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 |
|