Author

R. Heermann

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 3

Signature Assays, Organisms & Methods

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Organism:C. elegans· 2 Organism:E. coli· 2 Approach:experimental assay· 2 Approach:biophysical modeling· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:drug response / drug discovery· 1 Research Focus:gene regulatory network inference· 1 Assay:metagenomics· 1

Frequent Co-Authors

J. Frunzke· 2 shared A. Filipchyk· 1 shared B. Graf von Armansperg· 1 shared C. Gätgens· 1 shared F. Koller· 1 shared J. Brehm· 1 shared J. Hennig· 1 shared J. Lassak· 1 shared

Activity by Year

2020-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 15 mutual co-author links

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2 shared papersMicrobiology

J. Frunzke

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Author profile →

3 papers

Recent·Most cited

Identification of Gip as a novel phage-encoded gyrase inhibitor protein featuring a broad activity profile

L. Kever, M. Huennefeld, J. Brehm, R. Heermann, J. Frunzke

This study identifies Gip, a phage-encoded protein that inhibits gyrase across multiple bacterial species, suggesting potential for drug development targeting DNA gyrase.

bioRxiv · Jan 28, 2021Microbiology

Deciphering the rules underlying xenogeneic silencing and counter-silencing of Lsr2-like proteins

J. Wiechert, A. Filipchyk, M. Hünnefeld, C. Gätgens, R. Heermann, J. Frunzke

This study investigates how Lsr2-like proteins silence and counter-silence horizontally acquired genomic regions in actinobacteria, revealing binding preferences and demonstrating synthetic counter-silencing strategies.

mBio · Feb 25, 2020Peer-reviewedMicrobiology

Transcriptional regulation of the Nε-fructoselysine metabolism in Escherichia coli by global and substrate-specific cues

B. Graf von Armansperg, F. Koller, N. Gericke, M. Hellwig, P. K. A. Jagtap, R. Heermann, J. Hennig, T. Henle, J. Lassak

The paper shows that Escherichia coli regulates fructoselysine metabolism through global and substrate-specific transcriptional regulators to efficiently utilize this compound in the gut.

bioRxiv · Jan 13, 2020Microbiology