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各种哺乳动物组织和细胞培养物破碎细胞制剂中的无活性3-羟基-3-甲基戊二酰辅酶A还原酶。

Inactive 3-hydroxy-3-methylglutaryl-coenzyme A reductase in broken cell preparations of various mammalian tissues and cell cultures.

作者信息

Saucier S E, Kandutsch A A

出版信息

Biochim Biophys Acta. 1979 Mar 29;572(3):541-56. doi: 10.1016/0005-2760(79)90162-0.

Abstract

Preincubation of broken cell preparations from a variety of tissues and cell cultures resulted in an apparent increase in the level of 3-hydroxy-3-methylglutaryl-CoA reductase activity. However, apparent activation of the reductase in mouse liver, hepatomas and primary liver cell cultures was attributed largely to the loss, during the preincubation period, of an interfering enzyme, 3-hydroxy-3-methylglutaryl-CoA lyase. Among non hepatic cells and tissues (which did not contain appreciable lyase activity) the proportion of latent reductase was high in sonicates of fetal brain and in L cells and was independent of the level of total enzyme activity present. Activation of the reductase was blocked by hydroxymethylglutaryl-CoA and NADPH as well as by KF so that activation did not occur under the conditions of the enzyme assay. The enzyme was activated slowly at 4 degrees C, so that partial activation of the latent form occurred during isolation of the microsomal fraction by differential centrifugation. The reductase present in sonicates of cells with either a high or low proportion of the latent enzyme was inactivated by incubation with ATP and Mg2+. Suppression of reductase activity in L cell cultures by treatment with 25-hydroxycholesterol and an age-related decline in brain enzyme activity did not involve reversible conversion of the reductase to an inactive form.

摘要

对来自多种组织和细胞培养物的破碎细胞制剂进行预温育,结果显示3-羟基-3-甲基戊二酰辅酶A还原酶活性水平明显升高。然而,小鼠肝脏、肝癌和原代肝细胞培养物中还原酶的明显激活,很大程度上归因于在预温育期间一种干扰酶——3-羟基-3-甲基戊二酰辅酶A裂解酶的丧失。在非肝细胞和组织(不含有明显的裂解酶活性)中,胎儿脑超声裂解物和L细胞中潜在还原酶的比例较高,且与总酶活性水平无关。还原酶的激活被羟甲基戊二酰辅酶A、NADPH以及KF阻断,因此在酶测定条件下不会发生激活。该酶在4℃时缓慢激活,因此在通过差速离心分离微粒体部分的过程中,潜在形式会发生部分激活。用ATP和Mg2 +孵育后,潜在酶比例高或低的细胞超声裂解物中存在的还原酶会失活。用25-羟基胆固醇处理抑制L细胞培养物中的还原酶活性以及脑酶活性随年龄的下降,都不涉及还原酶可逆转化为无活性形式。

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