Related Experiment Video
Updated: Jul 11, 2026

Inhibition of Aspergillus flavus Growth and Aflatoxin Production in Transgenic Maize Expressing the α-amylase Inhibitor from Lablab purpureus L.
Published on: February 15, 2019
Aflatoxin formation and gene expression in response to carbon source media shift in Aspergillus parasiticus
J R Wilkinson1, J Yu, H K Abbas
1Department of Biochemistry and Molecular Biology, Mississippi State, MS 39762, USA. jwilkinson@bch.msstate.edu
Abstract:
Aflatoxins are toxic and carcinogenic polyketide metabolites produced by fungal species, including Aspergillus flavus and A. parasiticus. The biosynthesis of aflatoxins is modulated by many environmental factors, including the availability of a carbon source. The gene expression profile of A. parasiticus was evaluated during a shift from a medium with low concentration of simple sugars, yeast extract (YE), to a similar medium with sucrose, yeast extract sucrose (YES). Gene expression and aflatoxins (B1, B2, G1, and G2) were quantified from fungal mycelia harvested pre- and post-shifting. When compared with YE media, YES caused temporary reduction of the aflatoxin levels detected at 3-h post-shifting and they remained low well past 12 h post-shift. Aflatoxin levels did not exceed the levels in YE until 24 h post-shift, at which time point a tenfold increase was observed over YE. Microarray analysis comparing the RNA samples from the 48-h YE culture to the YES samples identified a total of 2120 genes that were expressed across all experiments, including most of the aflatoxin biosynthesis genes. One-way analysis of variance (ANOVA) identified 56 genes that were expressed with significant variation across all time points. Three genes responsible for converting norsolorinic acid to averantin were identified among these significantly expressed genes. The potential involvement of these genes in the regulation of aflatoxin biosynthesis is discussed.
Insights
Environmental factors like carbon sources impact aflatoxin production by Aspergillus parasiticus. Shifting to sucrose-rich media temporarily reduced aflatoxin levels, revealing key genes involved in biosynthesis regulation.
Area of Science:
- Mycology
- Biochemistry
- Molecular Biology
Background:
- Aflatoxins are toxic, carcinogenic metabolites from fungi like Aspergillus parasiticus.
- Environmental factors, particularly carbon sources, influence aflatoxin biosynthesis.
- Understanding gene regulation is crucial for controlling aflatoxin production.
Purpose of the Study:
- To investigate the effect of a carbon source shift on aflatoxin production in A. parasiticus.
- To analyze gene expression profiles in response to changing media conditions.
- To identify genes involved in the regulation of aflatoxin biosynthesis.
Main Methods:
- Culturing A. parasiticus in yeast extract (YE) and yeast extract sucrose (YES) media.
- Quantifying aflatoxin levels (B1, B2, G1, G2) at various time points post-shift.
- Employing microarray analysis to compare gene expression between YE and YES cultures.
- Utilizing ANOVA to identify significantly varied gene expression.
Main Results:
- YES medium caused a temporary reduction in aflatoxin levels compared to YE medium.
- A tenfold increase in aflatoxin levels was observed 24 hours after shifting to YES medium.
- Microarray analysis revealed 2120 consistently expressed genes, including aflatoxin biosynthesis genes.
- 56 genes showed significant expression variation, including three involved in norsolorinic acid to averantin conversion.
Conclusions:
- Carbon source availability significantly modulates aflatoxin biosynthesis in A. parasiticus.
- Specific genes identified in this study may play regulatory roles in aflatoxin production.
- Further research into these genes could offer strategies for aflatoxin mitigation.
Related Concept Videos
Fungal Phylum Ascomycota
Gene Regulation During Sporulation
Stringent Response in E. coli
