Lactiplantibacillus paraplantarum BPF2 and Pediococcus acidilactici ST6, Two Bacteriocinogenic Isolated Strains from Andalusian Spontaneous Fermented Sausages

Traditional spontaneously fermented foods are well known for their sensory and safety properties, which is mainly due to their indigenous microflora. Within this group of food, Mediterranean dry-cured sausages stand out as a significant source of lactic-acid bacterial strains (LAB) with biotechnological properties, such as their antimicrobial activity. The aim of this study was to investigate the biodiversity of antagonistic LAB strains from different Andalusian traditional sausages, such as salchichón and chorizo. First, a screening was carried out focusing on the antimicrobial activity against foodborne pathogens, such as Listeria monocytogenes, Escherichia coli, Clostridium perfringens, and Staphylococcus aureus, selecting two strains due to their higher antibiosis properties, both in agar and liquid media. These bacteria were identified as Lactiplantibacillus paraplantarum BPF2 and Pediococcus acidilactici ST6. In addition, genomic studies confirmed the presence of certain structural genes related to the production of bacteriocins. Finally, the culture supernatants of both strains were purified and analyzed by LC-MS/MS, obtaining the relative molecular mass and the amino acid sequence and identifying the peptides as the bacteriocins Pediocin-PA and Leucocin K. In conclusion, genomes and antimicrobial substances of P. acidilactici ST6, a Pediocin-PA producer, and Lpb. paraplantarum BPF2, a Leucocin K producer, isolated from Andalusian salchichón and chorizo, respectively, are presented in this work. Although further studies are required, these strains could be used alone or in combination as starters or protective cultures for the food industry.


Introduction
Fermentation is one of the oldest known preservation methods and has been one of the most used in Mediterranean countries since ancient times [1][2][3]. Spontaneously fermented meat sausages have a long tradition in Mediterranean countries as one of the most important traditional foods consumed throughout Europe [4]. Spanish fermented meat sausages such as chorizo or salchichón are generally made with small pieces of pork, back fat, sodium chloride, sodium nitrate-nitrite, and different spices, which are mixed homogeneously and stuffed into casings. The fermentation/maturation process occurs by storing the sausage in a well-ventilated chamber for 20-30 days under approximate temperature conditions of 25 ± 2 • C and 75-80% relative humidity. These conditions stimulate acidification and dehydration. The participation of different groups of bacteria is

Isolation of LAB Species from Dry-Fermented Sausages
LAB strains were isolated from traditional dry sausages collected from Andalusia, in the south of Spain. The isolation of LAB was performed based on the method described by Zhu [13]. A total of 14 samples of artisanal salchichón and chorizo from different locations of Andalusia (Spain), produced without starter addition, were collected: a salchichón from Alhendín (SA), a salchichón from Bérchules (SB), a salchichón from Écija (SE), a salchichón from Olvera (SCT), a salchichón from Grazalema (ST), a salchichón from Baños de la Encina (SBE), a chorizo from Bérchules (CPN), a chorizo from Chirivel (CCH), a chorizo from Prado Negro (BPF), a chorizo from Ubrique (CCU), a chorizo from Cazorla (CCA), a chorizo from Écija (CHE), a chorizo from Órgiva (CD), and a chorizo from Olvera (CT). For sampling purposes, we collected three samples from each sausage: two samples from the distal ends and one sample from the central portion. Sausage samples (25 g) were cut into pieces and added to 225 mL of sterile saline solution (0.85%, w/v). The samples were processed in sterile bags with filters (GASPAK Cromakit, Granada, Spain), and homogenized for 3 min in a paddle homogenizer (MASTICATOR, IUL Instruments, Barcelona, Spain). Subsequently, 0.1 mL of each 10-fold dilution series was spread on Man Rogosa Sharpe Agar, medium for selective isolation and culture lactic-acid bacteria (MRS Agar, Scharlab, Barcelona, Spain) and incubated at 30 • C for 48 h. Colonies were selected by streak plating three times until uniform colonies were obtained as candidate LAB strains. Candidate isolates were stored at refrigeration temperature before use.

