Talarolides Revisited: Cyclic Heptapeptides from an Australian Marine Tunicate-Associated Fungus, Talaromyces sp. CMB-TU011

• Published in: Marine drugs Vol. 21; no. 9; p. 487
• Main Authors: Salim, Angela A., Hussein, Waleed M., Dewapriya, Pradeep, Hoang, Huy N., Zhou, Yahao, Samarasekera, Kaumadi, Khalil, Zeinab G., Fairlie, David P., Capon, Robert J.
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 11-09-2023; MDPI
• Subjects: Amino acids; Bioavailability; Biological properties; Bridges; Conformation; Cultivation; cycloheptapeptide; Fungi; GNPS molecular networking; Marine invertebrates; MATRIX; N-OH glycine; Natural products; Optimization; Peptides; talarolides; Talaromyces; Queensland Australia; Australia
• ISSN: 1660-3397; 1660-3397
• DOI: 10.3390/md21090487

Application of a miniaturized 24-well plate system for cultivation profiling (MATRIX) permitted optimization of the cultivation conditions for the marine-derived fungus Talaromyces sp. CMB-TU011, facilitating access to the rare cycloheptapeptide talarolide A (1) along with three new analogues, B–D (2–4). Detailed spectroscopic analysis supported by Marfey’s analysis methodology was refined to resolve N-Me-l-Ala from N-Me-d-Ala, l-allo-Ile from l-Ile and l-Leu, and partial and total syntheses of 2, and permitted unambiguous assignment of structures for 1 (revised) and 2–4. Consideration of diagnostic ROESY correlations for the hydroxamates 1 and 3–4, and a calculated solution structure for 1, revealed how cross-ring H-bonding to the hydroxamate moiety influences (defines/stabilizes) the cyclic peptide conformation. Such knowledge draws attention to the prospect that hydroxamates may be used as molecular bridges to access new cyclic peptide conformations, offering the prospect of new biological properties, including enhanced oral bioavailability.