- Research article
- Open Access
Proteomic analysis of iron acquisition, metabolic and regulatory responses of Yersinia pestis to iron starvation
BMC Microbiology volume 10, Article number: 30 (2010)
The Gram-negative bacterium Yersinia pestis is the causative agent of the bubonic plague. Efficient iron acquisition systems are critical to the ability of Y. pestis to infect, spread and grow in mammalian hosts, because iron is sequestered and is considered part of the innate host immune defence against invading pathogens. We used a proteomic approach to determine expression changes of iron uptake systems and intracellular consequences of iron deficiency in the Y. pestis strain KIM6+ at two physiologically relevant temperatures (26°C and 37°C).
Differential protein display was performed for three Y. pestis subcellular fractions. Five characterized Y. pestis iron/siderophore acquisition systems (Ybt, Yfe, Yfu, Yiu and Hmu) and a putative iron/chelate outer membrane receptor (Y0850) were increased in abundance in iron-starved cells. The iron-sulfur (Fe-S) cluster assembly system Suf, adapted to oxidative stress and iron starvation in E. coli, was also more abundant, suggesting functional activity of Suf in Y. pestis under iron-limiting conditions. Metabolic and reactive oxygen-deactivating enzymes dependent on Fe-S clusters or other iron cofactors were decreased in abundance in iron-depleted cells. This data was consistent with lower activities of aconitase and catalase in iron-starved vs. iron-rich cells. In contrast, pyruvate oxidase B which metabolizes pyruvate via electron transfer to ubiquinone-8 for direct utilization in the respiratory chain was strongly increased in abundance and activity in iron-depleted cells.
Many protein abundance differences were indicative of the important regulatory role of the ferric uptake regulator Fur. Iron deficiency seems to result in a coordinated shift from iron-utilizing to iron-independent biochemical pathways in the cytoplasm of Y. pestis. With growth temperature as an additional variable in proteomic comparisons of the Y. pestis fractions (26°C and 37°C), there was little evidence for temperature-specific adaptation processes to iron starvation.
Yersinia pestis, a Gram-negative bacterium, is the causative agent of the bubonic and pneumonic plague. The pathogenic lifestyle of this microbe involves two distinct life stages, one in the flea vector, the other in mammalian hosts, primarily rodents . Genome sequencing and analyses have been completed for four major Y. pestis biovars, including the chromosome  and three virulence/transmission-associated plasmids [3, 4] of the KIM strain, which belongs to the biovar mediaevalis. In addition to plasmid-encoded virulence factors, the genetically unstable chromosomal 102-kb pgm locus is also important for full virulence of Y. pestis in mammals and for its transmission via blocked fleas [5, 6]. This locus encodes the yersiniabactin-dependent iron transport (Ybt) system and the hemin storage (Hms)-dependent biofilm system. Biofilm formation allows colonization of the flea proventriculus causing blockage which in turn induces active feeding behavior [7, 8].
Efficient iron acquisition systems are critical to the ability of Yersinia pestis to infect, spread and grow in mammalian hosts, because iron is sequestered and is considered part of the innate host immune defence against invading pathogens . The Ybt system includes a series of enzymes responsible for the siderophore's biosynthesis. Following secretion and iron chelation, the iron/yersiniabactin complex is bound by the outer membrane (OM) receptor Psn and transferred into the periplasm via TonB-dependent energy transmission. Binding of the complex to the periplasmic surface of the inner membrane-localized ATP-binding cassette (ABC) transporter YbtP/YbtQ, which contains two permease and two ATP-binding domains, initiates iron import into the cytoplasm. A functional Ybt transporter is required for bacterial infection by subcutaneous routes and important for iron acquisition in early stages of the bubonic plague in mice [10–12]. The manganese- and iron-specific ABC transporter Yfe is also important for full Y. pestis virulence according to data from a bubonic plague mouse model . Other ABC transporters for iron (Yfu and Yiu) and hemin (Hmu) were functionally characterized, but were not found to be required for virulence in the mouse model [14–16]. The transporters Yfe and Feo serve somewhat redundant roles in ferrous iron uptake under microaerophilic growth conditions . Genomic analysis suggests the existence of other transporters and OM receptors for iron/siderophores but have not been functionally characterized to date [2, 18].
The ferric uptake regulator Fur is a dominant transcription factor controlling iron assimilation in many bacterial species . Iron transporters, iron storage proteins and some proteins requiring iron cofactors for function feature conserved binding sites for Fur upstream of their genes. These sites are termed Fur-boxes . Under iron-rich conditions, Fur binds Fe2+, assumes a conformation resulting in tight binding to the Fur-box and repression of gene transcription . Low iron levels result in the loss of this metal ion and allosteric conformational changes in Fur that alleviate transcriptional repression. Positive regulation by Fur in Gram-negative bacteria seems to be primarily indirect via negative transcriptional control of small RNAs [22–24]. The Fur-dependent E. coli small RNA is termed RyhB, and two RyhB orthologs were discovered in the Y. pestis CO92 genome . E. coli RyhB controls the expression of genes whose products store iron or contain iron cofactors such as heme and iron-sulfur (Fe-S) clusters [25, 26]. The Fe-S cluster proteins FNR, IscR and SoxR are important global regulators . Some enzymes with functions in diverse branches of cellular energy metabolism [28–30] also contain Fe-S clusters. Thus, widespread changes in the proteome and metabolome of bacteria occur due to iron starvation. In E. coli, the Fur regulon was reported to overlap functionally with the regulons of the catabolite repressor protein  and the oxidative stress regulator OxyR . These overlaps suggest intriguing networks of metabolic inter-connectivity, allowing bacterial survival and growth under iron-deficient conditions. Iron homeostasis has not been thoroughly investigated to date in Y. pestis. Human plasma is an iron-limiting environment, and growth condition-dependent comparisons of Y. pestis transcriptional patterns have included growth in human plasma . Many genes involved in iron acquisition and storage and the response to oxidative stress were found to be differentially expressed [33–35]. There was reasonably good agreement between the aforementioned studies and DNA microarray data comparing a Δfur mutant with its Fur+ parent strain .
