The Bacteriostatic Activity of 2-Phenylethanol Derivatives Correlates with Membrane Binding Affinity
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-pheny...
Main Authors: | Isabel S. Kleinwächter, Stefanie Pannwitt, Alessia Centi, Nadja Hellmann, Eckhard Thines, Tristan Bereau, Dirk Schneider |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2021-03-01
|
Series: | Membranes |
Subjects: | |
Online Access: | https://www.mdpi.com/2077-0375/11/4/254 |
Similar Items
-
Metabolic Engineering of Escherichia coli for para-Amino-Phenylethanol and para-Amino-Phenylacetic Acid Biosynthesis
by: Behrouz Mohammadi Nargesi, et al.
Published: (2019-01-01) -
Occurrence, Function, and Biosynthesis of the Natural Auxin Phenylacetic Acid (PAA) in Plants
by: Veronica C. Perez, et al.
Published: (2023-01-01) -
Metabolic engineering of Escherichia coli to high efficient synthesis phenylacetic acid from phenylalanine
by: Lihua Zhang, et al.
Published: (2017-05-01) -
Uremic Toxins and Ciprofloxacin Affect Human Tenocytes In Vitro
by: Erman Popowski, et al.
Published: (2020-06-01) -
The Phenylacetic Acid Catabolic Pathway Regulates Antibiotic and Oxidative Stress Responses in Acinetobacter
by: Anna J. Hooppaw, et al.
Published: (2022-06-01)