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Insights into the Underlying Mechanism of Ochratoxin A Production in Aspergillus niger CBS 513.88 Using Different Carbon Sources.

Authors :
Wei S
Hu C
Nie P
Zhai H
Zhang S
Li N
Lv Y
Hu Y
Source :
Toxins [Toxins (Basel)] 2022 Aug 12; Vol. 14 (8). Date of Electronic Publication: 2022 Aug 12.
Publication Year :
2022

Abstract

Aspergillus niger produces carcinogenic ochratoxin A (OTA), a serious food safety and human health concern. Here, the ability of A. niger CBS 513.88 to produce OTA using different carbon sources was investigated and the underlying regulatory mechanism was elucidated. The results indicated that 6% sucrose, glucose, and arabinose could trigger OTA biosynthesis and that 1586 differentially expressed genes (DEGs) overlapped compared to a non-inducing nutritional source, peptone. The genes that participated in OTA and its precursor phenylalanine biosynthesis, including pks , p450 , nrps , hal , and bzip , were up-regulated, while the genes involved in oxidant detoxification, such as cat and pod , were down-regulated. Correspondingly, the activities of catalase and peroxidase were also decreased. Notably, the novel Gal4 -like transcription factor An12g00840 ( AnGal4 ), which is vital in regulating OTA biosynthesis, was identified. Deletion of AnGal4 elevated the OTA yields by 47.65%, 54.60%, and 309.23% using sucrose, glucose, and arabinose as carbon sources, respectively. Additionally, deletion of AnGal4 increased the superoxide anion and H <subscript>2</subscript> O <subscript>2</subscript> contents, as well as the sensitivity to H <subscript>2</subscript> O <subscript>2</subscript> , using the three carbon sources. These results suggest that these three carbon sources repressed AnGal4 , leading to the up-regulation of the OTA biosynthetic genes and alteration of cellular redox homeostasis, ultimately triggering OTA biosynthesis in A. niger .

Details

Language :
English
ISSN :
2072-6651
Volume :
14
Issue :
8
Database :
MEDLINE
Journal :
Toxins
Publication Type :
Academic Journal
Accession number :
36006213
Full Text :
https://doi.org/10.3390/toxins14080551