A stereospecific phosphotriesterase in hen liver and brain

被引:20
作者
Díaz-Alejo, N
Monroy, A
Vilanova, E [1 ]
Vicedo, JL
Sogorb, MA
机构
[1] Univ Miguel Hernandez, Dept Neuroquim, E-03550 San Juan De Alicante, Spain
[2] Univ Miguel Hernandez, Inst Neurociencias, E-03550 San Juan De Alicante, Spain
关键词
organophosphorus compound; phosphotriesterase; hen; stereospecific; liver; brain;
D O I
10.1016/S0009-2797(97)00106-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
O-Hexyl, O-2,5-dichlorophenyl phosphoramidate (HDCP) is a chiral compound that induces delayed neuropathy in hens. This compound is hydrolyzed by a phosphotriesterase known as HDCPase in hen and rat plasma, liver and brain. We studied the stereospecificity of HDCPase in hen tissues and in human and rabbit plasma employing a chromatographic method for analysis and quantification of HDCP stereoisomers. Hen and human plasma HDCPases were not stereospecific. However, rabbit plasma showed a remarkable stereospecificity to S-(-)-HDCP. High levels of stereospecific HDCPase were found in the particulate fraction of hen liver, where S-(-)-HDCP is hydrolyzed faster than R-(+)-HDCP. However, in hen brain the stereospecificity was found in the soluble fraction, where R-(+)-HDCP is hydrolyzed faster than S-(-)-HDCP. It is concluded that liver particulate fraction must be the main tissue responsible for the HDCP stereospecific biotransformation in hens. In an oral administration, the steroisomer R-(+)-HDCP would survive after passing through the liver and would interact with acetylcholinesterase and neuropathy target esterase in the nervous system. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:187 / 196
页数:10
相关论文
共 24 条
[1]
STEREOSPECIFIC ENZYMATIC-HYDROLYSIS OF PHOSPHORUS-SULFUR BONDS IN CHIRAL ORGANOPHOSPHATE TRIESTERS [J].
CHAE, MY ;
POSTULA, JF ;
RAUSHEL, FM .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 1994, 4 (12) :1473-1478
[2]
Cloning and expression of a gene encoding a bacterial enzyme for decontamination of organophosphorus nerve agents and nucleotide sequence of the enzyme [J].
Cheng, TC ;
Harvey, SP ;
Chen, GL .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (05) :1636-1641
[3]
STEREOSELECTIVE HYDROLYSIS OF SOMAN IN HUMAN-PLASMA AND SERUM [J].
DEBISSCHOP, HCJV ;
DEMEERLEER, WAP ;
VANHECKE, PRJ ;
WILLEMS, JL .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (21) :3579-3585
[4]
SCREENING OF HALOPHILIC BACTERIA AND ALTEROMONAS SPECIES FOR ORGANOPHOSPHORUS HYDROLYZING ENZYME-ACTIVITY [J].
DEFRANK, JJ ;
BEAUDRY, WT ;
CHENG, TC ;
HARVEY, SP ;
STROUP, AN ;
SZAFRANIEC, LL .
CHEMICO-BIOLOGICAL INTERACTIONS, 1993, 87 (1-3) :141-148
[5]
DEJONG LPA, 1989, ENZYMES HYDROLYSING ORGANOPHOSPHORUS COMPOUNDS, P65
[6]
HEN LIVER AND PLASMA CAN METABOLIZE HEXYL-DCP PHOSPHORAMIDATE AT A RATE COMPARABLE TO THAT OF RAT [J].
DIAZALEJO, N ;
PELLIN, MC ;
VICEDO, JL ;
VILANOVA, E .
NEUROTOXICOLOGY AND TERATOLOGY, 1990, 12 (06) :615-617
[7]
CHIRAL HIGH-PERFORMANCE LIQUID-CHROMATOGRAPHY AND GAS-CHROMATOGRAPHY OF THE STEREOISOMERS OF HEXYL 2,5-DICHLOROPHENYL PHOSPHORAMIDATE [J].
DIAZALEJO, N ;
VILANOVA, E .
JOURNAL OF CHROMATOGRAPHY-BIOMEDICAL APPLICATIONS, 1993, 622 (02) :179-186
[8]
Metal-substrate interactions facilitate the catalytic activity of the bacterial phosphotriesterase [J].
Hong, SB ;
Raushel, FM .
BIOCHEMISTRY, 1996, 35 (33) :10904-10912
[9]
STEREOSELECTIVITY OF SOMAN DETOXICATION BY ORGANOPHOSPHORUS ACID ANHYDRASES FROM ESCHERICHIA-COLI [J].
HOSKIN, FCG ;
GALLO, BJ ;
STEEVES, DM ;
WALKER, JE .
CHEMICO-BIOLOGICAL INTERACTIONS, 1993, 87 (1-3) :269-278
[10]
STEREO-SPECIFIC DEGRADATION OF THE R-(+) ISOMER OF O-N-HEXYL-S-METHYLPHOSPHOROTHIOAMIDATE CATALYZED BY RABBIT SERUM [J].
JOHNSON, MK ;
READ, DJ .
CHEMICO-BIOLOGICAL INTERACTIONS, 1993, 87 (1-3) :133-139