Publikationsliste Prof. Dr. Michael Müller (Stand ) 1. A. Yenesew, Ermias Dagne, Michael Müller, Wolfgang Steglich, An anthrone, an

Size: px
Start display at page:

Download "Publikationsliste Prof. Dr. Michael Müller (Stand ) 1. A. Yenesew, Ermias Dagne, Michael Müller, Wolfgang Steglich, An anthrone, an"

Transcription

1 Publikationsliste Prof. Dr. Michael Müller (Stand ) 1. A. Yenesew, Ermias Dagne, Michael Müller, Wolfgang Steglich, An anthrone, an anthraquinone and two oxoanthrones from Kniphofia foliosa, Phytochemistry 1994, 37, Ermias Dagne, B. van Wyk, Michael Müller, Wolfgang Steglich, Three dihydroanthracenones from Gasteria bicolor, Phytochemistry 1996, 41, Michael Wolberg, Michael Müller, Werner Hummel, Verfahren zur enantioselektiven Reduktion von 3,5-Dioxocarbonsäuren sowie deren Ester, Patent DE , (Patentanmeldung vom ). 4. Michael Müller, Rolf Müller, Tin-Wein Yu, Heinz G. Floss, Synthesis of (-)-3-Amino-3-deoxyquinic Acid, J. Org. Chem. 1998, 63, Thomas Dünnwald, Lasse Greiner, Hans Iding, Andreas Liese, Michael Müller, Martina Pohl, Stereoselektive Synthese von 2-Hydroxyketonen, Patentanmeldung DE , Michael Müller, Michael Wolberg, Werner Hummel, Christian Wandrey, Verfahren zur Reduktion von Keto-Carbonsäuren und deren Estern., US Patent 6,689,591 B2, (Patentanmeldung DE , ). 7. Sungsook Lee, Andreas Kirschning, Michael Müller, Chris Way, Heinz G. Floss, Enzymatic synthesis of [7-14 C, 7-3 H]- and [1-13 C]sedoheptulose 7-phosphate and [1-13 C]ido-heptulose 7-phosphate, J. Mol. Catalysis B: Enzymatic 1999, 6, Thomas Schubert, Maria-Regina Kula, Michael Müller, Chemoenzymatic Synthesis of (S)-8-O-Methylmellein by Candida parapsilosis Carbonyl Reductase, Synthesis 1999, Ayhan S. Demir, Thomas Dünnwald, Hans Iding, Martina Pohl, Michael Müller, Asymmetric Benzoin Reaction Catalyzed by Benzoylformate Decarboxylase, Tetrahedron: Asymmetry 1999, 10, Ayhan S. Demir, Martina Pohl, Michael Müller, Nukleotidsequenz kodierend für eine Benzaldehyd-Lyase und Verfahren zur stereoselektiven Synthese von 2-Hydroxyketonen, Patentanmeldung DE , Dirk Franke, Georg Sprenger, Rolf Müller, Ralf Takors, Volker Lorbach, Jörg Thömmes, Markus Halfar, Michael Müller, Verfahren zur verbesserten Herstellung und Isolierung von trans-dihydroxycyclohexadiencarbonsäuren und/oder deren Folgeprodukte sowie ein dazu geeigneter genetisch veränderter Organismus, Patentanmeldung DE , Michael Müller, Kai Lamottke, Erich Löw, Eva Magor-Veenstra, Wolfgang Steglich, Stereoselective total syntheses of atrochrysone, torosachrysone and related 3,4-dihydroanthracen- 1(2H)-ones, J. Chem. Soc., Perkin Trans , Hans Iding, Thomas Dünnwald, Lasse Greiner, Andreas Liese, Michael Müller, Petra Siegert, Joachim Grötzinger, Ayhan S. Demir, Martina Pohl, Benzoylformate Decarboxylase from Pseudomonas putida as Stable Catalyst for the Synthesis of Chiral 2-Hydroxy Ketones, Chem. Eur. J. 2000, 6, Thomas Dünnwald, Ayhan S. Demir, Petra Siegert, Martina Pohl, Michael Müller, Enantioselective Synthesis of (S)-2-Hydroxy propanone Derivatives by Benzoylformate Decarboxylase catalyzed C-C-bond formation, Eur. J. Org. Chem. 2000, Michael Wolberg, Werner Hummel, Christian Wandrey, Michael Müller, Highly Regio- and Enantioselective Reduction of 3,5-Dioxocarboxylates, Angew. Chem. 2000, 112, ; Angew. Chem. Int. Ed. 2000, 39, Thomas Dünnwald, Michael Müller, Stereoselective Formation of Bis(α-Hydroxy Ketones) via Enzymatic Carboligation, J. Org. Chem. 2000, 65,

