Emanuele M C, Scaloni A, Lavermicocca P, Jacobellis N S, Camoni L, Di Giorgio D, Pucci P, Paci M, Segre A, Ballio A
Istituto di Strutturistica Chimica G. Giacomello, CNR, Montelibretti, Rome, Italy.
FEBS Lett. 1998 Aug 21;433(3):317-20. doi: 10.1016/s0014-5793(98)00933-8.
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.