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Bacterial bioluminescence as a bioassay for mycotoxins.

机译:细菌生物发光作为霉菌毒素的生物测定。

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摘要

The use of bacterial bioluminescence as a toxicological assay for mycotoxins was tested with rubratoxin B, zearalenone, penicillic acid, citrinin, ochratoxin A, PR-toxin, aflatoxin B1, and patulin. The concentrations of mycotoxins causing 50% light reduction (EC50) in Photobacterium phosphoreum were determined immediately and at 5 h after reconstitution of the bacteria from a freeze-dried state. Generally, less toxins were required to obtain an EC50 at 5 h. The effects of the above mycotoxins on bioluminescence were determined after 5, 10, 15, and 20 min of incubation with the bacterial suspensions. The concentration of rubratoxin B necessary to elicit an EC50 increased with time, whereas the concentration of citrinin, penicillic acid, patulin, and PR-toxin necessary decreased with time. There was very little change in the concentration of zearalenone, aflatoxin B1, and ochratoxin A required to elicit an EC50 with time. The bacterial bioluminescence assay was most sensitive to patulin and least sensitive to rubratoxin B.
机译:用曲霉毒素B,玉米赤霉烯酮,青霉酸,citrinin,曲霉毒素A,PR毒素,黄曲霉毒素B1和棒曲霉素测试了细菌生物发光作为霉菌毒素的毒理学检测方法。立即和在从冷冻干燥状态复原细菌后的5 h处测定引起在荧光细菌中减少50%减光(EC50)的霉菌毒素的浓度。通常,在5小时内获得EC50所需的毒素较少。在与细菌悬浮液温育5、10、15和20分钟后,确定上述霉菌毒素对生物发光的影响。引发EC50所必需的rubratoxin B的浓度随时间增加,而西林素,青霉素,patulin和PR毒素所必需的浓度随时间降低。随时间变化引起EC50所需的玉米赤霉烯酮,黄曲霉毒素B1和曲霉毒素A的浓度变化很小。细菌生物发光测定法对展青霉素最敏感,对红曲霉毒素B最不敏感。

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