Bulygina E R, Voronina O L, Tsyplenkova M S, Telepneva V I
Biokhimiia. 1988 Sep;53(9):1557-62.
Two SH-groups per enzyme subunit have been identified in the native preparation of rabbit liver NAD kinase, using DTNB. The titration curve is biphasic; one SH-group is modified at each step. There is a strict correlation between the loss of the enzyme activity and the rate of modification of fast and slow SH-groups. Substrates afford only a partial protection of NAD kinase against the DTNB-induced inactivation. The data obtained suggest that two SH-groups of NAD kinase are essential for the enzyme activity; however, these groups are not directly involved in the active center formation.
利用5,5'-二硫代双(2-硝基苯甲酸)(DTNB),在兔肝NAD激酶的天然制剂中,已鉴定出每个酶亚基有两个巯基(SH)基团。滴定曲线呈双相;每一步修饰一个SH基团。酶活性的丧失与快速和慢速SH基团的修饰速率之间存在严格的相关性。底物仅对NAD激酶提供部分保护,使其免受DTNB诱导的失活。所获得的数据表明,NAD激酶的两个SH基团对酶活性至关重要;然而,这些基团并不直接参与活性中心的形成。