Author

B. Di Ventura

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 Biophysics· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 4 Research Focus:cell signaling & trafficking· 3 Organism:E. coli· 3 Assay:fluorescence / live-cell microscopy· 2 Research Focus:protein folding & dynamics· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

M. A. Oeztuerk· 3 shared N. Palanisamy· 2 shared A. Baumschlager· 1 shared A. G. Iken· 1 shared A. Guenter· 1 shared A. Ruggieri· 1 shared D. Armbruster· 1 shared E. A. Mueller· 1 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 16 mutual co-author links

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3 shared papersMicrobiology

M. A. Oeztuerk

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

Temporal control of the integrated stress response by a stochastic molecular switch

P. Klein, S. M. Kallenberger, H. Roth, K. Roth, T. B. N. Ly-Hartig, V. Magg, J. Ales, S. Rastgou Talemi, Y. Qiang, S. Wolf, O. Oleksiuk, R. Kurilov, B. Di Ventura, R. Bartenschlager, R. Eils, , A. Ruggieri

The paper identifies a stochastic molecular switch controlling the integrated stress response through cooperative activation of PKR, ultrasensitive eIF2 phosphorylation, and negative feedback via GADD34.

bioRxiv · Jan 1, 2022Cell Biology

An inducible AraC that responds to blue light instead of arabinose

E. Romano, A. Baumschlager, E. B. Akmeric, N. Palanisamy, M. Houmani, G. Schmidt, M. A. Oeztuerk, L. Ernst, M. Khammash, B. Di Ventura

This paper introduces BLADE, a blue light-inducible AraC variant in E. coli that enables reversible control of gene expression and morphology, and uses it to study gene function and create bacteriographs.

Nature Chemical Biology · Apr 26, 2021Peer-reviewedMicrobiology

Experimental characterization of in silico red-shift predicted iLOVL470T/Q489K and iLOVV392K/F410V/A426S mutants

P. Wehler, D. Armbruster, A. Guenter, E. Schleicher, B. Di Ventura, M. A. Oeztuerk

The paper experimentally tests two computationally predicted red-shifted iLOV mutants, finding they have reduced brightness, blue shifts, and low expression, limiting their imaging utility.

bioRxiv · Mar 25, 2021Biophysics

The active repertoire of Escherichia coli peptidoglycan amidases varies with physiochemical environment

E. A. Mueller, A. G. Iken, M. A. Oeztuerk, M. Schmitz, B. Di Ventura, P. A. Levin

This study identifies pH-dependent activity of E. coli amidases AmiB and AmiC, mediated by EnvC, NlpD, and YgeR, revealing non-redundant roles in cell separation.

bioRxiv · Oct 19, 2020Microbiology

C-terminal eYFP fusion impairs Escherichia coli MinE function

N. Palanisamy, M. A. Öztürk, B. Di Ventura

This study shows that C-terminal eYFP fusion to MinE impairs its function in Escherichia coli, affecting its ability to displace MinC, stimulate MinD ATPase activity, and bind to the membrane.

Open Biology · May 27, 2020Peer-reviewedMicrobiology