Landry J, Slama J T, Sternglanz R
Department of Biochemistry and Cell Biology, State University of New York, Stony Brook, New York, 11794-5215, USA.
Biochem Biophys Res Commun. 2000 Nov 30;278(3):685-90. doi: 10.1006/bbrc.2000.3854.
In this report we describe the role of NAD(+) in the deacetylation reaction catalyzed by the SIR2 family of enzymes. We first show that the products of the reaction detected by HPLC analysis are ADP-ribose, nicotinamide, and a deacetylated peptide substrate. These products are in a 1:1:1 molar ratio, indicating that deacetylation involves the hydrolysis of one NAD(+) to ADP-ribose and nicotinamide for each acetyl group removed. Three results suggest that deacetylation requires an enzyme-ADP-ribose intermediate. First, the enzyme can promote an NAD(+) if nicotinamide exchange reaction that depends on an acetylated substrate. Second, a non-hydrolyzable NAD(+) analog is a competitive inhibitor of the enzyme, and, third, nicotinamide shows product inhibition of deacetylase activity.
在本报告中,我们描述了NAD(+)在SIR2家族酶催化的脱乙酰化反应中的作用。我们首先通过高效液相色谱分析表明,该反应的产物是ADP-核糖、烟酰胺和一个脱乙酰化的肽底物。这些产物的摩尔比为1:1:1,这表明对于每一个去除的乙酰基,脱乙酰化反应涉及将一分子NAD(+)水解为ADP-核糖和烟酰胺。三个结果表明脱乙酰化需要一个酶-ADP-核糖中间体。第一,如果存在依赖于乙酰化底物的烟酰胺交换反应,该酶可以促进NAD(+)的反应。第二,一种不可水解的NAD(+)类似物是该酶的竞争性抑制剂,第三,烟酰胺对脱乙酰酶活性表现出产物抑制作用。