Naslov
New antimicrobial candidates – quaternary ammonium compounds based on natural scaffold quinuclidine

Autori
Mastelić, Linda ; Maravić, Ana ; Krce, Lucija ; Soldo, Barbara ; Odžak, Renata ; Bučević Popović, Viljemka ; Aviani, Ivica ; Primožič, Ines ; Šprung, Matilda

Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni

Izvornik
FEBS Open Bio, Volume 11, Issue S1. / - , 2021, 101-102

Skup
45th FEBS Congress: Molecules of Life: Towards New Horizons (FEBS 2021)

Mjesto i datum
Ljubljana, Slovenija, 03.07.2021. - 08.07.2021

Vrsta sudjelovanja
Predavanje

Vrsta recenzije
Međunarodna recenzija

Ključne riječi
quaternary ammonium compounds ; quinuclidine

Sažetak
Quaternary Ammonium Compounds (QACs) are amphiphilic molecules of antimicrobial properties with applications in numerous industries. Recent studies show that environmental bacteria acquire resistance to QACs at an alarming pace, and that this resistance is mostly but not exclusively related to Qac efflux pump expression. Motivated by these findings, our research group has been mainly focused in developing new potent QACs derived from natural precursor(s). One such precursor that caught our attention is quinuclidine, a bicyclic part of alkaloids isolated from the bark of the Cinchona tree. In our two recent studies we have shown that quaternization of quinuclidine improves its bioactivity by several hundred folds (Previously published in: Odžak R et al. (2017), Open Chem. 15, 320­331 and Bazina L et al. (2019) Eur. J. Med. Chem. 163, 626­635). The most active identified candidate was QOH­C14. This compound, with the longest alkyl chain, exhibited the lowest MIC values across a selected panel of the bacteria, had good activity toward Staphylococcus aureus biofilms and had the lowest toxicity toward healthy human cell lines. Moreover, atomic force microscopy and flow cytometry indicated that QOH­ C14 acts by disrupting the cell membrane provoking membrane disintegration and cell death. In addition, physicochemical characterization showed that derivatives with longer alkyl chains spontaneously form micelle and that their stability is also related to the number of carbon atoms in the chain (Previously published in: Bošković P et al. (2019) J. Surfact. Deterg. 23, 207­214). From these studies two main conclusions could be drown. First, quaternization of natural precursors could be a promising strategy in new QACs development. Second, alkyl chains are an important part of the structure whereby antimicrobial activity directly correlates with the number of carbon atoms in the chain.

Izvorni jezik
Engleski

Znanstvena područja
Kemija

POVEZANOST RADA