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Biosynthesis of vitamin B12: identity of fragment extruded during ring contraction to the corrin macrocycle.
Author(s) -
Alan R. Battersby,
M J Bushell,
Christopher G. Jones,
Norman Lewis,
Anja Pfenninger
Publication year - 1981
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.78.1.13
Subject(s) - corrin , vitamin b12 , chemistry , stereochemistry , ring (chemistry) , acetic acid , biosynthesis , cyanocobalamin , contraction (grammar) , biochemistry , organic chemistry , biology , endocrinology , enzyme
Incorporation experiments with labeled sirohydrochlorin and trimethylisobacteriochlorin demonstrate that ring contraction in vivo to the corrin macrocycle of vitamin B12 liberates acetic acid. The C-20 atom of the precursors becomes the acetate carboxyl carbon.

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