Screening and Selection of Antagonist LAB Strains
Antimicrobial activity by candidate LAB strains was determined by the diffusion agar method according to Alonso et al. [23], against L. monocytogenes DSM 112142, S. aureus CECT 520, and E. coli CECT 516. Bacteria were grown in the general enriched media Brain Heart Infusion (BHI, Scharlab, Barcelona, Spain). The pathogenic cultures were incubated overnight at 37 • C. Then, these bacteria were spread in Brain Heart Infusion Agar (BHA, Scharlab) dishes using a bacterial suspension adjusted to 1 × 10 6 CFU/mL to form a bacterial lawn. Once the plate was dried, drops of 10 µL of different isolated strains. After incubation at 30 • C for 48 h, the plates were examined to determine the absence/presence of inhibition zones and results were interpreted as positive (+) or negative (−). For positives, three levels of intensity were established depending on the diameter of the inhibition zone: + (1-10 mm); ++ (11-15 mm); +++ (>15 mm). Independent tests were carried out in duplicate for each pathogenic bacterium. From this point forward, a screening process was initiated to select the isolates that demonstrated higher antibacterial activity. The next step was to detect the production of extracellular antimicrobial inhibitors by each of the isolates that previously produced antibiosis in a solid medium against the target pathogens. Thus, the selected strains were inoculated in sterile tubes with 9 mL of BHI and incubated for 24 h at 30 • C. Then, 1.5 mL of each culture was centrifuged (13,000× g) and filtered using 3 mL syringes to which was attached a polyethersulfone (PES) filtration membrane (Merck Millipore, Carrigtwohill, Ireland) with a pore size of 0.22 µm, the filtrates were collected in sterile microcentrifuge tubes. To assess the antimicro- bial activity of the filtrates, the well technique described by Tagg and McGiven [23,24] was employed, using L. monocytogenes CECT 4032, Cl. perfringens CECT 821, and S. aureus CECT 239 as the target bacteria [24,25]. All target bacteria were incubated at 30 • C for 24-48 h. Cl. perfringens was incubated under anaerobic conditions (AnaeroGen; Thermo Fisher Scientific, Landsmeer, The Netherlands). Each sample was tested in duplicate. Once the indicator strain has grown, the appearance of inhibition halos around the wells was observed and measured in millimeters. Therefore, we were able to determine if the strain had produced the compound responsible for the antimicrobial activity observed in culture supernatants. Finally, the two strains that exhibited greater antibiosis and a broader spectrum of inhibition against target strains were selected.

Strain Identification and Characterization
Identification was based upon phenotypic characteristics, including cell morphology and Gram-staining, catalase activity, API50 system (BioMérieux, Craponne, France), ability to grow at 10 and 45 • C and the presence of 6.5% (w/v) NaCl.
For genotypic characterization, genomic DNA was extracted from pure cultures according to Martín-Platero et al. [26]. Identification of the selected strains was carried out by searching homologies of 16S ribosomal RNA in the BLASTN database (National Center for Biotechnology Information) using BLAST [27]. In addition, both genomes were sequenced with the Illumina HiSeq4000 platform by STAB VIDA (Caparica, Portugal), assembled with SPAdes 3.13 [28], and annotated with Prokka 1.13.3 [29]. Homologies between gene clusters were revealed by aligning in pairs using Blastn suit-2 sequences [30]. Functional analysis of genomes was performed through InterProScan v5.50-84.0 [31,32], which classifies proteins into families, predicting domains and important sites. InterproScan generates Gene ontology terms associated with each gene. Afterwards, the Gene Ontology Database [33][34][35] was used to perform a functional analysis of genes and their products.
Finally, to determine if the genomes were associated with the structural gene of any bacteriocin, a tblastn (version 2.10.1+) was run with a 10-6 e-value threshold [36,37] between our genomes and bacteriocins from the BACTIBASE databases [38].

