“…Five major compounds, including 3-(hydromethyl)-8, 9-dihydro-2H-furo[2, 3-h]chromen-8-ol, 1-hydroxy-2-oxo-5-(2, 4, 6-trihydroxy-2, 3, 3a, 8a-tetrahydrofuro[2, 3-b]benzofuran-5-yl)cyclopentanecarboxylic acid, 2-(2, 4-dihydroxy-2, 3, 3a, 8a-tetrahydrofuro[2, 3-b]benzofuran-5-yl)-5-hydroxycyclopent-1-enecarboxylic acid, 1-hydroxy-2-(4-hydroxy-6-methoxy-2-oxo-2, 3, 3a, 8a-tetrahydrofuro[2, 3-b]benzofuran-5-yl)-5-oxocyclopentanecarboxylic acid, and 1, 2-dihydroxy-5-(4-hydroxy-2-oxo-2, 3, 3a, 8a-tetrahydrofuro[2, 3-b]benzofuran-5-yl)cyclopentanecarboxylic acid, were revolved and identified from the degradation product by using UPLC-Q-TOP-MS, and the addition reaction was mainly responsible for AFB 1 decomposition. All the five degradation products lost their double bonds in the terminal furan ring and hence theoretically had reduced toxicity compared with AFB 1 according to the structure-activity by many microorganisms, enzymes [9], and the extract of some plants [11], and hence, the biological decontamination of AFB 1 appears attractive, but this method may have certain disadvantages in that the organisms would utilize food nutrients for their growth and release undesirable metabolites [12].…”