| Literature DB >> 28288097 |
Fumihito Hasebe1, Kenichi Matsuda1, Taro Shiraishi1, Yushi Futamura2, Takeshi Nakano3,4, Takeo Tomita1, Ken Ishigami5, Hikari Taka6, Reiko Mineki6, Tsutomu Fujimura6, Hiroyuki Osada2, Tomohisa Kuzuyama1, Makoto Nishiyama1.
Abstract
Amino-group carrier proteins (AmCPs) mediate the biosynthesis of lysine and arginine in some bacteria and archaea. Here we demonstrate that an uncharacterized AmCP-mediated biosynthetic system functions to biosynthesize the previously uncharacterized and nonproteinogenic amino acid (2S,6R)-diamino-(5R,7)-dihydroxy-heptanoic acid (DADH) in Streptomyces sp. SANK 60404. DADH is incorporated into a novel peptide metabolite, vazabitide A, featuring an azabicyclo-ring structure, by nonribosomal peptide synthetases and successive modification enzymes in this bacterium. As the AmCP-mediated machinery for DADH biosynthesis is widely distributed in bacteria, further analysis of uncharacterized AmCP-containing gene clusters will lead to the discovery of novel bioactive compounds and novel biosynthetic enzymes.Entities:
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Year: 2016 PMID: 28288097 DOI: 10.1038/nchembio.2181
Source DB: PubMed Journal: Nat Chem Biol ISSN: 1552-4450 Impact factor: 15.040