Bacteriocin Production and Purification Assay
First, production in a liquid medium and purification by cation exchange chromatography was performed. Therefore, flasks with 1 L of MRS medium in 0.1 mol/L sodium phosphate buffer (pH 7.2) were inoculated at 5% with an overnight culture of each of the strains of interest (culture in stationary phase). The cultured flasks (1 L) were incubated at 30 • C overnight and centrifuged for 20 min at 4 • C and 4750 rpm, collecting the supernatant to assess their inhibition by the well technique [24]. The recovery of the bacteriocins was carried out following Abriouel et al. [39]. The supernatants at pH7 were mixed with 1 N NaOH, 200 mL of Carboxymethyl Sephadex CM-25 (GE Healthcare, Madrid, Spain), and stirred for 30 min. Then, they were left to settle for 30 min. Afterwards, the supernatants were removed, and the CM-25 gel was transferred to a cylindrical filtering funnel with a plate with a porosity of 100-160 microns (Pobel, Madrid, Spain). The gel was washed with three volumes of distilled water, followed by two volumes of 1 M NaCl and two volumes of 1.5 M to elute the adsorbed bacteriocin. During the process, 50 mL fractions were collected manually, these were sterilized by filtration 0.22 µm PES (Merck Millipore, Cork, Ireland), and the activity was measured using the abovementioned well technique.
Subsequently, the determination of the molecular weight of both bacteriocins was carried out by LC-MS/MS. For this purpose, a tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) (Sigma-Aldrich, Madrid, Spain) system was used [40]. A total of 20 µL of the sample was mixed with 6 µL of Laemmli sample buffer (Bio-Rad), heated to 100 • C for 3 min and cooled to room temperature. The mixtures were injected into the wells of the 12% precast polyacrylamide gel (Criterion TGX™, Bio-Rad, Hercules, CA, USA), using standard proteins as molecular weight markers (Spectra™ Multicolor Low Range Protein Ladder, Thermo Scientific™, Madrid, Spain), Electrophoresis was carried out using the Criterion™ Cell (300 V, 20 min) (Hercules, CA, USA). The gel was washed with sterile distilled H 2 O and divided into three equal-sized fragments, each including a band of molecular weight markers. Two of the gel fragments were fixed with 25% (v/v) isopropanol and 10% (v/v) glacial acetic acid (Sigma) for 4 h, then washed with sterile distilled H 2 O. One of the fixed gels was stained with Coomassie blue (Sigma) overnight with constant shaking at room temperature. Finally, a solution of water and methanol was used to attenuate the gel. The bands were revealed by a gel documentation system. For the antimicrobial activity test, the gel fragment without fixation process was placed in a sterile Petri dish, then covered with BHA agar containing the indicator strain L. monocytogenes DSM 112142. The dish was kept at 4 • C for 30 min and then incubated at 30 • C overnight. The last sample of fixed gel was stored in sterile distilled H 2 O for identification by LC-MS/MS. Molecular mass determination and amino acid analysis of the bacteriocins from two selected strains were carried out by the Proteomics Unit at the López-Neyra Institute of Parasitology and Biomedicine, (IPBLN-CSIC, Granada, Spain). The pieces of gel that showed antimicrobial activity and contained the proteins of interest, were analyzed by LC-MS/MS. For this, they were cut manually and digested with trypsin gel (Promega, Madison, WI, USA) using a Digest MSPro (Intavis, Koeln, Germany) following standard procedures. Briefly, gel slices were reduced with 10 mM DTT, alkylated with 55 mM iodoacetamide, dehydrated with acetonitrile, and then digested with trypsin for 18 h at 30 • C. Peptides were extracted with 0.2% TFA and eluted with 30% acetonitrile (Sigma). The eluates from both extractions were dried in a vacuum centrifuge and stored at −20 • C. Analysis by mass spectrometry (LC-MS/MS) was performed by nLC (easy nanoLC, Proxeon, Thermo Fisher) coupled to an ion trap type mass spectrometer (Amazon Speed ETD, Bruker, Madrid, Spain) equipped with a captive source. The chromatographic separation was carried out on a C18 column (15 µm × 15 cm, 3 µm, 100 A) using a flow 300 nL/min with gradients from 5 to 30% B in 120 min (buffer A: 0.1% Fluoroacetic (FA) in water; buffer B: 0.1% FA in AcN). The mass analysis has been carried out in the range of 390-1400 (m/z). A total of 10 precursors per cycle were selected for fragmentation, establishing a dynamic exclusion of 0.5 min. Protein identification was performed using the ProteinScape program (Bruker) and MASCOT (Matrix Science, Boston, MA, USA) as search engines. The search was carried out using the Swiss-Prot database with a filter for the bacteria isolates, both downloaded from UniProt. In all cases, carbamidomethylation was considered to be a fixed modification, and oxidation was a variable modification.

Bacteriocin Stability against Heat, pH, and Enzymes
The two bacteriocin-producing strains were grown in 0.5 L of MRS broth (30 • C, 24 h) then 4750 g centrifuged at 4 • C for 35 min and filtered through a 500 mL Vacuum Filtration System, (0.22 µm PES Membrane, VWR International) to obtain a cell-free filtrate. The methodology indicated by Ahn et al. [41] was followed to test pH and thermal stability, the cell-free filter was adjusted to pH 6.5 with 4 N-HCl or NaOH and then heated at 60 • C, 80 • C, and 100 • C for 30 min each, or autoclaved (121 • C, 15 min). The activity was examined at various pHs by adjusting the cell-free filtered to pH 2, 3, 5, 7, 9, and 11 with 4 N-HCl or NaOH, which was then held at 30 • C for 2 h. Each sample was neutralized to pH 6.5. The samples were then membrane filtered (PES filter of 0.22 µm) and analyzed by the agar well diffusion assay as described above. Enzymatic degradation assay as proposed by Zhao et al. [42] was carried out to verify the protein nature of the inhibitor produced by the bacteria under study. For this, three proteinase enzymes were used: papain (≥10 units/mg, Sigma), trypsin (2000 units/mg, Sigma), and proteinase K (30 units/mg, Sigma). For each bacteria cell-free filter, the enzymes were added to each one at a concentration of 0.5 mg/mL and incubated at 37 • C for 2 h [43,44]. They were heated at 80 • C for 5 min to make those enzymes inactivated. After that, the antimicrobial activity was tested against L. monocytogenes DSM 112142 using the previously described well diffusion agar technique.

