about
Human FMO2-based microbial whole-cell catalysts for drug metabolite synthesis.Biocatalytic ketone reduction--a powerful tool for the production of chiral alcohols-part II: whole-cell reductions.Biocatalytic ketone reduction--a powerful tool for the production of chiral alcohols--part I: processes with isolated enzymes.Recombinant human cytochrome P450 monooxygenases for drug metabolite synthesis.Human xanthine oxidase recombinant in E. coli: A whole cell catalyst for preparative drug metabolite synthesis.Towards preparative scale steroid hydroxylation with cytochrome P450 monooxygenase CYP106A2.Challenges of steroid biotransformation with human cytochrome P450 monooxygenase CYP21 using resting cells of recombinant Schizosaccharomyces pombe.Ionic liquids as performance additives for electroenzymatic syntheses.Application of immobilized bovine enterokinase in repetitive fusion protein cleavage for the production of mucin 1.Enzyme-assisted physicochemical enantioseparation processes-Part III: Overcoming yield limitations by dynamic kinetic resolution of asparagine via preferential crystallization and enzymatic racemization.Indirect electrochemical reduction of nicotinamide coenzymes.Complementation of biotransformations with chemical C-H oxidation: copper-catalyzed oxidation of tertiary amines in complex pharmaceuticals.Metabolomics for biotransformations: Intracellular redox cofactor analysis and enzyme kinetics offer insight into whole cell processes.Stable electroenzymatic processes by catalyst separation.Kinetic modeling of acetophenone reduction catalyzed by alcohol dehydrogenase from Thermoanaerobacter sp.Immobilisation of bovine enterokinase and application of the immobilised enzyme in fusion protein cleavage.Enzyme-Based Electrobiotechnological Synthesis.The First Biocatalytic Carbon-Silicon Bond Formation.Continuous asymmetric ketone reduction processes with recombinant Escherichia coli.Process development for the electroenzymatic synthesis of (R)-methylphenylsulfoxide by use of a 3-dimensional electrode.The production of (R)-2-hydroxy-1-phenyl-propan-1-one derivatives by benzaldehyde lyase from Pseudomonas fluorescens in a continuously operated membrane reactor.Biocatalytic production of enantiopure cyclohexane-trans-1,2-diol using extracellular lipases from Bacillus subtilis.Expression of recombinant human flavin monooxygenase and moclobemide-N-oxide synthesis on multi-mg scale.Technische Anwendung von Enzymen: Weiße Wäsche und Grüne ChemieAn Efficient Route to Both Enantiomers of allo-Threonine by Simultaneous Amino Acid Racemase-Catalyzed Isomerization of Threonine and CrystallizationChemo-enzymatic cascade oxidation in supercritical carbon dioxide/water biphasic mediaA novel cytochrome P450 mono-oxygenase from Streptomyces platensis resembles activities of human drug metabolizing P450sScreening and Identification of Novel cGAS Homologues Using a Combination of in Vitro and In Vivo Protein SynthesisRecent advances in heme biocatalysis engineeringA Gram-Scale Limonene Production Process with Engineered Escherichia coli30 Years of Safe Genetic Engineering in Germany
P50
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P50
description
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name
Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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type
label
Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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Stephan Lütz
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P214
P227
P244
P1053
B-9304-2009
P108
P19
P21
P213
0000 0003 7827 4741
P214
P227
P244
n2007013232
P31
P3829
P496
0000-0001-8534-0554
P569
1976-01-01T00:00:00Z
P7859
lccn-n2007013232