4.7 Article

Antifungal properties of recombinant Puroindoline B protein against aflatoxigenic Aspergillus flavus

期刊

LWT-FOOD SCIENCE AND TECHNOLOGY
卷 144, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.lwt.2021.111130

关键词

Puroindoline B; Aspergillus flavus; Aflatoxin B1; Maize

资金

  1. National Science Foundation of China [31871852, 31972176]
  2. Innovation Funds Plan of Henan University of Technology [2020ZKCJ01]
  3. National Thirteenth Five-Year Plan Key RD Plan: Integration and Demonstration of Grain and Oil Quality and Safety Process Guarantee and Traceability Technology-Optimization of Intelligent Detection and Early Warning System for Mildew of Grain and Oil Ra [2019YFC1605303-04]

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The study demonstrated that rPINB has antifungal properties against A. flavus spores, inhibiting toxin production on maize. It showed dose-dependent inhibition of spore germination and growth in vitro, altering spore morphology and damaging the cell wall and membrane. The observed direct antifungal activity of rPINB suggests its potential use in preventing fungal contamination of stored foods and agricultural products in the future.
Aspergillus flavus contamination is of great concern to food safety. Our previous studies demonstrated that recombinant Puroindoline B protein (rPINB) has an inhibitory effect on A. flavus mycelium development. However, fungal contamination often begins with spore germination within food shelf life. Here, rPINB was evaluated for its antifungal properties against A. flavus spores in vivo and in vitro. The results showed that rPINB could inhibit spore formation and aflatoxin B1 of A. flavus on maize. In vitro analysis revealed its dose-dependent antifungal effect on spore germination and germ tube growth of A. flavus. Scanning electron microscopy revealed that rPINB exposure altered spore morphology, indicating it damaged the cell wall. Transmission electron microscopy and the inhibition of ergosterol synthesis further revealed that rPINB exposure significantly damaged the cell membrane. The mitochondrial membrane potential decreased, and DNA fragments were scattered in the cytoplasm as detected using 5,5',6,6'-tetrachloro-1,1',3,3'-tetraethylbenzimidazolocarbocyanine iodide and 4',6-diamidino-2-phenylindole staining. The direct antifungal activity of rPINB observed both in vivo and in vitro suggests that rPINB may be used to prevent fungal contamination of stored foods and agricultural products in the future.

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