Fujiwara K, Motokawa Y
J Biol Chem. 1983 Jul 10;258(13):8156-62.
Chicken liver P-protein of the multienzyme glycine cleavage system catalyzes the first partial reaction of glycine cleavage. In the partial reaction, glycine and H-protein serve as substrates and the products are CO2 (not bicarbonate) and the decarboxylated portion of glycine attached to H-protein. The reaction exhibited Michaelis-Menten kinetics with respect to both substrates. The optimum pH for the reaction is 7.1, with 6.5 for the reverse reaction. Km values for glycine and H-protein are independent of the concentration of the the co-substrate, and calculated values are 5.8 mM for glycine and 3.4 microM for H-protein. Initial velocity experiments gave intersecting double reciprocal plots that conform to a sequential mechanism. Product inhibition studies revealed that both products inhibited competitively with respect to the varied substrate. Glycine methyl ester was found to be a competitive inhibitor of glycine and noncompetitive inhibitor of H-protein. H-protein whose lipoic acid prosthetic group and cysteinyl residues were modified with N-ethylmaleimide was a noncompetitive inhibitor of glycine and a competitive inhibitor of H-protein. These results are most consistent with a sequential random Bi Bi mechanism in which no abortive dead end complex is formed. This was supported by an isotope exchange experiment.
多酶甘氨酸裂解系统的鸡肝P蛋白催化甘氨酸裂解的第一步部分反应。在该部分反应中,甘氨酸和H蛋白作为底物,产物是二氧化碳(而非碳酸氢盐)以及与H蛋白相连的甘氨酸脱羧部分。该反应对两种底物均表现出米氏动力学。反应的最适pH为7.1,逆反应的最适pH为6.5。甘氨酸和H蛋白的Km值与共底物浓度无关,计算得出甘氨酸的Km值为5.8 mM,H蛋白的Km值为3.4 μM。初始速度实验得到符合有序机制的相交双倒数图。产物抑制研究表明,两种产物对可变底物均有竞争性抑制作用。发现甘氨酸甲酯是甘氨酸的竞争性抑制剂和H蛋白的非竞争性抑制剂。其硫辛酸辅基和半胱氨酰残基用N - 乙基马来酰亚胺修饰的H蛋白是甘氨酸的非竞争性抑制剂和H蛋白的竞争性抑制剂。这些结果与不形成无效终止复合物的有序随机双双机制最为一致。这得到了同位素交换实验的支持。