Martina Pohl focuses on Benzoylformate decarboxylase, Stereochemistry, Enzyme, Biochemistry and Organic chemistry. Her studies in Benzoylformate decarboxylase integrate themes in fields like Enzyme catalysis and Enantiomeric excess, Enantioselective synthesis. Her work deals with themes such as Decarboxylation, Lyase, Substrate and Pyruvate decarboxylase, which intersect with Stereochemistry.
Martina Pohl mostly deals with Carboxy-lyases in her studies of Enzyme. Biocatalysis and Benzoin are among the areas of Organic chemistry where she concentrates her study. She combines subjects such as Directed evolution, Benzaldehyde and Active site with her study of Pseudomonas putida.
Martina Pohl mostly deals with Stereochemistry, Enzyme, Biochemistry, Organic chemistry and Biocatalysis. Martina Pohl interconnects Catalysis, Enantioselective synthesis, Stereoselectivity, Benzoylformate decarboxylase and Pyruvate decarboxylase in the investigation of issues within Stereochemistry. Her research combines Enzyme catalysis and Benzoylformate decarboxylase.
Her Pyruvate decarboxylase study integrates concerns from other disciplines, such as Decarboxylation and Biotransformation. Her research brings together the fields of Thiamine and Enzyme. Her research investigates the connection between Biocatalysis and topics such as Inclusion bodies that intersect with issues in Nanotechnology.
The scientist’s investigation covers issues in Biocatalysis, Enzyme, Inclusion bodies, Organic chemistry and Combinatorial chemistry. Her work in Biocatalysis addresses issues such as Immobilized enzyme, which are connected to fields such as Benzoylformate decarboxylase. Martina Pohl has researched Enzyme in several fields, including Computational biology and Catalysis.
To a larger extent, Martina Pohl studies Biochemistry with the aim of understanding Inclusion bodies. Her research in Organic chemistry intersects with topics in Phenylalanine ammonia-lyase and Stereochemistry. Her work in Stereochemistry tackles topics such as Enantioselective synthesis which are related to areas like Phenylacetylcarbinol.
Her primary areas of study are Biocatalysis, Organic chemistry, Inclusion bodies, Biochemistry and Immobilized enzyme. Her Biocatalysis research entails a greater understanding of Catalysis. Her research on Organic chemistry often connects related areas such as Active ingredient.
Her study in Enzyme, Hydroxynitrile lyase, Escherichia coli, Diacetyl reductase and Deamination is carried out as part of her studies in Biochemistry. Martina Pohl studies NAD+ kinase which is a part of Enzyme. Her Immobilized enzyme study incorporates themes from Benzoylformate decarboxylase, Cascade, Process optimization, Aldehyde lyases and Colocalization.
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Improved biocatalysts by directed evolution and rational protein design.
Uwe T Bornscheuer;Martina Pohl.
Current Opinion in Chemical Biology (2001)
Development of a donor-acceptor concept for enzymatic cross-coupling reactions of aldehydes: the first asymmetric cross-benzoin condensation.
Pascal Dünkelmann;Doris Kolter-Jung;Adam Nitsche;Ayhan S. Demir.
Journal of the American Chemical Society (2002)
Stabilization of NAD-dependent formate dehydrogenase from Candida boidinii by site-directed mutagenesis of cysteine residues.
Heike Slusarczyk;Stephan Felber;MariaâRegina Kula;Martina Pohl.
FEBS Journal (2000)
Thiamin-diphosphate-dependent enzymes: new aspects of asymmetric C-C bond formation.
Martina Pohl;Bettina Lingen;Michael Müller.
Chemistry: A European Journal (2002)
Enantioselective Synthesis of α‐Hydroxy Ketones via Benzaldehyde Lyase‐Catalyzed C−C Bond Formation Reaction
Ayhan S. Demir;Özge Şeşenoglu;Elif Eren;Birsu Hosrik.
Advanced Synthesis & Catalysis (2002)
Effect of Oxygen Limitation and Medium Composition on Escherichia coli Fermentation in Shake‐Flask Cultures
Mario Losen;Bettina Frölich;Martina Pohl;Jochen Büchs.
Biotechnology Progress (2004)
A new perspective on thiamine catalysis.
Martina Pohl;Georg A Sprenger;Michael Müller.
Current Opinion in Biotechnology (2004)
Benzoylformate Decarboxylase from Pseudomonas putida as Stable Catalyst for the Synthesis of Chiral 2‐Hydroxy Ketones
Hans Iding;Thomas Dünnwald;Lasse Greiner;Andreas Liese.
Chemistry: A European Journal (2000)
Enantioselective synthesis of hydroxy ketones through cleavage and formation of acyloin linkage. Enzymatic kinetic resolution via C-C bond cleavage
Ayhan S. Demir;Ayhan S. Demir;Martina Pohl;Elena Janzen;Michael Müller.
Journal of The Chemical Society-perkin Transactions 1 (2001)
Two Steps in One Pot: Enzyme Cascade for the Synthesis of Nor(pseudo)ephedrine from Inexpensive Starting Materials
Torsten Sehl;Helen C. Hailes;John M. Ward;Rainer Wardenga.
Angewandte Chemie (2013)
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