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Effects of lipid composition on the membrane activity and lipid phase behaviour of Vibrio sp. DSM14379 cells grown at various NaCl concentrations
Authors:Tja&scaron  a Danev?i?,Janez &Scaron  trancar,David Stopar
Affiliation:a University of Ljubljana, Biotechnical Faculty, Biological Centre, Department of Food Technology, Laboratory of Microbiology, Vecna pot 111, 1000 Ljubljana, Slovenia
b Umeå University, Department of Chemistry, Biophysical Chemistry, SE-90187 Umeå, Sweden
c Institute Jozef Stefan, Solid State Department, Laboratory of Biophysics, EPR Centre, Jamova 39, 1000 Ljubljana, Slovenia
Abstract:The membrane lipid composition of living cells generally adjusts to the prevailing environmental and physiological conditions. In this study, membrane activity and lipid composition of the Gram-negative bacterium Vibrio sp. DSM14379, grown aerobically in a peptone-yeast extract medium supplemented with 0.5, 1.76, 3, 5 or 10% (w/v) NaCl, was determined. The ability of the membrane to reduce a spin label was studied by EPR spectroscopy under different salt concentrations in cell suspensions labeled with TEMPON. For lipid composition studies, cells were harvested in a late exponential phase and lipids were extracted with chloroform-methanol-water, 1:2:0.8 (v/v). The lipid polar head group and acyl chain compositions were determined by thin-layer and gas-liquid chromatographies. 31P-NMR spectroscopy was used to study the phase behaviour of the cell lipid extracts with 20 wt.% water contents in a temperature range from −10 to 50 °C. The results indicate that the ability of the membrane to reduce the spin label was highest at optimal salt concentrations. The composition of both polar head groups and acyl chains changed markedly with increasing salinity. The fractions of 16:0, 16:1 and 18:0 acyl chains increased while the fraction of 18:1 acyl chains decreased with increasing salinity. The phosphatidylethanolamine fraction correlated inversely with the lysophosphatidylethanolamine fraction, with phosphatidylethanolamine exhibiting a minimum, and lysophosphatidylethanolamine a maximum, at the optimum growth rate. The fraction of lysophosphatidylethanolamine was surprisingly high in the lipid extracts. This lipid can form normal micellar and hexagonal phases and it was found that all lipid extracts form a mixture of lamellar and normal isotropic liquid crystalline phases. This is an anomalous behaviour since the nonlamellar phases formed by total lipid extracts are generally of the reversed type.
Keywords:PG, phosphatidylglycerol   PE, phosphatidylethanolamine   lyso-PE, lysophosphatidylethanolamine   DPG, diphosphatidylglycerol   TLC, thin-layer chromatography   GLC, gas-liquid chromatography   16:0, hexadecanoic acid   18:0, octadecanoic acid   14:1, cis-9-tetradecenoic acid   16:1, cis-9-hexadecenoic acid   18:1, cis-9-octadecenoic acid
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