Deletion of fbiC in Streptomyces venezuelae removes autofluorescence in the excitation-emission range of cyan fluorescent protein
(2025) In Microbiology (Reading, England) 171(4).- Abstract
Autofluorescence poses an impediment to fluorescence microscopy of biological samples. In the Gram-positive, soil-dwelling bacteria of the genus Streptomyces, sources of autofluorescence have not been examined systematically to date. Here, we show that the model organism for the genus, Streptomyces venezuelae, shows autofluorescence in two of the commonly used fluorescence channels for visualizing cyan and green/yellow fluorescent proteins. We identify the source of autofluorescence in the cyan fluorescence channel as redox cofactor factor 420 (F420) and target its synthesis to remove it. By deleting the vnz15170 (fbiC) gene, which is a key biosynthetic gene for the production of F420, we were able to create an autofluorescence-free... (More)
Autofluorescence poses an impediment to fluorescence microscopy of biological samples. In the Gram-positive, soil-dwelling bacteria of the genus Streptomyces, sources of autofluorescence have not been examined systematically to date. Here, we show that the model organism for the genus, Streptomyces venezuelae, shows autofluorescence in two of the commonly used fluorescence channels for visualizing cyan and green/yellow fluorescent proteins. We identify the source of autofluorescence in the cyan fluorescence channel as redox cofactor factor 420 (F420) and target its synthesis to remove it. By deleting the vnz15170 (fbiC) gene, which is a key biosynthetic gene for the production of F420, we were able to create an autofluorescence-free strain in the cyan range of fluorescence excitation-emission. We demonstrate the usefulness of this strain by imaging the mTurquoise-tagged polar growth-related protein DivIVA and the cell division-related protein FtsZ in the fbiC deletion background. Using live-cell imaging to follow the dynamics of DivIVA and FtsZ, we demonstrate an improved signal-to-noise ratio in the mutant strain. We show that this strain can be a suitable tool for visualizing the localization of proteins in Streptomyces spp. and can facilitate the utilization of multi-colour imaging and fluorescence resonance energy transfer-based imaging.
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- author
- Mavi, Parminder Singh LU and Flärdh, Klas LU
- organization
- publishing date
- 2025-04
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- Streptomyces/genetics, Bacterial Proteins/genetics, Green Fluorescent Proteins/genetics, Gene Deletion, Microscopy, Fluorescence/methods, Fluorescence
- in
- Microbiology (Reading, England)
- volume
- 171
- issue
- 4
- publisher
- MAIK Nauka/Interperiodica
- external identifiers
-
- scopus:105003615854
- pmid:40232129
- ISSN
- 1465-2080
- DOI
- 10.1099/mic.0.001552
- language
- English
- LU publication?
- yes
- id
- 60faed2b-4aeb-49d1-9900-73e8aea6da1c
- date added to LUP
- 2025-04-23 10:52:52
- date last changed
- 2025-07-09 09:58:38
@article{60faed2b-4aeb-49d1-9900-73e8aea6da1c,
abstract = {{<p>Autofluorescence poses an impediment to fluorescence microscopy of biological samples. In the Gram-positive, soil-dwelling bacteria of the genus Streptomyces, sources of autofluorescence have not been examined systematically to date. Here, we show that the model organism for the genus, Streptomyces venezuelae, shows autofluorescence in two of the commonly used fluorescence channels for visualizing cyan and green/yellow fluorescent proteins. We identify the source of autofluorescence in the cyan fluorescence channel as redox cofactor factor 420 (F420) and target its synthesis to remove it. By deleting the vnz15170 (fbiC) gene, which is a key biosynthetic gene for the production of F420, we were able to create an autofluorescence-free strain in the cyan range of fluorescence excitation-emission. We demonstrate the usefulness of this strain by imaging the mTurquoise-tagged polar growth-related protein DivIVA and the cell division-related protein FtsZ in the fbiC deletion background. Using live-cell imaging to follow the dynamics of DivIVA and FtsZ, we demonstrate an improved signal-to-noise ratio in the mutant strain. We show that this strain can be a suitable tool for visualizing the localization of proteins in Streptomyces spp. and can facilitate the utilization of multi-colour imaging and fluorescence resonance energy transfer-based imaging.</p>}},
author = {{Mavi, Parminder Singh and Flärdh, Klas}},
issn = {{1465-2080}},
keywords = {{Streptomyces/genetics; Bacterial Proteins/genetics; Green Fluorescent Proteins/genetics; Gene Deletion; Microscopy, Fluorescence/methods; Fluorescence}},
language = {{eng}},
number = {{4}},
publisher = {{MAIK Nauka/Interperiodica}},
series = {{Microbiology (Reading, England)}},
title = {{Deletion of fbiC in Streptomyces venezuelae removes autofluorescence in the excitation-emission range of cyan fluorescent protein}},
url = {{http://dx.doi.org/10.1099/mic.0.001552}},
doi = {{10.1099/mic.0.001552}},
volume = {{171}},
year = {{2025}},
}