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Functional Mechanisms Underlying the Antimicrobial Activity of the Oryza sativa Trx-like Protein

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dc.contributor.authorPark, Seong-Cheol-
dc.contributor.authorKim, Il Ryong-
dc.contributor.authorHwang, Jung Eun-
dc.contributor.authorKim, Jin-Young-
dc.contributor.authorJung, Young Jun-
dc.contributor.authorChoi, Wonkyun-
dc.contributor.authorLee, Yongjae-
dc.contributor.authorJang, Mi-Kyeong-
dc.contributor.authorLee, Jung Ro-
dc.date.accessioned2024-12-02T23:30:55Z-
dc.date.available2024-12-02T23:30:55Z-
dc.date.issued2019-03-
dc.identifier.issn1661-6596-
dc.identifier.issn1422-0067-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/73059-
dc.description.abstractPlants are constantly subjected to a variety of environmental stresses and have evolved regulatory responses to overcome unfavorable conditions that might reduce or adversely change a plant's growth or development. Among these, the regulated production of reactive oxygen species (ROS) as a signaling molecule occurs during plant development and pathogen defense. This study demonstrates the possible antifungal activity of Oryza sativa Tetratricopeptide Domain-containing thioredoxin (OsTDX) protein against various fungal pathogens. The transcription of OsTDX was induced by various environmental stresses known to elicit the generation of ROS in plant cells. OsTDX protein showed potent antifungal activity, with minimum inhibitory concentrations (MICs) against yeast and filamentous fungi ranging between 1.56 and 6.25 and 50 and 100 mu g/mL, respectively. The uptake of SYTOX-Green into fungal cells and efflux of calcein from artificial fungus-like liposomes suggest that its killing mechanism involves membrane permeabilization and damage. In addition, irregular blebs and holes apparent on the surfaces of OsTDX-treated fungal cells indicate the membranolytic action of this protein. Our results suggest that the OsTDX protein represents a potentially useful lead for the development of pathogen-resistant plants.-
dc.language영어-
dc.language.isoENG-
dc.publisherMDPI-
dc.titleFunctional Mechanisms Underlying the Antimicrobial Activity of the Oryza sativa Trx-like Protein-
dc.typeArticle-
dc.publisher.location스위스-
dc.identifier.doi10.3390/ijms20061413-
dc.identifier.scopusid2-s2.0-85063693005-
dc.identifier.wosid000465523400053-
dc.identifier.bibliographicCitationINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, v.20, no.6-
dc.citation.titleINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES-
dc.citation.volume20-
dc.citation.number6-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusSTRESS RESPONSES-
dc.subject.keywordPlusABIOTIC STRESS-
dc.subject.keywordPlusTHIOREDOXIN H-
dc.subject.keywordPlusARABIDOPSIS-
dc.subject.keywordPlusPEPTIDE-
dc.subject.keywordPlusCROSSTALK-
dc.subject.keywordPlusHP(2-20)-
dc.subject.keywordPlusPATHOGEN-
dc.subject.keywordPlusRICE-
dc.subject.keywordPlusPORE-
dc.subject.keywordAuthorantifungal activity-
dc.subject.keywordAuthorplant defense-
dc.subject.keywordAuthorreactive oxygen species-
dc.subject.keywordAuthorthioredoxin-
dc.subject.keywordAuthortetratricopeptide repeat domain-
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