Our objective was to assess iron acquisition and intracellular consequences of iron deficiency in the Y. pestis strain KIM6+ at two physiologically relevant temperatures (26°C and 37°C). Bacterial cultures weregrown in the absence and presence of 10 μM FeCl3. Cell lysis was followed by fractionation into periplasm, cytoplasm and mixed membranes. Upon pooling of two biological replicate samples for each growth condition, proteins were analysed by differential 2D gel display. Considering the high number of distinct experimental groups (fractions) and at least three required technical 2D gel replicates per experiment for meaningful statistical analyses, the rationale for sample pooling was to keep 2D gel runs at a manageable level. Sample pooling has the disadvantage that information on quantitative variability of proteins comparing biological replicates is not obtained. Proteome analysis was performed for two equivalent growth time points (13-15 h), which represented the stationary phase for iron-replete conditions (OD600 ~2.0) and growth arrest at the OD600 of ~0.8 for iron-deficient conditions.
Bacterial strains and culture conditions
The Y. pestis strain KIM6+ used in this study is an avirulent derivative of the fully virulent KIM strain, which was cured of the pCD1 plasmid but retained the chromosomal pgm locus and the plasmids pMT1 and pPCP1 . We used strain maintenance and cell growth procedures and verified the presence of the pgm locus on Congo Red agar as described previously . Bacterial colonies were grown on tryptose blood agar at 30°C, harvested after 48 h and stored at -80°C. Aliquots of these cell stocks were used to grow 5-10 mL cultures in chemically defined PMH2 medium  supplemented with 10 μM FeCl3, followed by dilution to an OD600 of ~0.05 with 0.3-1 L of PMH2. PMH2 was deferrated by incubation with Chelex-100 resin overnight at 4°C . Two passages of cell stocks in 10-30 mL of this medium were followed by dilution to an OD600 of ~0.05 with 0.3-1 L of deferrated PMH2. Overnight cell cultures (13-15 h) reached OD600s of ca. 1.8-2.5 and 0.6-0.9 for iron-rich and iron-deficient cells, respectively. Chelex-100 treatment was previously shown to reduce contaminating iron levels to 0.2-0.3 μM, and replenishment of this medium with 10 μM FeCl3 resulted in full recovery of the normal Y. pestis growth rate and yield. Chelex-100 treatment likely removes some other metal ions as well. However, in contrast to iron, addition of Mn, Zn and Cu did not enhance the observed growth rate or yield. Cell pellets were harvested by centrifugation at 8,000 × g for 15 min at 4°C and washed with ca. 30 volumes of 33 mM K2HPO4 (pH 7.5).
Subcellular fractionation of Y. pestis cells
K2HPO4-washed Y. pestis cells were subjected to a lysozyme/EDTA spheroplasting method, followed by lysis of spheroplasts via sonication in a hypotonic buffer as previously described [38, 39]. Soluble periplasmic and cytoplasmic fractions were exchanged into buffer A (25 mM NH4HCO3, 1 mM Na-EDTA and 1 mM benzamidine) and concentrated to 2-5 mg/mL protein at 3,000 × g using membrane filtration units (NMWL ~10,000). Protein concentrations were measured with the bicinchoninic acid assay, unless stated otherwise. Mixed membrane pellets were isolated from spheroplast lysates by centrifugation at 50,000 × g for 1 h at 4°C. These pellets were homogenized in 0.25 M sucrose, 150 mM NaCl, 10 mM Tris-OAc, pH 7.8, 5 mM Na-EDTA, 0.2 mM DTT, 10 μg/ml Leupeptin, 5 μg/ml Pepstatin, 10 μg/ml Nα-p-Tosyl-L-arginine methyl ester and 2 mM PMSF (ca. 10 mL/g pellet weight), and washed to remove most soluble protein contaminants. Sodium bromide (2.5 M final concentration) was added to the suspended membrane pellet, stirred for 1 h at 20°C and centrifuged at 50,000 × g for 1 h at 4°C. Insoluble pellets were then extracted with an ice-cold solution of 0.18 M Na2CO3, pH 11.3, 50 mM DTT, 1 mM CaCl2, 1 mM MgCl2 and 1 mM MnCl, stirred for 1 h and spun at 50,000 × g for 1 h at 4°C. The supernatants were not processed further. The membrane protein-enriched pellets were solubilised with 8 M urea, 2 M thiourea, 1% (w/v) amidosulfobetaine 14, 2 mM tributylphosphine and 0.5% Bio-Lyte pH 3-10 carrier ampholytes for analysis in 2D gels. Following incubation for 30 min at 20°C and centrifugation at 16,200 × g for 15 min, soluble aliquots of the extract, termed urea/amidosulfobetaine 14-extracted membrane (usb-MBR) fraction, were run in SDS-PAGE gels. Protein amounts were estimated from Coomassie Brilliant Blue G-250 (CBB)-stained band intensities. Integral OM proteins were more enriched than lipoproteins and integral IM proteins. The latter proteins tend to resist solubilisation or re-precipitate during the IEF separation step.
Spectrophotometric enzyme assay were performed in 96-well microtiter plates using soluble fractions of Y. pestis cell lysates. Cells were harvested during the mid-exponential phase (OD600 ~0.5-0.7) and stationary phase (OD600 ~1.8-2.1) time points from iron-replete conditions in PMH2 medium at 26°C. Cells from two equivalent time points (OD600 ~0.4-0.6 and OD600 ~0.7-0.9, respectively) were harvested when growth occurred in iron-free media at 26°C. In a 100 mM NaH2PO4 buffer (pH 6.5) with 75 μg/mL lysozyme, 1 mM Na-EDTA, 1 mM PMSF and 0.1% Triton X-100, cells were subjected to pressure cycling (12 cycles of 35 kPsi for 5 sec and 0 Psi for 20 sec). After the addition of 5 mM MgCl, 10 μg/mL DNAse I and 10 μg/mL RNAse cell lysates were incubated for 45 min at 20°C and centrifuged at 16,200 × g for 30 min at 4°C. The supernatants were frozen at -80°C in the presence of 15% glycerol until used for enzyme assays.
