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构建兔醛氧化酶cDNA表达系统以阐明种属差异。

Construction of expression system of rabbit aldehyde oxidase cDNA for the clarification of species differences.

作者信息

Liu Ping, Liang Sun, Wang Ben-Jie, Guo Rui-Chen

机构信息

Institute of Clinical Pharmacology, Qilu Hospital of Shandong University, Jinan 250012, China.

出版信息

Eur J Drug Metab Pharmacokinet. 2009 Jul-Sep;34(3-4):205-11. doi: 10.1007/BF03191175.

Abstract

A remarkably large species difference in cinchonidine oxidation activity catalyzed by aldehyde oxidase (AO) has been known, in particular between rabbit and monkey. As the first step in clarifying the phenomenon from the view point of structures of the active site, we attempted to construct an expression system of rabbit AO cDNA. The nucleotide sequences of cloned full-length rabbit AO cDNA were determined and confirmed to agree completely with those of genome DNA. The expression system in Escherichia coli was constructed in reference to the previously established method for monkey AO. Both expressed rabbit and monkey AO proteins correctly reproduced the remarkable species differences observed in their liver cytosols towards cinchonidine and methotrexate. Namely, the expressed rabbit AO protein showed extremely high activities than did that of monkey AO. A difference in the structure of the active site might be responsible for the substrate-dependent species difference towards the relatively bulky molecules of cinchonidine and methotrexate. The use of molecular biology techniques will be very useful to verify the hypothesis.

摘要

醛氧化酶(AO)催化的辛可尼定氧化活性存在显著的物种差异,尤其是在兔和猴之间。作为从活性位点结构角度阐明该现象的第一步,我们试图构建兔AO cDNA的表达系统。测定了克隆的兔全长AO cDNA的核苷酸序列,并确认其与基因组DNA的序列完全一致。参照先前建立的猴AO表达方法,构建了大肠杆菌中的表达系统。表达的兔和猴AO蛋白都正确再现了它们肝细胞溶胶中对辛可尼定和甲氨蝶呤所观察到的显著物种差异。也就是说,表达的兔AO蛋白比猴AO蛋白表现出极高的活性。活性位点结构的差异可能是对辛可尼定和甲氨蝶呤等相对大分子底物依赖性物种差异的原因。分子生物学技术的应用将非常有助于验证这一假设。

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