Neoteric approach for peanuts biofilm using the merits of Moringa extracts to control aflatoxin contamination

Aflatoxigenic fungi and aflatoxins are still a principal challenge that threatened peanut production, marketing, and handling. This study aimed to face the problem using bioactive materials, which reduce fungi and mycotoxin contamination, Moringa extracts may be suitable for solving this challenge. Also, the study was compared the extracts of leaves and oil-free seeds. Fresh leaves and seeds were collected, dried, and milled, while oil was collected by cold pressing. The extracts were evaluated for total phenols, flavonoids, and antioxidants, the oil contents of fatty acids, tocopherol, and sterols were determined. An emulsion for protecting peanuts compositing of leaves extract carried by Moringa oil, and commercial emulsifier. Leaves extract evaluation reflected distinct properties of its fibers, total phenols, and flavonoids. It was recorded a microbial inhibition of bacteria and fungi. The values for both minimal inhibition and fungicidal concentrations were recorded at 3.2 mg/mL and 490 mu g/L, respectively. For oil, it showed a unique content, as oleic acid was the main fatty acid, with an affinity between palmitic and behenic in their ratios. Also, oil was recorded by high contents of alpha-tocopherol and Delta 7-Campesterol, with 1.166 mg/kg oil as total sterols content. The leaves extract has also a unique capacity to inhibit toxigenic fungi. By applying the composite emulsion for peanut coating, results expressed a high CFU-count inhibition when it was inoculated by A. flavus strain compared to the control.

Automated summary

This study aimed to address the challenge of aflatoxigenic fungi and aflatoxins in peanut production by using bioactive Moringa extracts. The results showed that Moringa leaf and oil-seed extracts have microbial inhibition properties and unique fatty acid compositions. The application of a composite emulsion for peanut coating with Moringa extract demonstrated significant inhibition of A. flavus strain compared to the control.