2 17. Thomas Schubert, Werner Hummel, Michael Müller, Verfahren zur Herstellung von optisch aktiven, propargylischen, terminalen Epoxiden, Patentanmeldung DE , Silke Bode, Michael Wolberg, Michael Müller Verfahren zur Trennung diastereomerer 1,3-Diol-Acetale, Patentanmeldung DE , Michael Müller, Wolfgang Sauer, Gunter Laban, Verfahren zur Herstellung von (R)- und (S)-8-Chlor-6-hydroxy-octansäurealkylestern durch enzymatische Reduktion von 8-Chlor-6-oxo-octansäurealkylestern, Patent DE , (Patentanmeldung vom , AWD Dresden Viatris GmbH). 20. Tin-Wein Yu, Rolf Müller, Michael Müller, Xiaohong Zhang, Gerald Draeger, Chun-Gyu Kim, Eckhard Leistner, Heinz G. Floss, Mutational Analysis and Reconstitution Expression of the Biosynthetic Genes Involved in the Formation of 3-Amino-5-hydroxybenzoic Acid, the Starter Unit of Rifamycin Biosynthesis in Amycolatopsis mediterannei S699, J. Biol. Chem. 2001, 276, Aiguo Ji, Michael Wolberg, Werner Hummel, Christian Wandrey, Michael Müller, Dynamic kinetic resolution of tert-butyl 4-methyl-3,5-dioxohexanoate through enzymatic reduction, Chem. Commun. 2001, Daniel Drochner, Michael Müller, Total Synthesis of (R)- and (S)-semi-Vioxanthin, Eur. J. Org. Chem. 2001, Dirk Franke, Georg A. Sprenger, Michael Müller, Synthese funktionalisierter Cyclohexadien-trans-diole durch rekombinante Escherichia-coli-Zellen, Angew. Chem. 2001, 113, ; Angew. Chem. Int. Ed. 2001, 40, Ayhan S. Demir, Martina Pohl, Elena Janzen, Michael Müller, Enantioselective synthesis of hydroxy ketones via cleavage and formation of acyloin linkage. Enzymatic kinetic resolution via C-C bond cleavage, J. Chem. Soc., Perkin Trans , Michael Wolberg, Aiguo Ji, Werner Hummel, Michael Müller, Enzymatic reduction of hydrophobic β,δ-diketo esters, Synthesis 2001, Michael Wolberg, Werner Hummel, Michael Müller, Biocatalytic Reduction of β,δ-diketo Esters: A Highly Stereoselective Approach to All Four Stereoisomers of a Chlorinated β,δ-dihydroxy Hexanoate, Chem. Eur. J. 2001, 7, Thomas Schubert, Werner Hummel, Maria-Regina Kula, Michael Müller, Enantioselective Synthesis of both Enantiomers of various Propargylic Alcohols by Use of Two Oxidoreductases, Eur. J. Org. Chem. 2001, Andreas Job, Michael Wolberg, Michael Müller, Dieter Enders, Asymmetric Synthesis of S-(+)-Argentilactone and S-(-)-Goniothalamin, Synlett 2001, Aiguo Ji, Michael Müller, Michael Wolberg, Werner Hummel, Christian Wandrey, Chemoenzymatic Synthesis of Optically Pure tert-butyl (4S,5R)-4-Methyl-5-hydroxy-3-oxo-hexanoate, Chinese Journal of Organic Chemistry 2002, 22, Murillo Villela Filho, Michael Wolberg, Michael Müller, Werner Hummel, Andreas Liese, Christian Wandrey, Verfahrensentwicklung zur Synthese eines δ-hydroxy-β-ketohexanoates Chemie Ingenieur Technik 2002, 74, Thomas Schubert, Werner Hummel, Michael Müller, Highly Enantioselective Preparation of Novel Multifunctionalized Propargylic Building Blocks, Angew. Chem. 2002, 114, ; Angew. Chem. Int. Ed. 2002, 41, Silke E. Bode, Michael Müller, Michael Wolberg, Diastereomer-differentiating hydrolysis of 1,3-diol-acetonides: a simplified procedure for the separation of syn- and anti-1,3-diols, Org. Lett. 2002, 4,

3 33. Volker Lorbach, Dirk Franke, Martin Nieger, Michael Müller, Cyclohexadiene-trans-diols as versatile starting material in natural product synthesis: Short and efficient synthesis of iso-crotepoxide and ent-senepoxide, Chem. Commun. 2002, Ayhan S. Demir, Özge Şeşenoglu, Elif Eren, Birsu Hosrik, Martina Pohl, Elena Janzen, Doris Kolter, Ralf Feldmann, Pascal Dünkelmann, Michael Müller, Enantioselective Synthesis of α-hydroxy Ketones via Benzaldehyde Lyase Catalyzed C-C Bond Formation Reaction, Adv. Synth. Catal. 2002, 344, Jose L. Vicario, Andreas Job, Michael Wolberg, Michael Müller, Dieter Enders, Asymmetric Total Synthesis of (-)-Callystatin A Employing the SAMP/RAMP Hydrazone Alkylation Methodology, Org. Lett. 2002, 4, Dieter Enders, Jose L. Vicario, Andreas Job, Michael Wolberg, Michael Müller, Asymmetric Total Synthesis of (-)-Callystatin A and (-)-20-epi-Callystatin A Employing the SAMP/RAMP Hydrazone Alkylation Methodology, Chem. Eur. J. 2002, 8, Pascal Dünkelmann, Doris Kolter-Jung, Adam Nitsche, Ayhan S. Demir, Petra Siegert, Bettina Lingen, Martin Baumann, Martina Pohl, Michael Müller, Development of a donor-acceptor concept for catalytic asymmetric cross-coupling reactions of aldehydes: first asymmetric cross-benzoin condensation, J. Am. Chem. Soc. 2002, 124, Martina Pohl, Bettina Lingen, Michael Müller, Thiamin diphosphate-dependent Enzymes: New Aspects of Asymmetric C-C Bond Formation Chem. Eur. J. 2002, 8, (Concepts paper, invited). 39. Michael Müller, Anabel Cosp, Pascal Dünkelmann, Simon Esser, Daniel Drochner, Highlights 2002: Enzyme in der Organischen Synthese, Nachr. Chem. 2003, 51, Daniel Drochner, Wolfgang Hüttel, Martin Nieger, Michael Müller, Unselective Phenolic Coupling of Methyl 2-Hydroxy-4-methoxy-6-methylbenzoate A Valuable Tool for the Total Synthesis of Natural Product Families, Angew. Chem. 2003, 115, ; Angew. Chem. Int. Ed. 2003, 42, Holger Wildemann, Pascal Dünkelmann, Michael Müller, Bernd Schmidt, A short olefin metathesis-based route to enantiomerically pure arylated dihydropyrans, J. Org. Chem. 2003, 68, Ayhan S. Demir, Özge Sesenoglu, Pascal Dünkelmann, Michael Müller, Benzaldehyde Lyase-Catalyzed Enantioselective Carboligation of Aromatic Aldehydes with Mono- and Dimethoxy Acetaldehyde, Org. Lett. 2003, 5, Murillo Villela Filho, Thomas Stillger, Michael Müller, Andreas Liese, Christian Wandrey, Is log P a Convenient Criterion to Guide the Choice of Solvents for Biphasic Enzymatic Reactions?, Angew. Chem. 2003, 115, ; Angew. Chem. Int. Ed. 2003, 42, Bettina Lingen, Doris Kolter, Pascal Dünkelmann, Ralf Feldmann, Joachim Grötzinger, Martina Pohl, Michael Müller, Alteration of the Substrate Specificity of Benzoylformate Decarboxylase from Ps. putida by Directed Evolution, ChemBioChem 2003, 4, Dirk Franke, Georg A. Sprenger, Michael Müller, Easy access to monofunctionalized trans-3,4-dihydroxycyclohexa-1,5-diens with engineered strains of Escherichia coli, ChemBioChem 2003, 4, Dirk Franke, Volker Lorbach, Simon Esser, Christian Dose, Georg A. Sprenger, Markus Halfar, Jörg Thömmes, Rolf Müller, Ralf Takors, Michael Müller, (S,S)-2,3-Dihydroxy-2,3-dihydrobenzoic Acid: Microbial Access with Engineered Cells of Escherichia coli and Applicability as Starting Material in Natural Product Synthesis, Chem. Eur. J. 2003, 9,

