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FEBS Lett ; 433(3): 317-20, 1998 Aug 21.
Article in English | MEDLINE | ID: mdl-9744818

ABSTRACT

The structure of the corpeptins, bioactive lipodepsipeptides produced in culture by Pseudomonas corrugata, the causal agent of tomato pith necrosis, has been determined. The combined use of FAB-mass spectrometry, NMR spectroscopy and chemical procedures has allowed us to assign the following primary structure to the peptide moiety: Dhb-Pro-Ala-Ala-Ala-Val-Val-Dhb-Hse-Val-alle-Dhp-Ala-Ala-Ala-Val-D hb-aThr-Ala-Dab-Ser-Ile with the terminal carboxy group closing a macrocyclic ring on the hydroxy group of the allo-threonine residue. The N-terminus is in turn acylated by 3-hydroxydecanoate in corpeptin A and by cis-3-hydroxy-5-dodecenoate in corpeptin B. Some preliminary data on the biological activity of corpeptins are included.


Subject(s)
Peptides, Cyclic/chemistry , Pseudomonas/physiology , Acylation , Amino Acid Sequence , Chromatography, High Pressure Liquid , Culture Media , Decanoic Acids/analysis , Hydrolysis , Molecular Sequence Data , Nuclear Magnetic Resonance, Biomolecular , Peptides, Cyclic/isolation & purification , Peptides, Cyclic/pharmacology , Spectrometry, Mass, Fast Atom Bombardment
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