Degradation of VX and sulfur mustard by enzymatic haloperoxidation

被引:36
作者
Amitai, G [1 ]
Adani, R [1 ]
Hershkovitz, M [1 ]
Bel, P [1 ]
Rabinovitz, I [1 ]
Meshulam, H [1 ]
机构
[1] Israel Inst Biol Res, Div Med Chem, IL-74100 Ness Ziona, Israel
关键词
VX; sulfur mustard; HD; HD sulfoxide; HD sulfone; HD sulfoxide-vinyl; enzymatic degradation; chloroperoxidase; horseradish peroxidase; pig-ear skin;
D O I
10.1002/jat.911
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Chloroperoxidase (CPO) isolated from Caldariomyces fumago (20 U ml(-1)) together with urea hydrogenperoxide (UPER, 0.5 mM) and sodium chloride as co-substrate (NaCl, 0.5 M) caused rapid breakdown of VX (10 muM) (t(1/2) 8 s, 25 degreesC, 50 mM tartarate, pH 2.75). Glucose oxidase (GOX, Aspergillus niger) and glucose were used as an alternative source for H2O2. A mixture of GOX (20 U ml(-1)), glucose (GLU 0.45 M), CPO (20 U ml(-1)) and NaCl (0.5 M) caused a 3.8-fold slower degradation of VX (10 muM) (t(1/2) = 30 s, 25 degreesC, 50 mM tartarate, pH 2.75). The concentrations of H2O2 and chlorine produced by this enzyme/substrate mixture depended mainly on the GLU concentration. Horseradish peroxidase (HRP) together with UPER (1 mM) and sodium iodide (NaI, 0.05 M) caused progressive degradation of VX that was more than 400-fold slower than with CPO (20 U ml(-1)), UPER (0.5 mM) and NaCl (0.5 M) (t(1/2) = 55 min, 25 degreesC, pH 8). Skin decontamination of VX by CPO was tested in pig-ear skin in vitro. The chemical agent VX (0.01 M, 100 mul) was degraded by 98% within 3 h of skin diffusion when a mixture of UPER/NaCl/CPO was applied 60 min prior to VX application. A mixture of UPER/NaCl without CPO also caused significant VX degradation (94%) during skin diffusion whereas it did not cause any VX degradation in solution. Degradation of VX in skin, obtained without exogenous CPO, may indicate involvement of endogenous intradermal haloperoxidase-like enzyme. Reagent UPER (1 mM) did not cause any degradation of VX in solution or during its skin diffusion. Furthermore, a mixture of CPO, UPER and NaCl caused rapid degradation of sulfur mustard (HD). Sulfur mustard (50 muM) incubated in the presence of CPO (4 U ml(-1)), UPER (0.05 M) and NaCl (0.5 M) at pH 2.75 and 30 degreesC was oxidized by 97% and 99% within 5 and 10 min, respectively. The oxidation products HD sulfoxide, HD sulfoue and HD sulfoxidevinyl were identified by GC/MS in the enzymatic chloroperoxidation mixture. Copyright (C) 2003 John Wiley Sons, Ltd.
引用
收藏
页码:225 / 233
页数:9
相关论文
共 24 条
[1]   Oxidative biodegradation of phosphorothiolates by fungal laccase [J].
Amitai, G ;
Adani, R ;
Sod-Moriah, G ;
Rabinovitz, I ;
Vincze, A ;
Leader, H ;
Chefetz, B ;
Leibovitz-Persky, L ;
Friesem, D ;
Hadar, Y .
FEBS LETTERS, 1998, 438 (03) :195-200
[2]  
AMITAI G, 2002, IN PRESS BIOSCI MED
[3]  
BRIANDUNFORD H, 2000, REDOX REP, V5, P169
[4]  
CHANG M, 1984, SURVEY EVALUATION CH
[5]   In vitro skin absorption and decontamination of sulphur mustard:: Comparison of human and pig-ear skin [J].
Chilcott, RP ;
Jenner, J ;
Hotchkiss, SAM ;
Rice, P .
JOURNAL OF APPLIED TOXICOLOGY, 2001, 21 (04) :279-283
[6]  
Dacre JC, 1996, PHARMACOL REV, V48, P289
[7]   INACTIVATION OF ORGANOPHOSPHORUS NERVE AGENTS BY THE PHOSPHOTRIESTERASE FROM PSEUDOMONAS-DIMINUTA [J].
DUMAS, DP ;
DURST, HD ;
LANDIS, WG ;
RAUSHEL, FM ;
WILD, JR .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 277 (01) :155-159
[8]  
Elashvilli E, 2001, P ENZ M ORL FL, P54
[9]   A NEW AND RAPID COLORIMETRIC DETERMINATION OF ACETYLCHOLINESTERASE ACTIVITY [J].
ELLMAN, GL ;
COURTNEY, KD ;
ANDRES, V ;
FEATHERSTONE, RM .
BIOCHEMICAL PHARMACOLOGY, 1961, 7 (02) :88-&
[10]   Hypochlorite-induced oxidation of proteins in plasma: formation of chloramines and nitrogen-centred radicals and their role in protein fragmentation [J].
Hawkins, CL ;
Davies, MJ .
BIOCHEMICAL JOURNAL, 1999, 340 :539-548