Dynamics of Germinosome Formation and FRET-Based Analysis of Interactions between GerD and Germinant Receptor Subunits in Bacillus cereus Spores

Autor: Yan Wang, Lars Bults, Ronald M. P. Breedijk, Stanley Brul, Peter Setlow, Norbert O. E. Vischer, Mark A. Hink

Publikováno v: International Journal of Molecular Sciences, Vol 22, Iss 11230, p 11230 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 20
International Journal of Molecular Sciences, 22(20):11230. Multidisciplinary Digital Publishing Institute (MDPI)

Spores of the bacterium Bacillus cereus can cause disease in humans due to contamination of raw materials for food manufacturing. These dormant, resistant spores can survive for years in the environment, but can germinate and grow when their surround

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95ce46ad0e66a991d935f00caf50131f
https://hdl.handle.net/11245.1/afe42f63-e1a6-4ed5-ba69-db62ce318d7a

A live-cell super-resolution technique demonstrated by imaging germinosomes in wild-type bacterial spores

Autor: Norbert O. E. Vischer, T Bernas, Stanley Brul, Erik M. M. Manders, Peter Setlow, Venkataraman Krishnaswami, Juan Wen, Ronald M. P. Breedijk

Publikováno v: Scientific Reports
Scientific Reports, 10:5312. Nature Publishing Group
Scientific Reports, Vol 10, Iss 1, Pp 1-12 (2020)

Time-lapse fluorescence imaging of live cells at super-resolution remains a challenge, especially when the photon budget is limited. Current super-resolution techniques require either the use of special exogenous probes, high illumination doses or mu

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81f50543ce5180378048f0c0eaf248d2
https://doi.org/10.1038/s41598-020-62377-1

Re-scan confocal microscopy (RCM) improves the resolution of confocal microscopy and increases the sensitivity

Autor: Ron A. Hoebe, Sjoerd Stallinga, Giulia M. R. De Luca, Ronald M. P. Breedijk, Erik M. M. Manders

Publikováno v: METHODS AND APPLICATIONS IN FLUORESCENCE, 5(1). IOP Publishing Ltd.
Methods and applications in fluorescence, 5(1):015002. IOP Publishing Ltd.

Re-scan confocal microscopy (RCM) is a new super-resolution technique based on a standard confocal microscope extended with a re-scan unit in the detection path that projects the emitted light onto a sensitive camera. In this paper the fundamental pr

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98751befd8373e61fdb0564dad4f24a4
https://pure.amc.nl/en/publications/rescan-confocal-microscopy-rcm-improves-the-resolution-of-confocal-microscopy-and-increases-the-sensitivity(460578c6-dde7-4129-8800-d705bb050cf7).html

Re-scan confocal microscopy: Scanning twice for better resolution

Autor: Christiaan H.C. Zeelenberg, Ron A. Hoebe, Wendy Timmermans, Babette E. de Jong, Leila Nahidi Azar, Rick A.J. Brandt, Erik M. M. Manders, Giulia M. R. De Luca, Ronald M. P. Breedijk, Sjoerd Stallinga

Publikováno v: Biomedical Optics Express, 4 (11), 2013
Biomedical optics express, 4(11), 2644-2656. The Optical Society

We present a new super-resolution technique, Re-scan Confocal Microscopy (RCM), based on standard confocal microscopy extended with an optical (re-scanning) unit that projects the image directly on a CCD-camera. This new microscope has improved later

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::761b3f5dc15639f477956ba3bed0b7d6
http://resolver.tudelft.nl/uuid:03f51884-8326-48a6-9437-414b553ea420