在囯内首先建立了大肠杆菌DNA修复试验(E,coli recA/uvrB differential DNA repair test,E. coli DDRT),用21种各类化合物进行方法学验证。结果提示,与Ames 试验的符合率为65/%(13/20),与丈献报道E.coli DDRT(其它菌株)试验结果的符合率为80%(12/15〉,与幼物致癌试验结果的符合牟为76.5%(13/17),其中E.coli DDRT试验结果阳性而Ames城验阴性的有4-Aminophenol.Catechol,DES,Thioacetamide;而E.coli DDRT试验结果阴性,Ames试验阳性的有4-AAF,Benzidine,CP,DMSO。基于这些结果,可以认为本实验室建立的大肠杆菌recA/uvrB DNA修复试验方法具有实用价值和重现性,可进一步建立该菌株的体内试验方法。
Abstract
The E. coli recA/uvrB differential DNA repair test(E.coli DDRT) was first established and validated with 21 various compounds in China. The results showed that 13 were positive among 21 chemicals tested. The general concordance was 65% (13/20) with Ames test,80% (12/15) with E.coli DDRT(using different strains) results published in the literature,and 76. 5%(13/17) with animal carcinogenecity test. Among these compounds,4-aminophenol,catechol ,DES,thioacetamide were positive in E.coli DDRT but negetive in Ames test ,and conversely,4-AAF,benzidine ,CP,DMSO were negetive in E.coli DDRT but positive in Ames test.The reasons for this disagreement were discussed. The differential killing index (DKI) was caculated to quantitatively compare relative genotoxic potency among chemicals tested. These results suggest that the method established by now is practical and reproducible and can be applied to screen the mutageneeity of chemicals.
关键词
大肠杆菌K-12 /
DNA修复 /
致突变试验
{{custom_keyword}} /
Key words
E. colik-12. DNA repair /
mutageneeity test
{{custom_keyword}} /
{{custom_sec.title}}
{{custom_sec.title}}
{{custom_sec.content}}
参考文献
1 Mohn G,Kerklaan P,Ellenberger J.Methodologes for the direct and animal-mediated determination of vatious genetic efficts in derivativatives of strain 343/113 of E.coli K-12,in:Kilbey BJ,et al,ed.Handbook of mutagenicity test proce-dures.ed 2.Elsevier,Amsterdam;Elsevier Science Publish-er BV,1984:189-215.
2 Mohn GR.The DNA repair host-mediated assay as a rapid and sensitive in vivo present in various organs of mice.Some prclinuinary results with mitomycin C.Arch Toxicol,1984,55:268.
3 Hellmer L,Bolcsfoldi G.An evalution of the E.coli K-12 u-vrB/DNA repair host-mediated assay.I.In vitro sen-sitivity of the bacteria to 61 comounds.Mutat Res,1992,272:145.
4 Hellmer L,Bolcsfoldi G.An evalution of the E.coli K-12 u-vrB/R=recA DNA repair host-mediated asssay.Ⅱ.in vivo re-sults for 36 compornds tested i the mouse.Mutat Res,1992,72:161.
5 Kerklaan PRM,Bouter S,van Elburg PA,et al.Evaluation of the DNA repair host-mediated assay.I.Induction of re-pairable DNA damage in E.coli cells recovered from liver,spleen,lungs,kidneys,and the blood stream of mice treated with methylating carcinogens.Mrtat Res,1985,148:1.
6 Kerklaan PRM,Bouter S,van Elburg PE,et al.Evaluation of the DNA repair host-mediated assay.Ⅱ.Presence of geno-tixuc factirs ub various organs of mice treated with chemotherpeutic agents.Mutat Res,1986,164:19.
7 Zeilmaker MJ,van Teylylingen CMM,Mohn GR.Evaluation of the DNA-repair host-mediated assay.Ⅱ.Relationship be-tween metabolic activation of dimethylitrosamine and or-gan-specific differential lethality induced in E,Coli indicator strains.Mutat Res,1991,247:87.
8 De Flore S,Zanacchi P,Camoirano A,et Genotoxic activi-ty and potency of 135 compounds in the Ames reversion test and in a bacterial DNA repair test.Mutat Res,1984,133:161
{{custom_fnGroup.title_cn}}
脚注
{{custom_fn.content}}