Laboratoire de Toxicologie et Hygiène Appliquée, UFR de Pharmacie, 3 ter place de la Victoire, 33000, Bordeaux, France.
Mycotoxin Res. 1995 Mar;11(1):37-47. doi: 10.1007/BF03192060.
The toxicity of ochratoxin A (OTA), a mycotoxin produced by fungi ofAspergillus orPenicillium genera is now well documented. Its nephrotoxicity, immunosuppression, teratogenicity, and carcinogenicity have been widely studied. Physical and biochemical methods have been studied to prevent these toxinogenicAspergillus andPenicillium from producing OTA, and/or to destroy the mycotoxin when already produced in a liquid or a solid medium. Repeated freezing at - 20†C and thawing at + 26†C aleatory reduce OTA production in a liquid medium. Exposure to UV B for different periods of time is efficient in preventing OTA production in a liquid medium. Gamma-irradiation from 2 to 5 kGy gives good results in preventing the production of OTA or destroying it when already produced. Carboxypeptidase is very efficient at 5 units/50 ml in a liquid medium for cleaving the OTA already produced.
赭曲霉毒素 A(OTA)是一种由曲霉属和青霉属真菌产生的真菌毒素,其毒性现已得到充分证实。其肾毒性、免疫抑制作用、致畸性和致癌性已得到广泛研究。人们研究了物理和生化方法来防止这些产毒曲霉属和青霉属产生 OTA,以及/或在液体或固体培养基中已经产生时破坏真菌毒素。在-20°C 反复冷冻和解冻可随机减少液体培养基中 OTA 的产生。在液体培养基中,暴露于不同时间的 UV B 是有效防止 OTA 产生的方法。2 至 5 kGy 的γ辐射在防止 OTA 产生或在其产生后破坏它方面效果良好。在液体培养基中,5 单位/50ml 的羧肽酶对于切割已产生的 OTA 非常有效。