The lowest dilution that allowed detection of the gene within the linear working range was chosen as the dilution

to be used for the analysis of the genes of interest. To control for contaminating DNA in the reaction, tubes with template from control 1 (see above) and tubes with water instead of template were included in the analysis. The controls gave Ct values (Ct is the threshold cycle) below detection level or at least 8 cycles later than the corresponding cDNA. Relative copy numbers (RCN) of selected genes were expressed in relation to the expression of the housekeeping gene tul4 [24] and calculated according Momelotinib ic50 to the following equation: RCN = 2- ΔCt × 100 where ΔCt is Ct (target) – Ct(tul4) [25]. Thus, the copy number of a given gene is related to the copy number of tul4. Normalized Ct-values were used for NVP-BGJ398 statistical evaluation of the data. Chromazurol-S (CAS) plate assay Chrome-azurol sulfonate-C-CDM agar plates (CAS plates) were prepared essentially as described [13]. Briefly, 40 ml of CAS/Fe(III)-hexadecyltrimethylammonium solution was mixed with 50 ml of a 4% (wt/vol)

solution of GC II Agar buy LY2874455 Base (BD Diagnostic Systems, Franklin Lakes, NJ, USA) and 110 ml of C-CDM. The resulting CAS-C-CDM agar solution (1% agar) was poured into 20 ml Petri dishes. All components of the CAS-solution were purchased from Sigma-Aldrich, Buchs, Switzerland. Bacteria were cultivated overnight in C-CDM and thereafter washed three times in C-CDM before dilution in C-CDM to 1.0 OD600. The suspension was added as a droplet of 2.5 μl to the center of the CAS plate. The plates were incubated at 37°C in 5% CO2 and the size and appearance of the halo formed around the bacterial colony was scored at 72 h. Ferrozine assay A ferrozine-based method was used to measure the total amount of iron in the bacterial samples and in culture medium [26]. Ferrozine forms a complex with Fe2+ that absorbs light at 562 nm.

To determine the iron content of bacteria, a volume corresponding to 1.0 OD600 was withdrawn from the culture and bacteria collected by centrifugation for 5 min at 13,000 rpm. The bacteria were resuspended in PBS and collected Aurora Kinase by centrifugation. The resulting bacterial pellet was lysed with 100 μl of 50 mM NaOH. The solution was mixed thoroughly to ensure complete lysis of the bacteria. One hundred μl of 10 mM HCl was added to the lysate. To release protein-bound iron, the samples were treated with 100 μl of a freshly prepared solution of 0.7 M HCl and 2.25% (w/v) KMnO4 in H2O and incubated for 2 h at 60°C. All chemicals used were from Sigma-Aldrich. Thereafter, the samples were mixed with 100 μl of the iron detection reagent composed of 6.5 mM ferrozine, 6.5 mM neocuproine, 2.5 M ammonium acetate, and 1.0 M ascorbic acid dissolved in water. For determination of iron in medium, 30 μl of iron detection reagent was mixed with 170 μl of bacterial-free culture medium.