Cornelia Große
Martin Luther University of Halle-Wittenberg
19 Papers
15 Citations
Cornelia Große is an academic researcher from Martin Luther University of Halle-Wittenberg. The author has contributed to research in topics: Cupriavidus metallidurans & Biology. The author has an hindex of 10, co-authored 13 publications.
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Papers
CzcD is a heavy metal ion transporter involved in regulation of heavy metal resistance in Ralstonia sp. strain CH34.
TL;DR: CzcD appeared to repress the Czc system by an export of the inducing cations in Ralstonia, and this resistance was based on a reduced accumulation of the cations.
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Effect of Different Metal Ions on the Biological Properties of Cefadroxil
Sayed H. Auda,Ilka Knütter,Beate Bretschneider,Matthias Brandsch,Yahya Mrestani,Cornelia Große,Reinhard H.H. Neubert +6 more
TL;DR: The interaction of cephalosporins with the metal ions could suggest negative effects of some metal ions on the clinical aspects of small intestinal peptide and drug transport.
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The Third Pillar of Metal Homeostasis in Cupriavidus Metallidurans CH34: Preferences Are Controlled by Extracytoplasmic Function Sigma Factors
Cornelia Große,Anja Poehlein,Kathrin Blank,Claudia Schwarzenberger,Grit Schleuder,Martin Herzberg,Dietrich H. Nies +6 more
TL;DR: Data demonstrate on a global and systemic level how a robust network of ECF sigma factors and other regulators allow C. metallidurans to handle a mixture of toxic transition metal cations, which are conditions the bacterium faces in its natural environment.
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Importance of RpoD- and Non-RpoD-Dependent Expression of Horizontally Acquired Genes in Cupriavidus metallidurans
TL;DR: It is shown here that the main housekeeping sigma factor RpoD plays an important role in the expression of horizontally acquired genes in the metal-resistant hydrogen-oxidizing bacterium C. metallidurans.
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Full Copper Resistance in Cupriavidus metallidurans Requires the Interplay of Many Resistance Systems
TL;DR: In this article , the authors investigated the interplay of PIB1-type ATPases, periplasmic copper-and oxygen-dependent copper oxidases, transenvelope efflux systems, and glutathione.
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