Mohamram M, Rucker R B, Hodges R E
Biochim Biophys Acta. 1976 Jun 23;437(1):305-10. doi: 10.1016/0304-4165(76)90374-3.
The sulfation of ascorbic acid by an ascorbic acid sulphotransferase was investigated using rat liver and colon homogenates. When Na2 35 SO4 or 3'-phosphoadenylyl [35S]sulfate (P-Ado-P-35S) and ascorbic acid were used as substrates, chromatographic behavior of the reaction products on thin-layer cellulose suggested that ascorbic acid 2-[35S]sulfate was formed. With Na2 35SO4 as the source of radioactive sulfate in the assay system, ATP was found to be an obligatory cofactor. Incorporation of [35S]sulfate frofrom Na2 35SO4 into ascorbic acid 2-[35S]sulfate was also decreased when ATP sulfurylase inhibitors were added to the system. P-Ado-O35S alone in the assay without ATP was an extemely effective sulfating agent. In addition, liver and colon homogenates from vitamin A deficient and sufficient rats were used in one of the studies. Vitamin A deficiency appeared to have little effect on ascorbic acid 2-sulfate formation.
使用大鼠肝脏和结肠匀浆研究了抗坏血酸磺基转移酶对抗坏血酸的硫酸化作用。当使用Na2 35SO4或3'-磷酸腺苷[35S]硫酸盐(P-Ado-P-35S)和抗坏血酸作为底物时,反应产物在薄层层析纤维素上的色谱行为表明形成了抗坏血酸2-[35S]硫酸盐。在测定系统中以Na2 35SO4作为放射性硫酸盐的来源时,发现ATP是必需的辅助因子。当向系统中添加ATP硫酸化酶抑制剂时,从Na2 35SO4掺入抗坏血酸2-[35S]硫酸盐中的[35S]硫酸盐也会减少。在无ATP的测定中单独使用P-Ado-O35S是一种极其有效的硫酸化剂。此外,在其中一项研究中使用了来自维生素A缺乏和充足大鼠的肝脏和结肠匀浆。维生素A缺乏似乎对抗坏血酸2-硫酸盐的形成影响很小。