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通过cDNA表达的细胞色素P450 1A1、1A2和环氧化物水解酶对多环芳烃K区域进行立体选择性环氧化和水合作用。

Stereoselective epoxidation and hydration at the K-region of polycyclic aromatic hydrocarbons by cDNA-expressed cytochromes P450 1A1, 1A2, and epoxide hydrolase.

作者信息

Shou M, Gonzalez F J, Gelboin H V

机构信息

Laboratory of Molecular Carcinogenesis, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Biochemistry. 1996 Dec 10;35(49):15807-13. doi: 10.1021/bi962042z.

Abstract

Stereoselective epoxidation by cytochrome P450s (P450s) and regioselective hydration by epoxide hydrolase determine the carcinogenic potency of some polycyclic aromatic hydrocarbons (PAHs). In this report, cDNA-expressed human and mouse P450s 1A1 and 1A2 and epoxide hydrolase were used to characterize the stereoselective epoxidation and regioselective hydration at the K-region of benz[a]-anthracene (BA), 7,12-dimethylbenz[a]anthracene (DMBA), chrysene (CR), benzo[a]pyrene (B[a]P), dibenz[a,h]anthracene (DB[a,h]A), and benzo[c]phenanthrene (B[c]Ph) by direct chiral stationary-phase HPLC (CSP-HPLC) analyses. Our results indicated that all P450 isoforms preferentially produced major K-region, S,R-epoxides of BA (95-98%), DMBA (94-97%), B[a]P (91-96%), DB[a,h]A (94-98%), and B[c]Ph (87-92%), and major R,S-epoxide of CR (74-85%) in the presence of 3,3,3-trichloropropylene 1,2-oxide (TCPO), an inhibitor of epoxide hydrolase, suggesting that P450 enzymes exhibited the high stereoselectivity toward one of two stereoheterotopic faces of K-region double bond of the PAHs. Epoxide hydrolase either expressed from recombinant vaccinia virus or contained in human hepatoma G2 cells (HepG2) hydrated the C-O bond of epoxy-ring at the S-carbon of major metabolically-formed K-region epoxide enantiomers of BA, CR, DMBA, B[a]P, and DB[a,h]A to yield 80-98% dihydrodiols enriched in R,R-form and that at the R-carbon of B[c]Ph epoxide to yield 77-92% dihydrodiol enriched in S,S-form, suggesting that epoxide hydrolase was highly regioselective. The various enantiomeric components of dihydrodiol products in the metabolism of PAHs were apparently due to the combined effect of stereoselectivity of the P450s and regioselectivity of epoxide hydrolase. Our results provide a clear understanding of how these enzymes catalyze overall stereoselective metabolism at the K-region of the PAHs.

摘要

细胞色素P450(P450s)介导的立体选择性环氧化作用以及环氧水解酶介导的区域选择性水化作用决定了某些多环芳烃(PAHs)的致癌潜能。在本报告中,利用cDNA表达的人及小鼠P450s 1A1和1A2以及环氧水解酶,通过直接手性固定相高效液相色谱(CSP-HPLC)分析,对苯并[a]蒽(BA)、7,12-二甲基苯并[a]蒽(DMBA)、 Chrysene(CR)、苯并[a]芘(B[a]P)、二苯并[a,h]蒽(DB[a,h]A)和苯并[c]菲(B[c]Ph)在K区域的立体选择性环氧化和区域选择性水化作用进行了表征。我们的结果表明,在环氧水解酶抑制剂3,3,3-三氯丙烯1,2-氧化物(TCPO)存在的情况下,所有P450同工型均优先生成BA(95-98%)、DMBA(94-97%)、B[a]P(91-96%)、DB[a,h]A(94-98%)和B[c]Ph(87-92%)的主要K区域S,R-环氧化物,以及CR(74-85%)的主要R,S-环氧化物,这表明P450酶对PAHs的K区域双键的两个立体异位面之一表现出高立体选择性。由重组痘苗病毒表达或存在于人类肝癌G2细胞(HepG2)中的环氧水解酶,使BA、CR、DMBA、B[a]P和DB[a,h]A主要代谢形成的K区域环氧化物对映体的S-碳上环氧环的C-O键水化,生成80-98%富含R,R-形式的二氢二醇,使B[c]Ph环氧化物的R-碳上的C-O键水化,生成77-92%富含S,S-形式的二氢二醇,这表明环氧水解酶具有高度的区域选择性。PAHs代谢中二氢二醇产物的各种对映体成分显然是由于P450s的立体选择性和环氧水解酶的区域选择性共同作用的结果。我们的结果为这些酶如何催化PAHs在K区域的整体立体选择性代谢提供了清晰的认识。

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