| Title: | "Antagonistic activity of Lactobacillus plantarum C11: two new two-peptide bacteriocins, plantaricins EF and JK, and the induction factor plantaricin A" |
| Author(s): | Anderssen EL; Diep DB; Nes IF; Eijsink VG; Nissen-Meyer J; |
| Address: | "Department of Biochemistry, University of Oslo, Oslo, Norway" |
| DOI: | 10.1128/AEM.64.6.2269-2272.1998 |
| ISSN/ISBN: | 0099-2240 (Print) 1098-5336 (Electronic) 0099-2240 (Linking) |
| Abstract: | "Six bacteriocinlike peptides (plantaricin A [PlnA], PlnE, PlnF, PlnJ, PlnK, and PlnN) produced by Lactobacillus plantarum C11 were detected by amino acid sequencing and mass spectrometry. Since purification to homogeneity was problematic, all six peptides were obtained by solid-phase peptide synthesis and were tested for bacteriocin activity. It was found that L. plantarum C11 produces two two-peptide bacteriocins (PlnEF and PlnJK); a strain-specific antagonistic activity was detected at nanomolar concentrations when PlnE and PlnF were combined and when PlnJ and PlnK were combined. Complementary peptides were at least 10(3) times more active when they were combined than when they were present individually, and optimal activity was obtained when the complementary peptides were present in approximately equal amounts. The interaction between complementary peptides was specific, since neither PlnE nor PlnF could complement PlnJ or PlnK, and none of these peptides could complement the peptides constituting the two-peptide bacteriocin lactococcin G. Interestingly, PlnA, which acts as an extracellular signal (pheromone) that triggers bacteriocin production, also possessed a strain-specific antagonistic activity. No bacteriocin activity could be detected for PlnN" |
| Keywords: | "Amino Acid Sequence Bacteriocins/genetics/isolation & purification/*pharmacology Drug Interactions Genes, Bacterial Lactobacillus/drug effects/genetics/*metabolism Molecular Sequence Data;" |
| Notes: | "MedlineAnderssen, E L Diep, D B Nes, I F Eijsink, V G Nissen-Meyer, J eng Research Support, Non-U.S. Gov't 1998/06/03 Appl Environ Microbiol. 1998 Jun; 64(6):2269-72. doi: 10.1128/AEM.64.6.2269-2272.1998" |
