Production of cobalamin and sirohaem in Bacillus megaterium: an investigation into the role of the branchpoint chelatases sirohydrochlorin ferrochelatase (SirB) and sirohydrochlorin cobalt chelatase (CbiX)

• Published in: Biochemical Society transactions Vol. 30; no. 4; p. 610
• Main Authors: Leech, H K, Raux-Deery, E, Heathcote, P, Warren, M J
• Format: Journal Article
• Language: English
• Published: England 01.08.2002
• Subjects: Bacillus megaterium - enzymology; Bacterial Proteins; Ferrochelatase - metabolism; Heme - analogs & derivatives; Heme - biosynthesis; Kinetics; Lyases - metabolism; Uroporphyrins - metabolism; Vitamin B 12 - biosynthesis
• ISSN: 0300-5127
• DOI: 10.1042/bst0300610

One of the four operons required for cobalamin biosynthesis in Bacillus megaterium is also associated with sirohaem synthesis, and contains three genes, sirA, sirB and sirC. By undertaking functional complementation experiments and in vitro assays using recombinantly produced enzymes, we have been able to demonstrate that (1) SirA acts as a uroporphyrinogen III methyltransferase, transforming uroporphyrinogen III into precorrin-2, (2) SirC acts as an NAD(+) dehydrogenase, responsible for the oxidation of precorrin-2 into sirohydrochlorin, and (3) SirB acts as a ferrochelatase, responsible for the insertion of a ferrous ion into sirohydrochlorin to give sirohaem. Comparative sequence analysis reveals that the primary structure of SirB is highly similar to that of the cobalt chelatase involved in cobalamin biosynthesis in Bacillus megaterium, CbiX, with the exception that CbiX contains a C-terminal histidine-rich motif. Surprisingly, CbiX has been shown (using EPR) to contain a 4Fe-4S centre, a redox centre that is absent from SirB.