Tate S S, Orlando J
J Biol Chem. 1979 Jul 10;254(13):5573-5.
A purification procedure, based on that previously used for rat kidney gamma-glutamyl transpeptidase, was used for the purification of glutathione oxidase (which converts glutathione to gluthathione disulfide). The two activities co-purified, the ratio of the activities remaining constant through all steps of the isolation procedure. The purified enzyme was separable into 12 isozymic species by isoelectric focusing. All 12 isozymes exhibited a constant ratio of transpeptidase to glutathione oxidase activities, strongly supporting the conclusion that conversion of glutathione to glutathione disulfide is a catalytic function of gamma-glutamyl transpeptidase. Modulation of oxidase activity by inhibitors and acceptor substrates of transpeptidase is discussed in relation to the possible glutathione binding sites involved in gamma-glutamyl transfer and oxidase activities of the enzyme.
一种基于先前用于大鼠肾脏γ-谷氨酰转肽酶的纯化方法,被用于纯化谷胱甘肽氧化酶(该酶将谷胱甘肽转化为谷胱甘肽二硫化物)。这两种活性共同纯化,在分离过程的所有步骤中,活性比例保持恒定。通过等电聚焦,纯化后的酶可分离为12种同工酶。所有12种同工酶都表现出转肽酶与谷胱甘肽氧化酶活性的恒定比例,有力地支持了谷胱甘肽向谷胱甘肽二硫化物的转化是γ-谷氨酰转肽酶的催化功能这一结论。本文讨论了转肽酶的抑制剂和受体底物对氧化酶活性的调节作用,涉及该酶γ-谷氨酰转移和氧化酶活性中可能的谷胱甘肽结合位点。