- Research article
- Open Access
Relatedness between the two-component lantibiotics lacticin 3147 and staphylococcin C55 based on structure, genetics and biological activity
BMC Microbiologyvolume 7, Article number: 24 (2007)
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 C55α) and 55% (LtnA2 and C55β) 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.
So close is this relatedness that the hybrid peptide pairs LtnA1:C55β and C55α: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 C55α, but not C55β. In order to investigate in closer detail the significance of the differences between LtnA1 and C55α, three residues in LtnA1 were replaced with the equivalent residues in C55α. Surprisingly, one such mutant LtnA1-Leu21Ala was not produced. This may be significant given the positioning of this residue in a putative lipid II binding loop.
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.
Lantibiotics are gene-encoded, ribosomally-synthesized antimicrobial peptides which are distinguishable by the presence of unusual amino acids including lanthionine (Lan), β-methyl-lanthionine (meLan) and a number of dehydrated amino acids (for comprehensive reviews see [1–4]). These unusual amino acids are formed as a result of post-translational modifications of precursor peptides; for example, serine and threonine residues are enzymatically dehydrated to give dehydroalanine and dehydrobutyrine, respectively. A cysteine residue can then react with one of the newly formed unsaturated sites in what is essentially a 1,4-Michael addition reaction to form the characteristic thioether amino acids Lan and meLan. Lantibiotics are synthesized as precursor peptides containing N terminal extensions or leader peptides which are removed during export through a dedicated bacteriocin transport system leading to the active mature peptide.
Lantibiotics are currently classified into eleven subgroups based on alignments of the unmodified structural peptides (for the most recent classification scheme see ). Two of these groups contain the individual components of a number of two component lantibiotics i.e. those lantibiotics which display enhanced bactericidal effects due to the complementary activity of two peptides. To date, seven two component lantibiotics have been identified and include lacticin 3147 , staphylococcin C55 , plantaricin W , cytolysin , haloduracin , Smb  and BHT-A . Of these, cytolysin is clearly the most distant relative based on homologies and biological activity, while lacticin 3147 and staphylococcin C55 peptides are particularly closely related. Staphylococcin C55 is produced by Staphylococcus aureus C55, the adopted prototype of phage II bacteriocin producers (7) and indeed, is widely produced by this group of S. aureus strains . Its genetic determinants are located on a 32 kb plasmid in the strain S. aureus C55  but have also been identified on a 37 kb plasmid in S. aureus U0007 (Warren et al., 1975) and on a 38 kb pETB plasmid from the clinical isolate S. aureus TY4 . Interestingly, in all cases, the bacteriocin structural genes are closely associated with an exfoliative toxin B determinant, an exotoxin associated with skin infections in humans . The structural peptides, staphylococcin C55α and C55β of molecular masses 3339 and 2993, respectively, are both required in equimolar amounts to act synergistically to give an antimicrobial effect against S. aureus, Micrococcus luteus but not S. epidermidis strains . Mode of action studies indicated that cell death was due to pore formation in the cytoplasmic membrane and widespread inhibition of macromolecular biosynthesis following exposure to the partially purified material (Dajani et al., 1973).