Antagonism Assays in Cocultures
The inhibition of foodborne pathogen growth was evaluated following Baños et al. [45]. Overnight cultures of the two LAB-selected strains and pathogenic strains (L. monocytogenes CECT 4032, DSM 112142, and C. perfringens CECT 821) were diluted at 10 3 CFU/mL into BHI (Scharlab), incubated at 30 • C and shaken at 130 rpm, individually and in cocultures [46]. In the case of Cl. perfringens, the samples were incubated under anaerobic conditions (AnaeroGen; Thermo Fisher Scientific). At selected times of 0, 1, 5, and 10 days, samples were collected and serially diluted into a sterile saline solution. Dilutions were plated in triplicate into MRS Agar for LAB bacteria, Compass ® Listeria Agar (Biokar Diagnostics SA, Allonne, France) and CHROMagar ® C. perfringens (Scharlab), two chromogenic and selective media for quantification of L. monocytogenes and C. perfringens, respectively. The average number of colonies obtained after 48 h incubation at 30 • C was used to establish the growth curves of those bacteria cultured alone and co-cultivated.

Statistical Analysis
Statistical analysis and figures were performed with GraphPad Prism 8.0 software (GraphPad Software Inc., San Diego, CA, USA). All results were expressed as the mean ± standard deviation (SD). Differences between means were tested for statistical significance using a one-way analysis of variance (ANOVA).

Isolation of LAB Species from Dry-Fermented Sausages
The microbiota present in 14 different samples of sausages from Andalusia was explored focusing on lactic-acid bacteria (LAB) with potential biopreservation properties [3,17,47,48]. A total of 640 colonies were obtained on the MRS agar, which were considered potential candidates for antagonistic LAB.

Screening and Selection of Antagonist LAB Strains
The antimicrobial activity of the 640 initially isolated strains was evaluated using the agar diffusion method, obtaining a total of 62 strains that produced some inhibition against target bacteria L. monocytogenes, S. aureus, or E. coli ( Table 2). As expected, the tested strains showed remarkable activity against Gram-positive bacteria [47,49,50] but did not exhibit activity against Gram-negative bacteria. In a second screening, 12 bacteria ( Table 2) that showed the highest antagonist activity against the target bacteria were selected. These bacteria were employed to perform extracellular antimicrobial activity assays according to the previously described methodology, and the findings are reported in Table 3.
All strains exhibited antibiosis against the three target strains, with most of them being particularly active against L. monocytogenes ( Table 3). The BPF2 and ST6 strains were ultimately chosen due to their significant anti-Listeria activity as well as their inhibitory effects against S. aureus and Cl. perfringens.
After selecting the two strains with the most favorable antimicrobial properties, an antibiosis test was performed, confirming the absence of antagonism between both strains and therefore allowing for their potential combined use as starters cultures [51,52].

