胞浆
化学
动力学
体外
荧光
酶动力学
生物化学
硫酸化
结合
色谱法
酶
活动站点
物理
量子力学
数学分析
数学
作者
Risto O. Juvonen,Olli T. Pentikäinen,J. Huuskonen,Juri M. Timonen,Olli Kärkkäinen,Aki T. Heikkinen,Muluneh M. Fashe,Hannu Raunio
出处
期刊:Xenobiotica
[Taylor & Francis]
日期:2020-01-04
卷期号:50 (8): 885-893
被引量:2
标识
DOI:10.1080/00498254.2020.1711544
摘要
Sulfonation is an important high affinity elimination pathway for phenolic compounds.In this study sulfonation of 7-hydroxycoumarin and 13 its derivatives were evaluated in liver cytosols of human and six animal species. 7-hydroxycoumarin and its derivatives are strongly fluorescent, and their sulfate conjugates are nonfluorescent at excitation 405 nm and emission 460 nm. A convenient fluorescence based kinetic assay of sulfonation was established.The sulfonation rate of most of the 7-hydroxycoumarin derivatives was low in liver cytosol of human and pig, whereas it was high with most compounds in dog and intermediate in rat, mouse, rabbit, and sheep. Sulfonation of the 7-hydroxycoumarin derivatives followed Michaelis-Menten kinetics with Km values of 0.1–12 µM, Vmax of 0.005–1.7 µmol/(min * g protein) and intrinsic clearance (Vmax/Km) of 0.004–1.9 L/(min * g cytosolic protein).Fluorescence based measurement of sulfonation of 7-hydroxycoumarin derivatives provides a sensitive and convenient high-throughput assay to determine sulfonation rate in different species and tissues and can be applied to evaluate sulfonation kinetics and inhibition.
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