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Beate Henrichfreise

Researcher at University of Bonn

Publications -  25
Citations -  655

Beate Henrichfreise is an academic researcher from University of Bonn. The author has contributed to research in topics: Peptidoglycan & Lipid II. The author has an hindex of 12, co-authored 22 publications receiving 559 citations. Previous affiliations of Beate Henrichfreise include University Hospital Bonn.

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Journal ArticleDOI

Resistance Mechanisms of Multiresistant Pseudomonas aeruginosa Strains from Germany and Correlation with Hypermutation

TL;DR: Eleven out of 12 strains and 3 out of 10 strains from CF patients and non-CF patients, respectively, were hypermutable, which should be taken into consideration for the treatment of multiresistant P. aeruginosa.
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Functional conservation of the lipid II biosynthesis pathway in the cell wall-less bacteria Chlamydia and Wolbachia: why is lipid II needed?

TL;DR: The hypothesis that the necessity for maintaining lipid II biosynthesis in cell wall‐lacking bacteria reflects an essential role of the precursor in prokaryotic cell division is discussed and the lipid II pathway may be exploited as an antibacterial target for chlamydial and filarial infections.
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Lipid Requirements for the Enzymatic Activity of MraY Translocases and in Vitro Reconstitution of the Lipid II Synthesis Pathway.

TL;DR: The efficient production of MraY homologues from various human pathogens by synthetic cell-free expression approaches and their subsequent characterization are reported and the inhibition of the in vitro lipid II biosynthesis with the specific inhibitors fosfomycin, feglymycin, and tunicamycin is demonstrated.
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Functional analysis of the cytoskeleton protein MreB from Chlamydophila pneumoniae.

TL;DR: The findings suggest that MreB is involved in tethering biosynthesis of lipid II and as such may be necessary for maintaining a functional divisome machinery in Chlamydiaceae.
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Detection of VIM-2 Metallo-β-Lactamase in Pseudomonas aeruginosa from Germany

TL;DR: The emergence of metallo-β-lactamase (MBL)-producing pathogens is an increasing therapeutic problem; there is no clinically useful inhibitor available.