In contrast, lacticin 3147 is produced by a food-grade L. lactis subsp. lactis DPC3147 strain and encoded on a 60.2 kb conjugative plasmid pMRC01 which encodes the genetic determinants for production and immunity . The two structural peptides of lacticin 3147 are LtnA1 and LtnA2 with molecular masses of 3306 and 2847, respectively. The optimal ratio of the two lacticin peptides has recently been established, suggesting a peptide stoichiometry of 1:1, effective at nanomolar concentrations (7 nM) . Lacticin LtnA1 does exhibit independent inhibitory activity which is greatly enhanced by the presence of the LtnA2 peptide. Sequential addition studies show that the LtnA1 peptide must be added before LtnA2 to observe inhibitory activity . This activity, which occurs at nanomolar concentrations for the lacticin peptides, suggests the involvement of a docking molecule speculated to be lipid II as is the case with nisin . In addition, lipid II has been identified as the target molecule for a number of other antimicrobial peptides including mersacidin and actagardin [18–20]. Interestingly, the 3D structure of lacticin 3147 has recently been elucidated  and reveals a specific lanthionine-bridging pattern in LtnA1 closely resembling that of the lipid II-binding globular lantibiotic mersacidin which acts by inhibition of cell wall biosynthesis. In contrast, the LtnA2 peptide has a more elongated linear structure potentially capable of pore formation. It is speculated that the lacticin peptides display a dual mode of action similar to nisin, however in the case of lacticin 3147 both functions are assigned to separate peptides . In essence, it is predicted that LtnA1 binds to lipid II in a similar way to mersacidin, thereby inhibiting cell wall biosynthesis through the prevention of transglycosylation. The second function of pore formation and rapid efflux of K+ and phosphate ions  is assigned to the linear more hydrophobic peptide LtnA2. Weidemann et al.  recently provided some experimental evidence that agreed with this speculation.
The focus of this communication was to investigate the similarities and differences between lacticin 3147 and staphylococcin C55. Primary sequence analysis of the prepeptides suggests that lacticin A1 and staphylococcin C55α resemble natural variants with a difference of only 4 amino acids between the two peptides, while the complementary peptides share less identity (55%). We demonstrate that purified peptides of the two bacteriocins can cross complement with negligible losses in activity, and that the post translational machinery of LtnA1 can produce a viable C55α peptide. Furthermore substitution of leucine 21 of LtnA1, located within a proposed lipid II binding pocket, for the corresponding alanine residue in C55α counterpart, was not produced.
Results and Discussion
Lacticin 3147 and staphylococcin C55 are closely related two component lantibiotics. LtnA1 and C55α share 86% identity with a difference of only 4 amino acids in the unmodified propeptide whereas LtnA2 and C55β share less identity (55%) with highest homology spanning a 16 amino acid region at the C terminal end of the propeptides (Fig. 1). Thus, it is not surprising that the predicted structure of C55α very closely resembles that which has been established for LtnA1 (Fig. 1) . In addition to the structural peptides the proposed modification and transport proteins exhibit significant homology. For example, the lacticin modification peptides lacticin LtnM1 and LtnM2 share 44.7% and 40.7% identity to their staphylococcin counterparts SacM1 and SacM2, respectively. In addition, the transport peptides lacticin LtnT and staphylococcin SacT are 48.9% identical, while lacticin LtnJ and staphylococcin SacJ (C55 orf45) share 47% identity. A clustal W alignment demonstrating the evolutionary divergence across the structural peptides of lacticin 3147 and staphylococcin C55 indicated that the number of substitution events between LtnA1 and C55α was considerably lower at 14.7 in comparison to 67 for LtnA2 and C55β (Fig. 1). In contrast, investigation of the evolutionary divergence between the modification peptides LtnM1 with SacM1 and LtnM2 with SacM2 indicated values of 93.8 and 104.5, respectively, while the transport peptides were slightly more conserved with a value of 81.6 for LtnT and SacT. These results indicate that the lanthionine containing peptides LtnA1 and C55α had a slow rate of divergence relative to the biosynthesis machinery and are highly conserved. Indeed, the amino acid identity and evolutionary divergence across both two component lantibiotics is indicative of a common ancestor.
Purified preparation of staphylococcin C55 displays a broad spectrum of inhibition analogous to lacticin 3147
Initially, the range of inhibitory activity of L. lactis DPC3147 and S. aureus C55 against a number of indicator strains was examined (Table 1). The strain S. aureus C55 inhibited L. lactis strains and M. luteus but failed to inhibit Enterococcus, mastitic S. aureus, Listeria, Bacillus, Leuconostoc, Pediococcus or Escherichia coli. However, all of these strains with the exception of Pediococcus and the Gram-negative E. coli strain were inhibited by a concentrated preparation of the staphylococcin C55 peptides. The L. lactis DPC3147 culture inhibited all strains listed with the exception of the S. aureus strains and E. coli. However, when the concentrated supernatant of lacticin 3147 was assayed it was found to inhibit the full list of Gram-positive indicator strains used (Table 1). Overall, this demonstrates that both bacteriocins are active against a wide range of Gram-positive strains.
