Zapaśnik Agnieszka, Bryła Marcin, Wojtczak Adrian, Sokołowska Barbara
Department of Microbiology, Waclaw Dabrowski Institute of Agricultural and Food Biotechnology-State Research Institute, Rakowiecka 36, 02-532 Warsaw, Poland.
Department of Food Safety and Chemical Analysis, Waclaw Dabrowski Institute of Agricultural and Food Biotechnology-State Research Institute, Rakowiecka 36, 02-532 Warsaw, Poland.
Metabolites. 2025 Jan 5;15(1):20. doi: 10.3390/metabo15010020.
BACKGROUND/OBJECTIVES: Mycotoxins, secondary metabolites synthesized by filamentous fungi, have been classified as dangerous substances and proven to be carcinogenic, as well as to have genotoxic, nephrotoxic, hepatotoxic, teratogenic, and mutagenic properties. Despite numerous trials to develop an effective and safe-for-human-health method of detoxification, there is still a high risk associated with the occurrence of these toxins in food and feed. Biological methods of food preservation are an alternative option to conventional chemical and physical methods, characterized by their less negative impact on human health as well as their high efficiency against filamentous fungi and other foodborne pathogens. Mycoremediation is a new biotechnique based on the capability of fungi to detoxify matrices from various pullulans. Ligninolytic enzymes produced by white rot fungi (WRF) characterize a high efficiency in the degradation of various mycotoxins.
In our study, , as a representative of WRF, was cultivated on a medium contaminated by AFB1 and ZEN (mushroom substrate and maize) in a few variants of concentration. After the cultivation, medium and fruiting bodies were collected and analyzed with the usage of HPLC and LC/MS methods.
The reduction oscillated between 53 and 87% (AFB1) and 73 and 97% (ZEN) depending on the initial concentration of toxins in the medium. Grown fruiting bodies contained insignificant amounts of both toxins.
These findings confirm the potential of as an effective biological agent for reducing mycotoxins in contaminated medium, highlighting its applicability in developing sustainable and safe methods for detoxification.
背景/目的:霉菌毒素是丝状真菌合成的次生代谢产物,已被列为危险物质,被证明具有致癌性,以及遗传毒性、肾毒性、肝毒性、致畸性和致突变性。尽管进行了大量试验以开发一种对人类健康有效且安全的解毒方法,但食品和饲料中这些毒素的存在仍然存在高风险。食品保鲜的生物方法是传统化学和物理方法的替代选择,其特点是对人类健康的负面影响较小,以及对丝状真菌和其他食源性病原体具有高效性。真菌修复是一种基于真菌对各种支链淀粉基质进行解毒能力的新生物技术。白腐真菌(WRF)产生的木质素分解酶在降解各种霉菌毒素方面具有高效性。
在我们的研究中,作为WRF的代表,在受黄曲霉毒素B1和玉米赤霉烯酮污染的培养基(蘑菇基质和玉米)上以几种浓度变体进行培养。培养后,收集培养基和子实体,并使用HPLC和LC/MS方法进行分析。
根据培养基中毒素的初始浓度,降解率在53%至87%(黄曲霉毒素B1)和73%至97%(玉米赤霉烯酮)之间波动。生长的子实体中两种毒素的含量均微不足道。
这些发现证实了作为一种有效的生物制剂在降低受污染培养基中霉菌毒素方面的潜力,突出了其在开发可持续和安全解毒方法中的适用性。