The Bacteriostatic Activity of 2-Phenylethanol Derivatives Correlates with Membrane Binding Affinity

Membranes 11 (2021)
Author

Kleinwächter, Pannwitt, Centi, Hellmann, Thines, Bereau, Schneider

Published

2021-03-31

Doi



The hydrophobic tails of aliphatic primary alcohols do insert into the hydrophobic core of a lipid bilayer. Thereby, they disrupt hydrophobic interactions between the lipid molecules, resulting in a decreased lipid order, i.e., an increased membrane fluidity. While aromatic alcohols, such as 2-phenylethanol, also insert into lipid bilayers and disturb the membrane organization, the impact of aromatic alcohols on the structure of biological membranes, as well as the potential physiological implication of membrane incorporation has only been studied to a limited extent. Although diverse targets are discussed to be causing the bacteriostatic and bactericidal activity of 2-phenylethanol, it is clear that 2-phenylethanol severely affects the structure of biomembranes, which has been linked to its bacteriostatic activity. Yet, in fungi some 2-phenylethanol derivatives are also produced, some of which appear to also have bacteriostatic activities. We showed that the 2-phenylethanol derivatives phenylacetic acid, phenyllactic acid, and methyl phenylacetate, but not Tyrosol, were fully incorporated into model membranes and affected the membrane organization. Furthermore, we observed that the propensity of the herein-analyzed molecules to partition into biomembranes positively correlated with their respective bacteriostatic activity, which clearly linked the bacteriotoxic activity of the substances to biomembranes.

from Orcid & CrossRef

It is shown that the 2-phenylethanol derivatives phenylacetic acid, phenyllactic acid, and methyl phenylacetate, but not Tyrosol, were fully incorporated into model membranes and affected the membrane organization, and the propensity of the herein-analyzed molecules to partition into biomembranes positively correlated with their respective bacteriostatic activity, which clearly linked the bacteriotoxic activity of the substances to biomemBRanes.

from Semantic Scholar
@article{Kleinw_chter_2021,
    doi = {10.3390/membranes11040254},
    url = {https://doi.org/10.3390%2Fmembranes11040254},
    year = 2021,
    month = {mar},
    publisher = {{MDPI} {AG}},
    volume = {11},
    number = {4},
    pages = {254},
    author = {Isabel S. Kleinwächter and Stefanie Pannwitt and Alessia Centi and Nadja Hellmann and Eckhard Thines and Tristan Bereau and Dirk Schneider},
    title = {The Bacteriostatic Activity of 2-Phenylethanol Derivatives Correlates with Membrane Binding Affinity},
    journal = {Membranes}
}
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