Yang Yang, Ji Jian, Wu Shang, Ye Yongli, Sheng Lina, Zhang Yinzhi, Sun Xiulan
School of Food Science, State Key Laboratory of Food Science and Technology, National Engineering Research Center for Functional Foods, School of Food Science Synergetic Innovation Center of Food Safety and Nutrition, Joint International Research Laboratory on Food Safety, Jiangnan University, Wuxi 214122, China.
College of Food Science and Pharmacy, Xinjiang Agricultural University, Ürümqi 830052, China.
Foods. 2023 Jan 13;12(2):382. doi: 10.3390/foods12020382.
Patulin, a mycotoxin commonly found in fruits and derived products, causes serious health problems for humans and animals worldwide. Several microbial strains have been observed to possess the ability to effectively remove patulin. However, these methods are presently associated with disadvantages such as low degradation efficiency and an unclear biodegradation mechanism. In the current study, the characteristics of patulin degradation via FS10 were evaluated, and the mechanisms involved were analyzed using metabolomics technologies. The results showed that the suspension of FS10 could degrade 94.72% of patulin within 36 h. The moment concentration pf patulin was 0.116 μg/mL, and the detection limit value was 0.01 μg/mL. In addition, the patulin content was reduced to levels below the detection limit within 48 h. FS10 mainly degrades patulin by producing intracellular enzymes, which can convert patulin into ascladiol. This degradation method can effectively reduce the damage caused by patulin to HepG2 cells. In addition, the patulin treatment significantly affects the pentose phosphate pathway and the glutathione pathway. These two metabolic pathways are speculated to be closely related to patulin degradation via FS10. The incubation of FS10 with patulin-contaminated apple pomace can not only eliminate patulin but also increase the utilization of apple pomace. Therefore, our research results provide a new method for addressing patulin contamination in the food and feed industries.
展青霉素是一种常见于水果及其衍生产品中的霉菌毒素,在全球范围内对人类和动物都造成严重的健康问题。已观察到几种微生物菌株具有有效去除展青霉素的能力。然而,目前这些方法存在降解效率低和生物降解机制不明确等缺点。在本研究中,评估了通过FS10降解展青霉素的特性,并使用代谢组学技术分析了其中涉及的机制。结果表明,FS10悬浮液在36小时内可降解94.72%的展青霉素。展青霉素的瞬间浓度为0.116μg/mL,检测限值为0.01μg/mL。此外,展青霉素含量在48小时内降至检测限以下。FS10主要通过产生细胞内酶来降解展青霉素,这些酶可将展青霉素转化为阿斯克拉二醇。这种降解方法可有效降低展青霉素对HepG2细胞造成的损害。此外,展青霉素处理显著影响磷酸戊糖途径和谷胱甘肽途径。推测这两条代谢途径与通过FS10降解展青霉素密切相关。将FS10与受展青霉素污染的苹果渣一起培养,不仅可以消除展青霉素,还可以提高苹果渣的利用率。因此,我们的研究结果为解决食品和饲料行业中的展青霉素污染提供了一种新方法。