Moss J, Garrison S, Oppenheimer N J, Richardson S H
J Biol Chem. 1979 Jul 25;254(14):6270-2.
Escherichia coli heat-labile enterotoxin (labile toxin, LT) catalyzed the hydrolysis of NAD to ADP-ribose and nicotinamide and the ADP-ribosylation of arginine (Moss, J., and Richardson, S.H. (1978) J. Clin. Invest. 62, 281-285). Analysis of the product of the ADP-ribosylation of arginine by nuclear magnetic resonance spectroscopy indicated that the reaction was stereospecific and resulted in the formation of alpha-ADP-ribosyl-L-arginine. This reaction product rapidly anomerized to yield a mixture of the alpha and beta forms. In the presence of [adenine-U-14C]NAD, E. coli enterotoxin catalyzed the transfer of the radiolabel to proteins; the ADP-ribosylation of proteins was inhibited by arginine methyl ester, an alternative substrate. Digestion of the 14C-protein with snake venom phosphodiesterase released predominantly 5'-AMP. No product was obtained with a mobility similar to that of 2'-(5''-phosphoribosyl)-5'-AMP. This result is consistent with the covalent attachment by the enterotoxin of ADP-ribose rather than poly(ADP-ribose) to protein. Thus, LT is catalytically equivalent to choleragen, an enterotoxin of Vibrio cholerae, and activates adenylate cyclase through a similar stereospecific ADP-ribosylation reaction.
大肠杆菌不耐热肠毒素(不稳定毒素,LT)催化NAD水解为ADP-核糖和烟酰胺以及精氨酸的ADP-核糖基化(莫斯,J.,和理查森,S.H.(1978年)《临床研究杂志》62,281 - 285)。通过核磁共振光谱对精氨酸ADP-核糖基化产物的分析表明,该反应具有立体特异性,导致形成α-ADP-核糖基-L-精氨酸。该反应产物迅速发生异头化,产生α和β形式的混合物。在[腺嘌呤-U-14C]NAD存在下,大肠杆菌肠毒素催化放射性标记物转移到蛋白质上;蛋白质的ADP-核糖基化被精氨酸甲酯(一种替代底物)抑制。用蛇毒磷酸二酯酶消化14C-蛋白质主要释放出5'-AMP。未获得迁移率与2'-(5''-磷酸核糖基)-5'-AMP相似的产物。该结果与肠毒素将ADP-核糖而非聚(ADP-核糖)共价连接到蛋白质上一致。因此,LT在催化作用上等同于霍乱弧菌的肠毒素霍乱毒素,并通过类似的立体特异性ADP-核糖基化反应激活腺苷酸环化酶。