Sie befinden Sich nicht im Netzwerk der Universität Paderborn. Der Zugriff auf elektronische Ressourcen ist gegebenenfalls nur via VPN oder Shibboleth (DFN-AAI) möglich. mehr Informationen...
Ergebnis 10 von 102

Details

Autor(en) / Beteiligte
Titel
Detection and Physicochemical Characterization of Membrane Vesicles (MVs) of Lactobacillus reuteri DSM 17938
Ist Teil von
  • Frontiers in microbiology, 2017-06, Vol.8, p.1040-1040
Ort / Verlag
Switzerland: Frontiers Media S.A
Erscheinungsjahr
2017
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • Membrane vesicles (MVs) are bilayer structures which bleb from bacteria, and are important in trafficking biomolecules to other bacteria or host cells. There are few data about MVs produced by the Gram-positive commensal-derived probiotic ; however, MVs from this species may have potential therapeutic benefit. The aim of this study was to detect and characterize MVs produced from biofilm (bMVs), and planktonic (pMVs) phenotypes of DSM 17938. MVs were analyzed for structure and physicochemical characterization by Scanning Electron Microscope (SEM) and Dynamic Light Scattering (DLS). Their composition was interrogated using various digestive enzyme treatments and subsequent Transmission Electron Microscopy (TEM) analysis. eDNA (extracellular DNA) was detected and quantified using PicoGreen. We found that planktonic and biofilm of cultures generated MVs with a broad size distribution. Our data also showed that eDNA was associated with pMVs and bMVs (e DNA). DNase I treatment demonstrated no modifications of MVs, suggesting that an eDNA-MVs complex protected the e DNA. Proteinase K and Phospholipase C treatments modified the structure of MVs, showing that lipids and proteins are important structural components of MVs. The biological composition and the physicochemical characterization of MVs generated by the probiotic may represent a starting point for future applications in the development of vesicles-based therapeutic systems.
Sprache
Englisch
Identifikatoren
ISSN: 1664-302X
eISSN: 1664-302X
DOI: 10.3389/fmicb.2017.01040
Titel-ID: cdi_doaj_primary_oai_doaj_org_article_32be00db8883497abb51174040d4e748

Weiterführende Literatur

Empfehlungen zum selben Thema automatisch vorgeschlagen von bX