Krivobok S, Olivier P, Marzin D R, Seigle-Murandi F, Steiman R
UER de Pharmacie, Grenoble, France.
Mutagenesis. 1987 Nov;2(6):433-9. doi: 10.1093/mutage/2.6.433.
Seventeen mycotoxins [aflatoxins B1 (AFB1), B2 (AFB2), G1 (AFG1), G2 (AFG2), aflatoxicol, sterigmatocystin, patulin, citrinin, penicillic acid, T-2 toxin, diacetoxyscirpenol, zearalenone, zearalenol (alpha and beta isomers 1:1), ochratoxin A, norsolorinic acid, averufin, versicolorin A] were tested using the SOS Chromotest (PQ37 and PQ35). Six of the mycotoxins (AFB1, AFG1, AFB2, aflatoxicol, sterigmatocystin and versicolorin A) were genotoxic on PQ37 strain with and without metabolic activation. The results obtained with metabolic activation are in agreement with positive results obtained in other tests of genotoxicity. Except for AFB2, the presence of a double bond C8-C9 in the dihydrobenzofurane (DHBF) ring explained the activity due to the formation of an epoxide, but the coumarin cyclopentenone ring also plays a role in the qualitative differences of genotoxic activity. The wild-type uvrB gene in PQ35 decreases the genotoxic response with and without metabolic activation. Without metabolic activation, only mycotoxins possessing the DHBF ring group and double linkage C8-C9 exhibit a genotoxic effect.
使用SOS色测试(PQ37和PQ35)对17种霉菌毒素[黄曲霉毒素B1(AFB1)、B2(AFB2)、G1(AFG1)、G2(AFG2)、黄曲霉毒素醇、杂色曲霉素、展青霉素、桔霉素、青霉酸、T-2毒素、二乙酰基麦角甾醇、玉米赤霉烯酮、玉米赤霉醇(α和β异构体1:1)、赭曲霉毒素A、诺索林酸、黄绿青霉素、杂色曲菌素A]进行了测试。其中6种霉菌毒素(AFB1、AFG1、AFB2、黄曲霉毒素醇、杂色曲霉素和杂色曲菌素A)在有无代谢活化的情况下,对PQ37菌株均具有遗传毒性。代谢活化后获得的结果与其他遗传毒性测试中获得的阳性结果一致。除AFB2外,二氢苯并呋喃(DHBF)环中C8-C9双键的存在解释了由于环氧化物形成而产生的活性,但香豆素环戊烯酮环在遗传毒性活性的定性差异中也起作用。PQ35中的野生型uvrB基因在有无代谢活化的情况下均降低了遗传毒性反应。在没有代谢活化的情况下,只有具有DHBF环基团和C8-C9双键的霉菌毒素表现出遗传毒性作用。