Related Experiment Video
Updated: May 12, 2026

Quantification of Fungal Colonization, Sporogenesis, and Production of Mycotoxins Using Kernel Bioassays
Published on: April 23, 2012
Improved methodology for detecting aflatoxin production quantitatively in natural media
M A Moreno1, A Olivares, G Suárez
1UD Microbiología e Inmunología, Departamento Patología Animal I (Sanidad Animal), Facultad de Veterinaria, Universidad Complutense de Madrid, 28040, Madrid, Spain.
A new, simple method quickly screens for aflatoxin production by Aspergillus flavus moulds. This rapid screening technique uses natural media and thin-layer chromatography for early detection within three days.
Area of Science:
- Food safety and mycology
- Microbiology and analytical chemistry
Background:
- Aflatoxins are toxic secondary metabolites produced by certain moulds, notably within the Aspergillus flavus group.
- Accurate and rapid screening methods are crucial for controlling aflatoxin contamination in food and agricultural products.
- Existing methods can be time-consuming or require specialized equipment, limiting their widespread application.
Purpose of the Study:
- To develop and validate a simple, rapid, and quantitative method for screening aflatoxin production.
- To assess the efficacy of the proposed method for early detection of aflatoxin-producing moulds.
Main Methods:
- Utilized a natural medium (moist wheat or rice) for mould cultivation.
- Employed a single chloroform extraction step to isolate aflatoxins.
- Detected and quantified aflatoxins using thin-layer chromatography (TLC).
Main Results:
- The method demonstrated simplicity, rapidity, and quantitative capability.
- Aflatoxin production was detected by the third day of incubation in over 85% of tested strains.
- The method proved effective for both laboratory culture collection strains and field isolates.
Conclusions:
- The proposed method offers a practical and efficient approach for screening aflatoxin production by Aspergillus flavus group moulds.
- Early detection within three days facilitates timely intervention to prevent contamination.
- This technique is suitable for routine screening in various settings due to its simplicity and speed.
More Related Videos
10:24Non-destructive SPE-UPLC-based Quantification of Aflatoxins and Stilbenoid Phytoalexins in Single Peanut (Arachis spp.) Seeds
Published on: April 19, 2024
09:21Inhibition of Aspergillus flavus Growth and Aflatoxin Production in Transgenic Maize Expressing the α-amylase Inhibitor from Lablab purpureus L.
Published on: February 15, 2019