Identification and Genomic Studies
Before carrying out the genomic studies, the phenotypic characterization revealed that ST6 and BPF2 strains were Gram-positive cocci and bacilli, respectively. In addition, initial identification using the API50 system indicated that ST6 was associated with Pediococcus spp., while BPF2 was related to the Lactobacillus genus. Both strains were catalase-negative and demonstrated the ability to grow within a temperature range of 20-40 • C and in the presence of 6.5% (w/v) NaCl.
After sequencing, assembly, and annotation, analysis of the 16S gene predicted that our strains ST6 and BPF2 correspond to Pedicoccus acidilactici and Lactiplantibacillus paraplantarum species, respectively. The genome of P. acidilactici has a size of 1.95 Mb, with  [53][54][55][56][57]. Other characteristics of these genomes are summarized in Table 4.   Gene Ontology (GO) analysis showed that the cellular component category membrane was the most abundant term in both genomes ( Figure 1A). In the molecular function category, DNA binding and ATP binding were the most abundant terms in Lpb. paraplantarum and P. acidilactici, respectively ( Figure 1B). In addition, in the biological processes category, the regulation of DNA-templated transcription prevailed in P. acidilactici, while transmembrane transport was in Lpb. paraplantarum ( Figure 1C). Other GO results are summarized in Table 5.     InterProScan classified 1721 and 2850 proteins from P. acidilactici and Lpb. Paraplantarum, respectively. A total of 6059 families were assigned to 1671 of the total proteins (97.1%, 1671/1721) in P. acidilactici. In the case of Lpb. paraplantarum, 9049 families were assigned to The results of tblastn against the BACTIBASE database showed that Pediocin-PA was found in both genomes. In addition, five other bacteriocins were found in the Lpb. paraplantarum BPF2 genome: Mutacin III/1140, Leucocin K, Plantaricin A, Plantaricin E, and Plantaricin F. Furthermore, the gene clusters responsible for the production of bacteriocin were found (Figure 3 A,B). The Pediocin-PA gene cluster was formed by four genes, pedABCD, in both cases. The Plantaricin A gene cluster found in Lpb. paraplantarum BPF2 shows high similarities to the pln loci previously described from Lactobacillus plantarum C11 and WCFS1 [58,59] (Figure  4). The pln locus contains five inducible operons: plnABCD, plnEFI, plnJKLR, plnMNOP, and plnGHSTUVW. In our Lpb. paraplantarum, plnABCD, plnEFI, and plnGHSTUVW The results of tblastn against the BACTIBASE database showed that Pediocin-PA was found in both genomes. In addition, five other bacteriocins were found in the Lpb. paraplantarum BPF2 genome: Mutacin III/1140, Leucocin K, Plantaricin A, Plantaricin E, and Plantaricin F. Furthermore, the gene clusters responsible for the production of bacteriocin were found ( Figure 3A,B). The results of tblastn against the BACTIBASE database showed that Pediocin-PA was found in both genomes. In addition, five other bacteriocins were found in the Lpb. paraplantarum BPF2 genome: Mutacin III/1140, Leucocin K, Plantaricin A, Plantaricin E, and Plantaricin F. Furthermore, the gene clusters responsible for the production of bacteriocin were found (Figure 3 A,B). The Pediocin-PA gene cluster was formed by four genes, pedABCD, in both cases. The Plantaricin A gene cluster found in Lpb. paraplantarum BPF2 shows high similarities to the pln loci previously described from Lactobacillus plantarum C11 and WCFS1 [58,59] ( Figure  4). The pln locus contains five inducible operons: plnABCD, plnEFI, plnJKLR, plnMNOP, and plnGHSTUVW. In our Lpb. paraplantarum, plnABCD, plnEFI, and plnGHSTUVW The Pediocin-PA gene cluster was formed by four genes, pedABCD, in both cases. The Plantaricin A gene cluster found in Lpb. paraplantarum BPF2 shows high similarities to the pln loci previously described from Lactobacillus plantarum C11 and WCFS1 [58,59] (Figure 4). The pln locus contains five inducible operons: plnABCD, plnEFI, plnJKLR, plnMNOP, and plnGHSTUVW. In our Lpb. paraplantarum, plnABCD, plnEFI, and plnGHSTUVW operons are present, but the list is not complete. Operon plnJKLR appears to be truncated as it lacks the bacteriocin genes plnJK. plnT gene and plnMNOP operons are absent. The plnEFI genes code for two-peptide bacteriocin (plantaricins EF) and their cognate immunity protein (PlnI). plnLR encodes for a putative immunity protein containing a protease CAAX signature and a putative protein with an unknown function, respectively. plnGH codes for an ABC-transporter and an accessory protein, respectively. Both of these constitute an ABC-transport system involved in peptide secretion, utilizing a double-glycine leader. plnSTUVW exhibits considerable homology among itself and with proteins belonging to the type II CAAX amino protease family. Finally, plnABCD codes for a quorum-sensing network that is essential for expressing all the genes in the pln locus [60], where the pheromone peptide, Plantaricin A, is involved. In addition, the gene responsible for Leucocin K appears upstream of plnABCD in Lpb. paraplantarum ( Figure 3B). operons are present, but the list is not complete. Operon plnJKLR appears to be truncated as it lacks the bacteriocin genes plnJK. plnT gene and plnMNOP operons are absent. The plnEFI genes code for two-peptide bacteriocin (plantaricins EF) and their cognate immunity protein (PlnI). plnLR encodes for a putative immunity protein containing a protease CAAX signature and a putative protein with an unknown function, respectively. plnGH codes for an ABC-transporter and an accessory protein, respectively. Both of these constitute an ABC-transport system involved in peptide secretion, utilizing a doubleglycine leader. plnSTUVW exhibits considerable homology among itself and with proteins belonging to the type II CAAX amino protease family. Finally, plnABCD codes for a quorum-sensing network that is essential for expressing all the genes in the pln locus [60], where the pheromone peptide, Plantaricin A, is involved. In addition, the gene responsible for Leucocin K appears upstream of plnABCD in Lpb. paraplantarum ( Figure 3B). Numerous bacteriocinogenic strains of P. acidilactici have been isolated from fermented food products derived from both plants and animals. Furthermore, these strains have been extensively studied for their probiotic and biopreservative properties [17]. Consistent with our findings, some authors have also reported the isolation of Lpb. paraplantarum strains with biotechnological interest, including bacteriocin production, from spontaneously fermented foods such as fermented mushrooms, Chinese pickles, and Korean fermented foods [61][62][63]. The color scale represents the similarity between the different genes: light red and blue = 68% similarity; dark red and blue = up to 100% similarity; red corresponds to direct similarity and blue to inverse similarity. Similarities found upstream and downstream between Lpb. paraplantarum BPF2 and WCF1 correspond, respectively, to the genes brnQ1 and napA1, which are not part of the pln regulon, and to the helD gene that encodes for a DNA helicase IV.

