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谷胱甘肽S-芳烷基转移酶

Glutathione S-aralkyltransferase.

作者信息

Boyland E, Chasseaud L F

出版信息

Biochem J. 1969 Dec;115(5):985-91. doi: 10.1042/bj1150985.

Abstract
  1. The name ;glutathione S-aralkyltransferase' is proposed for the enzyme catalysing the reaction of benzyl chloride with GSH. 2. Results from heat-inactivation studies, ammonium sulphate-fractionation and acid-precipitation experiments, and studies of the distribution of activities in rat liver, in rat kidney and in the livers of other animals indicate that glutathione S-aralkyltransferase differs from glutathione S-alkyltransferase, S-aryltransferase, S-epoxidetransferase and an S-alkenetransferase. 3. The distribution of these enzymes in the livers of the animal species examined was different. 4. Glutathione S-alkyltransferase, S-aralkyltransferase and the S-alkenetransferase that are present in rat liver supernatant were inhibited by GSSG, and the nature of the inhibition varied in each case. 5. 3,5-Di-tert.-butyl-4-hydroxybenzyl acetate reacts spontaneously with GSH, but the rat liver-supernatant-catalysed reaction of GSH with this and other aralkyl esters was weak. 6. A probable function of the glutathione S-transferases is the protection of cellular constituents from strong electrophilic agents.
摘要
  1. 催化苄基氯与谷胱甘肽反应的酶被命名为“谷胱甘肽S-芳烷基转移酶”。2. 热失活研究、硫酸铵分级分离和酸沉淀实验的结果,以及对大鼠肝脏、大鼠肾脏和其他动物肝脏中活性分布的研究表明,谷胱甘肽S-芳烷基转移酶不同于谷胱甘肽S-烷基转移酶、S-芳基转移酶、S-环氧化物转移酶和一种S-烯烃转移酶。3. 在所检测的动物物种肝脏中,这些酶的分布有所不同。4. 大鼠肝脏上清液中存在的谷胱甘肽S-烷基转移酶、S-芳烷基转移酶和S-烯烃转移酶受到氧化型谷胱甘肽(GSSG)的抑制,且每种情况下抑制的性质有所不同。5. 3,5-二叔丁基-4-羟基苄基乙酸酯可与谷胱甘肽自发反应,但大鼠肝脏上清液催化的谷胱甘肽与该酯及其他芳烷基酯的反应较弱。6. 谷胱甘肽S-转移酶可能的功能是保护细胞成分免受强亲电试剂的侵害。

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