Cross complementation between lacticin 3147 and staphylococcin C55 evident at a nanomolar range
The synergistic effect of staphylococcin peptides C55α and C55β and the lacticin 3147 peptides LtnA1 and LtnA2 against the indicator strain L. lactis HP is clearly shown by the well diffusion assay technique (Fig. 2A and 2B). When the lacticin 3147 and staphylococcin C55 peptides were cross combined, complementation was observed. For instance, when LtnA1 and C55β were combined, a zone of inhibition against the sensitive indicator strain L. lactis HP was evident (Fig. 2C). Indeed, the combination of C55α and LtnA2 also appeared to exhibit cross synergism to the level of activity presented by both parent strains (Fig. 2D). This cross complementation which was evident between the two strains was further examined by microtitre plate assays using purified preparations of both peptides and is presented as isobolograms (Fig. 2E–H). The MIC50 for the lacticin peptides was in the single-nanomolar range; i.e. 5 nM of LtnA1 titrated against 7 nM of LtnA2 inhibited the growth of the indicator L. lactis HP by 50%, as similarly reported by Morgan et al., (2005) (Fig. 2E). Likewise, combinations of staphylococcin C55 peptides also displayed inhibitory activity in the singular nanomolar range (4 nM) at a peptide stoichiometry of 1:1 (Fig. 2F). Similarly, hybrid pairs of the bacteriocins, LtnA1 with C55β (Fig. 2G) and C55α with LtnA2 (Fig. 2H), displayed a high specific activity of 4:3 nM and 8:6 nM, respectively. Overall, the level of inhibition across the four combinations was in the nanomolar range.
Effect of swapping structural genes
The ltnA1 and ltnA2 genes in the large conjugative plasmid pMRC01 were precisely replaced with the staphylococcin C55 structural genes sacαA and sacβA using a strategy involving amplification and spliced overlap extension (SOEing) PCR  (Fig. 3A). This construct inhibited the indicator strain L. lactis HP, albeit the inhibitory activity was significantly reduced (Fig. 3A). The supernatant of mutant A was purified (solid phase extraction) and mass spectrometry analysis revealed that the structural peptide C55β was not produced whereas a mass corresponding to C55α was evident. When the purified HPLC fraction putatively containing C55α was combined with pure peptides of either LtnA2 or C55β the activity was greatly enhanced. This demonstrated that the modification and transport machinery of lacticin 3147 could modify and export the C55α peptide resulting in an extracellular mature active peptide. Notably, no complementation effect was seen when HPLC fractions were combined with either LtnA1 or C55α, supporting the mass spectrometry finding that C55β was not produced. It was thought possible that heterologous production of C55α and C55β could be enhanced through fusion of the corresponding LtnA1 and LtnA2 leaders, respectively, (which are more divergent than the corresponding propeptides) if it aided recognition of the peptides by the lacticin 3147 biosynthetic machinery.
Thus the leader of LtnA1 was fused by SOEing to the C55α propeptide segment of the structural gene generating an LtnA1/Sacα hybrid (Fig. 3B) and the leader of LtnA2 was fused to the propeptide segment of the structural gene of C55β generating an LtnA2/Sacβ hybrid (Fig. 3C). Purified preparations (solid phase extraction) from both hybrid bacteriocins produced a zone of inhibition against the indicator strain L. lactis HP, however, the activity was significantly reduced with respect to the parent strains. The reduced zone of inhibition was attributed to a concentrated level of one peptide alone, either LtnA2 (Fig. 3B) or LtnA1 (Fig. 3C). Following HPLC purification, neither hybrid peptide could be detected by mass spectrometry analysis. Notably, no complementation effect was seen when HPLC fractions of LtnA1/Sacα hybrid were combined with either LtnA2 or C55β (Fig. 3B) and similarly no complementation effect was seen when HPLC fractions of LtnA2/Sacβ hybrid were combined with either LtnA1 or C55α, supporting the mass spectrometry finding that the hybrid peptides were not produced. These results indicate that while the lacticin biosynthesis machinery can produce the active mature peptide C55α, it cannot produce either of the hybrid bacteriocins where Ltn leaders are used in attempt to enhance the generation of active mature processed C55 peptides.
