File:Explosive-cell-lysis-as-a-mechanism-for-the-biogenesis-of-bacterial-membrane-vesicles-and-biofilms-ncomms11220-s12.ogv
From Wikimedia Commons, the free media repository
Jump to navigation
Jump to search
Size of this JPG preview of this OGG file: 800 × 380 pixels. Other resolutions: 320 × 152 pixels | 640 × 304 pixels | 1,010 × 480 pixels.
Original file (Ogg Theora video file, length 4.0 s, 1,010 × 480 pixels, 225 kbps, file size: 110 KB)
File information
Structured data
Captions
Captions
Add a one-line explanation of what this file represents
Summary
[edit]DescriptionExplosive-cell-lysis-as-a-mechanism-for-the-biogenesis-of-bacterial-membrane-vesicles-and-biofilms-ncomms11220-s12.ogv |
English: Supplementary Movie 10 MVs are formed through curling of membrane fragments produced by explosive cell lysis. A P. aeruginosa PAK biofilm cultured on media containing the lipid stain FM1-43FX was imaged using f3D-SIM (DeltaVision OMX Blaze). A single rod cell transitions to a round-shaped cell and explodes (left panel). A magnified view of the boxed area (right panel) shows the release of shattered membrane fragments which curl and vesicularise into MVs. These newly formed MVs then come to rest on the surface of a neighboring cell. Time is shown in bottom right corner in seconds and milliseconds. |
||
Date | |||
Source | Video file from Turnbull L, Toyofuku M, Hynen A, Kurosawa M, Pessi G, Petty N, Osvath S, Cárcamo-Oyarce G, Gloag E, Shimoni R, Omasits U, Ito S, Yap X, Monahan L, Cavaliere R, Ahrens C, Charles I, Nomura N, Eberl L, Whitchurch C (2016). "Explosive cell lysis as a mechanism for the biogenesis of bacterial membrane vesicles and biofilms". Nature Communications. DOI:10.1038/ncomms11220. PMID 27075392. PMC: 4834629. | ||
Author | Turnbull L, Toyofuku M, Hynen A, Kurosawa M, Pessi G, Petty N, Osvath S, Cárcamo-Oyarce G, Gloag E, Shimoni R, Omasits U, Ito S, Yap X, Monahan L, Cavaliere R, Ahrens C, Charles I, Nomura N, Eberl L, Whitchurch C | ||
Permission (Reusing this file) |
![]() ![]() This file is licensed under the Creative Commons Attribution 4.0 International license.
|
||
Provenance InfoField |
|
File history
Click on a date/time to view the file as it appeared at that time.
Date/Time | Thumbnail | Dimensions | User | Comment | |
---|---|---|---|---|---|
current | 08:02, 28 October 2016 | 4.0 s, 1,010 × 480 (110 KB) | Open Access Media Importer Bot (talk | contribs) | Automatically uploaded media file from Open Access source. Please report problems or suggestions here. |
You cannot overwrite this file.
File usage on Commons
There are no pages that use this file.
Transcode status
Update transcode statusMetadata
This file contains additional information such as Exif metadata which may have been added by the digital camera, scanner, or software program used to create or digitize it. If the file has been modified from its original state, some details such as the timestamp may not fully reflect those of the original file. The timestamp is only as accurate as the clock in the camera, and it may be completely wrong.
Short title | Supplementary Movie 10 |
---|---|
Author | Turnbull L, Toyofuku M, Hynen A, Kurosawa M, Pessi G, Petty N, Osvath S, Cárcamo-Oyarce G, Gloag E, Shimoni R, Omasits U, Ito S, Yap X, Monahan L, Cavaliere R, Ahrens C, Charles I, Nomura N, Eberl L, Whitchurch C |
Usage terms | http://creativecommons.org/licenses/by/4.0/ |
Image title | MVs are formed through curling of membrane fragments produced by explosive cell lysis. A P. aeruginosa PAK biofilm cultured on media containing the lipid stain FM1-43FX was imaged using f3D-SIM (DeltaVision OMX Blaze). A single rod cell transitions to a round-shaped cell and explodes (left panel). A magnified view of the boxed area (right panel) shows the release of shattered membrane fragments which curl and vesicularise into MVs. These newly formed MVs then come to rest on the surface of a neighboring cell. Time is shown in bottom right corner in seconds and milliseconds. |
Software used | Xiph.Org libtheora 1.1 20090822 (Thusnelda) |
Date and time of digitizing | 2016-04-14 |