Studies on antibiotics from the genus Bacillus. X. The structure of brevistin.
- 1 January 1976
- journal article
- research article
- Published by Japan Antibiotics Research Association in The Journal of Antibiotics
- Vol. 29 (4), 380-389
- https://doi.org/10.7164/antibiotics.29.380
Abstract
Acid hydrolysis revealed the constituent amino acids of brevistin as follows: asparatic acid (D-form 2, L-form 1), L-threonine (1), glycine (1), sum of L-valine and L-isoleucine (1), L-phenylalanine (1), L-tryptophan (1) and 2,4-diamenobutyric acid (D-form 1, L-form 1). The constituent fatty acid was elucidated to be anteisononanoic acid by gas chromatography-mass spectrometry. A lactone linkage was proved between phenylalanine and the hydroxy group of threonine. Opening the lactone ring with dilute alkali afforded brevistinic acid. Deacylation with an enzyme preparation, polymyxin acylase, gave deacyl brevistinic acid. Cleavage reaction with N-bromosuccinimide, sequential analysis by Edman degradation and some additional evidences clarified the total structure of brevistin.This publication has 2 references indexed in Scilit:
- Studies on antibiotics from the genus Bacillus. IX. Isolation of brevistin, a new peptide antibiotic.The Journal of Antibiotics, 1976
- Structural studies on the minor components of quinoxaline antibioticsTetrahedron, 1967