4 47. Wolfgang Hüttel, Martin Nieger, Michael Müller, A Short and Efficient Total Synthesis Synthesis of the Naturally Occuring Coumarins Siderin, Kotanin, Isokotanin A and Desertorin C, Synthesis 2003, Georg A. Sprenger, Marcel Wubbolts, Johannes Bongaerts, Michael Müller, Stefan Kozak, R Bovenberg, Biosynthetic production of 4-amino-4-deoxychorismate (ADC) and [3R,4R]-4-amino-3- hydroxycyclohexa-1,5-diene-1-carboxylic ACID (3,4-CHA.) EP , PCT/EP2005/005988, eingereicht Michael Müller, Highlights 2003: Enzyme in der organischen Synthese, Nachr. Chem. 2004, 52, Wolfgang Hüttel, Michael Müller, Buchrezension: Pocket Guide Biotechnology, by Rolf D. Schmid, Nachr. Chem. 2004, 52, Pascal Dünkelmann, Martina Pohl, Michael Müller, Enantiomerically pure 2-hydroxy carbonyl compounds through enzymatic C-C bond formation, Chemistry Today 2004, Volker Lorbach, Dirk Franke, Simon Esser, Christian Dose, Georg A. Sprenger, Michael Müller, Microbially produced functionalized cyclohexadiene-trans-diols as a new class of chiral building blocks in organic synthesis: on the way to green and combinatorial chemistry, in Bioorganic Chemistry II, VCH-Wiley, 2004, Volker Lorbach, Dirk Franke, Georg A. Sprenger, Michael Müller, Metabolic pathway engineering, in Bioorganic Chemistry II, VCH-Wiley, 2004, Bettina Lingen, Martina Pohl, Ayhan S. Demir, Andreas Liese, Michael Müller, Enantioselective Synthesis of Hydroxy Ketones via Benzoylformate Decarboylase- and Benzaldehyde Lyase-catalyzed C-C Bond Formation, in Thiamine: Catalytic Mechanisms and Role in Normal and Disease States, Marcel Dekker, New York, 2004, Michael Müller, Georg A. Sprenger, Thiamine-dependent enzymes as catalysts of C-C-bonding reactions: The role of orphan enzymes, in Thiamine: Catalytic Mechanisms and Role in Normal and Disease States, Marcel Dekker, New York, 2004, Michael Müller, Kai Lamottke, Wolfgang Steglich, Steffan Busemann, Matthias Reichert, Gerhard Bringmann, Peter Spiteller, Biosynthesis and Stereochemistry of Phlegmacin-Type Fungal Pigments, Eur. J. Org. Chem. 2004, Dieter Enders, Achim Lenzen, Michael Müller, Efficient Asymmetric Syntheses of (+)-Strictifolione, Synthesis 2004, Martina Pohl, Georg A. Sprenger, Michael Müller A new perspective on thiamine catalysis, Current Opinion Biotechnol. 2004, 15, Michael Wolberg, Iwona A. Kaluzna, Michael Müller, Jon D. Stewart, Regio and enantioselective reduction of t-butyl 6-chloro-3,5-dioxohexanoate with baker s yeast Tetrahedron: Asymmetry 2004, 15, Michael Müller Chemical diversity through biotransformations, Current Opinion Biotechnol. 2004, 15, Johannes Bongaerts, Leon Raeven, Michael Müller, Volker Lorbach, Biosynthetic production of 2-amino-2-deoxyisochorismate (ADIC) and [5R,6S]-6-amino-5- hydroxycyclohexa-1,3-diene-1-carboxylic ACID (2,3-CHA) (WO 2006/128706)). 62. Michael Müller, Highlights 2004: Enzyme in der organischen Synthese, Nachr. Chem. 2005, 53, 270.

5 63. Michael Müller, Michael Wolberg, Thomas Schubert, Werner Hummel, Enzyme-catalyzed regio- and enantioselective ketone reductions, in Advances in Biochemical Engineering/Biotechnology, Volume Title: Technology Transfer in Biotechnology: From Lab to Industry to Production, Springer Verlag, Heidelberg 2005, 92, Michael Müller, Chemoenzymatic synthesis of statin side-chain building blocks, Angew. Chem. 2005, 117, ; Angew. Chem. Int. Ed. 2005, 44, Marianne Ernst, Björn Kaup, Michael Müller, Stephanie Bringer-Meyer, Hermann Sahm, Enantioselective reduction of carbonyl-compounds by whole-cell biotransformation, combining a formate dehydrogenase and a (R)-specific alcohol dehydrogenase, Appl. Microbiol. Biotechnol. 2005, 66, Tanja G. Mosbacher, Michael Müller, Georg E. Schulz Structure and mechanism of the ThDP-dependent benzaldehyde lyase from Pseudomonas fluorescens, FEBS Journal 2005, 272, Philippe Bisel, Michael Müller, Highlights 2005: Enzyme in der organischen Synthese, Nachr. Chem. 2006, 54, Silke Bode, Michael Wolberg, Michael Müller, Stereoselective Synthesis of 1,3-Diols, Synthesis 2006, Jean Detry, Thorsten Rosenbaum, Stephan Lütz, Doris Hahn, Karl-Erich Jaeger, Michael Müller, Thorsten Eggert, Biocatalytic production of enantiopure cyclohexane-trans-1,2-diol using extracellular lipases from Bacillus subtilis, Appl. Microbiol. Biotechnol. 2006, 72, C. Bihlmaier, E. Welle, C. Hofmann, K. Welzel, A. Vente, E. Breitling, M. Müller, S. Glaser, A. Bechthold, Biosynthetic Gene Cluster for the Polyenoyltetramic Acid α-lipomycin, Antimicrobiol. Agents Chemother. 2006, 50, Elena Janzen, Michael Müller, Doris Kolter-Jung, Malea M. Kneen, Michael J. McLeish, Martina Pohl, Characterization of benzaldehyde lyase from Pseudomonas fluorescens: A versatile enzyme for asymmetric C-C bond formation, Bioorg. Chem. 2006, 34, Helge Henning, Christian Leggewie, Martina Pohl, Michael Müller, Thorsten Eggert, Karl-Erich Jäger, Identification of novel benzyolformate decarboxylases by growth selection, Appl. Environ. Micobiol. 2006, 72, Michael Knoll, Michael Müller, Jürgen Pleiss, Martina Pohl, Factors mediating Activity, Selectivity, and Substrate Specificity for the Thiamin Diphosphate- Dependent Enzymes Benzaldehyde Lyase and Benzoylformate Decarboxylase, ChemBioChem 2006, 7, Michael Müller, Marcel Wubbolts, Biotransformation Methods for Preparing Chiral Drugs and Drug Intermediates, in Chirality in Drug Research, Methods and Principles in Medicinal Chemistry, Volume 33, (Eds. E. Francotte, W. Lindner) Wiley-VCH, Weinheim, 2006, Marion Wendorff, Thorsten Eggert, Martina Pohl, Carola Dresen, Michael Müller, Karl-Erich Jaeger, Directed Evolution to Increase the Substrate Range of Benzoylformate Decarboxylase from Pseudomonas putida, in Asymmetric Synthesis with Chemical and Biological Methods, Wiley-VCH, Weinheim, 2007, Andrea Weckbecker, Michael Müller, Werner Hummel, Preparative Syntheses of Chiral Alcohols using (R)-Specific Alcohol Dehydrogenases from Lactobacillus Strains, in Asymmetric Synthesis with Chemical and Biological Methods, Wiley-VCH, Weinheim, 2007, Michael Müller, Michael Wolberg, Silke E. Bode, Ralf Feldmann, Petra Geilenkirchen, Thomas Schubert, Lydia Walter, Werner Hummel, Thomas Dünnwald, Ayhan S. Demir, Doris Kolter-Jung, Adam Nitsche, Pascal Dünkelmann, Annabel Cosp, Martina Pohl, Bettina Lingen, Maria-Regina Kula, Flexible asymmetric redoxreactions and C-C bond formations by bioorganic synthetic strategies, in Asymmetric Synthesis with Chemical and Biological Methods, Wiley-VCH, Weinheim, 2007,

