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. 1983 Dec;36(12):1735-42.
doi: 10.7164/antibiotics.36.1735.

The biosynthesis of brominated pyrrolnitrin derivatives by Pseudomonas aureofaciens

Free article

The biosynthesis of brominated pyrrolnitrin derivatives by Pseudomonas aureofaciens

K H van Pée et al. J Antibiot (Tokyo). 1983 Dec.
Free article

Abstract

The mutant strain ACN of Pseudomonas aureofaciens ATCC 15926 produces several bromo derivatives of pyrrolnitrin. Five brominated amino- and three brominated nitrophenyl pyrrole compounds could be isolated, and their structures were established by 1H NMR, UV and mass spectroscopy. The isolated amino compounds showed no biological activity; the nitro derivatives inhibited the growth of Neurospora crassa ATCC 9276, though not as effective as pyrrolnitrin itself. 2-Carboxy-4-(2-amino-3-bromophenyl)pyrrole (X) is demonstrated to be an intermediate in the biosynthesis of brominated pyrrolnitrin; the biosynthetic pathway to bromo derivatives of pyrrolnitrin is discussed.

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