Site-directed mutagenesis reveal that residue L21 is essential for LtnA1 production
Site-directed mutagenesis of LtnA1 was carried out in order to assess the biological significance of changing any of the 4 amino acids in LtnA1 (N15, A17, L21 and A27) to their staphylococcin C55 counterparts. Several attempts to generate an A27S mutant failed. However, mutants N15K, A17N and L21A were introduced into the genes for the prepeptides. Therefore N15K, A17N amd L21A mutant peptides were successfully engineered. While concentrated preparations (solid phase extraction) of N15K and A17N supernatants retained high activity (20,240 AU/ml) the amino acid change of leucine to an alanine at position 21, which is in the putative lipid II binding region completely abolished the inhibitory capacity of the corresponding strain (0 AU/ml) (Fig. 4). Notably, when the purified preparation (solid phase extraction) of L21A was combined with LtnA1 peptide a complementation effect was evident confirming the mass spectrometry finding that LtnA2 was produced. On the other hand, when L21A was combined with LtnA2 peptide no complementation effect was evident supporting the mass spectrometry result that the LtnA1 mutant was not produced. In this case, a reduced zone of inhibition was evident; however, this was due to the presence of concentrated LtnA2 peptide alone. In fact it would appear that an LtnA1 derivative is not produced by this strain suggesting that the lacticin 3147 biosynthetic machinery could not tolerate this change. This is further evidence of a difference in the processing machinery of lacticin 3147 and staphylococcin C55, given that the SacM1 modification enzyme tolerates the presence of an alanine at position 21 in C55α.
L. lactis DPC3147 and S. aureus C55 contain plasmids which encode highly similar two component lantibiotics. Indeed, evolutionary divergence and amino acid identity across the two lantibiotics confirm a common ancestor. The structural genes for the LtnA1 and C55α peptides have diverged to a much lesser extent than their associated modification and processing machinery, indicating a high degree of conservation between sequence, structure and function in these peptides, almost certainly imposed by the role of these peptides in mediating binding to a highly conserved target in lipid II and subsequently promoting interaction with their LtnA2/C55β partner peptides. It is interesting to note in this respect that the leader regions do diverge to the extent which would be predicted by the divergent modification genes. In contrast, far less conservation is required for the α-helical section of the LtnA2/C55β peptides, where it is envisaged that amphiphatic conservative changes would not negatively affect the overall function of the peptide in pore formation. In addition, the difference in inhibitory spectra for both strains is negligible, both inhibiting a wide range of Gram-positive bacteria. When combinations of purified peptides were assayed, for example, LtnA1 with C55β and C55α with LtnA2, they display a cross synergistic effect against the indicator strain L. lactis HP. In addition to this cross complementation between the lantibiotics, their specific activity was in the singular nanomolar range. This finding suggests that both lantibiotics use the lipid II target, despite differences in their lipid II binding pocket. It is not surprising that LtnA1 and C55α can be interchangeable as they share 86% identity while on the other hand, LtnA2 and C55β only share 55% identity. Nonetheless, when LtnA2 and C55β were exchanged for each other no loss of activity was observed. This suggests that the region responsible for peptide:peptide (and possibly peptide lipid II) interaction spans the 16 amino acid region at the C terminus of both peptides (81% identity), while the more permissive N-terminus is responsible for membrane insertion and pore formation. While these results are obviously of interest with respect to lacticin 3147 and staphylococcin C55 in particular, there are a number of broader implications. This is the first occasion upon which it has been demonstrated that the individual components of any sort of two-component bacteriocin, be they lantibiotics or non-lantibiotics, are interchangeable. It would also indicate that one could take advantage of the fact that functional domains are separated across two peptides. Theoretically A1/α and A2/β from different sources could be combined with a view to identifying pairs that have more potent activity against a particular target organism.