6 78. Philippe Bisel, Michael Müller, Highlights 2006: Enzyme in der organischen Synthese, Nachr. Chem. 2007, 55, Falk Hildebrand, Sven Kühl, Martina Pohl, Durda Vasic-Racki, Michael Müller, Christian Wandrey, Stephan Lütz, The production of (R)-2-hydroxy-1-phenyl-propan-1-one derivatives by benzaldehyde lyase from Pseudomonas fluorescens in a continuously operated membrane reactor, Biotechnol. Bioengineering 2007, 96, Wolfgang Hüttel, Michael Müller, Regio- and Stereoselective intermolecular oxidative phenol coupling in kotanin biosynthesis by Aspergillus niger, ChemBioChem 2007, 8, Daniel Drochner, Wolfgang Hüttel, Silke E. Bode, Michael Müller, Ulrich Karl, Martin Nieger, Wolfgang Steglich, Dimeric Orsellinic Acid Derivatives: Valuable Intermediates for Natural Product Synthesis, Eur. J. Org. Chem. 2007, Yin-Ru Chiang, Wael Ismail, Michael Müller, Georg Fuchs, Initial steps in the anoxic metabolism of cholesterol by the denitrifying Sterolibacterium denitrificans, J. Biol. Chem. 2007, 282, Pablo Domínguez de María, Martina Pohl, Dörte Gocke, Harald Gröger, Harald Trauthwein, Thomas Stillger, Lydia Walter, Michael Müller, Asymmetric synthesis of aliphatic 2-hydroxy ketones by enzymatic carboligation of aldehydes, Eur. J. Org. Chem. 2007, Dörte Gocke, Con Luan Nguyen, Martina Pohl, Thomas Stillger, Lydia Walter, Michael Müller, Branched-chain ketoacid decarboxylase from Lactococcus lactis (KdcA), a new thiamin diphosphatedependent enzyme for asymmetric C-C bond formation, Adv. Synth. Catal. 2007, 349, Philippe Bisel, Lydia Walter, Martin Nieger, Michael Müller, Stereochemical clarification of the enzyme-catalysed reduction of 2-acetylchromen-4-one, Tetrahedron: Asymmetry 2007, 18, Tobias J. Erb, Ivan A. Berg, Volker Brecht, Michael Müller, Georg Fuchs, Birgit E. Alber, Synthesis of C 5 -dicarboxylic acids from C 2 -units involving crotonyl-coa carboxylase/reductase: The ethylmalonyl-coa pathway, PNAS 2007, 104, Silke E. Bode, Daniel Drochner, Michael Müller, Synthesis, Biosynthesis and absolute Configuration of Vioxanthin, Angew. Chem. 2007, 119, ; Angew. Chem. Int. Ed. 2007, 46, Sven Kühl, Daniela Zehentgruber, Martina Pohl, Michael Müller, Stephen Lütz Process development for enzmye catalysed asymmetric C-C bond formation Chemical Engineering Science 2007, 62, Carola Dresen, Michael Richter, Michael Müller, Verwendung de PigD-Proteins zur Katalyse von 1,4-Additionen von 2-Oxoalkanoaten an alpha-, betaungesättigte Ketone, DE , Christoph Krekel, Stella Eichner, Karin Geißinger, Michael Müller, Efeulacca - Bericht von einem vergessenen Farbmittel, Zeitschrift für Kunsttechnologie und Konservierung 2007, 21, Philippe Bisel, Michael Müller, Highlights 2007: Enzymreaktionen, Nachr. Chem. 2008, 56, Dörte Gocke, Lydia Walter, Ekaterina Gauchenova, Geraldine Kolter, Michael Knoll, Catrine L. Berthold, Gunter Schneider, Jürgen Pleiss, Michael Müller, Martina Pohl, Rational Protein Design of ThDP-Dependent Enzymes - Engineering Stereoselectivity, ChemBioChem 2008, 9, Jan Zarzycki, Ansgar Schlichting, Nina Strychalski, Michael Müller, Birgit E. Alber, Georg Fuchs, Mesaconyl-Coenzyme A Hydratase, a New Enzyme of Two Central Carbon Metabolic Pathways in Bacteria, J. Bacteriol. 2008, 190,

