Takayanagi Toshio, Okazaki Risa, Gotoda Karen, Mine Masanori, Mizuguchi Hitoshi
Graduate School of Technology, Industrial and Social Sciences, Tokushima University, 2-1 Minamijyousanjima-cho, Tokushima, 770-8506, Japan.
Faculty of Science and Technology, Tokushima University, 2-1 Minamijyousanjima-cho, Tokushima, 770-8506, Japan.
Anal Sci. 2025 Aug 28. doi: 10.1007/s44211-025-00844-3.
In-capillary enzymatic reaction was investigated in electrophoretically mediated microanalysis to achieve plateau response of the reaction product. Hydrolysis of 4-nitrophenyl phosphate (NPP) with alkaline phosphatase (ALP) was used as a model enzymatic reaction. The reaction product of 4-nitrophenol (NP) was photometrically detected as a plateau response based on the continuous enzymatic reaction in the separation capillary and the ongoing electrophoretic resolution of the product from the reaction zone. Two types of injection were compared between an enzyme injection and a substrate injection, whereas the counterpart reagent was contained in the separation buffer. In both approaches, the plateau response of NP developed linearly with increasing sample injection period, as well as the enzyme concentration. At low separation voltages, NP accumulated at the reaction zone, and the plateau height was inversely proportional to the applied voltage. Comparing enzyme and substrate injection methods, a stable plateau response was more easily achieved with the enzyme injection. It is because the concentration of the substrate in the injected plug decreases during the electrophoresis, leading to a reduced reaction rate. In contract, enzyme injection maintains consistent reaction conditions. The Michaelis-Menten constant was determined with the plateau response by both injection modes, and the values were comparable with each other.
在电泳介导的微分析中研究了毛细管内酶促反应,以实现反应产物的平稳响应。以碱性磷酸酶(ALP)催化4-硝基苯磷酸酯(NPP)水解作为模型酶促反应。基于分离毛细管中的连续酶促反应以及产物从反应区的持续电泳分离,通过光度法检测4-硝基苯酚(NP)的反应产物,将其作为平稳响应。比较了酶进样和底物进样两种进样方式,而对应试剂包含在分离缓冲液中。在这两种方法中,NP的平稳响应均随进样时间以及酶浓度的增加而呈线性发展。在低分离电压下,NP在反应区积累,平稳峰高与施加电压成反比。比较酶进样和底物进样方法,酶进样更容易实现稳定的平稳响应。这是因为在电泳过程中,进样塞中底物的浓度降低,导致反应速率降低。相比之下,酶进样可保持一致的反应条件。通过两种进样模式的平稳响应测定了米氏常数,其值彼此相当。