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dc.contributor.author Baglyas, Márton
dc.contributor.author Ott, Péter G.
dc.contributor.author Bozsó, Zoltán
dc.contributor.author Schwarczinger, Ildikó
dc.contributor.author Bakonyi, József
dc.contributor.author Dlauchy, Dénes
dc.contributor.author Darcsi, András
dc.contributor.author Varga, Szilárd
dc.contributor.author Móricz, Ágnes M.
dc.date.accessioned 2025-08-12T12:33:52Z
dc.date.available 2025-08-12T12:33:52Z
dc.date.issued 2025
dc.identifier.citation journalVolume=14;journalIssueNumber=14;journalTitle=PLANTS-BASEL;pagination=2152, pages: 19;journalAbbreviatedTitle=PLANTS-BASEL;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/10148
dc.identifier.uri doi:https://doi.org/10.3390/plants14142152
dc.description.abstract A previously undescribed cis-clerodane diterpenoid, diangelate solidagoic acid J (1), along with two known cis-clerodane diterpenoids, solidagoic acid C (2) and solidagoic acid D (3), as well as two known unsaturated monoacylglycerols, 1-linoleoyl glycerol (4) and 1-α-linolenoyl glycerol (5), were isolated and characterized from the n-hexane leaf extract of Solidago gigantea (giant goldenrod). Compounds 2–5 were identified first in this species, and compounds 4 and 5 are reported here for the first time in the Solidago genus. The bioassay-guided isolation procedure included thin-layer chromatography (TLC) coupled with a Bacillus subtilis antibacterial assay, preparative flash column chromatography, and TLC–mass spectrometry (MS). Their structures were elucidated via extensive spectroscopic and spectrometric techniques such as one- and two-dimensional nuclear magnetic resonance (NMR) spectroscopy and high-resolution tandem mass spectrometry (HRMS/MS). The antimicrobial activities of the isolated compounds were evaluated by a microdilution assay. All compounds exhibited weak to moderate antibacterial activity against the Gram-positive plant pathogen Clavibacter michiganensis, with MIC values ranging from 17 to 133 µg/mL, with compound 5 being the most potent. Only compound 1 was active against Curtobacterium flaccumfaciens pv. flaccumfaciens, while compound 3 demonstrated a weak antibacterial effect against B. subtilis and Rhodococcus fascians. Additionally, the growth of B. subtilis and R. fascians was moderately inhibited by compounds 1 and 5, respectively. None of the tested compounds showed antibacterial activity against Gram-negative Pseudomonas syringae pv. tomato and Xanthomonas arboricola pv. pruni. No bactericidal activity was observed against the tested microorganisms. Compounds 2 and 3 displayed weak antifungal activity against the crop pathogens Bipolaris sorokiniana and Fusarium graminearum. Our results demonstrate the efficacy of bioassay-guided strategies in facilitating the discovery of novel bioactive compounds.
dc.format.extent 2152-2152
dc.relation.ispartof urn:issn:2223-7747
dc.title Bioassay-Guided Isolation of cis-Clerodane Diterpenoids and Monoglycerides from the Leaves of Solidago gigantea and Their Antimicrobial Activities
dc.type Journal Article
dc.date.updated 2025-07-14T21:34:54Z
dc.language.rfc3066 en
dc.rights.holder NULL
dc.identifier.mtmt 36244467
dc.contributor.institution Doktori Iskola
dc.contributor.institution Növénykórtani Osztály
dc.contributor.institution TTK hallgatók
dc.contributor.institution Növényi Kórélettani Osztály
dc.contributor.institution Hevesy György Kémia Doktori Iskola
dc.contributor.institution Növényvédelmi Intézet


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