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Vitamin B-12 and methionine synthesis: A critical review. Is nature's most beautiful cofactor(*) misunderstood?

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BIOFACTORS
卷 26, 期 1, 页码 45-57

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WILEY
DOI: 10.1002/biof.5520260105

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5'-deoxyadenosyl radical; hyperhomocysteinemia; methionine synthesis; methionine transamination; cobalamins; polyamines; methylthio growth factor

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The mechanism by which Vitamin B-12 prevents demyelination of nerve tissue is still not known. The evidence indicates that the critical site of B12 function in nerve tissue is in the enzyme, methionine synthase, in a system which requires S-adenosylmethionine. In recent years it has been recognized that S-adenosylmethionine gives rise to the deoxyadenosyl radical which catalyzes many reactions including the rearrangement of lysine to beta-lysine. Evidence is reviewed which suggests that there is an analogy between the two systems and that S-adenosyl methionine may catalyze a rearrangement of homocysteine on methionine synthase giving rise to iso- or beta-methionine. The rearranged product is readily degraded to CH3-SH, providing a mechanism for removing toxic homocysteine.

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