Identification of the Bacteriocins by LC-MS/MS
In this study, an SDS-PAGE was performed on the samples that showed the highest activity after the purification step. The SDS-PAGE gel coupled to an antimicrobial activity test showed a zone of inhibition in the lanes corresponding to the P. acidilactici ST6 and Lpb. paraplantarum BPF2 samples. The bands responsible for the zone of inhibition The color scale represents the similarity between the different genes: light red and blue = 68% similarity; dark red and blue = up to 100% similarity; red corresponds to direct similarity and blue to inverse similarity. Similarities found upstream and downstream between Lpb. paraplantarum BPF2 and WCF1 correspond, respectively, to the genes brnQ1 and napA1, which are not part of the pln regulon, and to the helD gene that encodes for a DNA helicase IV.
Numerous bacteriocinogenic strains of P. acidilactici have been isolated from fermented food products derived from both plants and animals. Furthermore, these strains have been extensively studied for their probiotic and biopreservative properties [17]. Consistent with our findings, some authors have also reported the isolation of Lpb. paraplantarum strains with biotechnological interest, including bacteriocin production, from spontaneously fermented foods such as fermented mushrooms, Chinese pickles, and Korean fermented foods [61][62][63].

Identification of the Bacteriocins by LC-MS/MS
In this study, an SDS-PAGE was performed on the samples that showed the highest activity after the purification step. The SDS-PAGE gel coupled to an antimicrobial activity test showed a zone of inhibition in the lanes corresponding to the P. acidilactici ST6 and Lpb. paraplantarum BPF2 samples. The bands responsible for the zone of inhibition corresponded to a molecular weight in both cases between 10 and 4.6 kDa. The amino acid sequence and the molecular mass were analyzed using an LC-MS/MS system. The results obtained in the case of the bacteriocin from P. acidilactici ST6 were 5378 Da for the molecular mass. The MS/MS graph was analyzed ( Figure 5) to determine the amino acid sequence of ST6 as a function of the ionic strength of each fragment. The amino acid sequence of bacteriocin ST6 was His-Ser-Cys-Ser-Val-Asp-Trp-Gly-Lys (HSCSVDWGK). Comparison with known proteins in the UniProt database revealed that the amino acid sequence of ST6 matches the amino acid sequence of the antimicrobial peptide Pediocin-PA. The results obtained are consistent with the genomic study carried out previously in which P. acidilactici ST6 presented only the Pediocin-PA gene, which belongs to class IIa, linear peptides with 25 to 58 residues containing one or two disulfide bridges [64]. These have been named the "family of pediocins" in honor of the first representative of this class and the most widely studied, pediocin-PA-1 [65].
corresponded to a molecular weight in both cases between 10 and 4.6 kDa. The amino acid sequence and the molecular mass were analyzed using an LC-MS/MS system. The results obtained in the case of the bacteriocin from P. acidilactici ST6 were 5378 Da for the molecular mass. The MS/MS graph was analyzed ( Figure 5) to determine the amino acid sequence of ST6 as a function of the ionic strength of each fragment. The amino acid sequence of bacteriocin ST6 was His-Ser-Cys-Ser-Val-Asp-Trp-Gly-Lys (HSCSVDWGK). Comparison with known proteins in the UniProt database revealed that the amino acid sequence of ST6 matches the amino acid sequence of the antimicrobial peptide Pediocin-PA. The results obtained are consistent with the genomic study carried out previously in which P. acidilactici ST6 presented only the Pediocin-PA gene, which belongs to class IIa, linear peptides with 25 to 58 residues containing one or two disulfide bridges [64]. These have been named the "family of pediocins" in honor of the first representative of this class and the most widely studied, pediocin-PA-1 [65].
In the case of Lpb. paraplantarum BPF2, the molecular mass was 5825 Da, and the MS/MS graph ( Figure 6) was analyzed to determine the amino acid sequence of the BPF2 peptide as a function of the ionic strength of each fragment. The amino acid sequence was Phe-Leu-Ala-Ser-Ala-Thr-His-Tyr-Try-Gly-Lys (FLASATHYYGK). Comparison with known proteins in the UniProt database revealed that the amino acid sequence matches the amino acid sequence of the antimicrobial peptide Leucocin K. The results obtained in the genomic study revealed genes to produce six different bacteriocins: Pediocin-PA, Mutacin III, Leucocin K, Plantaricin A, Plantaricin E, and Plantaricin F. However, the LC-MS/MS analysis revealed the presence of only Leucocin K, which presented a value of emPAI (exponentially modified protein abundance index) of 0.77 [66], which indicates a high concentration of Leucocin K in the analyzed sample. Finally, the amino acid sequence obtained by LC-MS/MS was compared with the encoded sequence in genomes of BPF2 and ST6 strains, confirming the identification of both bacteriocins. The presence of Pediocin-PA genes in the genomes of Lpb. paraplantarum BPF2 and P. acidilactici ST6 could indicate the resistance of both strains to Pediocin-PA. On the other hand, although most of the Leucocin produced by Leuconostoc has been reported to exhibit anti-listerial activity, this fact is not extensible to other Gram-positive bacteria, which could explain the resistance of P. acidilactici ST6 to Leucocin K [67]. These aforementioned facts may indicate the compatibility of both bacteria and their potential synergistic use to produce fermented foods. In the case of Lpb. paraplantarum BPF2, the molecular mass was 5825 Da, and the MS/MS graph ( Figure 6) was analyzed to determine the amino acid sequence of the BPF2 peptide as a function of the ionic strength of each fragment. The amino acid sequence was Phe-Leu-Ala-Ser-Ala-Thr-His-Tyr-Try-Gly-Lys (FLASATHYYGK). Comparison with known proteins in the UniProt database revealed that the amino acid sequence matches the amino acid sequence of the antimicrobial peptide Leucocin K. The results obtained in the genomic study revealed genes to produce six different bacteriocins: Pediocin-PA, Mutacin III, Leucocin K, Plantaricin A, Plantaricin E, and Plantaricin F. However, the LC-MS/MS analysis revealed the presence of only Leucocin K, which presented a value of emPAI (exponentially modified protein abundance index) of 0.77 [66], which indicates a high concentration of Leucocin K in the analyzed sample. Finally, the amino acid sequence obtained by LC-MS/MS was compared with the encoded sequence in genomes of BPF2 and ST6 strains, confirming the identification of both bacteriocins.
The presence of Pediocin-PA genes in the genomes of Lpb. paraplantarum BPF2 and P. acidilactici ST6 could indicate the resistance of both strains to Pediocin-PA. On the other hand, although most of the Leucocin produced by Leuconostoc has been reported to exhibit anti-listerial activity, this fact is not extensible to other Gram-positive bacteria, which could explain the resistance of P. acidilactici ST6 to Leucocin K [67]. These aforementioned facts may indicate the compatibility of both bacteria and their potential synergistic use to produce fermented foods.