7 94. Anabel Cosp, Carola Dresen, Martina Pohl, Lydia Walter, Caroline Röhr, Michael Müller α,β-unsaturated aldehydes as substrates for asymmetric C-C bond forming reactions with thiamine diphosphate (ThDP)-dependent enzymes, Adv. Synth. Catal. 2008, 350, Michael Wolberg, Murillo Villela Filho, Silke Bode, Petra Geilenkirchen, Ralf Feldmann, Andreas Liese, Werner Hummel, Michael Müller, Chemoenzymatic synthesis of the chiral side-chain of statins: application of an alcohol dehydrogenase-catalysed ketone reduction on a large scale, Bioprocess Biosyst. Eng. 2008, 31, Philippe Bisel, Loay Al-Momani, Michael Müller, The tert-butyl group in Chemistry and Biology, Organic Biomol. Chem. 2008, 6, Bärbel Thiele, Oliver Rieder, Nico Jehmlich, Martin von Bergen, Michael Müller, Matthias Boll, Aromatizing Cyclohex-1,5-diene-1-carbonyl-Coenzyme A Oxidase: Characterization and its Role in Anaerobic Aromatic Metabolism, J. Biol. Chem. 2008, 283, Alexander Pontius, Anja Krick, Stefan Kehraus, Silke E. Foegen, Michael Müller, Karin Klimo, Clarissa Gerhäuser, Gabriele M. König, Noduliprevenone, a novel heterodimeric chromanone with cancer chemopreventive potential Chem. Eur. J. 2008, 14, Alexander Pontius, Anja Krick, Ronak Mesry, Stefan Kehraus, Silke E. Foegen, Michael Müller, Karin Klimo, Clarissa Gerhäuser, Gabriele M. König, Monodictyochrome A and B, Dimeric Xanthone Derivatives from the Marine Algicolous Fungus Monodictys putredinis, J. Nat. Prod. 2008, 71, Bärbel Thiele, Oliver Rieder, Bernard Golding, Michael Müller, Matthias Boll, Mechanism of Enzymatic Birch Reduction: Stereochemical Course and Exchange Reactions of Benzoyl-CoA Reductase, J. Am. Chem. Soc. 2008, 130, Martina Pohl, Dörte Gocke, Michael Müller, Thiamin-based Enzymes for Biotransformations, in Green Chemistry, Anastas PT, editor. Handbook of Green Chemistry, Green Catalysis, Vol. 3 Biocatalysis. Weinheim: Wiley-VCH. 2008, p Patrizia Lehwald, Michael Richter, Michael Müller, Verfahren zur stereospezifischen Synthese von Verbindungen mit einem Enzym aus Yersinia, EP , Steffen Lüdeke, Michael Richter, Michael Müller, Stereoselective synthesis of three isomers of tert-butyl 5-hydroxy-4-methyl-3-oxohexanoate through alcohol dehydrogenase-catalyzed dynamic kinetic resolution, Adv. Synth. Catal. 2009, 351, Volker Auwärter, Sebastian Dresen, Wolfgang Weinmann, Michael Müller, Michael Pütz, Nerea Ferreirós Spice and other herbal blends: harmless incense or cannabinoid designer drugs?, Journal of Mass Spectrometry 2009, 44, Wolfgang Hüttel, Michael Müller Highlights 2008: Enzyme in der organischen Synthese, Nachr. Chem. 2009, 57, Dörte Gocke, Thorsten Graf, Helen Brosi, Ilona Frindi-Wosch, Lydia Walter, Michael Müller, Martina Pohl, Comparative characterisation of thiamin diphosphate-dependent decarboxylases, J. Mol. Catal., B: Enzym. 2009, 61, Anja Kurutsch, Michael Richter, Volker Brecht, Georg A. Sprenger, Michael Müller, MenD as a versatile catalyst for asymmetric synthesis, J. Mol. Catal., B: Enzym , Andreas Liese, Michael Müller, Martina Pohl, Dieter Sell, Kai Tittmann, Special Issue: Chemical Biology of Thiamine (Editorial), J. Mol. Catal., B: Enzym. 2009, 61, 1.

8 109. Michael Müller, Dörte Gocke, Martina Pohl, Exploitation of ThDP-dependent enzymes for asymmetric chemoenzymatic synthesis, FEBS Journal , Tobias J. Erb, Volker Brecht, Michael Müller, Georg Fuchs, Birgit E. Alber, Carboxylation mechanism and stereochemistry of crotonyl.coa carboxylase/reductase, a carboxylating enoyl-thioester reductase, PNAS 2009, 106, Michael Müller, Christian Klein, Bookreview: Practical Biotransformations. A Beginner's Guide. von Gideon Grogan. Angewandte Chemie. 2009, 121, ; Angewandte Chemie Int. Ed. 2009, 48, Jan Zarzycki, Volker Brecht, Michael Müller, Georg Fuchs, Final steps of an autotrophic pathway: closing the 3-hydroxypropionate bicycle in Chloroflexus aurantiacus, PNAS 2009, 106, Patrizia Lehwald, Michael Richter, Caroline Röhr, Hung-wen Liu, Michael Müller, Enantioselective Intermolecular Aldehyde-Ketone Cross-Coupling through an Enzymatic Carboligation Reaction, Angew. Chem. 2010, 122, ; Angew. Chem. Int. Ed. 2010, 49, Dörte Gocke, Geraldine Kolter, Michael Müller, Martina Pohl Entwicklung einer Enzymplattform für die biokatalytische C-C-Verknüpfung Chemie Ingenieur Technik 2010, 82, Wolfgang Hüttel, Michael Müller, Highlights 2009: Enzyme in der organischen Synthese, Nachr. Chem. 2010, 58, Martina Daum, Hans-Jörg Schnell, Simone Herrmann, Andreas Günther, Renato Murillo, Rolf Müller, Philippe Bisel, Michael Müller, Andreas Bechthold, Functions of Genes and Enzymes Involved in Phenalinolactone Biosynthesis, ChemBioChem 2010, 11, Carola Dresen, Michael Richter, Martina Pohl, Steffen Lüdeke, Michael Müller, The Enzymatic Asymmetric Conjugate Umpolung Reaction, Angew. Chem. 2010, 122, ; Angew. Chem. Int. Ed. 2010, 49, Johannes W. Kung, Sven Baumann, Martin von Bergen, Michael Müller, Peter-Leon Hagedoorn, Wilfred R. Hagen, Matthias Boll, Reversible Biological Birch Reduction at an Extremely Low Redox Potential, J. Am. Chem. Soc. 2010, 132, Wolfgang Hüttel, Michael Müller, Highlights 2010: Enzyme in der organischen Synthese, Nachr. Chem. 2011, 59, Danilo Meyer, Lydia Walter, Geraldine Kolter, Martina Pohl, Michael Müller, Kai Tittmann, Conversion of Pyruvate Decarboxylase into an Enantioselective Carboligase with Biosynthetic Potential, J. Am. Chem. Soc. 2011, 133, Dörte Rother, Geraldine Kolter, Tina Gerhards, Catrine L. Berthold, Ekaterina Gauchenova, Michael Knoll, Jürgen Pleiss, Michael Müller, Gunter Schneider, Martina Pohl, S-selective mixed carboligation by structure-based design of the pyruvate decarboxylase from Acetobacter pasteurianus, ChemCatChem 2011, 3, Syed Masood Husain, Thomas Stillger, Pascal Dünkelmann, Melanie Lödige, Lydia Walter, Elke Breitling, Martina Pohl, Mara Bürchner, Ingo Krossing, Michael Müller, Diego Romano, Francesco Molinari, Stereoselective Reduction of 2-Hydroxy Ketones towards syn- and anti-1,2-diols, Adv. Synth. Catal. 2011, 353, Johannes Bongaerts, Simon Esser, Volker Lorbach, Lóay Al-Momani, Michael A. Müller, Dirk Franke, Christoph Grondal, Anja Kurutsch, Robert Bujnicki, Ralf Takors, Leon Raeven, Marcel Wubbolts, Roel Bovenberg, Martin Nieger, Melanie Schürmann, Natalie Trachtmann, Stefan Kozak, Georg A. Sprenger, Michael Müller, Diversity-oriented production of metabolites derived from chorismate and their use in organic synthesis, Angew. Chem. 2011, 123, ; Angew. Chem. Int. Ed. 2011, 50,

