Sequences of Tolypins, Insecticidal Efrapeptin‐Type Peptaibiotics from Species of the Fungal Genus Tolypocladium. Issue 7 (23rd June 2020)

• Record Type: Journal Article
• Authors: Brückner, Hans; Degenkolb, Thomas
• Is Part Of: Chemistry & biodiversity. Volume 17:Issue 7(2020)
• Page Start: n/a
• Page End: n/a
• Publication Date: 2020-06-23
• Subjects: peptide antibiotics -- antiviral agent -- uncoupling of oxidative phosphorylation -- Tolypocladium inflatum -- acretocin -- Aib, l-isovaline -- amino acids; Biochemistry -- Periodicals; Molecular biology -- Periodicals; Biodiversity -- Periodicals; 572
• DOI: 10.1002/cbdv.202000276
• Languages: English
• ISSNs: 1612-1872

Abstract

Abstract: A peptide mixture named tolypin, originally isolated from species of the fungal genus Tolypocladium, was structurally characterised and sequences compared to those reported for efrapeptins isolated from strains of Tolypocladium inflatum . Chiral amino acid analysis, direct infusion, and online HPLC electrospray ionization tandem mass spectrometry provided composition, molecular weights of peptides, and series of diagnostic fragment ions. Sequences deduced from ESI‐MS revealed that tolypins C−G are identical to efrapeptins C−G. The results were corroborated by ESI‐MS and HPLC of an authentic efrapeptin sample from Eli Lilly Research Laboratories (USA). Comparison of the HPLC elution profiles of efrapeptin and tolypin indicated a pronounced microheterogeneity of the former. A high‐resolution HPLC of authentic efrapeptin has not been published before. Close relationship and partial identity of sequences of tolypins and efrapeptins, which had previously been postulated, were definitely proven. The geographical origin of the two most important T. inflatum strains used for sequencing of efrapeptins/tolypins could unambiguously be clarified. A new minor compound, designated tolypin H1, was sequenced. High proportions of helicogenic Aib ( α ‐aminoisobutyric acid) and l ‐isovaline, N ‐terminal acetyl‐l ‐pipecolic acid and the unusual, amide‐bound C ‐terminal residue, named ( S )‐2‐amino‐1‐(1, 5‐diazabicyclo[4.3.0]non‐5‐ene‐5‐ylium)‐4‐methylpentane corresponding to 1‐[(2 S )‐2‐amino‐4‐methylpentyl]‐2, 3, 4, 6, 7, 8‐hexahydropyrrolo[1, 2‐ a ]pyrimidin‐1‐ium, define these peptides as linear, cationic peptaibiotics. Abstract :