iTRAQ proteome analysis of the antifungal mechanism of citral on mycelial growth and OTA production in Aspergillus ochraceus
文献类型： 外文期刊
作者： Wang, Yan 1 ; Lin, Wei 1 ; Yan, Hao 2 ; Neng, Jing 1 ; Zheng, Yong 1 ; Yang, Kai 1 ; Xing, Fuguo 3 ; Sun, Peilong 1 ;
作者机构： 1.Zhejiang Univ Technol, China Natl Light Ind, Key Lab Food Macromol Resources Proc Technol Res, Coll Food Sci & Technol, Hangzhou 310014, Peoples R China
2.Zhejiang Prov Ctr Dis Control & Prevent, Hangzhou 310051, Peoples R China
3.Minist Agr & Rural Affairs, Key Lab Agroprod Qual & Safety Control Storage &, Chinese Acad Agr Sci, Inst Food Sci & Technol, Beijing, Peoples R China
关键词： Aspergillus ochraceus; ochratoxin A; citral; proteomics; oxidative stress; secondary metabolism
期刊名称：JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE （ 影响因子：3.638； 五年影响因子：3.802 ）
ISSN： 0022-5142
年卷期：
页码：
收录情况： SCI
摘要： BACKGROUND Aspergillus ochraceus causes food spoilage and produces mycotoxin ochratoxin A (OTA) during storage of agricultural commodities. In this study, citral was used to inhibit A. ochraceus growth and OTA accumulation, proteomic analysis was employed to verify the mechanism of citral. RESULTS Citral was found to significantly inhibit fungal growth and mycotoxin production in A. ochraceus. Specifically, 75, 125, 150 and 200 mu L L-1 citral suppressed mycelial growth by 33%, 46%, 50% and 100%, respectively. Additionally, 75 mu L L-1 citral inhibited OTA accumulation by 25%. Proteomic analysis was performed to elucidate the inhibitory mechanism of citral on mycelial growth and OTA production at subinhibitory concentrations (75 mu L L-1). Proteomics analysis identified 2646 proteins in A. ochraceus fc-1, of which 218 were differentially expressed between control and 75 mu L L-1 citral treatment samples. Differentially expressed proteins were identified by Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses of biological process, cellular component and molecular function terms. Potential factors affecting mycelial growth and OTA production were analysed, and OTA production was revealed to be a complex process involving many associated factors related to various processes including nutrient intake, sterol biosynthesis, ribosome biogenesis, energy metabolism, oxidative stress and amino acid metabolism. In addition, citral at 75 mu L L-1 down-regulated OTA biosynthetic genes including pks and nrps, but slightly up-regulated the global regulatory factors veA, velB and laeA. CONCLUSION The findings further demonstrate the potential of citral for the preservation of grains and other agricultural products, and provide new insight into its antifungal mechanisms at subinhibitory concentrations. (c) 2021 Society of Chemical Industry
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