Abstract
Lipid As are the main components of the external leaflet of the outer membrane of Gram-negative bacteria. Their molecular structure has evolved to allow the bacteria survival in specific environments. In the present work, we investigate how and to what extent lipid membranes that include in their composition lipid A molecules of a bacterium of the gut microbiota, Stenotrophomonas maltophilia, differ from those formed by the lipid A of the common Gram-negative bacterium Salmonella enterica, which is not specific to the gut and is here used as a reference. Electron Paramagnetic Resonance (EPR) spectroscopy, using spin-labelled lipids as molecular probes, allows the segmental order of the acyl chain and the polarity across the bilayer to be analyzed in detail. Both considered lipid As cause a stiffening of the outermost segments of the acyl chains. This effect increases with increasing the lipid A content and is stronger for the lipid A extracted from Stenotrophomonas maltophilia than for that extracted from Salmonella enterica. At the same time, the local polarity of the bilayer region just below the interface increases. As the inner core of the bilayer is considered, it is found that the lipid A from Salmonella enterica causes a local disorder and a significant reduction of the local polarity, an effect not found for the lipid A from Stenotrophomonas maltophilia. These results are interpreted in terms of the different lengths and distributions of the acyl tails in the two lipid As. It can be concluded that the symmetrically distributed short tails of the lipid A from Stenotrophomonas maltophilia favors a regular packing within the bilayer.
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