Karakaya A, Suzen S, Sardas S, Karakaya A E, Vural N
Ankara University, Faculty of Pharmacy, Department of Toxicology, Tandogan, Turkey.
Pharmacogenetics. 1991 Oct;1(1):58-61. doi: 10.1097/00008571-199110000-00009.
Human serum paraoxonase is a polymorphic enzyme that is capable of catalyzing the hydrolysis of paraoxon and other organophosphates, some carbamates and certain aromatic carboxylic acid esters. This enzyme is specified by two allelic genes at one autosomal locus (isozymes 'A' and 'B'). The purpose of this study was to examine the paraoxonase activity of 105 Turkish subjects. Paraoxonase activities ranged from 39.6 to 278.2 nmol p-nitrophenol formed per ml of serum per min. Paraoxonase phenotypes could be clearly identified by salt and paraoxonase:arylesterase activity ratio characteristics. The gene frequencies were 0.632 for the low activity allele (A) and 0.368 for the high activity allele (B).
人血清对氧磷酶是一种多态性酶,能够催化对氧磷及其他有机磷酸酯、一些氨基甲酸酯和某些芳香族羧酸酯的水解。该酶由常染色体上一个位点的两个等位基因(同工酶“A”和“B”)决定。本研究的目的是检测105名土耳其受试者的对氧磷酶活性。对氧磷酶活性范围为每分钟每毫升血清生成39.6至278.2纳摩尔对硝基苯酚。通过盐析及对氧磷酶:芳基酯酶活性比率特征能够清晰鉴定对氧磷酶表型。低活性等位基因(A)的基因频率为0.632,高活性等位基因(B)的基因频率为0.368。