustu S, et al.: Toward a protein profile of Escherichia coli: comparison to its transcription profile. Proc Natl Acad Sci USA. 2003, 100 (16): 9232-9237.PubMed CentralView ArticlePubMedGoogle Scholar
- Oltvai ZN, Barabasi AL: Systems biology. Life's complexity pyramid. Science. 2002, 298 (5594): 763-764.View ArticlePubMedGoogle Scholar
- Balazsi G, Barabasi AL, Oltvai ZN: Topological units of environmental signal processing in the transcriptional regulatory network of Escherichia coli. Proc Natl Acad Sci USA. 2005, 102 (22): 7841-7846.PubMed CentralView ArticlePubMedGoogle Scholar
- Arifuzzaman M, Maeda M, Itoh A, Nishikata K, Takita C, Saito R, Ara T, Nakahigashi K, Huang HC, Hirai A, et al.: Large-scale identification of protein-protein interaction of Escherichia coli K-12. Genome Res. 2006, 16 (5): 686-691.PubMed CentralView ArticlePubMedGoogle Scholar
- Su C, Peregrin-Alvarez JM, Butland G, Phanse S, Fong V, Emili A, Parkinson J: Bacteriome.org--an integrated protein interaction database for E. coli. Nucleic Acids Res. 2008, D632-636. 36 Database
- Jeong H, Tombor B, Albert R, Oltvai ZN, Barabasi AL: The large-scale organization of metabolic networks. Nature. 2000, 407 (6804): 651-654.View ArticlePubMedGoogle Scholar
- Covert MW, Knight EM, Reed JL, Herrgard MJ, Palsson BO: Integrating high-throughput and computational data elucidates bacterial networks. Nature. 2004, 429 (6987): 92-96.View ArticlePubMedGoogle Scholar
- Guimera R, Nunes Amaral LA: Functional cartography of complex metabolic networks. Nature. 2005, 433 (7028): 895-900.PubMed CentralView ArticlePubMedGoogle Scholar
- Ouzounis CA, Karp PD: Global properties of the metabolic map of Escherichia coli. Genome Res. 2000, 10 (4): 568-576.PubMed CentralView ArticlePubMedGoogle Scholar
- Saavedra S, Reed-Tsochas F, Uzzi B: A simple model of bipartite cooperation for ecological and organizational networks. Nature. 2009, 457 (7228): 463-466.View ArticlePubMedGoogle Scholar
- Barabasi AL, Albert R: Emergence of scaling in random networks. Science. 1999, 286 (5439): 509-512.View ArticlePubMedGoogle Scholar
- Clauset A, Newman ME, Moore C: Finding community structure in very large networks. Phys Rev E Stat Nonlin Soft Matter Phys. 2004, 70 (6 Pt 2): 066111-View ArticlePubMedGoogle Scholar
- Bascompte J, Jordano P, Melian CJ, Olesen JM: The nested assembly of plant-animal mutualistic networks. Proc Natl Acad Sci USA. 2003, 100 (16): 9383-9387.PubMed CentralView ArticlePubMedGoogle Scholar
- Csonka LN: Physiological and genetic responses of bacteria to osmotic stress. Microbiol Rev. 1989, 53 (1): 121-147.PubMed CentralPubMedGoogle Scholar
- Purvis JE, Yomano LP, Ingram LO: Enhanced trehalose production improves growth of Escherichia coli under osmotic stress. Appl Environ Microbiol. 2005, 71 (7): 3761-3769.PubMed CentralView ArticlePubMedGoogle Scholar
- Ling M, Allen SW, Wood JM: Sequence analysis identifies the proline dehydrogenase and delta 1-pyrroline-5-carboxylate dehydrogenase domains of the multifunctional Escherichia coli PutA protein. J Mol Biol. 1994, 243 (5): 950-956.View ArticlePubMedGoogle Scholar
- Richard HT, Foster JW: Acid resistance in Escherichia coli. Adv Appl Microbiol. 2003, 52: 167-186.View ArticlePubMedGoogle Scholar
- Klauck E, Typas A, Hengge R: The sigmaS subunit of RNA polymerase as a signal integrator and network master regulator in the general stress response in Escherichia coli. Sci Prog. 2007, 90 (Pt 2-3): 103-127.PubMedGoogle Scholar
- Stim-Herndon KP, Flores TM, Bennett GN: Molecular characterization of adiY, a regulatory gene which affects expression of the biodegradative acid-induced arginine decarboxylase gene (adiA) of Escherichia coli. Microbiology. 1996, 142: 1311-1320.View ArticlePubMedGoogle Scholar
- De Biase D, Tramonti A, Bossa F, Visca P: The response to stationary-phase stress conditions in Escherichia coli: role and regulation of the glutamic acid decarboxylase system. Mol Microbiol. 1999, 32 (6): 1198-1211.View ArticlePubMedGoogle Scholar
