Journal
JOURNAL OF NATURAL PRODUCTS
Volume 72, Issue 6, Pages 1036-1044Publisher
AMER CHEMICAL SOC
DOI: 10.1021/np900190w
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Funding
- NSFC [30672607]
- National Hi-Tech Projects [2006AA09Z446, 2006DFA31100, 2007AA09Z448, 2006AA09Z405, 2007AA09Z435]
- China Uni-PhD Base Project [20060001149]
- International Cooperation Projects of BMBF-MOST
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Fermentation of the marine-derived fungus Trichoderma asperellum, collected from the sediment of the Antarctic Penguin Island, resulted in the isolation of six new peptaibols named asperelines A-F (1-6), which are characterized by an acetylated N-terminus and a C-terminus containing an uncommon prolinol residue. Structures were determined by extensive 1D and 2D NMR (H-1-H-1 COSY, HMQC, HMBC, NOESY) spectroscopic data analysis combined with ESIMS/MS fragmentation. The absolute configurations of the amino acid residues possessing a chiral alpha-carbon and of the prolinol residue were determined to be L and S, respectively, using a new method of H-1 NMR spectroscopic comparison of complexes formed between the chiral reagent Ru(D-4-Por*)CO and amino acids derived from the peptaibols with those formed with reference standards.
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