{ "labelLang" : "eng", "responseDate" : "2024-03-28 23:15", "content" : { "otype" : "JournalArticle", "mtid" : 31259936, "status" : "VALIDATED", "published" : true, "comment" : "Institute of Plant Biology, Biological Research Centre, Temesvári krt. 62, Szeged, H-6726, Hungary \n Institute of Biochemistry, Biological Research Centre, Temesvári krt. 62, Szeged, H-6726, Hungary \n Department of Plant Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary \n Department of Medical Chemistry, Faculty of Medicine, University of Szeged, Dóm tér 8, Szeged, H-6720, Hungary \n Institute of Molecular Biology, Biocenter, Medical University of Innsbruck, Innrain 80-82, Innsbruck, A-6020, Austria \n MTA-SZTE Biomimetic Systems Research Group, University of Szeged, Dóm tér 8, Szeged, H-6720, Hungary \n Department of Biotechnology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary \n Institute of Biophysics, Biological Research Centre, Temesvári krt. 62, Szeged, H-6726, Hungary \n Cited By :1 \n Export Date: 19 October 2020 \n Correspondence Address: Galgóczy, L.; Institute of Plant Biology, Biological Research Centre, Institute of Molecular Biology, Biocenter, Medical University of Innsbruck, Department of Biotechnology, Faculty of Science and Informatics, University of Szeged, Temesvári krt. 62, Hungary; email: galgoczi@bio.u-szeged.hu\nInstitute of Plant Biology, Biological Research Centre, Temesvári krt. 62, Szeged, H-6726, Hungary \n Institute of Biochemistry, Biological Research Centre, Temesvári krt. 62, Szeged, H-6726, Hungary \n Department of Plant Biology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary \n Department of Medical Chemistry, Faculty of Medicine, University of Szeged, Dóm tér 8, Szeged, H-6720, Hungary \n Institute of Molecular Biology, Biocenter, Medical University of Innsbruck, Innrain 80-82, Innsbruck, A-6020, Austria \n MTA-SZTE Biomimetic Systems Research Group, University of Szeged, Dóm tér 8, Szeged, H-6720, Hungary \n Department of Biotechnology, Faculty of Science and Informatics, University of Szeged, Közép fasor 52, Szeged, H-6726, Hungary \n Institute of Biophysics, Biological Research Centre, Temesvári krt. 62, Szeged, H-6726, Hungary \n Cited By :4 \n Export Date: 25 August 2021 \n Correspondence Address: Galgóczy, L.; Institute of Plant Biology, Temesvári krt. 62, Hungary; email: galgoczi@bio.u-szeged.hu \n Correspondence Address: Marx, F.; Institute of Molecular Biology, Innrain 80-82, Austria; email: florentine.marx@i-med.ac.at \n Correspondence Address: Galgóczy, L.; Department of Biotechnology, Közép fasor 52, Hungary; email: galgoczi@bio.u-szeged.hu \n Chemicals/CAS: Antifungal Agents; Fungal Proteins; Peptides\nFunding Agency and Grant Number: Hungarian National Research, Development and Innovation Office (NKFI Office) [PD 131340, ANN 131341]; Austrian Science Fund FWFAustrian Science Fund (FWF) [I3132-B21]; Janos Bolyai Research Scholarship of the Hungarian Academy of SciencesHungarian Academy of Sciences; Aktion Osterreich-Ungarn (AOU); New National Excellence Program of the Ministry for Innovation and Technology [UNKP-19-4]; NTP-NFTO-18 Scholarship; [TUDFO/47138-1/2019-ITM FIKP]; [GINOP-2.3.2-15-2016-00014]; [20391-3/2018/FEKUSTRAT]\n Funding text: LG is financed from the Postdoctoral Excellence Programme (PD 131340) and the bilateral Austrian-Hungarian Joint Research Project (ANN 131341) of the Hungarian National Research, Development and Innovation Office (NKFI Office). This work was supported by the Austrian Science Fund FWF (I3132-B21) to FM. Research of LG and PP has been supported by the Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences. JH was financed by the exchange fellowship of the Aktion Osterreich-Ungarn (AOU). Present work of LG and PP was supported by the UNKP-19-4 New National Excellence Program of the Ministry for Innovation and Technology. This work was supported from the following grants TUDFO/47138-1/2019-ITM FIKP, GINOP-2.3.2-15-2016-00014, 20391-3/2018/FEKUSTRAT to ZK, GV and GKT. 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Application of alternative fungicides, such as antifungal proteins and peptides, provides a promising basis to overcome this problem; however, their direct use in fields suffers limitations, such as high cost of production, low stability, narrow antifungal spectrum and toxicity on plant or mammalian cells. Recently, we demonstrated that a Penicillium chrysogenum-based expression system provides a feasible tool for economic production of P. chrysogenum antifungal protein (PAF) and a rational designed variant (PAFopt ), in which the evolutionary conserved γ-core motif was modified to increase antifungal activity. In the present study, we report for the first time that γ-core modulation influences the antifungal spectrum and efficacy of PAF against important plant pathogenic ascomycetes, and the synthetic γ-core peptide Pγopt , a derivative of PAFopt , is antifungal active against these pathogens in vitro. Finally, we proved the protective potential of PAF against Botrytis cinerea infection in tomato plant leaves. 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