9 124. Pascal Dünkelmann, Michael Müller, Enzymatic C-C coupling in the synthesis of fine chemcials, Speciality Chemicals Magazine 2011, 31, Regine Süss, Rolf Schubert, Irmgard Merfort, Michael Müller, Andreas Bechthold, Manfred Jung, Martin Müller, Rüdiger Holzbach, Ernst Pallenbach, Arzneimittelabhängigkeit und Suchtkrankheiten ein Beitrag der Klinischen Pharmazie Pharm. Ztg. 2011, 156, Michael Müller, Diversität asymmetrischer Thiamin-Katalyse, Biospektrum 2011, 17, ; und in Biochemie und molekulare Biologie Das Beste aus BIOspektrum, Ed. J. Alves, Springer Spektrum, Michael A. Schätzle, Stephan Flemming, Syed Masood Husain, Michael Richter, Stefan Günther, Michael Müller, Tetrahydroxynaphthalene Reductase Catalytic Properties of an Enzyme Involved in Reductive Asymmetric Naphthol Dearomatization, Angew. Chem. 2012, 124, ; Angew. Chem. Int. Ed. 2012, 51, Stefan Kneisel, Philippe Bisel, Volker Brecht, Sebastian Broecker, Michael Müller, Volker Auwärter, Identification of the cannabimimetic AM-1220 and its azepane isomer (N-methylazepan-3-yl)-3-(1- naphthoyl)indole in a research chemical and several herbal mixtures, Forensic Toxicol. 2012, 30, Syed Masood Husain, Michael A. Schätzle, Caroline Röhr, Steffen Lüdeke, Michael Müller, Biomimetic asymmetric synthesis of (R)-GTRI-02 and (3S,4R)-3,4-dihydroxy-3,4-dihydronaphthalen- 1(2H)-ones, Org. Lett. 2012, 14, Christian Gil Girol, Katja M. Fisch, Thorsten Heinekamp, Stefan Günther, Wolfgang Hüttel, Jörn Piel, Axel A. Brakhage, Michael Müller, Regio- and Stereoselective Oxidative Phenol Coupling in Aspergillus niger, Angew. Chem. 2012, 124, ; Angew. Chem. Int. Ed. 2012, 51, Martina Pohl, Carola Dresen, Maryam Beigi, Michael Müller, Enzymatic Acyloin and Benzoin Condensations, in Enzyme Catalysis in Organic Synthesis, Third Edition. Edited by Karlheinz Drauz, Harald Gröger, and Oliver May: Wiley-VCH, Weinheim, 2012 chapter 22, Jennifer Andexer, Michael Müller, Highlights 2011: Enzymreaktionen, Nachr. Chem. 2012, 60, Christian Gil Girol, Wolfgang Hüttel, Silke Fögen, Katja M. Fisch, Jörn Piel, Thorsten Heinekamp, Axel Brakhage, Michael Müller, Regio- and stereoselektive intermolecular oxidative phenol coupling in filamentous fungi, Pharmaceutical Biology 2012, 50, Michael A. Schätzle, Syed Masood Husain, Sascha Ferlaino, Michael Müller, Enzymatic reduction of anthrahydoquinones: implications für chrysophanol, monodictyphenone and related xanthone biosyntheses, J. Am. Chem. Soc. 2012, 134, Nadine Roth, Ariane Wohlfarth, Michael Müller, Volker Auwärter, Regioselective synthesis of isotopically labeled 9-tetrahydrocannabinolic acid A (THCA-A-D 3 ) by reaction of 9-tetrahydrocannabinol-D 3 with magnesium methyl carbonate, Forensic Sci. Int. 2012, 222, Michael Müller, Recent Developments in Enzymatic Asymmetric C-C Bond Formation, Adv. Synth. Catal. 2012, 354, Maryam Beigi, Sabrina Loschonsky, Patrizia Lehwald, Volker Brecht, Susana L. A. Andrade, Finian J. Leeper, Werner Hummel, Michael Müller, α-hydroxy-β-keto Acid Rearrangement Decarboxylation: Impact on ThDP-Dependent Enzymatic Transformations, Org. Biomol. Chem. 2013, 11,