- Lin J, Lee IS, Frey J, Slonczewski JL, Foster JW: Comparative analysis of extreme acid survival in Salmonella typhimurium, Shigella flexneri, and Escherichia coli. J Bacteriol. 1995, 177 (14): 4097-4104.PubMed CentralPubMedGoogle Scholar
- Hopkin KA, Papazian MA, Steinman HM: Functional differences between manganese and iron superoxide dismutases in Escherichia coli K-12. J Biol Chem. 1992, 267 (34): 24253-24258.PubMedGoogle Scholar
- Benov LT, Fridovich I: Escherichia coli expresses a copper- and zinc-containing superoxide dismutase. J Biol Chem. 1994, 269 (41): 25310-25314.PubMedGoogle Scholar
- Li Y, Odumeru JA, Griffiths M, McKellar RC: Effect of environmental stresses on the mean and distribution of individual cell lag times of Escherichia coli O157:H7. Int J Food Microbiol. 2006, 110 (3): 278-285.View ArticlePubMedGoogle Scholar
- Stadtman ER: Protein oxidation and aging. Science. 1992, 257 (5074): 1220-1224.View ArticlePubMedGoogle Scholar
- Mecsas J, Rouviere PE, Erickson JW, Donohue TJ, Gross CA: The activity of sigma E, an Escherichia coli heat-inducible sigma-factor, is modulated by expression of outer membrane proteins. Genes Dev. 1993, 7 (12B): 2618-2628.View ArticlePubMedGoogle Scholar
- Yura T, Kawasaki Y, Kusukawa N, Nagai H, Wada C, Yano R: Roles and regulation of the heat shock sigma factor sigma 32 in Escherichia coli. Antonie Van Leeuwenhoek. 1990, 58 (3): 187-190.View ArticlePubMedGoogle Scholar
- De Las Penas A, Connolly L, Gross CA: SigmaE is an essential sigma factor in Escherichia coli. J Bacteriol. 1997, 179 (21): 6862-6864.PubMed CentralPubMedGoogle Scholar
- Nachin L, Nannmark U, Nystrom T: Differential roles of the universal stress proteins of Escherichia coli in oxidative stress resistance, adhesion, and motility. J Bacteriol. 2005, 187 (18): 6265-6272.PubMed CentralView ArticlePubMedGoogle Scholar
- Gaitanaris GA, Vysokanov A, Hung SC, Gottesman ME, Gragerov A: Successive action of Escherichia coli chaperones in vivo. Mol Microbiol. 1994, 14 (5): 861-869.View ArticlePubMedGoogle Scholar
- Patridge EV, Ferry JG: WrbA from Escherichia coli and Archaeoglobus fulgidus is an NAD(P)H:quinone oxidoreductase. J Bacteriol. 2006, 188 (10): 3498-3506.PubMed CentralView ArticlePubMedGoogle Scholar
- Keseler IM, Collado-Vides J, Gama-Castro S, Ingraham J, Paley S, Paulsen IT, Peralta-Gil M, Karp PD: EcoCyc: a comprehensive database resource for Escherichia coli. Nucleic Acids Res. 2005, D334-337. 33 Database
- Skibinski DA, Golby P, Chang YS, Sargent F, Hoffman R, Harper R, Guest JR, Attwood MM, Berks BC, Andrews SC: Regulation of the hydrogenase-4 operon of Escherichia coli by the sigma(54)-dependent transcriptional activators FhlA and HyfR. J Bacteriol. 2002, 184 (23): 6642-6653.PubMed CentralView ArticlePubMedGoogle Scholar
- Island MD, Kadner RJ: Interplay between the membrane-associated UhpB and UhpC regulatory proteins. J Bacteriol. 1993, 175 (16): 5028-5034.PubMed CentralPubMedGoogle Scholar
- Govantes F, Orjalo AV, Gunsalus RP: Interplay between three global regulatory proteins mediates oxygen regulation of the Escherichia coli cytochrome d oxidase (cydAB) operon. Mol Microbiol. 2000, 38 (5): 1061-1073.View ArticlePubMedGoogle Scholar
- Brondsted L, Atlung T: Anaerobic regulation of the hydrogenase 1 (hya) operon of Escherichia coli. J Bacteriol. 1994, 176 (17): 5423-5428.PubMed CentralPubMedGoogle Scholar
- Luna-Chavez C, Iverson TM, Rees DC, Cecchini G: Overexpression, purification, and crystallization of the membrane-bound fumarate reductase from Escherichia coli. Protein Expr Purif. 2000, 19 (1): 188-196.View ArticlePubMedGoogle Scholar
- Campbell JW, Morgan-Kiss RM, Cronan JE: A new Escherichia coli metabolic competency: growth on fatty acids by a novel anaerobic beta-oxidation pathway. Mol Microbiol. 2003, 47 (3): 793-805.View ArticlePubMedGoogle Scholar
