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1989 EMS Abstracts<br />

S . typhimurium TA98 <strong>and</strong> TA100, with <strong>and</strong> without metabolic activation . The samples from Notes<br />

the Katsura showed the highest mutagenic activity (3500 revertants with TA98, . +59 ; 87<br />

revertants with TA9B, -S9~ 141 revertants with TA100, +S9 ; negative with TA100, -S9,<br />

per 0 .1-g equivalent of'bIue rayon) . By further measurement at several different sites<br />

of this river, we found that the effluent from a waste-water treatment plant in Kyoto<br />

City is the possible source of the mutagenic pollution . When the samples collected<br />

from this river in the winter <strong>and</strong> summer of 1988 were fractionated by TLC, the mutagenic<br />

activity in TA98 with metabolic activation was found predominantly in single identical<br />

zones . It is suggested that River Katsura is constantly polluted with certain<br />

frameshift promutagens of polycyclic structures .<br />

490<br />

SALMONELLA MUTAGENICITY TEST ON VARIOUS KIND OF IRRADIATED SUGARS AND AMIlIO ACIDS<br />

K . Sakamoto, K . Kanazashi, S . Iwahara, K .Takatori, <strong>and</strong> R . Aibara, Hatano Research<br />

Institute, Food <strong>and</strong> Drug Safety Center, Hadano, [anagawa (Japan)<br />

Recently, various kind of irradiated foods were studied in mutagenicity tests .<br />

Every food comprises variety of components, but the volume of samples that can be<br />

used by these test systems is limited . Accordingly, even if certain components of<br />

the irradiated food should undergo mutagenic changes, it would be impossible to<br />

detect such changes if the volume of them are smaller than the detectable limit of<br />

the test systems .<br />

For this reason, it is necessary to study mutagenicity on each irradiated food<br />

components . And if the test results indicate the formation of mutagens in component<br />

by irradiation, we should evaluate the genetic toxicity of irradiated foods with the<br />

test results in due consideration of : 1) irradiation dose, 2) ratio of mutagenic<br />

products formed from the irradiated food components, 3) strength of mutagenic<br />

activity, 4) proportion of components in food changeable to mutagens <strong>and</strong> 5) possibility<br />

of elimination of the mutagenic products .<br />

We studied Salmonella/mammalian microsome mutagenicity test on various kinds ofsugars<br />

<strong>and</strong> amino acids irradiated in the dry condition <strong>and</strong> in liquid solution with<br />

gamma ray of maximum dosage upto 10 kGy . As a result, weak mutagenic activity was<br />

detected in the 5% solution of cystein <strong>and</strong> 10% solution of arabinose irradilted at<br />

the maximum dosage of 10 kGy, with metabolic activation system . The results indicate<br />

that the mutagenic products from each compound hardly forms in irradiated foods .<br />

491<br />

CLASTOGENIC EFFECT OF ELLIPTICINE ON DIFFERENT PHASES OF THE CELL CYCLE OF<br />

CULTURED HUMAN LYMPHOCYTES AND ITS SYNERGISTIC ACTION WITH INHIBITORSOF<br />

DNA REPAIR AT G2 . Elza T . Sakamoto-Hojo <strong>and</strong> Catarina S . Takahashi'(IBILCE-<br />

S . Jose Rio PreEo-UNESP <strong>and</strong> FFCL de Ribeir`ao Preto-USP, BRASIL) .<br />

Ellipticine, a pyridocarbazole alkaloid, has shown an antitumor effect<br />

on several types of experimental <strong>and</strong> human tumors, being an intercalating<br />

substance whose mutagenicity has been demonstrated in several systems .<br />

To characterize the mechanism of action of this compound at the cell cycle<br />

level, human lymphocyte cultures from 2 healthy donors were treated with<br />

3 pg/ml ellipticine in 30-minute pulses during different phases of the<br />

cycle <strong>and</strong> analyzed for chromosome aberrations <strong>and</strong> sister chromatid exchanges<br />

. The G2 phase was more sensitive in terms of induction of aberrations,<br />

followed by S <strong>and</strong> G1 . The 24-h treatment (S phase) induced a four<br />

fold increase compared to th8 control . SCE induction was significant only<br />

at G1, when SCE frequency doubled_3The effect of lymphocytg post-treatment<br />

with inhibitors of DNA repair (10 M caffeine <strong>and</strong> 5 x 10 M 1-B-D-arabino<br />

furanosylcytosine) was also tested by adding 3 yg/ml ellipticine at G in<br />

30-minute pulses <strong>and</strong> the inhibitors immediately afterward during the2last<br />

3 h before harvesting the cultures . In the two experiments performed on<br />

blood from the 2 donors there was a moderate effect of chromosome aberration<br />

potentiation (about 2-3 times), i .e ., ellipticine bad a synergistic<br />

effect with both inhibitors in terms of chromosome aberration induction .<br />

492<br />

THE ABSENCE OF PAH HYDROXYLATION ACTIVITY IN TOBACCO CALLUS S9 . M . F . Salamone',<br />

S . Richard', C . J . Gentile', J . M . Gentiles, <strong>and</strong> D . A . Rokosh', 'Ministry of the<br />

Environment, Toronto, Canada <strong>and</strong> *Hope College, Holl<strong>and</strong>, Michigan .<br />

Microsomal enzymes (S9) from four week old photosynthetic <strong>and</strong> nonphotosynthetic<br />

tobacco (Nicotiana tobacum) callus cultures were prepared by two separate laboratories .<br />

The ability of each callus S9 to activate 2-aminofluorene (2AF) <strong>and</strong> benzo(a)pyrene<br />

(BaP) was then tested with the Ames fluctuation <strong>and</strong> plate incorporation assays . With<br />

each assay the callus S9 preparations from both laboratories increased the mutagenic<br />

http://legacy.library.ucsf.edu/tid/clb93d00/pdf<br />

.<br />

169<br />

Y

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