10 138. Maryam Beigi, Simon Waltzer, Alexander Fries, Lothar Eggeling, Georg A. Sprenger, Michael Müller, TCA Cycle Involved Enzymes SucA and Kgd, as well as MenD: Efficient Biocatalysts for Asymmetric C C Bond Formation, Org. Lett. 2013, 15, Robert Westphal, Simon Waltzer, Ursula Mackfeld, Michael Widmann, Jürgen Pleiss, Maryam Beigi, Michael Müller, Dörte Rother, Martina Pohl, (S)-Selective MenD variants from Escherichia coli provide access to new functionalized chiral α- hydroxy ketones, Chem. Commun. 2013, 49, Jennifer Andexer, Michael Müller, Highlights 2012: Enzymreaktionen, Nachr. Chem. 2013, 61, Michael Müller, Georg A. Sprenger, Martina Pohl, C C Bond Formation Using ThDP-Dependent Lyases, Current Opinion Chem. Biol. 2013, 17, Michael Müller, Biokatalytische Synthese tertiärer Alkohole, Chemie Ingenieur Technik 2013, 85, Matthias Häckh, Michael Müller, Steffen Lüdeke, Substrate-Dependent Stereospecificity of Tyl-KR1, an Isolated Polyketide Synthase Ketoreductase Domain from Streptomyces fradiae, Chem. Eur. J. 2013, 19, Christian Eberlein, Sebastian Estelmann, Jana Seifert, Martin von Bergen, Michael Müller, Rainer U. Meckenstock, Matthias Boll, Identification and characterization of 2-naphthoyl-coenzyme A reductase, the prototype of a novel class of dearomatizing reductases, Mol. Microbiol. 2013, 88, Robert Westphal, Doris Hahn, Ursula Mackfeld, Simon Waltzer, Maryam Beigi, Michael Müller, Michael Widmann, Constatin Vogel, Jürgen Pleiss, Dörte Rother, Martina Pohl, Tailoring (S)-selectivity of MenD from Escherichia coli, ChemCatChem 2013, 5, Helen Hailes, Dörte Rother, Michael Müller, Robert Westphal, John Ward, Jürgen Pleiss, Constantin Vogel, Martina Pohl, Engineering Stereoselectivity of ThDP-dependent Enzymes, FEBS Journal 2013, 280, Robert Westphal, Sascha Jansen, Constantin Vogel, Jürgen Pleiss, Michael Müller, Dörte Rother, Martina Pohl, MenD from Bacillus subtilis: A Potent Catalyst for the Enantiocomplementary Asymmetric Synthesis of Functionalized α-hydroxy Ketones, ChemCatChem 2014, 6, Sabrina Loschonsky, Simon Waltzer, Sonja Fraas, Peter M. H. Kroneck, Tobias Wacker, Susana L. A. Andrade, Michael Müller, Catalytic Scope of Thiamine-Dependent Multifunctional Enzyme Cyclohexane-1,2-dione Hydrolase, ChemBioChem 2014, 15, Sabrina Loschonsky, Simon Waltzer, Michael Müller, Elucidation of the Enantioselective Cyclohexane-1,2-dione Hydrolase (CDH) Catalyzed Formation of (S)-Acetoin, ChemCatChem 2014, 6, Michael Müller, Enzymatic synthesis of tertiary alcohols, ChemBioEng Reviews 2014, 1, Petra Mußler, Michael Müller, Pharmazie quo vadis, Das Hochschulwesen 2014, (1+2),

11 152. Andreas Präg, Björn Andreas Grüning, Anika Erxleben, Matthias Häckh, Steffen Lüdeke, Andriy Luzhetskyy, Michael Richter, Marta Luzhetska, Stefan Günther, Michael Müller, Regio- and Stereoselective Intermolecular Oxidative Phenol Coupling in Streptomyces, J. Am. Chem. Soc. 2014, 136, Tobias Huber, Lisa Schneider, Andreas Präg, Stefan Gerhardt, Oliver Einsle, Michael Müller, Direct Reductive Amination of Ketones: Structure and Activity of (S)-Selective Imine Reductases from Streptomyces, ChemCatChem 2014, 6, Robert Westphal, Constantin Vogel, Carlo Schmitz, Jürgen Pleiss, Michael Müller, Martina Pohl, Dörte Rother, A Tailor-made Chimeric Thiamine Diphosphate Dependent Enzyme for the Direct Asymmetric Synthesis of (S)-Benzoins, Angew. Chem. 2014, 126, ; Angew. Chem. Int. Ed. 2014, 53, Syed Masood Husain, Michael A. Schätzle, Steffen Lüdeke, Michael Müller, Unprecedented role of hydronaphthoquinone tautomers in biosynthesis, Angew. Chem. 2014, 126, ; Angew. Chem. Int. Ed. 2014, 53, Elena Kasparyan, Michael Richter, Carola Dresen, Lydia S. Walter, Georg Fuchs, Finian J. Leeper, Tobias Wacker, Susana L. A. Andrade, Geraldine Kolter, Martina Pohl, Michael Müller, Asymmetric Stetter Reactions Catalyzed by Thiamine Diphosphate-Dependent Enzymes, Appl. Microbiol. Biotechnol. 2014, 98, Maryam Beigi, Simon Waltzer, Mostafa Zarfei, Michael Müller, New Stetter reactions catalyzed by Thiamine Diühosphate dependent MenD from E.coli, Journal of Biotechnology 2014, 191, Florian Hubrich, Michael Müller, Jennifer N. Andexer, In vitro production and purification of isochorismate using a two-enzyme cascade, Journal of Biotechnology 2014, 191, Sabrina Loschonsky, Tobias Wacker, Simon Waltzer, Pier Paolo Giovannini, Michael J. McLeish, Susana L. A. Andrade, Michael Müller, Extended Reaction Scope of Thiamine Diphosphate Dependent Cyclohexane-1,2-dione Hydrolase: From C C Bond Cleavage to C C Bond Ligation, Angew. Chem. 2014, 126, ; Angew. Chem. Int. Ed. 2014, 53, Martina Pohl, Cindy Wechsler, Michael Müller, Acyloin, Benzoin, and Related Reactions, in Science of Synthesis, Biocatalysis in Organic Synthesis 2 (Eds. K. Faber, W.-D. Fessner, N. J. Turner), Thieme, 2015, Giovanni Bernacchia, Olga Bortolini, Morena De Bastiani, Lindomar Alberto Lerin, Sabrina Loschonsky, Alessandro Massi, Michael Müller, Pier Paolo Giovannini, Enzymatic Chemoselective Aldehyde Ketone Cross-Couplings through the Polarity Reversal of Methylacetoin, Angew. Chem. 2015, 127, ; Angew. Chem. Int. Ed. 2015, 54, Dennis Wetzl, Marco Berrera, Nicolas Sandon, Dan Fishlock, Martin Ebeling, Michael Müller, Steven Paul Hanlon, Beat Wirz, Hans Iding, Expanding the imine reductase toolbox by exploring the bacterial protein-sequence space, ChemBioChem 2015, 16, David Conradt, Michael A. Schätzle, Julian Haas, Craig A. Townsend, Michael Müller, New Insights into the Conversion of Versicolorin A in the Biosynthesis of Aflatoxin B 1, J. Am. Chem. Soc. 2015, 137, Florian Hubrich, Puneet Juneja, Michael Müller, Kay Diederichs, Wolfram Welte, and Jennifer N. Andexer, Chorismatase Mechanisms Reveal Fundamentally Different Types of Reaction in a Single Conserved Protein Fold, J. Am. Chem. Soc. 2015, 137, David Conradt, Michael A. Schätzle, Syed Masood Husain, Michael Müller, Diversity in Reduction with Short-Chain Dehydrogenases: Tetrahydroxynaphthalene Reductase, Trihydroxynaphthalene Reductase, and Glucose Dehydrogenase, ChemCatChem 2015, 7,

