Abstract
The corrinoid/iron-sulfur protein (C/Fe-SP) from Clostridium thermoaceticum is an 88 kDa [alpha][beta]-dimer that cycles between a Co(I) and methyl-Co(III) form as it transfers a methyl group from methyltetrahydrofolate (methyl-H[sub 4]folate) to carbon monoxide dehydrogenase. Extended X-ray absorption fine structure (EXAFS) and X-ray edge spectroscopy of the as-isolated C/Fe-SP indicates that the inactive Co(II) state of the corrinoid has a four-coordinate distorted square-planar structure. To the authors' knowledge, this is the first observation of a four-coordinate Co(II) corrinoid. This unusual coordination state would be expected to poise the Co(II) state of the C/Fe-SP for facile reduction to four-coordinate Co(I), which is the active nucleophile that acts as the acceptor of the methyl group of methyl-H[sub 4]folate. Additionally, the first-derivative X-ray edge spectra for both the methyl-Co(III) and Co(II) forms of the C/Fe-SP show an unexpected shift to lower energy when compared to analogous free cobalamins indicating a potential role for the protein in mediating electronic as well as structural properties of the enzyme bound methylcobamide. 42 refs., 6 figs., 3 tabs.
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