Two microarray studies, however, reported increased transcript abundances for many of the putative iron transporters when iron was complexed with dipyridyl [35] or sequestered by iron-binding proteins in blood plasma [33].

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 [15]. The delivery of Fe3+ or Fe2+ from check details the extracellular milieu to periplasmic binding proteins of the ABC transporters

Yfe, Yfu and Yiu is unclear, although a YiuR AZD1080 ic50 surface receptor was expressed according to our data. The Hmu transporter acquires heme from blood plasma proteins such as myoglobin, hemoglobin and hemopexin [16]. Three Fe2+ transport systems (EfeUOB, Y2368-Y2370 and FeoAB, Figure 5) were shown to be functional in either Y. pestis [17] 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 Emricasan cell line 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 3-oxoacyl-(acyl-carrier-protein) reductase 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. [33] 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.