Dietmar Schlosser

Dr. Dietmar Schlosser

Environmental Mycology Group, Department of Environmental Microbiology, Helmholtz Centre for Environmental Research – UFZ, Leipzig, Germany
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Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 February 2011 in Nature Reviews Microbiology
Verified
Journal Article
Closed access
HHHauke Harms
Hauke Harms
DSDietmar Schlosser
Dietmar Schlosser
LWLukas Yvo Wick
Lukas Yvo Wick

30 August 2015 in Applied Microbiology and Biotechnology
Verified
Journal Article
Closed access
PDF file
MKMartin C. Krueger
Martin C. Krueger
HHHauke Harms
Hauke Harms
DSDietmar Schlosser
Dietmar Schlosser

1 July 2011 in FEMS Microbiology Reviews
Verified
Journal Article
Open access
PDF file
GKGerd-Joachim Krauss
Gerd-Joachim Krauss
MSMagali Solé
Magali Solé
GKGudrun Krauss
Gudrun Krauss
DSDietmar Schlosser
Dietmar Schlosser
DWDirk Wesenberg
Dirk Wesenberg
FBFelix Bärlocher
Felix Bärlocher
Research on freshwater fungi has concentrated on their role in plant litter decomposition in streams. Higher fungi dominate over bacteria in terms of

1 July 2002 in Applied and Environmental Microbiology
Verified
Journal Article
Open access
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DSDietmar Schlosser
Dietmar Schlosser
CHChristine HöfEr
Christine HöfEr
A purified and electrophoretically homogeneous blue laccase from the litter-decaying basidiomycete Stropharia rugosoannulata with a molecular mass of approximately 66 kDa oxidized Mn 2+ to Mn 3+ , as assessed in the presence of the Mn chelators oxalate, malonate, and pyrophosphate. At rate-saturating concentrations (100 mM) of these chelators and at pH 5.0, Mn 3+ complexes were produced at 0.15, 0.05, and 0.10 μmol/min/mg of protein, respectively. Concomitantly, application of oxalate and malonate, but not pyrophosphate, led to H 2 O 2 formation and tetranitromethane (TNM) reduction indicative for the presence of superoxide anion radical. Employing oxalate, H 2 O 2 production, and TNM reduction significantly exceeded those found for malonate. Evidence is provided that, in the presence of oxalate or malonate, laccase reactions involve enzyme-catalyzed Mn 2+ oxidation and abiotic decomposition of these organic chelators by the resulting Mn 3+ , which leads to formation of superoxide and its subsequent reduction to H 2 O 2 . A partially purified manganese peroxidase (MnP) from the same organism did not produce Mn 3+ complexes in assays containing 1 mM Mn 2+ and 100 mM oxalate or malonate, but omitting an additional H 2 O 2 source. However, addition of laccase initiated MnP reactions. The results are in support of a physiological role of laccase-catalyzed Mn 2+ oxidation in providing H 2 O 2 for extracellular oxidation reactions and demonstrate a novel type of laccase-MnP cooperation relevant to biodegradation of lignin and xenobiotics.

1 February 2006 in Journal of Biotechnology
Verified
Journal Article
Closed access
USUrs von Stockar
Urs von Stockar
Thomas MaskowThomas Maskow
Thomas Maskow
JLJingsong Liu
Jingsong Liu
IMIan W. Marison
Ian W. Marison
RPRodrigo Patiño
Rodrigo Patiño

7 July 2006 in Applied Microbiology and Biotechnology
Verified
Journal Article
Closed access
PDF file
PCP. F. X. Corvini
P. F. X. Corvini
ASA. Schäffer
A. Schäffer
DSDietmar Schlosser
Dietmar Schlosser