Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/173209
Title: Oligopolyphenylenevinylene-conjugated oligoelectrolyte membrane insertion molecules selectively disrupt cell envelopes of gram-positive bacteria
Authors: Hinks, J
Poh, WH
Hann Chu, JJ 
Chye Loo, JS
Bazan, GC
Hancock, LE
Wuertz, S
Keywords: Cell Membrane
Gram-Negative Bacteria
Gram-Positive Bacteria
Microscopy, Electron, Transmission
Polyvinyls
Issue Date: 1-Jan-2015
Publisher: American Society for Microbiology
Citation: Hinks, J, Poh, WH, Hann Chu, JJ, Chye Loo, JS, Bazan, GC, Hancock, LE, Wuertz, S (2015-01-01). Oligopolyphenylenevinylene-conjugated oligoelectrolyte membrane insertion molecules selectively disrupt cell envelopes of gram-positive bacteria. Applied and Environmental Microbiology 81 (6) : 1949-1958. ScholarBank@NUS Repository.
Abstract: © 2015, American Society for Microbiology. The modification of microbial membranes to achieve biotechnological strain improvement with exogenous small molecules, such as oligopolyphenylenevinylene-conjugated oligoelectrolyte (OPV-COE) membrane insertion molecules (MIMs), is an emerging biotechnological field. Little is known about the interactions of OPV-COEs with their target, the bacterial envelope. We studied the toxicity of three previously reported OPV-COEs with a selection of Gram-negative and Gram-positive organisms and demonstrated that Gram-positive bacteria are more sensitive to OPV-COEs than Gram-negative bacteria. Transmission electron microscopy demonstrated that these MIMs disrupt microbial membranes and that this occurred to a much greater degree in Gram-positive organisms. We used a number of mutants to probe the nature of MIM interactions with the microbial envelope but were unable to align the membrane perturbation effects of these compounds to previously reported membrane disruption mechanisms of, for example, cationic antimicrobial peptides. Instead, the data support the notion that OPV-COEs disrupt microbial membranes through a suspected interaction with diphosphatidylglycerol (DPG), a major component of Grampositive membranes. The integrity of model membranes containing elevated amounts of DPG was disrupted to a greater extent by MIMs than those prepared from Escherichia coli total lipid extracts alone.
Source Title: Applied and Environmental Microbiology
URI: https://scholarbank.nus.edu.sg/handle/10635/173209
ISSN: 00992240
10985336
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