Harm W
Basic Life Sci. 1975;5A:89-101. doi: 10.1007/978-1-4684-2895-7_12.
This paper summerizes experimental work (most of which is published) in which light flashes were used for an analysis of photoenzymatic repair in vivo and in vitro. The method permits determination of the reaction rate constants for the formation, dark dissociation, and repair photolysis of enzyme-substrate complexes under various conditions, and estimation of the number of photoreactivating enzyme molecules present. Investigation of these characteristics is basic for understanding of the overall photoreactivation kinetics observed in biological systems, its dependence on experimental parameters, and possibly its biological significance.
本文总结了(大部分已发表的)实验工作,其中利用光脉冲对体内和体外的光酶修复进行分析。该方法能够测定在各种条件下酶 - 底物复合物形成、暗解离和修复光解的反应速率常数,并估算存在的光复活酶分子数量。研究这些特性是理解在生物系统中观察到的整体光复活动力学、其对实验参数的依赖性以及可能的生物学意义的基础。