Pyruvate oxidase activities were determined using sodium pyruvate and Na3Fe(CN)6 as substrates and monitoring the rate of absorbance decrease of Na3Fe(CN)6 at A450 (E450 = 0.218 cm-1 mM-1) while incubating at 30°C. Cell lysates were adjusted to ~0.4 mg/mL protein and assayed at pH 6.0 in 120 mM NaH2PO4 as previously reported , with one modification: 1% Nonidet-P40 was added to the assay buffer, because this detergent increased the activity of PoxB. Aconitase activities were determined using a coupled enzyme assay converting citrate to isocitrate and, via activity of supplemented isocitric dehydrogenase (IcdA), isocitrate to α-ketoglutarate as previously described  (assay kit from Cayman Chemicals, Ann Arbor, MI). The rate of absorbance increases at A340 (E340 = 0.00622 cm-1 μM-1) due to formation of the IcdA product NADPH was monitored while incubating at 37°C. To increase the pH and stabilize aconitase, crude extracts were exchanged into 50 mM Tris-HCl (pH 7.5), 0.6 mM MnCl2 and 2 mM sodium citrate, and adjusted to ~0.5 mg/mL protein. To distinguish the aconitase/IcdA activity from other NADP+-dependent oxidoreductive enzymes, the aconitase inhibitor oxalomalate was added at a 18.7 mM concentration to the assay mixture. Catalase activities were determined assessing the peroxidatic function with methanol as a substrate and formaldehyde as a product in the presence of optimal concentrations of H2O2 at 22°C. Crude extracts were diluted to ~0.15 mg/mL protein, and formaldehyde was measured colorimetrically at A540 in an endpoint assay via addition of the chromogen 4-amino-3-hydrozino-5-mercapto-1,2,4-triazole, as previously described  (assay kit from Cayman Chemicals). Superoxide dismutase (SOD) activities were determined using a coupled enzyme assay measuring the dismutation of the superoxide radical formed by xanthine oxidase at 22°C. The reaction was coupled to the conversion of a tetrazolium salt to formazan whose absorbance was measured at A450 in an endpoint assay as described  (assay kit from Cayman Chemicals). Cell lysates were diluted to ~1.1 μg/mL protein to measure SOD activities.
Protein separation and differential display in 2D gels
Equal protein amounts from two biological replicates of periplasmic and cytoplasmic fractions were combined and diluted in a 1:5 to 1:10 ratio with RB buffer, which contained 8 M urea, 2 M thiourea, 4% (w/v) CHAPS, 18 mM DTT and 0.5% (v/v) Bio-Lyte pH 3-10 carrier ampholytes. Equal protein amounts from solubilised biological replicates of mixed membrane fractions were also combined. The rationale for sample pooling is described at the end of the 'Background' section. Circa 75 μg protein for Sypro Ruby®-stained gels and 130 μg for Coomassie Brilliant Blue G250 (CBB)-stained gels were loaded via rehydration loading onto 24 cm IPG gel strips (pH ranges 4-7 and 3-10) and separated in the 1st dimension as previously described . Established methods were also used for 2nd dimension slab gel electrophoresis (25 × 19.5 × 0.15 cm), gel staining with CBB, scanning and gel image import into the analysis software Proteomweaver v.4.0 . The scope of differential 2D display analysis was extensive, with three subcellular fractions and four growth conditions (fourteen experimental groups for seven group-to-group comparisons, among them two analyses for the periplasmic fraction with 2D gels in the pH ranges 4-7 and 6.5-10). Software-assisted gel image analysis included spot matching, pre-match and post-match spot normalization and spot intensity averaging. The analysis mode did not require internal standards for spot normalization. The Mann-Whitney Test was used for statistical significance analysis of spot abundance changes. It is a non-parametric two sample distribution-free t-test and assesses whether two independent samples of observations come from the same distribution: , where n1 and n2 are numbers of observations in the samples and R1 is the sum of the ranks of the observations in sample 1. P-values determined by this test are based on 3 ≤ n ≤ 5 observations, which reflect 2D spot intensity data from an equal number of replicate gels. Provided that spot abundance ratios were ≥1.5, p-values < 0.02 were considered statistically significant. Protein spots observed in only one the two sample groups required spot matches among at least three technical replicates, but p-values could not be determined.
Mass spectrometry and bioinformatic protein analysis
Nearly all spots derived from 2D gels of the three Y. pestis subcellular fractions were analyzed by mass spectrometry (MS) two or more times. This was necessary in order to link each spot abundance change unambiguously to identification of a distinct protein; limitation of spot resolution in 2D gels is a known problem when the analyzed samples are highly complex. Prerequisites for confident spot identification were known protein identities of surrounding spots with equal or higher abundance and the comparison of Mascot scores in those spots. Methods for spot cutting and protein digestion with trypsin were reported previously . Peptide digests were analyzed using a MALDI-TOFTOF mass spectrometer (4700 Proteomics Analyzer, Applied Biosystems) and a nano-electrospray LC-MS/MS system (LTQ ion trap mass spectrometer, Thermo-Finnigan, San Jose, CA) equipped with an Agilent 1100 series solvent delivery system (Agilent, Palo Alto, CA). Reversed phase peptide separations for LC-MS/MS analysis were performed at nanoflow rates (350 nL/min). Technical details of MS and MS2 analysis methods have been described . The data were searched against the latest release of the Y. pestis KIM strain subset of the NCBInr database, using the Mascot searching engine v.2.1 (Matrix Science, London, UK). Carbamidomethyl was invariably selected as a fixed modification and one missed tryptic cleavage was allowed. MALDI search parameters (+1 ions) included mass error tolerances of ± 100 ppm for peptide precursor ions and ± 0.2 Da for fragment ions. LTQ ion trap search parameters (+1, +2 and +3 ions) included mass error tolerances of ± 1.4 Da for peptide precursor ions and ± 0.5 Da for fragment ions. Protein identifications were accepted as significant when Mascot protein scores >75 were obtained. Using a randomized decoy database, setting a default significance threshold of 0.05 in the Mascot algorithm and requiring two peptide e-values < 0.1 per protein identification, the false positive rate of proteins by LC-MS/MS was estimated to be <0.5%. Bioinformatic predictions of Y. pestis KIM iron transporters and binding proteins, of transmembrane domains, of protein export signal motifs and of β-barrel OM protein motifs were derived from the algorithms utilized in TransportDB http://www.membranetransport.org, TMHMM and SignalP http://www.cbs.dtu.dk/services and PRED-TMBB , respectively.
Using subcellular fractionation and differential 2D gel display to assess the response of Y. pestis to iron starvation
Three subcellular fractions of the Y. pestis strain KIM6+, a periplasmic, a cytoplasmic and a membrane fraction enriched in integral OM proteins, were isolated from cells cultured at two growth temperatures (26°C and 37°C), without FeCl3 or supplemented with 10 μM FeCl3. Data published on the periplasmic and membrane proteomes of this strain facilitated the study [39, 44, 47]. Extensive protein identification efforts from soluble cytoplasmic fractions were performed for this study. We estimated the coverage of subcellular proteomes by comparing predicted localizations of experimentally identified proteins with those in silico assigned to the ORFs annotated in the Y. pestis KIM genome. The algorithm used here was PSORTb. Limiting this to the proteins clearly assigned to distinct 2D gel spots, the coverage was roughly 25% for the periplasm, 20% for the cytoplasm, 1% for the IM and 25% for the OM. The prediction of subcellular proteomes is incomplete because assignments are not made for all ORFs (e.g., 45% of the 4086 Y. pestis KIM ORFs using PSORTb). Many proteins were not profiled quantitatively. However, subcellular fractionation allowed us to increase the number of surveyed proteins and the dynamic range of abundance measurements.