Interestingly, at a molecular level, the lacticin 3147-biosynthetic machinery was capable of producing the lanthionine containing C55α peptide when preceded by the staphylococcin C55α leader. To our knowledge this is the first occasion upon which an active (β-methyl) lanthionine-containing peptide has been produced from its own gene by biosynthetic machinery other than its own, without some manipulation of its leader region. Previously it was established that processed, albeit inactive, nisin could only be produced by the subtilin biosynthetic machinery if a nisin-subtilin chimera containing the subtilin leader was first generated . It is thus surprising that when the C55 leader was precisely replaced with the lacticin LtnA1 leader (LtnA1/Sacα hybrid) production of C55α was eliminated rather than improved (Fig. 3B). It was previously established that processing of lacticin 481 by LctM occurred independently of the first 10 N-terminally located residues of the LctA leader . Significantly, although the LtnA1 and C55α leaders are only 48% identical, they are 74% identical with respect to the 19 C-terminally located residues. This identity is likely to be responsible for successful biosynthesis and production by the lacticin 3147 machinery. It may also mean that one or more of the five residue differences within this region could explain the negative impact of the LtnA1 leader. Thus, in this instance at least, the leader appears to be specific to the peptide that it exports rather than to the biosynthetic machinery. With respect to C55β it is not surprising, given the relatively lower levels of homology with LtnA2 both within the structural and leader regions, that heterologous production was not successful.
Mature LtnA1 differs from C55α with respect to at least four residues. There is, however, some ambiguity with respect to the identity of the amino acid at position 7 of C55α. It may be that this residue is a D-alanine, as is the case for LtnA1, rather than the Dha reported previously . This suggestion is based on the fact that amino acid analysis predicts the presence of three alanines in the mature form of C55α (data not shown) and that the C55 operon contains an LtnJ homolog . With respect to the four confirmed differences site directed mutagenesis was employed to convert the individual amino acids of LtnA1 into its C55 counterpart where three out of the four mutants were successfully created. Interestingly, it was found that an exchange of leucine 21 for alanine abolished peptide production of the associated mutant peptide. It is noteworthy that a corresponding leucine is also found in a number of other lantibiotics within the same subgroup as LtnA1 i.e. mersacidin , actagardine , and plantaricin W . Alignments of closely related globular peptides show that residues surrounding this leucine are highly conserved and in the case of mersacidin are found to be involved in lipid II binding . In contrast, the site directed mutants of N15K and A17N tolerated change and the peptides were highly active. It may be that the presence of an alanine at position 21 of these peptides is only successful if complementary residues are located at positions 15, 17 and/or 27. It will be interesting to determine in the future whether it is possible to restore production/activity of the LtnA1-L21A mutant through the introduction of compensatory mutations.
We have thus established that because of their two component nature it is possible to combine the attributes of two lantibiotics such as lacticin 3147 and staphylococcin C55 in vitro to produce new antimicrobials. Should it prove possible to build on these successes a great number of two-component mixtures, limited only by the number of two-component lantibiotics present in nature, would be possible. It is very interesting that such remarkably similar systems ended up in dissimilar organisms.
