4.8 Article

Anaerobic 5-Hydroxybenzimidazole Formation from Aminoinnidazole Ribotide: An Unanticipated Intersection of Thiamin and Vitamin B12 Biosynthesis

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 137, Issue 33, Pages 10444-10447

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.5b03576

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Funding

  1. Robert A. Welch Foundation [A-0034]
  2. National Institutes of Health [DK44083, DK067081]

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Comparative genomics of the bacterial thiamin pyrimidine synthase (thiC) revealed a paralogue of thiC (bzaF) clustered with anaerobic vitamin B-12 biosynthetic genes. Here we demonstrate that BzaF is a radical S-adenosylmethionine enzyme that catalyzes the remarkable conversion of aminoimidazole ribotide (AIR) to S-hydroxybenzimidazole (5-HBI). We identify the origin of key product atoms and propose a reaction mechanism. These studies represent the first step in solving a long-standing problem in anaerobic vitamin B-12 assembly and reveal an unanticipated intersection of thiamin and vitamin B-12 biosynthesis.

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