posted on 2017-09-21, 00:00authored byTânia
K. Shishido, Jouni Jokela, David P. Fewer, Matti Wahlsten, Marli F. Fiore, Kaarina Sivonen
Anabaenopeptins
are a diverse group of cyclic peptides, which contain
an unusual ureido linkage. Namalides are shorter structural homologues
of anabaenopeptins, which also contain an ureido linkage. The biosynthetic
origins of namalides are unknown despite a strong resemblance to anabaenopeptins.
Here, we show the cyanobacterium Nostoc sp. CENA543
strain producing new (nostamide B–E (2, 4, 5, and 6)) and known variants
of anabaenopeptins (schizopeptin 791 (1) and anabaenopeptin
807 (3)). Surprisingly, Nostoc sp. CENA543
also produced namalide B (8) and the new namalides D
(7), E (9), and F (10) in similar
amounts to anabaenopeptins. Analysis of the complete Nostoc sp. CENA543 genome sequence indicates that both anabaenopeptins
and namalides are produced by the same biosynthetic pathway through
module skipping during biosynthesis. This unique process involves
the skipping of two modules present in different nonribosomal peptide
synthetases during the namalide biosynthesis. This skipping is an
efficient mechanism since both anabaenopeptins and namalides are synthesized
in similar amounts by Nostoc sp. CENA543. Consequently,
gene skipping may be used to increase and possibly broaden the chemical
diversity of related peptides produced by a single biosynthetic gene
cluster. Genome mining demonstrated that the anabaenopeptin gene clusters
are widespread in cyanobacteria and can also be found in tectomicrobia
bacteria.