Vitamin cofactor, labeling

Much attention has focused on vitamin K 1 because of its function as an obligatory cofactor in enzymic sequences central to blood clotting. The role of molecular oxygen in the formation of vitamin K oxide 2 has been studied intensively, and the mechanism of the 1 —> 2 transformation has been the subject of much controversy. Oxidation of 1 with basic hydrogen peroxide also gives 2, and two obvious mechanisms can be postulated for this model oxidation. 180 labelling studies have been used to distinguish between these mechanisms. 

The nickel-containing factor F 430 (134) provides an example of how nature exploits the reactivity of organometallic compounds, as is the case with vitamin B12. Factor F 430 (134) plays a key role as cofactor for the coenzyme M reductase of primitive methanogenic bacteria in the formation of methane from 2-(methylthio)-ethanesulfonate (86). The structural elucidation of factor F 430 (134) is based on a combination of classical spectroscopic methods, chemical degradation, and biosynthetic studies with C-labelled precursors 83a,b). These biosynthetic investigations will be addressed in section 8.2. Chemical degradation products obtained by ozonolysis of factor F 430 (134) allowed the determination of the absolute configuration by comparison with reference compounds derived from chlorophyll a (2) and vitamin B12 (4) 83a,b). 

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