The genetic context and the experimental evidence previously published for the Vorinostat rpoNs from R. sphaeroides WS8 (Poggio et al., 2002, 2006) suggest that in these strains, rpoN1 could be required for the expression of nitrogen fixation genes, whereas rpoN2 is needed to express the flagellar genes. Finally, as it occurs in the strains that have rpoN3,

two genes probably involved in the incorporation of selenium into tRNAs and proteins (selD) are found upstream of rpoN3 in R. azotoformans, but in contrast to the other Rhodobacter strains, R. azotoformans and R. sphaeroides ATCC17025 have in the downstream region, a tRNA-Gly and a putative transcriptional regulator instead of a protein with a hyadantoinase domain. In the Rhodobacter species where a single copy of rpoN is present (R. capsulatus, R. blasticus Palbociclib and Rv. sulfidophilum), it is always located next to genes required for nitrogen fixation (nif or fix; Fig. 2). Furthermore, when rpoN is present in multiple copies, one of these copies is always

found in a nif-fix context (as occurs in all the R. sphaeroides strains, in R. sp SW2 and R. azotoformans). As stated before, the presence of rpoN1 in all the strains suggests that this may be the ancestral rpoN gene. This idea is supported by the association of this gene with the widespread role of rpoN in the expression of genes involved in nitrogen fixation. The limited distribution of rpoN4 to the strains closely related to R. sphaeroides 2.4.1 (R. sphaeroides WS8, ATCC17029, and KD131) suggests that this gene is of recent appearance. It should be noted that its genetic context is identical in all the strains that were analyzed. It has been reported that the rpoN genes of R. sphaeroides are functionally specialized to transcribe a particular subset of genes. RpoN1

is required to express the genes involved in nitrogen CYTH4 fixation (nif), whereas RpoN2 only promotes the expression of the flagellar genes (fli). So far, the genes expressed by RpoN3 and RpoN4 have not been identified; however, it was shown that these proteins were not able to transcribe the nif or fli genes, suggesting that an unidentified subset of genes may be dependent on them (Poggio et al., 2002, 2006). The functional specialization of the RpoN factors in R. sphaeroides encouraged us to test whether other sigma-54 factors from closely related species could complement the phenotype caused by the absence of rpoN1 (growth deficient under nitrogen fixation conditions) or rpoN2 (motility deficient) in R. sphaeroides WS8. For this purpose, each rpoN gene identified in this work was cloned into plasmid pRK415 in an orientation that allows transcription of the gene from an unidentified promoter, presumably the tet or the lac promoters present in this vector. The resultant constructions were introduced to SP7 (ΔrpoN2::kan) and SP8 (ΔrpoN1::aadA) strains. Swimming and growth under diazotrophic conditions were evaluated. When rpoN from R. blasticus, Rv. sulfidophilum or rpoN1 from R.