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Réjean Beaudet

Researcher at Institut national de la recherche scientifique

Publications -  65
Citations -  2441

Réjean Beaudet is an academic researcher from Institut national de la recherche scientifique. The author has contributed to research in topics: Desulfitobacterium & Desulfitobacterium hafniense. The author has an hindex of 31, co-authored 65 publications receiving 2342 citations. Previous affiliations of Réjean Beaudet include Université du Québec.

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The Desulfitobacterium genus

TL;DR: The release of the complete genome of Desulfitobacterium hafniense strain Y51 and information from the partial genome sequence of D. hafNIense strain DCB-2 will certainly help in predicting how desulf itobacteria interact with their environments and other microorganisms, and the mechanisms of actions related to reductive dehalogenation.
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Isolation and characterization of Desulfitobacterium frappieri sp. nov., an anaerobic bacterium which reductively dechlorinates pentachlorophenol to 3-chlorophenol

TL;DR: Results suggest that strain PCP-1T is a member of a new species and belongs to the recently proposed genus Desulfitobacterium, a spore-forming rod-shaped bacterium that is nonmotile, asaccharolytic, and Gram stain negative but Gram type positive.
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Optimization of high-molecular-weight polycyclic aromatic hydrocarbons' degradation in a two-liquid-phase bioreactor.

TL;DR: Micro‐organisms from the interface were slightly more effective in degrading PAHs than those from the aqueous phase.
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Bacterial Diversity of a Consortium Degrading High-Molecular-Weight Polycyclic Aromatic Hydrocarbons in a Two-Liquid Phase Biosystem

TL;DR: Information is provided on the bacterial composition of a HWM PAH-degrading consortium and its dynamics in a TLP biosystem during PAH degradation.
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Hydrolysis of 4-Hydroxybenzoic Acid Esters (Parabens) and Their Aerobic Transformation into Phenol by the Resistant Enterobacter cloacae Strain EM

TL;DR: Enterobacter cloacae strain EM harbored a high-molecular-weight plasmid and was resistant to high concentrations of parabens, and the transformation of 4-hydroxybenzoic acid into phenol was stoichiometric.