Molecular Characterization and Functional Analysis of Outer Membrane Vesicles from the Antarctic Bacterium Pseudomonas syringae Suggest a Possible Response to Environmental Conditions
journal contributionposted on 07.03.2014, 00:00 by Heramb M. Kulkarni, Ch. V. B. Swamy, Medicharla V. Jagannadham
Outer membrane vesicles (OMVs) of Gram-negative bacteria form an important aspect of bacterial physiology as they are involved in various functions essential for their survival. The OMVs of the Antarctic bacterium Pseudomonas syringae Lz4W were isolated, and the proteins and lipids they contain were identified. The matrix-assisted laser desorption/ionization time of flight (MALDI-TOF/TOF) analysis revealed that phosphatidylethanolamines and phosphatidylglycerols are the main lipid components. The proteins of these vesicles were identified by separating them by one-dimensional gel electrophoresis and liquid chromatography coupled to electrospray ionization tandem mass spectrometry (ESI–MS/MS). They are composed of outer membrane and periplasmic proteins according to the subcellular localization predictions by Psortb v.3 and Cello V2.5. The functional annotation and gene ontology of these proteins provided hints for various functions attributed to OMVs and suggested a potential mechanism to respond to the extracellular environmental changes. The OMVs were found to protect the producer organism against the membrane active antibiotics colistin and melittin but not from streptomycin. The 1-N-phenylnapthylamine (NPN)-uptake assay revealed that the OMVs protect the bacterium from membrane active antibiotics by scavenging them and also showed that membrane and protein packing of the OMVs was similar to the parent bacterium. The sequestering depends on the composition and organization of lipids and proteins in the OMVs.
Read the peer-reviewed publication
gene ontologyantibiotics colistinAntarctic Bacterium Pseudomonas syringaeEnvironmental ConditionsOuter membrane vesiclesFunctional AnalysisNPNgel electrophoresisPsortb v .3Molecular Characterizationlipid componentsproducer organismAntarctic bacterium Pseudomonas syringae Lz 4Welectrospray ionization tandem mass spectrometryOMVOuter Membrane VesiclesCello V 2.5.subcellular localization predictionsperiplasmic proteinsparent bacteriumPossible ResponseESI