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Spermidine as a potential biosynthetic precursor to the 1,5-diazabicyclo[4:3:o]nonene residue in the efrapeptins.

作者信息

Uma M V, Sudha R, Balaram P

机构信息

Molecular Biophysics Unit, Indian Institute of Science, Bangalore.

出版信息

J Pept Res. 2001 Nov;58(5):375-9. doi: 10.1034/j.1399-3011.2001.00915.x.

DOI:10.1034/j.1399-3011.2001.00915.x
PMID:11892846
Abstract

Efrapeptins are a group of microheterogeneous polypeptide antibiotics produced by the fungus Tolypocladium niveum, which are potent inhibitors of mitochondrial F1-ATPase. Efrapeptins contain an unusual 1,5-diazabicyclo[4:3:0]nonene (DBN) residue at the C-terminus. This study is driven by the hypothesis that the DBN residue could, in principle, arise by oxidative cyclization of a spermidine moiety. Electrospray ionization mass spectrometry of the peptide antibiotics 'elvapeptins' from T niveum establishes the presence of a C-terminal spermidine residue. Conversion of elvapeptins to efrapeptins by CuCl/pyridine demonstrates the transformation of the spermidine residue to the 1,5-diazabicyclo[4:3:0]nonene system by oxidative cyclization.

摘要

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