Discovery, Production and Modification of Five Novel Lantibiotics Using the Promiscuous Nisin Modification Machinery

• Published in: ACS synthetic biology Vol. 5; no. 10; pp. 1146 - 1154
• Main Authors: van Heel, Auke J, Kloosterman, Tomas G, Montalban-Lopez, Manuel, Deng, Jingjing, Plat, Annechien, Baudu, Baptiste, Hendriks, Djoke, Moll, Gert N, Kuipers, Oscar P
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 21-10-2016
• Subjects: Amino Acid Sequence; Anti-Bacterial Agents - chemistry; Anti-Bacterial Agents - pharmacology; Bacteriocins - chemistry; Bacteriocins - pharmacology; Cloning, Molecular; Corynebacterium - chemistry; Corynebacterium - genetics; Gene Expression Regulation, Bacterial; Multigene Family; Nisin - chemistry; Protein Sorting Signals - genetics; Streptococcus agalactiae - chemistry; Streptococcus agalactiae - genetics
• ISSN: 2161-5063; 2161-5063
• DOI: 10.1021/acssynbio.6b00033

To find the right conditions to isolate natively expressed antimicrobial peptides from a wide range of different microorganisms can be a challenge. Here, we exploited a heterologous expression system to produce and characterize several novel lantibiotics. We identified 54 novel putative class I and class II lantibiotics after inspecting all publicly available prokaryotic genomes using the in-house developed mining tool BAGEL3. The genes encoding these new lantibiotics fused to the nisin leader peptide gene sequence were synthesized, and the constructs were plugged into the nisin expression and modification system. Using this approach 30 peptides could be expressed, 27 of which were dehydrated by NisBC on at least 1 predicted position. Good antimicrobial activity against several pathogenic bacteria could be demonstrated for 5 novel heterologously modified lantibiotics. Lantibiotics from Corynebacterium lipophiloflavum DSM 44291 and Streptococcus agalactiae ATCC 13813, named flavucin and agalacticin, respectively, were fully modified and displayed high antimicrobial activity. The efficiency of functional expression was significantly enhanced when we made use of the native nisin leader cleavage site, instead of an artificial factor Xa site. Thus, we describe an efficient way for heterologous production of active lantibiotics, facilitating a rapid identification of promising molecules.