AFB[sub.1] Microbial Degradation by IBacillus subtilis/I WJ6 and Its Degradation Mechanism Exploration Based on the Comparative Transcriptomics Approach

• Published in: Metabolites Vol. 13; no. 7
• Main Authors: Yang, Peizhou, Wu, Wenjing, Zhang, Danfeng, Cao, Lili, Cheng, Jieshun
• Format: Journal Article
• Language: English
• Published: MDPI AG 01.06.2023
• Subjects: Analysis; Bacillus subtilis; Decomposition (Chemistry); Evaluation; Health aspects; Metabolites; China
• ISSN: 2218-1989; 2218-1989
• DOI: 10.3390/metabo13070785

Aflatoxin pollution poses great harm to human and animal health and causes huge economic losses. The biological detoxification method that utilizes microorganisms and their secreted enzymes to degrade aflatoxin has the advantages of strong specificity, high efficiency, and no pollution inflicted onto the environment. In this study, Bacillus subtilis WJ6 with a high efficiency in aflatoxin B[sub.1] degradation was screened and identified through molecular identification, physiological, and biochemical methods. The fermentation broth, cell-free supernatant, and cell suspension degraded 81.57%, 73.27%, and 8.39% of AFB[sub.1] , respectively. The comparative transcriptomics analysis indicated that AFB[sub.1] led to 60 up-regulated genes and 31 down-regulated genes in B. subtilis WJ6. A gene ontology (GO) analysis showed that the function classifications of cell aggregation, the organizational aspect, and the structural molecule activity were all of large proportions among the up-regulated genes. The down-regulated gene expression was mainly related to the multi-organism process function under the fermentation condition. Therefore, B. subtilis WJ6 degraded AFB[sub.1] through secreted extracellular enzymes with the up-regulated genes of structural molecule activity and down-regulated genes of multi-organism process function.