Effect of Temperature, pH, and Different Enzymes on Bacteriocins
The stability of the two bacteriocins was tested under different conditions of temperature, pH, and treatment with enzymes. The results presented in Table 6 show that Pediocin-PA activity was maintained in a wide pH range between 2 and 10 and it was sensitive to protease enzymes such as pepsin, papain, and trypsin. The antimicrobial activity was not affected by heating at 80 • C for 30 min. However, at higher temperatures, its activity began to reduce with a complete loss of efficacy observed at 121 • C for 15 min. This indicates that Pediocin is thermolabile [68][69][70]. In the case of Leucocin K from BPF2, results similar to those reported by other authors were obtained [71]. This bacteriocin was sensitive to the tested proteases and showed good thermal stability up to 80 • C similar to Pediocin, completely losing activity at 121 • C, with a wide active pH range from 2 to 10 without loss of efficacy (Table 6).
Other authors have recently reported bacteriocinogenic strains of P. acidilactici isolated from meat products. The strain P. acidilactici LMQS 154.1, isolated from traditionally produced fermented sausages in Germany, has been described [5]. Consistent with our findings, this strain also demonstrated significant anti-listerial activity associated with the production of Pediocin-PA-1 [5]. In another recent work, P. acidilactici ST3522BG isolated from silage has been identified as a pediocin-PA-1 producer with high antimicrobial activity against Listeria and vancomycin-resistant Enterococcus species [72]. Furthermore, P. acidilactici ST3522BG produces other antifungal metabolites with the potential for the inhibition of mycotoxigenic molds [72].
In relation to the bacteriocinogenic strains of Lpb. paraplantarum, recent studies have highlighted the capability of Lpb. paraplantarum RX-8, isolated from traditional pickles, to produce plantaricin, linked to its antibacterial activity [61]. Furthermore, other studies have highlighted the potential use of similar bacteriocinogenic strains of Lactiplantibacillus plantarum for animal nutrition, showing promising results in mitigating methane emissions in ruminants [73].

