Anton D L, Friedman P A
J Biol Chem. 1983 Dec 10;258(23):14084-7.
The gamma-glutamyl carboxylation reaction proceeds by an initial vitamin K-dependent gamma-C-H glutamyl bond cleavage and a subsequent carboxylation of the activated glutamyl residue. This system is easily uncoupled such that at low CO2 concentrations which limit the extent of carboxylation there is no effect on the rate of C-H bond cleavage. In an uncoupled system, the fate of activated glutamyl residues is to incorporate a hydrogen as demonstrated by the recovery of only unaltered glutamyl residues from digests of uncoupled reactions. In addition, in reactions carried out in tritiated, deuterated water mixtures, tritium is incorporated into the gamma positions of the glutamyl residues of peptide substrates in a vitamin K-dependent process, indicating that the hydrogen incorporated must ultimately come from solvent. These results, while not proof, put severe restraints on a radical mechanism while favoring a carbanion mechanism.
γ-谷氨酰羧化反应首先通过维生素K依赖的γ-C-H谷氨酰键断裂进行,随后是活化的谷氨酰残基的羧化反应。该系统很容易解偶联,以至于在限制羧化程度的低二氧化碳浓度下,对C-H键断裂速率没有影响。在解偶联系统中,活化的谷氨酰残基的最终结果是结合一个氢,这可以从未偶联反应消化物中仅回收未改变的谷氨酰残基得到证明。此外,在含有氚化水和氘化水混合物的反应中,氚在维生素K依赖的过程中掺入肽底物谷氨酰残基的γ位,这表明掺入的氢最终必定来自溶剂。这些结果虽然不是证据,但对自由基机制施加了严格限制,同时支持碳负离子机制。