Skip to main content
Article
Anaerobic 5-Hydroxybenzimidazole Formation from Aminoimidazole Ribotide: An Unanticipated Intersection of Thiamin and Vitamin B12 Biosynthesis
Chemistry & Physics Faculty Publications
  • Angad P. Mehta, Texas A&M University
  • Sameh H. Abdelwahed, Texas A&M University
  • Michael K. Fenwick, Cornell University
  • Amrita B. Hazra, Department of Plant & Microbial Biology
  • Michiko E. Taga, Department of Plant & Microbial Biology
  • Yang Zhang, Cornell University
  • Steven E. Ealick, Cornell University
  • Tadhg P. Begley, Texas A&M University
Document Type
Article
Publication Date
8-3-2015
Abstract

Comparative genomics of the bacterial thiamin pyrimidine synthase (thiC) revealed a paralogue of thiC (bzaF) clustered with anaerobic vitamin B12 biosynthetic genes. Here we demonstrate that BzaF is a radical S-adenosylmethionine enzyme that catalyzes the remarkable conversion of aminoimidazole ribotide (AIR) to 5-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 B12 assembly and reveal an unanticipated intersection of thiamin and vitamin B12 biosynthesis.

Citation Information
Angad P. Mehta, Sameh H. Abdelwahed, Michael K. Fenwick, Amrita B. Hazra, et al.. "Anaerobic 5-Hydroxybenzimidazole Formation from Aminoimidazole Ribotide: An Unanticipated Intersection of Thiamin and Vitamin B12 Biosynthesis" (2015)
Available at: http://works.bepress.com/Sameh-Abdelwahed/4/