- Jung H, Buchholz M, Clausen J, Nietschke M, Revermann A, Schmid R, Jung K: CaiT of Escherichia coli, a new transporter catalyzing L-carnitine/gamma-butyrobetaine exchange. J Biol Chem. 2002, 277 (42): 39251-39258.View ArticlePubMedGoogle Scholar
- Peekhaus N, Conway T: What's for dinner?: Entner-Doudoroff metabolism in Escherichia coli. J Bacteriol. 1998, 180 (14): 3495-3502.PubMed CentralPubMedGoogle Scholar
- Yew WS, Gerlt JA: Utilization of L-ascorbate by Escherichia coli K-12: assignments of functions to products of the yjf-sga and yia-sgb operons. J Bacteriol. 2002, 184 (1): 302-306.PubMed CentralView ArticlePubMedGoogle Scholar
- Cho BK, Knight EM, Barrett CL, Palsson BO: Genome-wide analysis of Fis binding in Escherichia coli indicates a causative role for A-/AT-tracts. Genome Res. 2008, 18 (6): 900-910.PubMed CentralView ArticlePubMedGoogle Scholar
- Finkel SE, Johnson RC: The Fis protein: it's not just for DNA inversion anymore. Mol Microbiol. 1992, 6 (22): 3257-3265.View ArticlePubMedGoogle Scholar
- Wei Y, Newman EB: Studies on the role of the metK gene product of Escherichia coli K-12. Mol Microbiol. 2002, 43 (6): 1651-1656.View ArticlePubMedGoogle Scholar
- Jung IL, Oh TJ, Kim IG: Abnormal growth of polyamine-deficient Escherichia coli mutant is partially caused by oxidative stress-induced damage. Arch Biochem Biophys. 2003, 418 (2): 125-132.View ArticlePubMedGoogle Scholar
- Stathopoulos C, Hendrixson DR, Thanassi DG, Hultgren SJ, St Geme JW, Curtiss R: Secretion of virulence determinants by the general secretory pathway in gram-negative pathogens: an evolving story. Microbes Infect. 2000, 2 (9): 1061-1072.View ArticlePubMedGoogle Scholar
- Francetic O, Pugsley AP: The cryptic general secretory pathway (gsp) operon of Escherichia coli K-12 encodes functional proteins. J Bacteriol. 1996, 178 (12): 3544-3549.PubMed CentralPubMedGoogle Scholar
- Ganduri YL, Sadda SR, Datta MW, Jambukeswaran RK, Datta P: TdcA, a transcriptional activator of the tdcABC operon of Escherichia coli, is a member of the LysR family of proteins. Mol Gen Genet. 1993, 240 (3): 395-402.PubMedGoogle Scholar
- Koch D, Nies DH, Grass G: The RcnRA (YohLM) system of Escherichia coli: a connection between nickel, cobalt and iron homeostasis. Biometals. 2007, 20 (5): 759-771.View ArticlePubMedGoogle Scholar
- Stewart EJ, Madden R, Paul G, Taddei F: Aging and death in an organism that reproduces by morphologically symmetric division. PLoS Biology. 2005, 3 (2): e45-PubMed CentralView ArticlePubMedGoogle Scholar
- Anjum MF, Lucchini S, Thompson A, Hinton JC, Woodward MJ: Comparative genomic indexing reveals the phylogenomics of Escherichia coli pathogens. Infect Immun. 2003, 71 (8): 4674-4683.PubMed CentralView ArticlePubMedGoogle Scholar
- Eriksson S, Lucchini S, Thompson A, Rhen M, Hinton JC: Unravelling the biology of macrophage infection by gene expression profiling of intracellular Salmonella enterica. Mol Microbiol. 2003, 47 (1): 103-118.View ArticlePubMedGoogle Scholar
- Pin C, Reuter M: Use of genomic DNA control features and predicted operon structure in microarray data analysis: ArrayLeaRNA - a Bayesian approach. BMC Bioinformatics. 2007, 8 (1): 455-PubMed CentralView ArticlePubMedGoogle Scholar
- Gama-Castro S, Jimenez-Jacinto V, Peralta-Gil M, Santos-Zavaleta A, Penaloza-Spinola MI, Contreras-Moreira B, Segura-Salazar J, Muniz-Rascado L, Martinez-Flores I, Salgado H: RegulonDB (version 6.0): gene regulation model of Escherichia coli K-12 beyond transcription, active (experimental) annotated promoters and Textpresso navigation. Nucleic Acids Res. 2008, D120-124. 36 DatabaseGoogle Scholar
- KEGG maps. http://www.genome.ad.jp/kegg/pathway.html
- CMR-TIGR database. http://cmr.tigr.org/tigr-scripts/CMR/CmrHomePage.cgi
- PAJEK. http://vlado.fmf.uni-lj.si/pub/networks/pajek/
- Cytoscape. http://cytoscape.org/