Yh. Ju et Mj. Plewa, PLANT-ACTIVATION OF THE BICYCLIC AROMATIC-AMINES BENZIDINE AND 4-AMINOBIPHENYL, Environmental and molecular mutagenesis, 29(1), 1997, pp. 81-90
Benzidine and 4-aminobiphenyl (4-ABP) are promutagenic bicyclic aromat
ic amines that are activated into frameshift and base pair substitutio
n mutagens by plant systems. Using the plant cell/microbe coincubation
assay, plant-activated benzidine from 0 to 50 mu M induced a concentr
ation-response in Salmonella typhimurium. At concentrations above 5 mu
M plant-activated benzidine induced frameshift and base pair substitu
tion mutations in the N- or O-acetyltransferase over-expressing strain
s, DJ460, YG1024, and YG1029. With plant-activated 4-ABP, concentratio
ns above 250 mu M induced a significant mutagenic response in strains
YG 1024 and YG 1029. A tobacco cell-free mixture, TX1MX, activated ben
zidine and 4-ABP Into mutagenic metabolites in S. typhimurium strains
YG1024, YG1029, and DJ460. The mutagenic sensitivities of plant-activa
ted benzidine and 4-ABP were the some with two different types of plan
t activation systems, TX1 sus pension cells and TX1MX cell-free medium
. The plant activation of these aromatic amines is mediated by tobacco
cell peroxidase. Plant-activated benzidine and 4-ABP are converted in
to intermediates that serve as substrates for bacterial or humanacetyl
CoA: N-hydroxyarylamine N-acetyltransferase to generate the ultimate m
utagenic products. (C) 1997 Wiley-Liss, Inc.