Basit öğe kaydını göster

dc.contributor.authorKılıç, Gözde
dc.contributor.authorTosun, Gonca
dc.contributor.authorBozdeveci, Arif
dc.contributor.authorErik, İshak
dc.contributor.authorÖztürk, Elif
dc.contributor.authorReis, Rengin
dc.contributor.authorSipahi, Hande
dc.contributor.authorCora, Merve
dc.contributor.authorKaraoğlu, Şengül Alpay
dc.contributor.authorYaylı, Nurettin
dc.date.accessioned2022-09-06T07:23:57Z
dc.date.available2022-09-06T07:23:57Z
dc.date.issued2021en_US
dc.identifier.citationKilic, G., Tosun, G., Bozdeveci, A., Erik, I., Ozturk, E., Reis, Rengin, Sipahi, H., Cora, M., Karaoglu, S.A. & Yayli, N. (2021). Antimicrobial, Cytotoxic, Antiviral Effects, and Spectroscopic Characterization of Metabolites Produced by Fusarium oxysporum YP9B. Records of Natural Products, 15(6), 547-567. : http://doi.org/10.25135/rnp.208.20.06.1674en_US
dc.identifier.issn1307-6167
dc.identifier.uri: http://doi.org/10.25135/rnp.208.20.06.1674
dc.identifier.urihttps://hdl.handle.net/11436/6396
dc.description.abstractThe goal of the work is to determine the bioactive pharmaceutical metabolites produced by the Fusarium oxysporum YP9B isolate. Ten new natural compounds were isolated from the ethyl acetate extract of the F. oxysporum YP9B strain. Their structures were elucidated by spectroscopic methods using 1D and 2D NMR, UV, FT-IR, and mass spectra (LC-QTOF MS and GC-FID/MS). Identified compounds were named as; (1-benzyl-2-methoxy-2-oxoethyl)-2-hydroxy-3-methylbutanoate (1), 2-oxo-8-azatricyclo[9.3.1.1(3,7)]-hexadeca-1(15),3(16),4,6,11,13-hexaen-10-one (2), 2,3-dihydroxypropanoic, hexadecanoic anhydride (3a), 2,3-dihydroxypropanoic (9Z)-octadecenoic anhydride (3b), 2,3-dihydroxy-propanoic (9Z,12Z)-octadecadienoic anhydride (3c), 2,3-dihydroxypropanoic (11Z)-octadecenoic anhydride (4a), 2,3-dihydroxypropanoic, (9E,12E)-octadecadienoic anhydride (4b), 3-hydroxy-1,2,6,10-tetramethylundecyl hexzadecanoate (5a), 3-hydroxy-1,2,6,10-tetramethylundecyl (9E)-octadecaenoate (5b), and 3-hydroxy-1,2,6,10-tetramethylundecyl octadecanoate (5c). Antimicrobial activities of the isolates obtained from the YP9B strain were determined. Cytotoxic and antiviral activities were tested for the isolates against VERO, MCF-7, PC-3, and A549. Compounds 5a-c, 1, and 3a-c showed bacteriostatic activity at low concentrations, and 4a-b and 2 were found to be bactericides. MIC and MBC values against Mycobacterium smegmatis for the compounds 5a-c and 1 were determined to be <0.5 mu g/mL and 0.46 mu g/mL, respectively. The experimental result showed that compounds 2, 5a-c and 1 have strong cytotoxic (7.51 +/- 1.38 and 19.13 +/- 0.68 (mu M) IC50) activity. The antiviral activity against HSV type-1 was determined to be 1.25 mu M for compounds 4a-c and 0.312 mu M for compound 1.en_US
dc.language.isoengen_US
dc.publisherACG Publicationsen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectFusarium oxysporum YP9Ben_US
dc.subjectSeconder metaboliteen_US
dc.subjectAntimicrobialen_US
dc.subjectCytotoxicen_US
dc.subjectAntiviralen_US
dc.titleAntimicrobial, cytotoxic, antiviral wffects, and apectroscopic characterization of metabolites produced by fusarium oxysporum YP9Ben_US
dc.typearticleen_US
dc.contributor.departmentRTEÜ, Fen - Edebiyat Fakültesi, Biyoloji Bölümüen_US
dc.contributor.institutionauthorBozdeveci, Arif
dc.contributor.institutionauthorKaraoğlu, Şengül Alpay
dc.identifier.doi10.25135/rnp.208.20.06.1674en_US
dc.identifier.volume15en_US
dc.identifier.issue6en_US
dc.identifier.startpage547en_US
dc.identifier.endpage567en_US
dc.relation.journalRecords of Natural Productsen_US
dc.relation.tubitak1002
dc.relation.tubitak117S937
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


Bu öğenin dosyaları:

Thumbnail

Bu öğe aşağıdaki koleksiyon(lar)da görünmektedir.

Basit öğe kaydını göster