Bacterial strains, culture conditions, inhibitory spectrum assays and cross complementation assays
Bacterial strains and plasmids used in this study are listed in Table 1 and Table 2. L. lactis subsp. lactis DPC3147, L. lactis subsp. cremoris HP and strains used in inhibitory spectra study (Table 1) were obtained from the culture collection at the Moorepark Food Research Centre, Teagasc, Fermoy, Co. Cork, Ireland. S. aureus C55, phage group II type71 strain , was obtained from Department of Microbiology, University of Otago. Lactococcal strains were grown at 30°C on M17  supplemented with 0.5% w/v lactose (LM17) or glucose (GM17). S. aureus C55 was grown at 37°C on Tryptic Soy broth (Difco). Solid media was prepared by the addition of 1% agar. L. lactis DPC3147 and S. aureus C55 were grown in modified tryptone-yeast (TY) broth  for the purpose of peptide purification. All strains were stocked at -20°C in 40% glycerol. Bacteriocin activity of cultures, L. lactis DPC3147 and S. aureus C55, was assessed using deferred antagonism assay technique . Briefly, 10 μl of overnight culture (108 cells per ml) was spotted on petri dishes containing 20 ml of solidified GM17 and allowed to grow overnight at 30°C or 37°C. The resultant growth was overlaid with molten agar containing 1 × 106 cells of indicator strain listed in Table 1. Inhibitory activity of the concentrated supernatant preparations from L. lactis and S. aureus was assessed using well diffusion assays described by Ryan et al., (1996). In this method, each indicator strain (106 cells per ml of an overnight culture), was seeded into molten agar (48°C). Following this, the concentrated supernatants of lacticin 3147 and staphylococcin C55 (50 μl) were dispensed into wells and the seeded plates were incubated at 30°C or 37°C. In addition, cross complementation assays of lacticin 3147 and staphylococcin C55 peptides was carried out by the well diffusion assay technique also, whereby molten LM17 agar was seeded with the indicator L. lactis HP and 25 μl of concentrated preparations of peptides were combined and assayed in wells.
Bioinformatic analysis and homology modelling
Nucleotide sequence analysis was performed using the DNAStar software package (DNAStar, Madison, WI, U.S.A.). Sequence alignments were performed using the CLUSTAL method  of the Megalign program of the DNAStar software package. The 3D structure of LtnA1 which differs in sequence from C55α by just four amino acids was used as a backbone to predict a model structure for C55α. Homology modelling was performed using SWISS MODEL and PDB Viewer , a fully automated protein structure homology-modelling server. The amino acid sequence was mapped onto LtnA1. The resulting superimposition of C55α on LtnA1 was then visualised using the molecular viewer CHIMERA .
Purification of lacticin (LtnA1 and LtnA2) and staphylococcin C55 (C55α and C55β) peptides
Overnight cultures of the producing strains, L. lactis DPC3147 and S. aureus C55 were inoculated into 2 L of modified TY broth (0.5% inoculum) and incubated overnight at 30°C and 37°C respectively. The cells were subsequently removed by centrifugation at 7,000 × g for 20 min. The resulting supernatant was applied to a column (3 by 23 cm) containing a 60 g bed of XAD-16 resin (Sigma-Aldrich Co. Ltd., Dorset, England) at a flow rate of 900 ml hour-1 and the column then washed with 1 L of 40% aqueous ethanol. Inhibitory activity was subsequently eluted with 1 L of 70% propan-2-ol, pH 2 (adjusted to pH 2 with concentrated HCL). The propan-2-ol was removed by rotary evaporation and the resultant preparation was applied to a Varian C18 Bond Elut Column (Varian, Harbor City, CA) pre-equilibrated with methanol and water. The column was subsequently washed with 120 ml of 40% ethanol and inhibitory activity eluted with 100 ml of 70% propan-2-ol, pH 2. The bacteriocin preparation was concentrated to a volume of ~5 ml through the removal of propan-2-ol by rotary evaporation. Aliquots of 1 ml were then purified by solid phase extraction whereby aliquots were applied to a phenomenex C18 reverse phase (RP)-HPLC column (Phenomenex, Macctesfield, Cheshire, UK) previously equilibrated with 0.1% aqueous trifluoroacetic acid (TFA). The column was subsequently developed in a gradient of 27 to 53% propan-2-ol containing 0.1% TFA at a flow rate of 2.9 ml min-1. Fractions were collected and assayed for activity against the indicator strain L. lactis HP as described above. Each culture was assessed according to their HPLC profile and proposed fractions representing lacticin 3147 peptides LtnA1 and LtnA2 and staphylococcin C55 peptides C55α and C55β were subjected to mass analysis with a Shimadzu Biotech MALDI-TOF Mass Spectrometer (model AXIMA-CFR plus). In order to locate complementary activity during the purification protocol, 25 μl aliquots of putative LtnA1 fractions were cross-tested with isolated peptide LtnA2 and vice versa. Similarly, putative C55α fractions were combined with C55β to investigate complementation. Amino acid analysis of the lacticin 3147 peptides and staphylococcin C55 were performed in the Department of Molecular and Cell Biology, University of Aberdeen, Scotland.