Proteome profiles derived from iron-starved and iron-replete growth conditions, often abbreviated as '-Fe and +Fe conditions' from here on, were compared. When cells were harvested, they were in the stationary phase for at least 3 h (+Fe conditions) or near complete growth arrest due to the lack of iron (-Fe conditions). This is visualized in growth curves at the temperatures of 37°C and 26°C provided in the graphics of Additional File 1. Cells grown in the absence of iron at 37°C consistently reached a 10-20% higher OD600 than those grown at 26°C. Earlier growth time points (exponential phase) would have been of interest, but were not included due to already extensive proteomic profiling efforts. Our rationale was that the greater difference in cell doubling times during the exponential phase (-Fe vs. +Fe) would have confounded identification of iron starvation-specific protein changes more than that for the late growth stage.
Differential display experiments were focused on the pH range 4-7 in 2D gels because the majority of mature proteins have pI values ranging from 4 to 7. The removal of basic N-terminal signal sequences from exported proteins, which are displayed in the periplasmic and mixed membrane fractions, often result in a shift towards more acidic pIs. Few integral IM proteins, typically those with low Mr values, were quantitatively profiled because TMD proteins are too hydrophobic to be sufficiently solubilised or resolved as spots in 2D gels. Periplasmic fractions consistently showed contamination with cytoplasmic proteins which was attributed to partial lysis of Y. pestis spheroplasts during the fractionation. The outcome of this cross-contamination was a moderately decreased depth of analysis for periplasmic proteins. Of nearly 250 statistically significant spot abundance changes with confident protein identifications, observed at 26°C and/or 37°C, some were associated with spot trains. Particularly the 2D profile of the usb-MBR fraction featured extensive spot trains. Based on MS2 data from MALDI-TOFTOF and ESI-ion trap experiments, we have evidence that Asn and Gln amino acid side chain deamidations, which lead to acidic 2D spot shifts of proteins, account for many of the spot trains . The Table of Additional File 2 lists all significant spot abundance changes (-Fe vs. +Fe conditions). Comprehensive MS and MS2 datasets are provided in the Table of Additional File 3. The concise protein lists in the Tables 1, 2 and 3 are of particular interest in the context of iron homeostasis. Only if protein abundance ratios differed substantially comparing the -Fe vs. +Fe datasets at 26°C and 37°C, the temperature dependency was pointed out in the following paragraphs.
Y. pestis iron acquisition systems
Proteomic profiling of characterized Y. pestis iron/siderophore and heme transporters (Ybt, Yfe, Yfu, Yiu and Hmu) was in good agreement with negative regulation of the respective operons by Fur and iron [15, 16, 20, 49, 50]. The subscript number following a protein name represents the spot number displayed in Figures 1, 2, 3 and 4, and is also denoted in the left-most column of Tables 1, 2 and 3. Periplasmic binding proteins of four of the ABC transporters (YfeA#68, YfuA#65, YiuA#82 and HmuT#56; Figures 1 and 2) were increased in abundance in iron-starved cells. The integral IM proteins YbtP and YbtQ were identified from streaky 2D spots of the usb-MBR fraction of iron-depleted cells, but could not be differentially quantitated. Two of these five transporters have an OM receptor responsible for iron/yersiniabactin or heme uptake (Psn#102 and HmuR#95, respectively; Figure 3), both of which were increased in iron-starved cells. Y0850#96 (Figure 3) is hypothesized to be a TonB-dependent OM receptor with Fe3+/siderophore uptake activity. This protein was also more abundant in iron-depleted cells. Detection in the usb-MBR fraction, its Mr of ca. 75-85 kDa and the presence of a highly conserved Fur-box upstream of the gene's transcriptional start site (AATGATAATTGATATCATT, -100 to -82) with a position weight matrix score of 13.2 using the patser-matrix tool  further supported the assignment as a Fur-regulated TonB-dependent OM receptor. Fur#18 was also detected in the cytoplasm, but not altered in abundance (Figure 4).
Abundance increases in iron-starved cells were observed for the multifunctional yersiniabactin synthase subunits HMWP1 and HMWP2 (products of the irp1 and irp2 genes, respectively) and other enzymes contributing to yersiniabactin biosynthesis (YbtS#73, YbtT#75, YbtE#76 and YbtU#74). The high Mr proteins HMWP1 and HMWP2 were reliably quantitated only from SDS-PAGE gels (data not shown). The ysu locus encodes an OM receptor (YsuR/Y2633), an ABC transporter (Y2634-Y2637) and a suite of siderophore biosynthetic enzymes (Y2638-Y2641). Two subunits, Y2638#78 (Figure 1) and YsuR#104 (Figure 3) were of low abundance and detected only in iron-starved cells at 26°C. Biosynthesis of a Ysu siderophore has not been proven, and a siderophore biosynthetic pseudogene precedes the y2633-y2637 locus . The OM β-barrel ferrichrome receptor FcuA#103 (Y2556) was identified as a protein of moderate abundance in usb-MBR fractions at 26°C (Figure 3) and 37°C, but not significantly altered in abundance comparing -Fe vs. +Fe conditions. Many membrane proteins ascribed to have putative functions in iron transport were not detected, e.g. the OM receptors Y3948 and IutA/Y3385 and the transport systems FitA-D (Y4043-Y4046), Y2837-Y2842 and FepB/Y3477. Our data support the notion of a hierarchy of iron (Fe3+)/siderophore transporters , with the Ybt and Yfe systems being dominant compared to the Yfu, Yiu and Hmu systems. Periplasmic subunits of two ferrous iron (Fe2+) transporters, EfeO/Y2451 and Y2368, were also profiled in 2D gels (Figure 1). The low Mr protein Y2368#72 was increased in iron-starved cells at 37°C. The tripartite Fe2+ transport protein EfeO#77 was increased in abundance in iron-starved cells at 26°C.
