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Status |
Public on Oct 09, 2018 |
Title |
Analysis of LOV-FPs-mediated stress response in E. coli. |
Platform organisms |
Gluconobacter oxydans; Escherichia coli; Corynebacterium glutamicum; Bacillus subtilis subsp. subtilis str. 168 |
Sample organism |
Escherichia coli str. K-12 substr. MG1655 |
Experiment type |
Expression profiling by array
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Summary |
Flavin-binding fluorescent proteins (FPs) are genetically encoded in vivo reporters, which are derived from microbial and plant LOV photoreceptors. In this study, we comparatively analyzed the ROS-induced stress responses of the two variants DsFbFP M49I and Pp2FbFP, exhibiting preferential photosensitization of superoxide and singlet oxygen, respectively, in E.coli.
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Overall design |
To analyze differences in global oxidative stress response in E. coli that were induced by Pp2FbFP and DsFbFP M49I, a DNA microarray-based analysis was conducted. E. coli cells expressing the respective photosensitizers were cultivated in LB media. LOV-FP expression was induced by addition of 0.4 mM IPTG during the logarithmic growth phase (~OD580 = 0.7). Three hours after induction, cultures were divided into two test cultures with a volume of 25 ml in 500 ml Erlenmeyer flaks and an OD580 of 0.5. For light treatment one of these cultures was placed between two blue-light emitting LED-panels, whereas the second culture was kept in the dark. Detailed transcriptome analyses of light-induced stress-response based on independent biological triplicates were finally carried out under best illumination conditions (i.e. Pp2FbFP: 5 min, DsFbFP M49I: 15 min).
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Contributor(s) |
Endres S, Polen T, Drepper T |
Citation(s) |
30301917 |
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Submission date |
Feb 05, 2018 |
Last update date |
Oct 17, 2018 |
Contact name |
Tino Polen |
E-mail(s) |
t.polen@fz-juelich.de
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Organization name |
Forschungszentrum Jülich GmbH
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Department |
IBG-1: Biotechnology
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Street address |
Leo Brandt Str.
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City |
Juelich |
State/province |
NRW |
ZIP/Postal code |
52425 |
Country |
Germany |
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Platforms (1) |
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Samples (6)
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Relations |
BioProject |
PRJNA433001 |