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Karl-Heinrich Engesser

Researcher at University of Stuttgart

Publications -  73
Citations -  2468

Karl-Heinrich Engesser is an academic researcher from University of Stuttgart. The author has contributed to research in topics: Ether & Pseudomonas putida. The author has an hindex of 28, co-authored 71 publications receiving 2279 citations.

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Assemblage of ortho cleavage route for simultaneous degradation of chloro- and methylaromatics

TL;DR: Critical enzymes from five different catabolic pathways of three distinct soil bacteria have been combined in patchwork fashion into a functional ortho cleavage route for the degradation of methylphenols and methylbenzoates and a new bacterium thereby evolved was able to degrade and grow on mixtures of chloro- and methylaromatics that were toxic even for the bacteria that could degrade the individual components of the mixtures.
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Metabolism of 2,4-dichlorophenoxyacetic acid, 4-chloro-2-methylphenoxyacetic acid and 2-methylphenoxyacetic acid by Alcaligenes eutrophus JMP 134

TL;DR: Of eleven substituted phenoxyacetic acids tested, only three (2,4-dichloro-, 4-chloro-2-methyl- and 2-methylphen Oxyacetic acid) served as growth substrates for Alcaligenes eutrophus JMP 134, and there was evidence for the presence of three different phenol hydroxylases in this strain.
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Effects of pH on the degradation of phenanthrene and pyrene by Mycobacterium vanbaalenii PYR-1

TL;DR: An acidic pH seemed to render the mycobacterial cells more permeable to hydrophobic substrates, and the non-K-region polycyclic aromatic hydrocarbon oxidation might be a significant burden to the cell due to the accumulation of toxic metabolites.
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Alkane hydroxylase homologues in Gram-positive strains.

TL;DR: It is shown that most Rhodococcus isolates contain three to five quite divergent homologues of the Pseudomonas putida GPo1 alkB gene, and two Mycobacterium isolates each contain one homologue, however there is no evidence for the presence of alkB homologue in the remaining strains.
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Dioxygenolytic cleavage of aryl ether bonds: 1, 10‐dihydro‐1, 10‐dihydroxyfluoren‐9‐one, a novel arene dihydrodiol as evidence for angular dioxygenation of dibenzofuran

TL;DR: Two dibenzofuran degrading bacteria were found to utilize fluorene as sole source of carbon and energy and the presence of a novel type of dioxygenase, attacking polynuclear aromatic systems in the unusual angular position was indicated.