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生物素酶的新实验

New experiments of biotin enzymes.

作者信息

Lynen F

出版信息

CRC Crit Rev Biochem. 1979 Dec;7(2):103-19. doi: 10.3109/10409237909105428.

Abstract

The objects of structural studies on biotin-enzymes were acetyl CoA-carboxylase and pyruvate carboxylase of Saccharomyces cerevisiae and beta-methylcrotonyl CoA-carboxylase and acetyl CoA-carboxylase of Achromobacter IV S. It was found that these enzymes can be arranged in three groups. In the first group, as represented by acetyl CoA-carboxylase of Achromobacter, the active enzyme could be resolved in three types of functional components: (1) the biotin-carboxyl carrier protein, (2) the biotin carboxylase, and (3) the carboxyl transferase. In the second group, as represented by beta-methylcrotonyl CoA-carboxylase from Achromobacter only two types of polypeptides are present. The one carries the biotin carboxylase activity together with the biotin-carboxyl-carrier protein, the other one carries the carboxyl transferase activity. In this third group, as represented by the two enzymes of yeast, all three catalytic functions are incorporated in one multifunctional polypeptide chain. The evolution of the different enzymes is discussed. The animal tissues acetyl CoA-carboxylase is under metabolic control, as known from previous studies. It thus has to be expected that the levels of malonyl CoA in livers of rats in all states of depressed fatty acid synthesis are much lower than under normal conditions because the carboxylation of acetyl CoA is strongly reduced and cannot keep pace with the consumption of malonyl CoA by fatty acid synthetase. A new highly sensitive assay method for malonyl CoA was developed which uses tritiated NADPH and measures the incorporation of radioactivity into the fatty acids formed from malonyl CoA in the presence of purified fatty acid synthetase. The application of this method to liver extracts showed that the level of malonyl CoA which amounts to about 7 nmoles per gram of wet liver drops to less than 10% within a starvation period of 24 hr and even further if the starvation period is extended to 48 hr. A low malonyl CoA concentration is also found in the alloxan diabetic animals and in animals being fed a fatty diet after starvation. On the other hand, feeding a carbohydrate rich diet leads to malonyl CoA levels surpassing the levels found after feeding a balanced diet. These observations reconfirm the concept that fatty acid synthesis is principally regulated by the carboxylation of acetyl CoA.

摘要

对生物素酶进行结构研究的对象是酿酒酵母的乙酰辅酶A羧化酶和丙酮酸羧化酶,以及无色杆菌IV S的β-甲基巴豆酰辅酶A羧化酶和乙酰辅酶A羧化酶。发现这些酶可分为三组。在第一组中,以无色杆菌的乙酰辅酶A羧化酶为代表,活性酶可分解为三种功能成分:(1)生物素羧基载体蛋白,(2)生物素羧化酶,(3)羧基转移酶。在第二组中,以无色杆菌的β-甲基巴豆酰辅酶A羧化酶为代表,仅存在两种类型的多肽。一种同时具有生物素羧化酶活性和生物素羧基载体蛋白,另一种具有羧基转移酶活性。在第三组中,以酵母的两种酶为代表,所有三种催化功能都包含在一条多功能多肽链中。讨论了不同酶的进化。如先前研究所知,动物组织中的乙酰辅酶A羧化酶受代谢控制。因此可以预期,在脂肪酸合成受抑制的所有状态下,大鼠肝脏中丙二酰辅酶A的水平远低于正常条件下,因为乙酰辅酶A的羧化作用大大降低,无法跟上脂肪酸合成酶对丙二酰辅酶A的消耗。开发了一种新的高灵敏度丙二酰辅酶A测定方法,该方法使用氚标记的NADPH,并在纯化的脂肪酸合成酶存在下测量放射性掺入由丙二酰辅酶A形成的脂肪酸中的情况。将该方法应用于肝脏提取物表明,每克湿肝中丙二酰辅酶A的含量约为7纳摩尔,在24小时饥饿期内降至不到10%,如果饥饿期延长至48小时,则下降得更多。在四氧嘧啶糖尿病动物和饥饿后喂食高脂肪饮食的动物中也发现丙二酰辅酶A浓度较低。另一方面,喂食富含碳水化合物的饮食会导致丙二酰辅酶A水平超过喂食均衡饮食后的水平。这些观察结果再次证实了脂肪酸合成主要受乙酰辅酶A羧化作用调节的概念。

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