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Nucleic Acids Res 18 : 4253– 4254 38. Paik SH, Chakicherla A, Hansen JN (1998) Identification and Characterization of the Structural and Transporter Genes for, and the Chemical and Biological Properties of Sublancin 168, a Novel lantibiotic Produced by Bacillus subtilis 168. J Biol Chem 273 : 23134–23142 39. Jung G (1991) Lantibiotics: a survey. In: Jung G, Sahl H-G (eds) Nisin and Novel Lantibiotics. ESCOM Science, Leiden, pp 1–34 52 E. Sablon et al. 40. De Vos WM, Kuipers OP, van der Meer JR, Siezen RJ (1995b) Maturation pathway of nisin and other lantibiotics: post-translational modified antimicrobial peptides exported by Gram-positive bacteria.
Therefore, the leader peptide might have an essential role in biosynthesis, either in that it could contain a specific recognition motif which would direct the precursor towards biosynthetic enzymes and/or in that the leader peptide may interact with the propeptide region to stabilize a conformation which is essential for correct modification . In contrast, the class IAII lantibiotics contain a double-glycine type processing site and a leader peptide that matches the consensus of the non-lantibiotic class II bacteriocins [21, 40] (Fig.
Besides PlnP, PlnM could hence be considered as a second valid candidate for PlnN immunity, although located in the 5¢ end of the operon. Two proteins, PlnG (ABC transporter) and plnH (accessory protein), shown to constitute an ATP-dependent transport apparatus, were located downstream of the plnABCD operon . The homologous counterparts in the sakacin A operon were named SapT and SapE, respectively . The region encoding plantaricin A activity has proven to be a multiple gene locus consisting of not less than 22 different open reading frames in the same or opposite orientation to the previously described plnABCD operon [49, 134].