Peer-Reviewed Journal Details
Mandatory Fields
O'Connor, EB;Cotter, PD;O'Connor, P;O'Sullivan, O;Tagg, JR;Ross, RP;Hill, C
2007
April
BMC Microbiology
Relatedness between the two-component lantibiotics lacticin 3147 and staphylococcin C55 based on structure, genetics and biological activity
Validated
WOS: 24 ()
Optional Fields
BROAD-SPECTRUM BACTERIOCIN PRECURSOR LIPID-II LACTOCOCCUS-LACTIS ANTIMICROBIAL ACTIVITY AUREUS C55 BIOSYNTHESIS PLASMID STREPTOCOCCI MERSACIDIN PEPTIDES
7
Background: Two component lantibiotics, such as the plasmid-encoded lacticin 3147 produced by Lactococcus lactis DPC3147 and staphylococcin C55 produced by Staphylococcus aureus C55, represent an emerging subgroup of bacteriocins. These two bacteriocins are particularly closely related, exhibiting 86% (LtnA1 and C55 alpha) and 55% (LtnA2 and C55 beta) identity in their component peptides. The aim of this study was to investigate, for the first time for any two component bacteriocins, the significance of the relatedness between these two systems. Results: So close is this relatedness that the hybrid peptide pairs LtnA1:C55 beta and C55 alpha: LtnA2 were found to have activities in the single nanomolar range, comparing well with the native pairings. To determine whether this flexibility extended to the associated post-translational modification/processing machinery, the staphylococcin C55 structural genes were directly substituted for their lacticin 3147 counterparts in the ltn operon on the large conjugative lactococcal plasmid pMRC01. It was established that the lacticin LtnA1 post-translational and processing machinery could produce functionally active C55 alpha, but not C55 beta. In order to investigate in closer detail the significance of the differences between LtnA1 and C55 alpha, three residues in LtnA1 were replaced with the equivalent residues in C55 alpha. Surprisingly, one such mutant LtnA1-Leu21 Ala was not produced. This may be significant given the positioning of this residue in a putative lipid II binding loop. Conclusion: It is apparent, despite sharing striking similarities in terms of structure and activity, that these two complex bacteriocins display some highly dedicated features particular to either system.
LONDON
1471-2180
10.1186/1471-2180-7-24
Grant Details