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Amino-group carrier-protein-mediated secondary metabolite biosynthesis in Streptomyces.
Hasebe, Fumihito; Matsuda, Kenichi; Shiraishi, Taro; Futamura, Yushi; Nakano, Takeshi; Tomita, Takeo; Ishigami, Ken; Taka, Hikari; Mineki, Reiko; Fujimura, Tsutomu; Osada, Hiroyuki; Kuzuyama, Tomohisa; Nishiyama, Makoto.
Afiliação
  • Hasebe F; Biotechnology Research Center, The University of Tokyo, Tokyo, Japan.
  • Matsuda K; Biotechnology Research Center, The University of Tokyo, Tokyo, Japan.
  • Shiraishi T; Biotechnology Research Center, The University of Tokyo, Tokyo, Japan.
  • Futamura Y; Chemical Biology Research Group, RIKEN Center for Sustainable Resource Science, Wako, Japan.
  • Nakano T; Gene Discovery Research Group, RIKEN Center for Sustainable Resource Science, Wako, Japan.
  • Tomita T; Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Agency (JST), Kawaguchi, Japan.
  • Ishigami K; Biotechnology Research Center, The University of Tokyo, Tokyo, Japan.
  • Taka H; Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, Japan.
  • Mineki R; Division of Biochemical Analysis, Central Laboratory of Medical Sciences, Juntendo University School of Medicine, Tokyo, Japan.
  • Fujimura T; Division of Biochemical Analysis, Central Laboratory of Medical Sciences, Juntendo University School of Medicine, Tokyo, Japan.
  • Osada H; Division of Biochemical Analysis, Central Laboratory of Medical Sciences, Juntendo University School of Medicine, Tokyo, Japan.
  • Kuzuyama T; Chemical Biology Research Group, RIKEN Center for Sustainable Resource Science, Wako, Japan.
  • Nishiyama M; Biotechnology Research Center, The University of Tokyo, Tokyo, Japan.
Nat Chem Biol ; 12(11): 967-972, 2016 Nov.
Article em En | MEDLINE | ID: mdl-28288097
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.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arginina / Streptomyces / Proteínas de Transporte / Metabolismo Secundário / Lisina Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Arginina / Streptomyces / Proteínas de Transporte / Metabolismo Secundário / Lisina Idioma: En Ano de publicação: 2016 Tipo de documento: Article