The energy metabolism of Y. pestis is affected by iron starvation
Lower growth rates of Y. pestis in deferrated medium followed by growth arrest at OD600s between 0.5 and 0.9 suggest perturbations of energy generation pathways. Many oxidoreductive processes are catalyzed by enzymes containing Fe-S clusters or heme, and we sought to understand the consequences of limited iron availability as it pertains to the Y. pestis energy metabolism. The EcoCyc database http://www.ecocyc.org with its extensive data on E. coli energy metabolic pathways and iron cofactors of proteins was a useful resource in this context. Y. pestis aconitases A and B (AcnA#34 and AcnB#8; Figure 4) have functions in the TCA cycle and were decreased in abundance or detected only in iron-starved cells. So were subunits of two other TCA cycle enzymes harboring Fe-S clusters (SdhA#43 and FumA#11; Figure 4). Some TCA cycle enzymes devoid of Fe-S clusters were decreased at moderate levels under -Fe conditions (IcdA#26, SucA#42, SucD#41 and SucB#111; Figure 4). Strongly decreased abundances were denoted for AceA#2 and AceB#1 (Figure 4), enzymes which catalyze the glyoxalate bypass reaction of the TCA cycle and are regulated by the catabolite repressor protein (CRP). Glycerol kinase, also regulated by CRP, was more moderately decreased in iron-starved cells (GlpK#3, Figure 4). GlpK catalyzes the rate-limiting step of glycerol utilization and feeds its metabolites into the glycolytic pathway. CRP#91 itself was identified with low abundance in the periplasmic fraction (Figure 2). In summary, the data suggested reduced pyruvate metabolism via the citrate cycle when iron resources are exhausted in Y. pestis cells. Aconitase activity assays supported this assumption; the reaction rates were 2.8-fold and 2-fold higher in lysates derived from iron-replete cells vs. those from iron-starved cells at 26°C (stationary and exponential phase, respectively; Table 4).
The question arose whether iron-starved Y. pestis cells activated a different metabolic route of pyruvate degradation able to produce reducing equivalents (NADH and UQH2) for the electron transport chain. Pyruvate oxidase (PoxB) degrades pyruvate to acetate and is a flavin-dependent, iron-independent enzyme that generates UQH2 . The pyruvate oxidase pathway indeed appeared to be important, as judged by the strong abundance increase of PoxB#39 (Figure 4) under -Fe conditions. The flavin cofactor may be recruited from redox activities of two flavodoxins. FldA3#44 was quite abundant and moderately increased in iron-depleted cells (Figure 4). FldA was identified in faint 2D spots and not reproducibly quantitated. PoxB activity measurements revealed excellent correlation between enhanced abundances and increased reaction rates in iron-starved cells. PoxB activities were 5.3-fold and 7.8-fold higher in lysates of iron-starved cells than in lysates of iron-replete cells at 26°C (stationary and exponential phase, respectively; Table 4).
Electron transport chains are localized in the IM, a fact that compromised the analysis of subunits of these IM protein complexes in 2D gels. NuoCD#99, a peripheral membrane protein of the NADH:ubiquinone oxidoreductase, was moderately decreased in abundance in iron-depleted cells (Figure 3). The E. coli NuoCD sub-complex is important for binding of some of the six Nuo-integrated Fe-S clusters . Subunits of Fe-S cluster proteins with roles in two anaerobic energy metabolism branches were also less abundant in iron-depleted cells. This pertained to PflB#37 and YfiD#19, proteins of the formate-pyruvate lyase complex, and FrdA#6, which is part of the terminal electron acceptor fumarate reductase (Figure 4). Decreased abundances of metabolically active Fe-S cluster enzymes were a notable feature of iron-starved Y. pestis proteome profiles, while the abundance and activity of PoxB suggested that this enzyme was important to maintain the aerobic energy metabolism and iron cofactor-independent generation of UQH2 in iron-deficient Y. pestis cells.
Oxidative stress response in Y. pestis under iron starvation conditions
Oxidative stress is caused by various oxygen radicals and H2O2, and catalyzed by redox enzymes in non-specific reactions. While the presence of free intracellular iron aggravates oxidative stress via the Fenton reaction, it is mitigated by cytoplasmic proteins that scavenge free iron, e.g. Dps and the ferritins FtnA and Bfr . The question arose how aerobically growing, iron-deficient Y. pestis cells coped with oxidative stress. One of the main E. coli global regulators of the oxidative stress response, the Fe-S cluster protein SoxR, is not encoded in the Y. pestis genome . The other global oxidative stress response regulator is OxyR. OxyR#4 (Figure 4) was not altered in abundance in Y. pestis comparing -Fe and+Fe conditions. Among the enzymes deactivating H2O2 and oxygen radicals are catalases/peroxidases and superoxide dismutases (SODs). Y. pestis produces two catalases with heme cofactors in high abundance. KatE#40 (Y2981) was predominantly expressed at 26°C (Figure 4) and KatY#12 (Y0870) at 37°C. Cytoplasmic SODs include SodB#31, which has an iron cofactor, and SodA#52, which has a manganese cofactor (Figure 4). Periplasmic SodC#84 has a copper/zinc cofactor (Figure 2). Iron availability-dependent patterns of abundance changes reminiscent of enzymes with functions in energy metabolism were observed. Only the iron-dependent proteins KatE, KatY and SodB were strongly diminished in abundance in iron-depleted cells (Table 3). We also determined overall catalase and SOD activities. Catalase reaction rates were 3.2-fold and 2.6-fold higher in lysates derived from iron-replete vs. iron-starved cells at 26°C (stationary and exponential phase, respectively; Table 4). SOD reaction rates were 2-fold higher in the exponential phase, but not significantly altered in the stationary phase (Table 4). This data was in good agreement with differential abundance data, although individual activities of SodA, SodB and SodC could not be discerned with the assay.
AhpC#14, Tpx#33, TrxB#38 and Gst#32, all of which are involved in redox homeostasis and deactivation of oxidative compounds, were similarly abundant in iron-rich vs. iron-starved Y. pestis cells (Figure 4). These enzymes contain either disulfide- or flavin-based redox centers. Dps#24, an iron-scavenging protein important for the protection and repair of DNA under general stress conditions, was moderately decreased in abundance under -Fe conditions, but only at 26°C. The OxyR H2O2-response system of E. coli was reported to restore Fur in its ability to repress gene expression in the presence of iron by increasing the protein's synthesis during oxidative stress , a mechanism that may be applicable to Y. pestis. We conclude that the bacterium adjusts its repertoire of oxidative stress response proteins when iron is in short supply, by reducing the abundance of those proteins that require iron cofactors for functional activity.
