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Bifunctional peptides as alternatives to copper-based formulations to control citrus canker

dc.contributor.authorDilarri, Guilherme
dc.contributor.authorde Lencastre Novaes, Leticia Celia
dc.contributor.authorJakob, Felix
dc.contributor.authorSchwaneberg, Ulrich
dc.contributor.authorFerreira, Henrique [UNESP]
dc.contributor.institutionSanta Catarina State University (UDESC)
dc.contributor.institutionDWI – Leibniz-Institute for Interactive Materials
dc.contributor.institutionRWTH Aachen University
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.date.accessioned2025-04-29T20:16:43Z
dc.date.issued2024-12-01
dc.description.abstractAbstract: Citrus canker is an infectious bacterial disease and one of the major threats to the orange juice industry, a multibillion-dollar market that generates hundreds of thousands of jobs worldwide. This disease is caused by the Gram-negative bacterium Xanthomonas citri subsp. citri. In Brazil, the largest producer and exporter of concentrate orange juice, the control of citrus canker is exerted by integrated management practices, in which cupric solutions are intensively used in the orchards to refrain bacterial spreading. Copper ions accumulate and are as heavy metals toxic to the environment. Therefore, the aim of the present work was to evaluate bifunctional fusion proteins (BiFuProts) as novel and bio-/peptide-based alternatives to copper formulations to control citrus canker. BiFuProts are composed of an anchor peptide able to bind to citrus leaves, and an antimicrobial “killer” peptide to protect against bacterial infections of plants. The selected BiFuProt (Mel-CgDEF) was bactericidal against X. citri at 125 μg mL−1, targeting the bacterial cytoplasmic membrane within the first minutes of contact. The results in the greenhouse assays proved that Mel-CgDEF at 250 μg mL−1 provided protection against X. citri infection on the leaves, significantly reducing the number of lesions by area when compared with the controls. Overall, the present work showed that the BiFuProt Mel-CgDEF is a biobased and biodegradable possible alternative for substitute cupric formulations. Key points: • The bifunctional fusion protein Mel-CgDEF was effective against Xanthomonas citri. • Mel-CgDEF action mechanism was the disruption of the cytoplasmic membrane. • Mel-CgDEF protected citrus leaves against citrus canker disease.en
dc.description.affiliationDepartment of Fisheries Engineering and Biological Sciences Santa Catarina State University (UDESC), Rua Coronel Fernandes Martins 270, Postal code, SC
dc.description.affiliationDWI – Leibniz-Institute for Interactive Materials, Forckenbeckstraße 50, Postal code
dc.description.affiliationInstitute of Biotechnology RWTH Aachen University, Worringerweg 3, Postal code
dc.description.affiliationInstitute of Biosciences Biochemistry Building Department of General and Applied Biology State University of Sao Paulo (UNESP), Avenida 24-A 1515, Postal code, SP
dc.description.affiliationUnespInstitute of Biosciences Biochemistry Building Department of General and Applied Biology State University of Sao Paulo (UNESP), Avenida 24-A 1515, Postal code, SP
dc.description.sponsorshipRWTH Aachen University
dc.identifierhttp://dx.doi.org/10.1007/s00253-023-12908-3
dc.identifier.citationApplied Microbiology and Biotechnology, v. 108, n. 1, 2024.
dc.identifier.doi10.1007/s00253-023-12908-3
dc.identifier.issn1432-0614
dc.identifier.issn0175-7598
dc.identifier.scopus2-s2.0-85184545089
dc.identifier.urihttps://hdl.handle.net/11449/309790
dc.language.isoeng
dc.relation.ispartofApplied Microbiology and Biotechnology
dc.sourceScopus
dc.subjectAnchor peptide
dc.subjectCitriculture defensive
dc.subjectCitrus leaf-binding
dc.subjectMelittin
dc.subjectXanthomonas citri
dc.titleBifunctional peptides as alternatives to copper-based formulations to control citrus cankeren
dc.typeArtigopt
dspace.entity.typePublication
unesp.author.orcid0000-0003-2625-7392[1]
unesp.author.orcid0000-0003-4488-2239[2]
unesp.author.orcid0000-0002-9815-2066[3]
unesp.author.orcid0000-0003-4026-701X[4]
unesp.author.orcid0000-0002-9183-9420[5]

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