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. 2022 May 8;12(6):536–544. doi: 10.1016/j.jtcme.2022.05.001

Table 1.

Mutagenicity assay of GEO on Salmonella typhimurium TA98, TA100, TA102, TA1535, and TA1537 in the presence or absence of metabolic activation.

Treatment Revertant colonies
TA98 TA100 TA102 TA1535 TA1537
Without S9 metabolic activation
Negative controla 51 ± 5.3 216 ± 5.0 299 ± 7.2 29 ± 2.6 13 ± 2.6
Positive controlb 132 ± 5.6∗∗ 606 ± 7.0∗∗ 761 ± 7.2∗∗ 133 ± 5.1∗∗ 53 ± 4.5∗∗
GEO (mg/plate)
0.05 56 ± 5.3## 219 ± 3.5## 294 ± 6.7## 28 ± 1.5## 12 ± 2.5##
0.1 47 ± 2.5## 211 ± 8.5## 310 ± 5.0## 30 ± 1.5## 13 ± 1.5##
0.125 55 ± 4.0## 220 ± 5.5## 280 ± 12.1## 29 ± 3.2## 12 ± 1.2##
0.25 51 ± 7.2## 206 ± 7.6## 290 ± 2.5## 28 ± 2.1## 11 ± 3.1##
0.5
58 ± 4.5##
205 ± 5.1##
301 ± 4.7##
30 ± 1.0##
12 ± 1.7##
With S9 metabolic activation
Negative controla 57 ± 2.5 224 ± 8.7 293 ± 12.2 30 ± 1.0 10 ± 2.1
Positive controlc 165 ± 3.2∗∗ 715 ± 4.5∗∗ 935 ± 4.7∗∗ 106 ± 5.1∗∗ 45 ± 4.5∗∗
GEO (mg/plate)
0.05 52 ± 3.0## 209 ± 13.4## 292 ± 4.5## 29 ± 1.5## 7 ± 0.6##
0.1 51 ± 5.5## 226 ± 6.1## 306 ± 5.0## 32 ± 2.1## 9 ± 0.6##
0.125 54 ± 4.6## 229 ± 5.0## 299 ± .4.0## 33 ± 2.1## 11 ± 1.2##
0.25 52 ± 2.3## 213 ± 10.1## 293 ± 5.7## 31 ± 2.1## 9 ± 0.6##
0.5 49 ± 5.3## 218 ± 11.0## 302 ± 3.1## 31 ± 2.5## 11 ± 2.1##

Data are presented as the mean ± SD (n = 3 plates/group). Statistical analysis was performed using one-way ANOVA followed by Tukey's post-hoc multiple comparison test. ∗∗, P < 0.01 denotes significant differences compared to negative control group. ##, P < 0.01 denotes significant differences compared to positive control group.

a

Dimethyl sulfoxide (DMSO).

b

4-nitro-o-phenylenediamine (0.5 μg/plate) for TA98; sodium azide (1 μg/plate) for TA100 and TA1535; mitomycin C (0.5 μg/plate) for TA102; 9-aminoacridine (0.5 μg/plate) for TA1537.

c

Benzo[a]pyrene (1.0 μg/plate) for TA98 and TA102; 2-aminoanthracene (4 μg/plate) for TA100, TA1535, and TA1537.