Iron storage and iron-sulfur cluster biosynthesis in Y. pestis
High concentrations of free Fe3+ are toxic to bacterial cells and require sequestration by proteins. FtnA and Bfr are the main cytoplasmic iron storage proteins. FtnA#36 was slightly increased in iron-depleted cells at 26°C (Figure 4), but not at 37°C. Bfr#51 (Figure 4) was of considerably lower abundance than FtnA and not significantly changed in abundance comparing -Fe vs. +Fe conditions. The Y. pestis KIM genome harbors two gene clusters orthologous to those of the E. coli isc and suf operons (y1333-y1341 and y1934-1939, respectively). The gene products are responsible for Fe-S cluster assembly under normal growth and stress conditions, respectively. E. coli sufABCDSE expression was reported to be controlled by the regulators OxyR (oxidative stress) and Fur (iron starvation) . Protein profiling revealed that the Y. pestis Suf proteins were considerably increased or detected only in iron-depleted cells (SufC#69 and SufD#70, Figure 1; SufA#27, SufB#28 and the cysteine desulfurase SufS#29; Figure 4). Four Y. pestis Isc subunits (IscS, NifU, HscA and HscB) were detected at very low abundance in cytoplasmic fractions. The cysteine desulfurase IscS#20 and the chaperone HscA#21 were diminished in abundance in iron-starved cells at 37°C (Table 3). In contrast, an ortholog of the E. coli essential respiratory protein A (ErpA#9) was increased in abundance in iron-starved cells, particularly at 26°C (Figure 4). This low Mr Fe-S cluster protein was proposed to serve in the transfer of Fe-S moieties to an enzyme involved in isoprenoid biosynthesis . Its expression was described to be under the control of E. coli IscR, the regulator of the isc gene locus. However, the abundance changes of Y. pestis ErpA (-Fe vs. +Fe) resemble those of the Suf rather than the Isc subunits.
The question arose whether sulfur-mobilizing proteins were also altered in abundance comparing -Fe and +Fe conditions, in order to support a Fe-S cluster rebalancing effort among proteins localized in the Y. pestis cytoplasm. Periplasmic binding proteins of sulfate/thiosulfate ABC transporters (Sbp, CysP) were not altered in abundance (data not shown). The flavoprotein subunit of sulfate reductase (CysJ#10) was strongly decreased in abundance under iron-limiting conditions (Figure 4). CysI, the Fe-S cluster subunit, was not detected. Taurine dioxygenase however (TauD#50, Figure 4), which utilizes aliphatic sulfonates as a sulfur source, was increased in iron-starved Y. pestis cells. The E. coli dioxygenase TauD seems to require iron for activity according to a note in the EcoCyc database. Whether the activity of TauB is linked to Fe-S cluster biosynthesis or repair remains to be shown. In summary, our data supported a functional role of the Y. pestis Suf system in Fe-S cluster assembly when cells are deprived of iron. Data related to CysIJ suggested that Fe-S cluster proteins active in pathways unrelated to energy metabolism were also down-regulated upon intracellular iron starvation.
Protein abundance changes less obviously linked to iron homeostasis
Iron is an essential cofactor for many cellular processes, and a network of global regulators (CRP, OxyR and Fur/RyhB; Figure 5) are affected by or implicated in responses to iron deficiency. We expected to detect protein abundance changes less obviously linked to iron homeostasis. S-ribosylhomocysteinase (LuxS#13) is an enzyme of central importance in the activated methyl cycle and plays a role in autoinducer 2-mediated quorum sensing in E. coli . The enzyme harbors tetrahedrally coordinated Fe2+ in its catalytic center. LuxS was moderately increased in iron-depleted cells at 26°C (Figure 4). In contrast, LsrB#87 whose E. coli ortholog facilitates periplasmic transport of the autoinducer 2 following cellular re-uptake was decreased in abundance in iron-starved cells (Figure 1), similar to YebC#35, a protein hypothesized to be involved in quorum sensing regulation . Y. pestis has been shown to produce the autoinducer 2, although genes controlled by this system have not been identified . Slightly increased abundances of four subunits of a putative type VI secretion system (T6SS) were also observed in iron-deficient vs. iron-rich cells. The proteins HCP1#47 and Y3675#48 (Figure 4), Y3676#86 (Figure 1) and Y3674#110 (Figure 3) were not at all detected in Y. pestis protein profiles at 37°C. The T6SS is temperature-regulated. The flea survival factor Ymt#15 (Figure 4) was moderately increased in iron-starved cells at 26°C. It was one of the most abundant proteins in cells grown at 26°C. N- and C-terminal fragments of Ymt, each ca. 30 kDa in size and with a single cleavage site between V300 and I304 (Ymt#16 and Ymt#17, respectively; Figure 4), were also increased under -Fe vs. +Fe conditions. There is no evidence for a connection between the functional roles of Ymt or the T6SS and the iron starvation response.
Periplasmic subunits of ABC transporters for amino acids, sugars and phosphate, various diffusion porins of the OM allowing passage of nutrients into the periplasm, and various amino acid tRNA-synthetases and enzymes implicated in amino acid biosynthesis were significantly increased in abundance in iron-replete cells. These observations were consistent with the notion that Y. pestis cells grown to stationary phase under +Fe conditions were depleted of various nutrients and induced the expression of high affinity transport systems for their import into the cell. Examples were the phosphate-specific OM porin PhoE#109 (Figure 3) and the periplasmic maltose-binding protein MalE#53 (Figure 1), each of which was much more abundant under +Fe vs. -Fe conditions.
Regulation of iron homeostasis
Fur in Y. pestis, as in many other Gram-negative bacteria, is a central transcriptional regulator responding to the cellular iron status [20, 50], as indicated in the schematic of Figure 5. Many iron uptake systems are transcriptionally repressed during iron-replete growth conditions to reduce accumulation of intracellular iron. Evidence has emerged that small RNA regulators are implicated in bacterial stress responses . These small RNAs act by base-pairing with specific mRNAs whose translation they stimulate or inhibit in the presence of a unique protein, the RNA chaperone Hfq. A small RNA of 90 nucleotides determined to regulate genes involved in iron homeostasis in E. coli  and Pseudomonas aeruginosa  was termed RyhB. It is negatively regulated by Fur and was shown to down-regulate the translation of many of the same iron-dependent enzymes we detected as decreased in iron-starved Y. pestis cells (SdhA, AcnA, FumA, FrdA, SodB, KatE and KatY) . We hypothesize that one or both of the conserved Y. pestis homologs of RyhB  co-regulate Y. pestis iron homeostasis and selectively decrease translation of mRNAs whose protein products depend on or store iron, as illustrated in Figure 5. Such a mechanism may restrict the use of scarce intracellular iron to processes pivotal to bacterial survival. Some of the encoding genes (e.g. ftnA, katE and sodB) may also be positively controlled by Fur as suggested by Yang et al. . Gel shift assays revealed binding of recombinant Fur to promoter regions upstream of the genes ftnA and katE .