Specific activity determination and generation of isobologram graphs
Ninety six well microtitre plates were used to determine the minimum inhibitory concentration of 50% (MIC50) of L. lactis HP, using a combination of purified preparations of LtnA1, LtnA2, C55α, and C55β. Triplicate wells, containing 3 separate L. lactis HP cultures were included in each microtitre plate. The total volume in each well was 200 μl and experimental wells comprised broth (media), combinations of purified peptides LtnA1, LtnA2, C55α, C55β and 150 μl of a 1 in 10 dilution of overnight L. lactis HP cultures (diluted in growth media, L-M17). In addition, plates contained a number of blank wells (media only) and a number of control wells (untreated L. lactis HP, or L. lactis HP treated alone with LtnA1, LtnA2, C55α, or C55β) and plates were incubated at 30°C. The optical density at 600 nm (OD600 nm) was recorded at time 0 and 5 h (Anthos 2001, Anthos Labtec Instruments). Triplicate readings were averaged, and blanks (media only) were subtracted from these readings. A 50% growth inhibition was determined as half the final OD600 nm ± 0.05. Concentrations of combinations of peptides, which caused 50% growth inhibition of L. lactis HP, were plotted to generate an isobologram.
Genetic replacement study
In order to exactly replace the lacticin 3147 structural genes ltnA1 and ltnA2 on pMRC01 with the staphylococcin C55 structural genes sacαA and sacβA, a spliced overlap extension (SOE) method was employed [23, 37]. To generate this SOE product, primers SOEA, SOEB, SOE1, SOE2, SOE3 and SOED were designed (Table 3). Expand High fidelity (Roche diagnostics, East Sussex, UK) was used to amplify fragments for cloning. Two PCR products (P1 and P3), each 291 bp in length, were amplified from pMRC01 using primer pairs SOEA, SOEB and SOE3, SOED which amplify from either side of the ltnA1A2 genes. The third product (P2), 433 bp in length, was amplified from S. aureus C55 using primer pair SOE1 and SOE2, representing sacαAsacβA. The resulting products were gel extracted using the genecleanII kit (Qbiogene, Inc., Carlsbad, CA). Product P1 and P2 were mixed in a 1:1 ratio, and reamplified by PCR, with the SOEA and SOE2 primers, resulting in a new (P1+P2) fragment. P1+P2 was then mixed in a 1:1 ratio with P3 and reamplified by PCR with primers SOEA and SOED generating a spliced product (P1+P2+P3), whereby the staphylococcin C55 structural genes precisely replace the lacticin structural genes. This product was cloned in to pCR®2.1-TOPO® vector (Invitrogen™ Life Technologies) and sequenced (Lark Technologies) and subsequently cloned into the erythromycin (Ery) resistant integration vector pORI280 generating the plasmid pORI-SOEA (Table 2). The plasmid pORI-SOEA was transformed into E. coli EC101 (RepA+) . Blue colonies on Ery (150 μg ml-1) and 5-bromo-4-chloro-3-indolyl-β-D-galactosidase (X-Gal; 40 μg ml-1) on Luria-Bertani agar (Difco) were selected, and restriction digest was used to confirm the correct insert. The plasmid pORI-SOEA was then electroporated into competent L. lactis MG1363 cells [39, 40] containing both pMRC01 and the temperature-sensitive chloramphenicol resistant (Cmr) RepA+ helper plasmid pVE6007 . Temperature induced curing of pVE6007 at 39°C along with the selective pressure of Ery resistance ensured the integration of pORI-SOEA into pMRC01. To excise pORI280, the Ery resistant and Cm sensitive