Cu Transport by the Extended Family of CcoA-like Transporters (CalT) in Proteobacteria

Abstract

Abstract Comparative genomic studies of the bacterial MFS-type copper importer CcoA, required for cbb 3 -type cytochrome c oxidase ( cbb 3 -Cox) biogenesis, revealed a widespread C co A - l ike t ransporters (CalT) family, containing the conserved CcoA Cu-binding M xxx M and H xxx M motifs. Surprisingly, this family also included the RfnT-like proteins, earlier suggested to transport riboflavin. However, presence of the Cu-binding motifs in these proteins raised the possibility that they might be Cu transporters. To test this hypothesis, the genomic context of the corresponding genes was examined, and three of such genes from Ochrobactrum anthropi , Rhodopseudomonas palustris and Agrobacterium tumefaciens were expressed in Escherichia coli (Δ ribB ) and Rhodobacter capsulatus (Δ ccoA ) mutants. Copper and riboflavin uptake abilities of these strains were compared with those expressing R. capsulatus CcoA and Rhizobium leguminosarum RibN as bona fide copper and riboflavin importers, respectively. Overall data demonstrated that the “RfnT-like” CalT proteins are unable to efficiently transport riboflavin, but they import copper like CcoA. Nevertheless, even though expressed and membrane-localized in a R. capsulatus mutant lacking CcoA, these transporters were unable to accumulate Cu or complement for cbb 3 -Cox defect. This lack of functional exchangeability between the different subfamilies of CalT homologs suggests that MFS-type bacterial copper importers might be species-specific.