Several of the enzymes decreased in abundance in iron-deficient Y. pestis harbor Fe-S clusters. Expression of the respective genes did not appear to be altered under conditions sequestering or depleting iron in Y. pestis according to two DNA microarray studies [33, 35] and suggests post-transcriptional mechanisms. The involvement of RyhB in controlling the abundances of proteins with iron cofactors when cells are iron-deficient needs to be verified. Since our data were derived from proteomic comparisons of Y. pestis cells harvested at different cell densities (OD600s of ~2.0 for stationary phase cells vs. OD600s of ~0.8 for growth arrested, iron-starved cells), the argument can be made that population density differences account for some of the protein abundance changes. Unpublished data (Pieper, R.) and a previous study analyzing the Y. pestis periplasmic proteome in the context of two growth phases  allow us to largely refute this notion. Among the proteins with iron or Fe-S cofactors, only PflB and KatE were increased in stationary vs. exponential phase proteomic profiles with ratios comparable to those observed in iron-rich vs. iron-starved cells. FtnA and Bfr are iron storage proteins and, via regulation by RyhB, were reported to be quantitatively decreased when iron supplies are limited in E. coli . Our data on the FtnA and Bfr orthologs of Y. pestis were not consistent with the results of the aforementioned studies, nor with two Y. pestis transcriptional profiling studies where increased bfr expression and, in one case, decreased ftnA expression were reported for iron-limiting growth environments [33, 35].
Post-transcriptional regulatory functions in iron-deficient cells have also been attributed to aconitases. In fact, eukaryotic AcnA has been termed iron-responsive protein 1 (IRP-1) . Apo-enzyme versions of E. coli aconitases stabilize their cognate mRNAs and influence the expression of sodA. AcnA enhanced sodA transcript stability and was induced by iron starvation and oxidative stress in E. coli [61, 62]. These findings could not be easily reconciled with our data onAcnA and AcnB abundance changes in Y. pestis. AcnA and AcnB were decreased in abundance, as were the combined aconitase activities, in iron-depleted cells. SodA abundance was not significantly affected by either growth phase  or iron depletion. The response of Y. pestis to iron starvation and cellular stress resulting from the loss of this metal ion seems to implicate a network of regulators, as presented in Figure 5. Indeed, functional relationships between Fur and OxyR , Fur and CRP  and Fur and apo-aconitases  were previously reported for E. coli.
Iron starvation stress responses
Numerous E. coli genes encoding oxidative stress response proteins are co-regulated by SoxR, Fur and OxyR according to information in the EcoCyc database. The OxyR H2O2-response system restored Fur repression in iron-replete media during oxidative stress in E. coli , a mechanism that we think is also relevant in Y. pestis. Strong abundance decreases in iron-starved Y. pestis cells were observed for three iron-dependent proteins, SodB, KatE and KatY. The three enzymes detoxify peroxides and radicals formed during oxidative stress. Proteins with similar functions but cofactors other than iron (e.g. SodA and AhpC) were not markedly changed in abundance. Functional assays supported such proteomic data; SOD activities in iron-depleted cells dropped markedly less than catalase activities. In conclusion, our data strongly support the notion that Y. pestis adapts its repertoire of oxidative stress response enzymes by limiting the expression of iron cofactor-dependent enzymes, when iron is in short supply. The coordination of bacterial responses to iron limitation and the defence against oxidative stress was proposed earlier .
Iron acquisition systems
All Y. pestis biovars have several proven iron acquisition systems, and transcriptional control by Fur has been demonstrated [18, 64]. The genes and operons for putative iron transporters (e.g. Ysu, Fit, Fhu, Iuc, Has) also feature conserved 19-nt Fur-binding sites to which recombinant Fur binds . Our data indicated that none of the abovementioned iron transporters were expressed at levels similar to those observed for subunits of proven iron transport systems (Ybt, Yfe, Yfu, Yiu and Hmu) under iron-deficient conditions. Two microarray studies, however, reported increased transcript abundances for many of the putative iron transporters when iron was complexed with dipyridyl  or sequestered by iron-binding proteins in blood plasma . 2D gel analysis has known limitations pertaining to protein detection sensitivity and the resolution of hydrophobic IM-localized proteins, e.g. many nutrient transporters. Except Ysu subunits, unproven iron transporters were also not profiled employing a peptide-based LC-MS/MS analysis approach with Y. pestis lysates [47, 65]. These lysates were derived from iron-replete growth conditions. Only functional iron transporters are presented in the schematic of Figure 5 and appear to follow a hierarchy of importance in the order of Ybt, Yfe (each important for virulence in a bubonic plague model), Yfu and Yiu . The delivery of Fe3+ or Fe2+ from the extracellular milieu to periplasmic binding proteins of the ABC transporters Yfe, Yfu and Yiu is unclear, although a YiuR surface receptor was expressed according to our data. The Hmu transporter acquires heme from blood plasma proteins such as myoglobin, hemoglobin and hemopexin . Three Fe2+ transport systems (EfeUOB, Y2368-Y2370 and FeoAB, Figure 5) were shown to be functional in either Y. pestis  or other bacteria [66–68]. We identified the subunits EfeO and Y2368 as periplasmic proteins, and their abundance increases in iron-deficient cells appeared to be moderately temperature-dependent. There is no evidence to date for their regulation by Fur. FeoB was recently identified in Y. pestis membrane proteome surveys [47, 65]. A protein highly abundant in membrane fractions of iron-depleted Y. pestis cells but not characterized in the context of iron transport was the orphan TonB-dependent OM receptor Y0850. The protein is a candidate for Fur regulation and the contribution to iron uptake, but its exact function remains to be elucidated. A conserved Fur box upstream of the gene and sequence similarity of Y0850 to Bordetella bronchiseptica BfrA and Campylobacter coli CfrA [69, 70] were established. Our proteomic surveys did not support the activation of specific iron uptake pathways at only one of the physiologically relevant temperatures. Based on multivariate transcriptional profiling data for Y. pestis (28°C vs. 37°C, iron-supplemented cell growth vs. iron sequestration in plasma), Carniel et al.  suggested that the Ybt system and the TonB protein are of particular importance for iron acquisition at 37°C.
