Theodorsen L, Stromme J H
Clin Chim Acta. 1976 Oct 15;72(2):205-10. doi: 10.1016/0009-8981(76)90074-7.
Gamma-Glutamyl-3-carboxy-4-nitroanilide has been tested as donor substrate in the assay of gamma-glutamyltransferase activity in serum, glycylglycine being used as acceptor substrate. This donor substrate is highly solube even in neutral solutions, in contrast to the commonly used gamma-glutamyl-4-nitroanilide. The enzyme which apparently acts accordingly to a ping-pong bi bi kinetic mechanism, shows an absolute KM value for gamma-glutamyl-3-carboxy-4-nitroanilide of about 0.64 mmol/l, and for glycylglycine of about 13.4 mmol/l. The former KM value is significantly lower than that previously found for gamma-glutamyl-4-nitroanilide. The carboxyl derivative exhibits a marked competitive inhibitory effect on the gamma-glutamyltransferase. This effect is more pronounced than that of gamma-glutamyl-4-nitroanilide. The carboxyl derivative has somewhat higher absorbance in the range of wave length (400-420 nm) used to monitor the formation of the product. It is concluded that as donor substrate in the assay of gamma-glutamyltransferase activity of serum, the new derivative is not substantially superior to the gamma-glutamyl-4-nitroanilide conventionally used.
γ-谷氨酰-3-羧基-4-硝基苯胺已被用作供体底物,用于检测血清中的γ-谷氨酰转移酶活性,甘氨酰甘氨酸用作受体底物。与常用的γ-谷氨酰-4-硝基苯胺不同,这种供体底物即使在中性溶液中也具有很高的溶解度。该酶显然按照乒乓双底物动力学机制起作用,对γ-谷氨酰-3-羧基-4-硝基苯胺的绝对米氏常数约为0.64 mmol/L,对甘氨酰甘氨酸的约为13.4 mmol/L。前一个米氏常数明显低于先前发现的γ-谷氨酰-4-硝基苯胺的米氏常数。羧基衍生物对γ-谷氨酰转移酶表现出明显的竞争性抑制作用。这种作用比γ-谷氨酰-4-硝基苯胺的更明显。羧基衍生物在用于监测产物形成的波长范围(400 - 420 nm)内具有稍高的吸光度。得出的结论是,作为血清γ-谷氨酰转移酶活性检测中的供体底物,新衍生物并不比传统使用的γ-谷氨酰-4-硝基苯胺有实质性优势。