Empty vector (pDB1568) was used as negative control and plasmids containing iscS or nifS from A. vinelandii as positive controls. No growth was observed on nonsupplemented medium after 72 h at 37 °C, click here although control strains grew as expected (Fig. 3a). These results indicate the E. faecalis SUF machinery is not able to complement the ISC system of Proteobacteria, even in E. coli, which is slightly evolutionarily different from A. vinelandii in terms of the presence of SUF machinery in the latter. Several Proteobacteria representatives possess the SUF. genes together with the

housekeeping ISC machinery. However, E. faecalis possess the only SUF system with high homology with the corresponding E. coli SUF genes, with the addition of sufU, similar to E. coli iscU. Genetic experiments were performed to assess the possibility that the cloned E. faecalis SUF genes can complement E. coli mutants lacking one or more of the components of the SUF system. SUF mutants of E. coli have no apparent growth phenotype. However, combination of an SUF mutation (or mutations)

with an iscS mutation is lethal unless a plasmid is present in trans that provides either iscS or the missing SUF function(s) (Trotter et al., 2009). To guarantee BYL719 price the complementation of the iscS mutant, the complementing element needs to fill the gaps caused by the absence of iscS. This is what seems to occur in vivo when the E. coli sufABCDSE system produces viable strains of E. coli ISC mutants (Takahashi & Tokumoto, 2002). This system plays roles related not only to [Fe–S] cluster formation, but also to nicotinic acid and thiamine biosynthesis. Escherichia coli strains JW1670-1 (ΔsufS), GSO97 (ΔsufSE), and GSO92 (ΔsufABCDSE) were used as recipient strains for phage P1 transduction

experiments in which the donor strain (EESC42) contained ΔiscS∷kan and a tightly linked Tn10, which Ceramide glucosyltransferase confers tetracycline resistance. In each transduction, tetracycline resistance was selected and kanamycin resistance scored as described by Outten et al. (2004). The appearance of viable kanR transductants would indicate complementation of either iscS or SUF function(s) by the resident plasmid. As negative and positive control plasmids, the empty vectors pDB1568 and pDB943 (which encodes iscS from A. vinelandii) were used. Azotobacter vinelandii IscS was able to complement all double mutants, whereas the only complementation observed using the test strains was with strain GSO92 (ΔsufABCDSE), containing pEFSE121 (which encodes sufCDSUB). Tetracycline-resistant transductants were obtained that displayed resistance to kanamycin and ampicillin, and grew on glucose minimal medium (containing arabinose) after 48 h of incubation (Fig. 3b).