| Literature DB >> 17925955 |
Kouhei Shinoda1, Takuji Hasegawa, Hiroaki Sato, Masaaki Shinozaki, Hirotomo Kuramoto, Yosuke Takamiya, Tsutomu Sato, Naoki Nikaidou, Takeshi Watanabe, Tsutomu Hoshino.
Abstract
A biosynthetic intermediate of violacein produced by the mixed enzymes of VioABDE was elucidated to be 5-(5-hydroxy-1H-indol-3-yl)-3-(1H-indol-3-yl)-1H-pyrrole-2-carboxylic acid, named protoviolaceinic acid, indicating that VioC, responsible for the final biosynthetic step, works to oxygenate at the 2-position of the right side indole ring, and that the oxygenation reaction to form the central pyrrolidone core proceeds in a non-enzymatic fashion.Entities:
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Year: 2007 PMID: 17925955 DOI: 10.1039/b705358d
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222