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Katrin Dohnt

Researcher at Braunschweig University of Technology

Publications -  13
Citations -  580

Katrin Dohnt is an academic researcher from Braunschweig University of Technology. The author has contributed to research in topics: Geobacter sulfurreducens & Bioelectrochemistry. The author has an hindex of 7, co-authored 11 publications receiving 476 citations.

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Industrial biotechnology of Pseudomonas putida and related species

TL;DR: Pseudomonas putida and related subspecies, traditionally known as well-performing xenobiotic degraders, are becoming efficient cell factories for various products of industrial relevance including a full range of unnatural chemicals.
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Robustness and Plasticity of Metabolic Pathway Flux among Uropathogenic Isolates of Pseudomonas aeruginosa

TL;DR: Pseudomonas aeruginosa is a human pathogen that frequently causes urinary tract and catheter-associated urinary tract infections as discussed by the authors, however, it does not have the ability to metabolize glucose.
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Core Fluxome and Metafluxome of Lactic Acid Bacteria under Simulated Cocoa Pulp Fermentation Conditions

TL;DR: Simulated cocoa fermentation was investigated at the level of metabolic pathway fluxes (fluxome) of lactic acid bacteria (LAB), which are typically found in the microbial consortium known to convert nutrients from the cocoa pulp into organic acids and revealed major differences in their fluxes.
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Long-Term Behavior of Defined Mixed Cultures of Geobacter sulfurreducens and Shewanella oneidensis in Bioelectrochemical Systems

TL;DR: The results demonstrate that S. oneidensis was not stably incorporated into the biofilm; rather, the planktonic presence of S.oneidensis has a positive effect on the bio film growth of G. sulfurreducens and thus on current production.
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Regulatory and metabolic networks for the adaptation of Pseudomonas aeruginosa biofilms to urinary tract-like conditions.

TL;DR: The obtained quorum sensing response results in an increased production of virulence factors like the extracellular lipase LipA and protease LasB and AprA explaining the harmful cause of these infections.