Antagonism Assays in Cocultures
The objective of these assays was to demonstrate the competitive exclusion of the P. acidilactici ST6 and Lpb. paraplantarum BPF2 against L. monocytogenes and Cl. perfringens pathogens. Competitive exclusion can be defined as the state in which coexisting bacterial species in the same ecological niche compete for limited resources such as nutrients and space through either competition or interference mechanisms [74]. In this instance, an interference mechanism was observed as both strains exhibited the ability to produce bacteriocins. As can be observed in Figure 7, the growth of LAB strains in both the control and the co-culture was similar, indicating that their growth is not affected by the presence of pathogens. Nevertheless, for L. monocytogenes DSM 112142 and CECT 4032, a rapid decline of bacterial counts was observed after 48 h, and complete absence was achieved after 5 days of coexistence with both lactic-acid bacteria strains. Although Cl. perfringens showed lower sensitivity compared to Listeria, a significant decrease in bacterial counts was observed during co-culture with both LAB strains, leading to the complete elimination of the pathogen after 10 days.
interference mechanism was observed as both strains exhibited the ability to produce bacteriocins. As can be observed in Figure 7, the growth of LAB strains in both the control and the co-culture was similar, indicating that their growth is not affected by the presence of pathogens. Nevertheless, for L. monocytogenes DSM 112142 and CECT 4032, a rapid decline of bacterial counts was observed after 48 h, and complete absence was achieved after 5 days of coexistence with both lactic-acid bacteria strains. Although Cl. perfringens showed lower sensitivity compared to Listeria, a significant decrease in bacterial counts was observed during co-culture with both LAB strains, leading to the complete elimination of the pathogen after 10 days.
In accordance with our results, other authors have described the activity of pediocin-PA-producing strains for the control of L. monocytogenes in both in vitro and in efficacy trials in different food models [75][76][77][78][79]. Other studies have similarly described the ability of certain bacteriocinogenic strains of Pediococcus to inhibit Clostridium species [75,76,80]. On the other hand, Leucocins are bacteriocins specific to Leuconostoc, with very little evidence of their production in other LAB genera. This fact makes the Lpb. paraplantarum BPF2 strain particularly unique as Leucocin K producer. As with our results, Leucocin K7 from L. mesenteroides has demonstrated anti-Listeria activity in vitro and in foods such as milk [71]. and Clostridium perfringens CECT821. The bars represent means ± standard deviations of three independent tests. ** p < 0.01; *** p < 0.001; **** p < 0.0001 respect to controls.

Conclusions
A biodiversity study of spontaneously fermented Andalusian sausages revealed the significant potential of these foods as a source for the isolation of lactic-acid bacteria with interesting technological and antibiosis properties. This work conducted a screening study from hundreds of isolated strains obtained from artisanal salchichones and chorizos, Figure 7. Bacterial survival in cocultures of Pediococcus acidilactici ST6 and Lactiplantibacillus paraplantarum BPF2 with Listeria monocytogenes DSM 112142 and CECT4032 and Clostridium perfringens CECT821. The bars represent means ± standard deviations of three independent tests. ** p < 0.01; *** p < 0.001; **** p < 0.0001 respect to controls.
In accordance with our results, other authors have described the activity of pediocin-PA-producing strains for the control of L. monocytogenes in both in vitro and in efficacy trials in different food models [75][76][77][78][79]. Other studies have similarly described the ability of certain bacteriocinogenic strains of Pediococcus to inhibit Clostridium species [75,76,80]. On the other hand, Leucocins are bacteriocins specific to Leuconostoc, with very little evidence of their production in other LAB genera. This fact makes the Lpb. paraplantarum BPF2 strain particularly unique as Leucocin K producer. As with our results, Leucocin K7 from L. mesenteroides has demonstrated anti-Listeria activity in vitro and in foods such as milk [71].

Conclusions
A biodiversity study of spontaneously fermented Andalusian sausages revealed the significant potential of these foods as a source for the isolation of lactic-acid bacteria with interesting technological and antibiosis properties. This work conducted a screening study from hundreds of isolated strains obtained from artisanal salchichones and chorizos, selecting two strains for showing the broadest spectrum of antibiosis against food pathogens. P. acidilactici ST6, a pediocin-PA producer isolated from salchichón, and Lpb. paraplantarum BPF2, a Leucocin K producer isolated from chorizo, are presented in this work. Both strains exhibited significant inhibitory activity against L. monocytogenes and Cl. perfringens.
Further studies are required to delve into the genomic characteristics and their potential use in food models. In addition, it would be advisable to investigate their influence on the technological and sensory properties of foods in which they could be used as potential starters or protective cultures.