Biosynthesis of Enduracidin: Origin of Enduracididine and Other Amino Acids
- 1 June 1984
- journal article
- research article
- Published by Oxford University Press (OUP) in Agricultural and Biological Chemistry
- Vol. 48 (6) , 1503-1508
- https://doi.org/10.1080/00021369.1984.10866355
Abstract
The biosynthetic origin of the amino acid moieties of enduracidin was investigated by feeding experiments with labeled compounds. Results of the incorporation and the distribution of radioactivity into the antibiotic revealed that glycine, l-serine, l-threonine, l-alanine, L-aspartic acid, l-ornithine and l-citrulline were incorporated into the corresponding amino acid moieties. Unique amino acids, enduracididine and its isomer with an imidazolidine ring, were derived from l-arginine, but not histidine. K1 (4-hydroxyphenylglycine) and K2 (3,5-dichloro-K1) moieties were derived from l-tyrosine. 36Cl-Sodium chloride was incorporated into the antibiotic in the early stage of fermentation.This publication has 2 references indexed in Scilit:
- Biosynthesis of Peptide AntibioticsPublished by Springer Nature ,1981
- Incorporation of14C-Amino Acids into Nocardicin A by Growing CellsAgricultural and Biological Chemistry, 1977