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Jensen, G. J.

Publications and source records attributed to Jensen, G. J..

56 records · Page 4Linked to original sources

The ultrastructure of Shewanella oneidensis MR-1 nanowires revealed by electron cryo-tomography

AbstractBacterial nanowires have garnered recent interest as a proposed Extracellular Electron Transfer (EET) pathway that links the bacterial electron transport chain to solid-phase electron acceptors away from the cell. In vivo fluorescence Light Microscopy (fLM) imaging recently showed that Shewanella oneidensis MR-1 nanowires are extensions of the outer membrane that contain EET components. However, their fine structure and distribution of cytochrome electron carriers remained unclear, making it difficult to evaluate the electron transport mechanism along the nanowires. Here, we report high-resolution images of nanowires using Electron Cryo-Tomography (ECT). We developed a robust method for fLM imaging of nanowire growth on electron microscopy grids and used correlative light and electron microscopy to identify and image the same nanowires by ECT. Our results confirm that S. oneidensis nanowires are outer membrane extensions, and further reveal that nanowires are dynamic chains of interconnected Outer Membrane Vesicles (OMVs) with variable dimensions, curvature, and extent of tubulation. Junction densities that potentially stabilize OMV chains are seen between neighboring vesicles in cryotomograms. Our ECT results also provide the first hints of the positions and packing of periplasmic and outer membrane proteins consistent with cytochromes. We observe tight packing of putative cytochromes along lateral patches that extend tens of nanometers, but not across the micrometer scale of whole nanowires. We therefore propose that electron transfer along nanowires involves a combination of direct hopping and diffusive events that link neighboring redox proteins.

microbiology↗

Structure of the Legionella Dot/Icm type IV secretion system in situ by electron cryotomography

Type IV secretion systems (T4SSs) are large macromolecular machines that translocate protein and DNA and are involved in the pathogenesis of multiple human diseases. Here, using electron cryotomography (ECT), we report the in situ structure of the Dot/Icm type IVB secretion system (T4BSS) utilized by the human pathogen Legionella pneumophila. This is the first structure of a type IVB secretion system, and also the first structure of any T4SS in situ. While the Dot/Icm system shares almost no sequence homology with type IVA secretion systems (T4ASSs), its overall structure shows remarkable similarities to two previously imaged T4ASSs, suggesting shared aspects of mechanism. However, compared to one of these, the negative-stain reconstruction of the purified T4ASS from the R388 plasmid, it is approximately twice as long and wide and exhibits several additional large densities, reflecting type-specific elaborations and potentially better structural preservation in situ.

microbiology↗