colonies were passaged in 10 ml of GM17 broth without antibiotic selection at 39°C. After 12 consecutive transfers (0.1% inoculum), white colonies appeared indicating a second crossover event leading to the loss of pORI280 and the generation of Mutant A (Table 2). PCR was used to assess deletion-replacement of target genes, using check primers (Table 3) outside the SOE product in pMRC01 and internal to the C55 structural genes. The above method was also employed to generate MG1363 pMRC01 ltnA1leadersacαAΔltnA1 (LtnA1/Sacα Hybrid) and MG1363 pMRC01 ltnA2leadersacβAΔltnA2 (LtnA2/Sacβ Hybrid) which exactly replaced either the lacticin 3147 ltnA1 gene with staphylococcin C55 propeptide segment of the structural sacαA gene or the lacticin 3147 ltnA2 gene with staphylococcin C55 propeptide segment of the structural sacβA gene respectively, in pMRC01 (Table 2). The primers used to generate LtnA1/Sacα Hybrid were as follows; SOEA, SOE6, SOE7, SOE4, SOE5, and SOED (Table 3). The primers used to generate LtnA2/Sacβ Hybrid were SOEA, SOE8, SOE9, SOE2, SOE3, and SOED (Table 3).
Residue specific mutagenesis
QuikChange XL site-directed mutagenesis (Stratagene) was used to incorporate changes into LtnA1 (changing it into its staphylococcin C55α counterpart) according to manufacturers instructions. Briefly, PCR of the template pORI280-ltnA1A2 generated by Cotter et al., (2005) was used to produce the DNA fragments incorporating the site directed changes encoded on the specifically designed oligonucleotide primers (Table 3). The products were digested with the enzyme Dpn1 and transformed into E. coli host EC101. In this way the following pORI280-LtnA1 derivatives were made: pORI-N15K, pORI-A17N and pORI-L21A (Table 2). PCR was used to screen for candidate E. coli EC101 transformants using check primers (Table 3). In all cases successful mutagenesis was confirmed by DNA sequencing. Mutants were electroporated into MG1363 pMRC01 pVE6007 and were incorporated into pMRC01 by double-crossover homologous recombination in place of the corresponding region (Table 2). DNA sequencing was used to confirm successful mutagenesis in the lactococcal hosts.
Determination of bacteriocin activity
Bacteriocin activity was determined by the agar well diffusion assay as described by Parente and Hill . Molten agar was seeded with an indicator strain and dispensed into petri dishes. Wells of approximately 4.6mm in diameter were bored in the agar and a 50 μl volume of a two fold serial dilution of a bacteriocin preparation was dispensed into each well.
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The authors would like to thank Elaine Lawton for technical assistance. Eileen O'Connor is in receipt of a Teagasc Walsh Fellowship. This work was funded by the National Development Plan 2000–2006 and the Science Foundation of Ireland funded Centre for Science, Engineering and Technology (SCI-CSET): the Alimentary Pharmabiotic Centre.
EBOC Primaryauthor and contributed to all experiments. PC reviewed, Site directed mutagenesis experiments, and intellectual contribution to the manuscript. POC Mass Spectrometry analysis, HPLC analysis and specific activity analysis. OOS performed the homology modelling. JRT intellectual input behind the cross complementation. RPR Principle investigator and intellectual input. CH Principle investigator and intellectual input. All authors have read and approved the final manuscript.