Fe-S cluster biosynthesis and energy metabolism in iron-starved Y. pestis
Growth of iron-depleted Y. pestis cells was arrested at an OD600 of ~0.8, indicative of the inability of iron-dependent enzymes to perform essential metabolic functions. In addition to the already discussed impact of iron depletion on oxidative stress response enzymes and aconitases, we explored how Fe-S cluster assembly systems and other energy metabolism enzymes were affected. Iron-sulfur clusters are critical to the function of many redox enzymes in bacteria . Incorporation of Fe-S into proteins requires Fe-S cluster assembly systems, which were named Suf and Isc in E. coli. Our data showed that SufA, SufB, SufC and SufS, four of the six subunits of the Suf complex, were more abundant under iron starvation conditions. Regulation of the Y. pestis suf operon by Fur and a functional Fur-binding site were reported previously . The cysteine desulfurase subunits of the Suf and Isc systems (SufS and CsdA, respectively) were quantitatively changed in opposite directions (-Fe vs. +Fe), suggesting that Suf functionally replaces Isc at the onset of iron starvation in Y. pestis. Mobilization of sulfur from cysteine appears to be catalyzed by SufS in E. coli . The increased abundance of TauD, an enzyme that mobilizes sulfite from taurine, in iron-depleted Y. pestis cells was intriguing. TauD is a dioxygenase, harbors a Fe2+ cofactor and was reported to be induced under sulfate starvation conditions in E. coli . We speculate that TauD plays an accessory role in sulphur mobilization for Fe-S cluster assembly via the Suf pathway. Furthermore, the Y. pestis ortholog of a recently discovered Fe-S cluster protein ErpA was also increased under iron-limiting conditions. Since ErpA was proposed to transfer Fe-S clusters to apo-enzymes , we hypothesize that Y. pestis ErpA may perform such activities cooperatively with the Suf system. Transcriptional data on erpA and tauD expression changes for -Fe vs. +Fe growth conditions are not available. Mammalian hosts starve Y. pestis of iron and, therefore, the Suf complex constitutes a good target for inhibitory drug design.
Enzymes with Fe-S clusters in their catalytic cores, many of them in the TCA cycle, are also displayed in Figure 5. Although in different ratios, subunits of such enzyme complexes (e.g. FumA, SdhA, FrdA and CysJ) were invariably decreased in abundance in iron-starved Y. pestis cells. Most of these quantitative decreases appear to be unrelated to population density differences, because they were not observed in cells cultured to stationary vs. exponential phase in iron-replete PMH2 medium(Pieper, R., unpublished data). A decreased pyruvate metabolism rate should be the consequence of the loss of Fe-S cluster enzyme activities in the TCA cycle and may be followed by reduced production of ATP and NADPH reducing equivalents in the electron transport chain. Furthermore, a decreased turnover of citrate may lead to its accumulation in the cytoplasm, which could chelate iron and exacerbate iron starvation . A highly interesting observation was the dramatic abundance and activity increase of PoxB in iron-starved Y. pestis cells, both at 26°C and 37°C. PoxB activity increases were independent of Y. pestis cell densities during growth in chemically defined media. poxB expression was reported to be moderately enhanced in Y. pestis cells grown in human plasma vs. LB media . We suggest that the metabolism of pyruvate via the PoxB route compensates for reduced activities of Fe-S cluster enzymes in the TCA cycle. The pathway catalyzed by PoxB is iron-independent. The E. coli ortholog, a thiamin/flavin-dependent enzyme activated by binding to IM phospholipids, was shown to feed electrons directly from the cytosol to the respiratory chain . To our knowledge, this is the first report linking enhanced PoxB activities in bacteria specifically to iron starvation. PoxB is a potential drug target in the context of intracellular pathogens surviving in environments where iron is sequestered.
Proteomic surveys of Y. pestis subcellular fractions grown under iron-replete vs. iron-starved conditions supported the physiological importance of the iron acquisition systems Ybt, Yfe, Yfu, Yiu and Hmu. An uncharacterized TonB-dependent OM receptor, Y0850, was also highly abundant in iron-depleted cells, appeared to be Fur-regulated and may participate in iron uptake. Numerous enzymes harboring iron and Fe-S cluster cofactors were significantly decreased in abundance in iron-starved cells, suggesting a regulatory process shifting the metabolism of Y. pestis to iron-independent pathways when the supply of this metal ion is limited. Small Fur-regulated RNAs termed RyhB in E. coli may be involved in this process. Finally, this study revealed biochemical pathways likely essential for the iron starvation response in Y. pestis. Examples are the energy metabolism via the pyruvate oxidase route and Fe-S cluster assembly mediated by the Suf system.
2-dimensional gel electrophoresis
Coomassie Brilliant Blue G250
immobilized pH gradient
type III secretion system
type VI secretion system
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This work was performed under the Pathogen Functional Genomics Resource Center contract (contract No. N01-AI15447), funded by the National Institute of Allergy and Infectious Diseases, National Institutes of Health. We thank Jasmine Pollard for the graphic presented in Figure 4, Christine Bunai for the development of the mass spectrometry analysis platform and John Braisted for advice on statistical data analysis methods.
The authors declare that they have no competing interests.
RP: primary role in designing the study, analyzing and interpreting the data, performing the enzyme assays, writing the article; STH: quantitative and bioinformatic data analysis, database queries, generation of Figures and Tables for the article; PPP: sample preparation, 2D gel experiments and proof-reading; DJC: acquisition of the LC-MS/MS data; HA: acquisition of the MALDI-MS data; RDF: generated the framework for the performance of this study; RDP: major role in the design and initial experiments of the study, biological interpretation of the data, writing parts of the article and its review; SNP: major role in the biological data interpretation and the review of the article.
Electronic supplementary material
Additional file 1: Yersinia pestis growth curves in PMH2 medium. Growth curves (OD600) are displayed in graphical form for Y. pestis KIM6+ cell cultures in iron rich and iron-depleted media, at 26°C and at 37°C. (DOC 133 KB)
Additional file 2: Yersinia pestis proteins comparing iron-replete and iron starvation conditions. A variety of qualitative and quantitative data are provided for differentially displayed proteins derived from + Fe vs. -Fe growth conditions, from cell cultures at 26°C and at 37°C. (XLS 130 KB)
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Pieper, R., Huang, S., Parmar, P.P. et al. Proteomic analysis of iron acquisition, metabolic and regulatory responses of Yersinia pestis to iron starvation. BMC Microbiol 10, 30 (2010). https://doi.org/10.1186/1471-2180-10-30
- Iron Starvation
- Pyruvate Oxidase
- Outer Membrane Receptor
- Iron Acquisition System