Three Antifungal Proteins From : Different Patterns of Production and Antifungal Activity.

Front Microbiol

Department of Biotechnology, Instituto de Agroquímica y Tecnología de Alimentos, Consejo Superior de Investigaciones Científicas, Valencia, Spain.

Published: October 2018

Antifungal proteins of fungal origin (AFPs) are small, secreted, cationic, and cysteine-rich proteins. Filamentous fungi encode a wide repertoire of AFPs belonging to different phylogenetic classes, which offer a great potential to develop new antifungals for the control of pathogenic fungi. The fungus is one of the few reported to encode three AFPs each belonging to a different phylogenetic class (A, B, and C). In this work, the production of the putative AFPs from was evaluated, but only the representative of class A, PeAfpA, was identified in culture supernatants of the native fungus. The biotechnological production of PeAfpB and PeAfpC was achieved in with the -based expression cassette, which had been proved to work efficiently for the production of other related AFPs in filamentous fungi. Western blot analyses confirmed that only produces PeAfpA naturally, whereas PeAfpB and PeAfpC could not be detected. From the three AFPs from , PeAfpA showed the highest antifungal activity against all fungi tested, including plant and human pathogens. . was also sensitive to its self-AFPs PeAfpA and PeAfpB. PeAfpB showed moderate antifungal activity against filamentous fungi, whereas no activity could be attributed to PeAfpC at the conditions tested. Importantly, none of the PeAFPs showed hemolytic activity. Finally, PeAfpA was demonstrated to efficiently protect against fungal infections caused by in tomato leaves and in oranges. The strong antifungal potency of PeAfpA, together with the lack of cytotoxicity, and significant protection against phytopathogenic fungi that cause postharvest decay and plant diseases, make PeAfpA a promising alternative compound for application in agriculture, but also in medicine or food preservation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182064PMC
http://dx.doi.org/10.3389/fmicb.2018.02370DOI Listing

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