Paper · 2026 · Journal of Chromatography A

2D-TLC–UV/Vis/FLD–direct bioautography–HRMS/MS-based identification of antibacterial compounds of Myrtus communis L

Ecesu Sezen; Ágnes M. Móricz; Péter G. Ott; et al.

3
claims
6
verbatim quotes
0
citations
2
research areas
✓
Open access · cc-by

Abstract

The search for new antibacterial agents is often hindered by the limited efficiency of traditional isolation-based workflows, which may result in low yields or insufficient detection of bioactive constituents. To address these limitations, an affordable two-dimensional thin-layer chromatography (2D-TLC) combined with direct bioautography was applied for the rapid screening of the hydroalcoholic leaf extract of Myrtus communis. The 2D-TLC-UV/Vis/FLD-Bacillus subtilis assay provided improved separation capacity, including in overloaded conditions, also enabling the visualization of minor antibacterial zones. Bioactivity-guided HRMS/MS analysis performed directly from the inhibition areas allowed the tentative identification of several triterpenoids and fifteen myrtucommulone-type non-prenylated acylphloroglucinol derivatives. Some of these metabolites have not been previously described in the context of antibacterial screening of M. communis. This is the first application of an eight-dimensional workflow integrating 2D-TLC-UV/Vis/FLD-B. subtilis bioassay-HESI-HRMS/MS for the screening and characterization of antibacterials in a complex matrix, exemplified here for M. communis, which provided previously unexplored compounds with potent antibacterial activity.

Abstract from the paper’s OpenAlex record; open copy licensed cc-by. Read at the source ↗

The text the model read, with the source record’s inline markup (italics, sub- and superscripts) rendered and its character entities decoded; quote offsets refer to the raw text.

Claims 3

Method / resourceobservedoriginal resultmeasured

Claim · model-written summary

The 2D-TLC bioautography workflow tentatively identified fifteen myrtucommulone-type acylphloroglucinol derivatives in Myrtus communis leaf extract.

Taxon
Myrtus communisMyrtus communise0
Outcome
tentative identificatione1
Value
fifteene1
Qualifier
myrtucommulone-type non-prenylated acylphloroglucinol derivativese1

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Myrtus communis
Myrtus communis · TaxonGeorge E. Koronaios · CC BY-SA 2.0 · Wikimedia Commons ↗

Verbatim

e0

“hydroalcoholic leaf extract of Myrtus communis”

✓ located verbatim in the source · abstract, characters 383–429 · show in text ↑
e1

“tentative identification of several triterpenoids and fifteen myrtucommulone-type non-prenylated acylphloroglucinol derivatives”

✓ located verbatim in the source · abstract, characters 707–834 · show in text ↑
Observationobservedoriginal resultmeasured

Claim · model-written summary

The workflow tentatively identified several triterpenoids in Myrtus communis leaf extract.

Taxon
Myrtus communisMyrtus communise0
Outcome
tentative identificatione1
Qualifier
several triterpenoidse1

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Myrtus communis
Myrtus communis · TaxonGeorge E. Koronaios · CC BY-SA 2.0 · Wikimedia Commons ↗

Verbatim

e0

“hydroalcoholic leaf extract of Myrtus communis”

✓ located verbatim in the source · abstract, characters 383–429 · show in text ↑
e1

“tentative identification of several triterpenoids and fifteen myrtucommulone-type non-prenylated acylphloroglucinol derivatives”

✓ located verbatim in the source · abstract, characters 707–834 · show in text ↑
Observationobservedoriginal resultpositivemeasured

Claim · model-written summary

Identified compounds showed potent antibacterial activity.

Taxon
Myrtus communisMyrtus communise0
Outcome
antibacterial activitye3
Qualifier
potente3

Organisms pictured · Representative pictures of the matched species, not figures from the paper.

Myrtus communis
Myrtus communis · TaxonGeorge E. Koronaios · CC BY-SA 2.0 · Wikimedia Commons ↗

Verbatim

e0

“hydroalcoholic leaf extract of Myrtus communis”

✓ located verbatim in the source · abstract, characters 383–429 · show in text ↑
e3

“previously unexplored compounds with potent antibacterial activity”

✓ located verbatim in the source · abstract, characters 1209–1275 · show in text ↑