Eftink M R, Biltonen R L
Biochemistry. 1983 Oct 25;22(22):5134-40. doi: 10.1021/bi00291a012.
Various kinetic aspects of the nonenzymatic hydrolysis of cytidine cyclic 2',3'-phosphate and uridine cyclic 2',3'-phosphate have been studied in order to provide a basis for comparison with the ribonuclease A catalyzed hydrolysis reaction. Studies of the pH dependence of the nonenzymatic reaction reveal mechanisms that are first order in hydroxide concentration and second order in hydrogen ion concentration, in addition to a "water" reaction. The rate constant for the water reaction was found to be very small, approximately equal to 2.5 X 10(-6) min-1. General base catalyzed hydrolysis reactions were also studied with imidazole as the catalyst. At pH values in which both the protonated and neutral forms of imidazole are present, a kinetic mechanism was observed that appears to be second order in total imidazole concentration, thus suggesting that bifunctional catalysis occurs. The activation enthalpy for the hydroxide, hydrogen ion, water, and imidazole catalyzed reactions was determined.
为了为与核糖核酸酶A催化的水解反应进行比较提供基础,对胞苷2',3'-环磷酸酯和尿苷2',3'-环磷酸酯的非酶促水解的各种动力学方面进行了研究。对非酶促反应的pH依赖性研究揭示了除“水”反应外,在氢氧根浓度上为一级且在氢离子浓度上为二级的反应机制。发现水反应的速率常数非常小,约等于2.5×10⁻⁶ min⁻¹。还以咪唑为催化剂研究了一般碱催化的水解反应。在咪唑的质子化形式和中性形式均存在的pH值下,观察到一种动力学机制,该机制在总咪唑浓度上似乎为二级,因此表明发生了双功能催化。测定了氢氧根、氢离子、水和咪唑催化反应的活化焓。