Issue 13, 1993

Biosynthesis of vitamin B12: structure of precorrin-3B, the trimethylated substrate of the enzyme catalysing ring contraction

Abstract

FAB-MS, FTIR spectroscopy, 13C labelling and NMR experiments establish the structure of precorrin-3B, a further trimethylated intermediate along the vitamin B12 pathway, thus demonstrating that precorrin-3B is synthesised from precorrin-3 (called precorrin-3A from now) by a complex oxidative reaction involving C-20 hydroxylation and γ-lactone formation from ring-A acetate to C-1, catalysed by the CobG protein in Pseudomonas denitrificans.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1993, 1100-1103

Biosynthesis of vitamin B12: structure of precorrin-3B, the trimethylated substrate of the enzyme catalysing ring contraction

L. Debussche, D. Thibaut, M. Danzer, F. Debu, D. Fréchet, F. Herman, F. Blanche and M. Vuilhorgne, J. Chem. Soc., Chem. Commun., 1993, 1100 DOI: 10.1039/C39930001100

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