Copsin, a Novel Peptide-based Fungal Antibiotic Interfering with the Peptidoglycan Synthesis

• Published in: The Journal of biological chemistry 2014-12, Vol.289 (50), p.34953-34964
• Main Authors: Essig, Andreas, Hofmann, Daniela, Münch, Daniela, Gayathri, Savitha, Künzler, Markus, Kallio, Pauli T., Sahl, Hans-Georg, Wider, Gerhard, Schneider, Tanja, Aebi, Markus
• Format: Article
• Language: English
• Subjects: Agaricales - growth & development; Agaricales - metabolism; Amino Acid Sequence; Anti-Bacterial Agents - chemistry; Anti-Bacterial Agents - metabolism; Anti-Bacterial Agents - pharmacology; Antibiotic Resistance; Antibiotics; Antimicrobial Peptide (AMP); Bacteria - drug effects; Bacteria - growth & development; Bacteria - metabolism; Bacterial-Fungal Interaction (BFI); Coculture Techniques; Defensins - chemistry; Defensins - metabolism; Defensins - pharmacology; Fungal Proteins - chemistry; Fungal Proteins - metabolism; Fungal Proteins - pharmacology; Fungal Secretome; Fungi; Lipid II; Microbiology; Models, Molecular; Molecular Sequence Data; Peptidoglycan - biosynthesis; Protein Conformation
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M114.599878

Fungi and bacteria compete with an arsenal of secreted molecules for their ecological niche. This repertoire represents a rich and inexhaustible source for antibiotics and fungicides. Antimicrobial peptides are an emerging class of fungal defense molecules that are promising candidates for pharmaceutical applications. Based on a co-cultivation system, we studied the interaction of the coprophilous basidiomycete Coprinopsis cinerea with different bacterial species and identified a novel defensin, copsin. The polypeptide was recombinantly produced in Pichia pastoris, and the three-dimensional structure was solved by NMR. The cysteine stabilized α/β-fold with a unique disulfide connectivity, and an N-terminal pyroglutamate rendered copsin extremely stable against high temperatures and protease digestion. Copsin was bactericidal against a diversity of Gram-positive bacteria, including human pathogens such as Enterococcus faecium and Listeria monocytogenes. Characterization of the antibacterial activity revealed that copsin bound specifically to the peptidoglycan precursor lipid II and therefore interfered with the cell wall biosynthesis. In particular, and unlike lantibiotics and other defensins, the third position of the lipid II pentapeptide is essential for effective copsin binding. The unique structural properties of copsin make it a possible scaffold for new antibiotics. Background: Secreted antibacterial substances of fungi provide a rich source for new antibiotics. Results: Copsin is a novel fungal antimicrobial peptide that binds in a unique manner to the cell wall precursor lipid II. Conclusion: As part of the defense strategy of a mushroom, copsin kills bacteria by inhibiting the cell wall synthesis. Significance: Copsin provides a novel highly stabilized scaffold for antibiotics.