Zearalenone (ZEN) and its derivatives pose a serious threat to global food quality and animal health. The use of enzymes to degrade mycotoxins has become a popular method to counter this threat. In this study, Aspergillus niger ZEN-S-FS10 extracellular enzyme solution with ZEN-degrading effect was separated and purified to prepare the biological enzyme, FSZ, that can degrade ZEN. The degradation rate of FSZ to ZEN was 75–80% (pH = 7.0, 28 °C). FSZ can function in a temperature range of 28–38 °C and pH range of 2.0–7.0 and can also degrade ZEN derivatives (α-ZAL, β-ZOL, and ZAN). According to the enzyme kinetics fitting, ZEN has a high degradation rate. FSZ can degrade ZEN in real samples of corn flour. FSZ can be obtained stably and repeatedly from the original strain. One ZEN degradation product was isolated: FSZ−P(C₁₈H26O₄), with a relative molecular weight of 306.18 g/mol. Amino-acid-sequencing analysis revealed that FSZ is a novel enzyme (homology < 10%). According to the results of molecular docking, ZEN and ZAN can utilize their end-terminal carbonyl groups to bind FSZ residues PHE307, THR55, and GLU129 for a high-degradation rate. However, α-ZAL and β-ZOL instead contain hydroxyl groups that would prevent binding to GLU129; thus, the degradation rate is low for these derivatives.

Ochratoxin A (OTA) is a mycotoxin that can contaminate a wide range of crops such as grains and grapes. In this study, a novel fungal mutant strain (FS-UV-21) with a high OTA degradation rate (74.5%) was obtained from Aspergillus niger irradiated with ultraviolet light (15 W for 20 min). The effect of pH, temperature, and inoculation concentration on the degradation of OTA by FS-UV-21 was investigated, and the results revealed that the detoxification effect was optimal (89.4%) at a pH of 8 and a temperature of 30 °C. Ultra-performance liquid chromatography-tandem mass spectrometry was used to characterize the degraded products of OTA, and the main degraded product was ochratoxin α. Triple quadrupole-linear ion trap-mass spectrometry combined with LightSight software was used to analyze the biotransformation pathway of OTA in FS-UV-21, to trace the degraded products, and to identify the main metabolite, P1 (C₁₉H₁₈ClNO₆, m/z 404). After the FS-UV-21 strain was treated with OTA, the HepG2 cellular toxicity of the degradation products was significantly reduced. For the real sample, FS-UV-21 was used to remove OTA from wheat bran contaminated by mycotoxins through fermentation, resulting in the degradation of 59.8% of OTA in wheat bran. Therefore, FS-UV-21 can be applied to the degradation of OTA in agricultural products and food.

A static magnetic field (SMF)-assisted liquid-state fermentation strategy using Lacticaseibacillus paracasei (L. paracasei) is proposed to improve the comprehensive utilization value of Ginkgo biloba leaves. Taking total flavonoid extraction yield as the objective, Box-Behnken response surface methodology was adopted to optimize the fermentation process. Meanwhile, the nutritional components and hypoglycemic activity of Ginkgo biloba leaves in vitro before and after fermentation were compared and analyzed. The optimal fermentation conditions were determined as follows: 3-fold-diluted De Man, Rogosa, and Sharpe (MRS) medium, an SMF intensity of 4.2 mT, an SMF duration of 2.9 h, and an inoculum size of 6.5%. Under these conditions, the total flavonoid extraction yield reached (3.41 ± 0.11)%, which was 3.33 times that of unfermented raw material. Analysis of the nutritional components revealed that after SMF-assisted fermentation, crude protein and crude fat contents increased by 59.58% and 13.72%, while ash and crude fiber contents decreased by 24.84% and 35.66%, respectively. SMF application also significantly affected the crude fiber content (p < 0.05). Meanwhile, the contents of phytic acid, tannins, phenolic acids, and ginkgolic acids in the SMF-assisted group declined by 29.56%, 43.10%, 23.42%, and 50.37%, respectively, and the SMF further promoted the degradation of anti-nutritional factors. Hypoglycemic activity analysis indicated that fermentation markedly enhanced the inhibitory effect of Ginkgo biloba leaf-derived flavonoids against α-glucosidase and α-amylase, and that SMF stimulation may also contribute to strengthening this inhibitory activity. This study demonstrates that SMF-coupled probiotic fermentation is an effective and environmentally friendly approach for processing Ginkgo biloba leaves, providing experimental support for high-value utilization of plant-based resources through physical-field-assisted microbial fermentation.