12 166. Laura S. Mazzaferro, Wolfgang Hüttel, Alexander Fries, Michael Müller, Cytochrome P450-Catalyzed Regio- and Stereoselective Phenol Coupling of Fungal Natural Products, J. Am. Chem. Soc. 2015, 137, Cindy Wechsler, Danilo Meyer, Sabrina Loschonsky, Lisa-Marie Funk, Piotr Neumann, Ralf Ficner, Florian Brodhun, Michael Müller, Kai Tittmann, Tuning and switching enantioselectivity of asymmetric carboligation in an enzyme through mutational analysis of a single hot spot, ChemBioChem 2015, 16, Stefanie Houwaart, Dominik Baltes, Jonas Pavelka, Michael Müller, Forschungsethik Verantwortung des Naturwissenschaftlers im interdisziplinären Dialog, in Zufallsbefunde bei molekulargenetischen Untersuchungen; Medizinische, juristische und ethische Perspektiven; (Hrsg. Martin Langanke, Pia Erdmann, Jürgen Robienski, Sabine Rudnik- Schöneborn), Springer Verlag, Berlin Heidelberg, 2015, Georg Fuchs, Michael Müller, Hermann Staudinger, in 80 Jahre Rotary Club Freiburg, Herder Verlag, 2015, Georg Fuchs, Michael Müller, Arthur Lüttringhaus, in 80 Jahre Rotary Club Freiburg, Herder Verlag, 2015, Michael Müller, Kurt Walther Merz, in 80 Jahre Rotary Club Freiburg, Herder Verlag, 2015, Markus Warnke, Tobias Jung, Juri Dermer, Karin Hipp, Nico Jehmlich, Martin von Bergen, Sascha Ferlaino, Alexander Fries, Michael Müller, Matthias Boll, 25-Hydroxyvitamin D3 synthesis by enzymatic steroid side chain hydroxylation with water, Angew. Chem. 2016, 128, ; Angew. Chem. Int. Ed. 2016, 55, Julian Haas, Michael A. Schätzle, Syed M. Husain, Johannes Schulz-Fincke, Manfred Jung, Werner Hummel, Michael Müller, Steffen Lüdeke, A quinone mediator drives oxidations catalysed by alcohol dehydrogenase-containing cell lysates, Chem. Commun. 2016, 52, Dennis Wetzl, Martin Gand, Alfred Ross, Hubertus Müller, Philipp Matzel, Steven Hanlon, Michael Müller, Beat Wirz, Matthias Höhne, Hans Iding, Asymmetric Reductive (Alkyl)Amination of Ketones catalyzed by Imine Reductases, ChemCatChem 2016, 8, Patrizia Lehwald, Olga Fuchs, Laurence A. Nafie, Michael Müller, Steffen Lüdeke, Substrate-determined diastereoselectivity in an enzymatic carboligation, ChemBioChem 2016, 17, Mayram Beigi, Ekatarina Gauchenova, Lydia Walter, Simon Waltzer, Fabrizio Bonina, Thomas Stillger, Dörte Rother, Martina Pohl, Michael Müller, Regio- and Stereoselective Aliphatic Aromatic Cross-Benzoin Reaction: Enzymatic Divergent Catalysis, Chem. Eur. J. 2016, 22, Pier Paolo Giovannini, Lindomar Alberto Lerin, Michael Müller, Giovanni Bernacchia, Morena De Bastiani, Martina Catani, Graziano di Carmine, Alessandro Massi, (S)-Selectivity in Phenylacetyl Carbinols Synthesis Using the Wild-Type Enzyme Acetoin:Dichlorophenolindophenol Oxidoreductase from Bacillus licheniformis, Adv. Synth. Catal. 2016, 358, Carola Dresen, Elena Kasparyan, Lydia S. Walter, Fabrizio Bonina, Simon Waltzer, Michael Müller, Stetter Reactions Catalyzed by Thiamine Diphosphate-Dependent Enzymes, in Practical Methods for Biocatalysis and Biotransformations 3 (Eds. J. Whittall, P. W. Sutton, W. Kroutil), Wiley, 2016, Michael A. Schätzle, Syed Masood Husain, Michael Müller, Tetrahydroxynaphthalene Reductase: Broad Substrate Range of an NADPH-Dependent Oxidoreductase Involved in Reductive Asymmetric Naphthol Dearomatization, in Practical Methods for Biocatalysis and Biotransformations 3 (Eds. J. Whittall, P. W. Sutton, W. Kroutil), Wiley, 2016, Thorsten Friedrich, Petra Mußler, Thomas Kenkmann, Michael Müller, Interdisziplinäre Studiengangsentwicklung der Fakultät für Chemie, Pharmazie und Geowissenschaften, in Kreativ, Innovativ, Motivierend Lehrkonzepte in der Praxis, Albert-Ludwigs-Universität Freiburg (Hg), Universitätsverlag Webler, 2016,

13 181. Oliver Tiedt, Mario Mergelsberg, Kerstin Boll, Michael Müller, Lorenz Adrian, Nico Jehmlich, Martin von Bergen, Matthias Boll, ATP-dependent C-F bond cleavage allows the complete degradation of 4-fluoroaromatics without oxygen, mbio 2016, 7(4):e doi: /mbio David Conradt, Bianca Hermann, Stefan Gerhardt, Oliver Einsle, Michael Müller, Identification and Biocatalytic Properties of Phloroglucinol Reductases, Angew. Chem. 2016, 128, (in press)

Publications. Prof. Dr. Martina Pohl

Publications. Prof. Dr. Martina Pohl Publications 2015 Diener M, Kopka B, Pohl M, Jaeger KE, Krauss U. 2015. Fusion of a coil-coiled domain facilitates the high-level production of catalytically-active enzyme inclusion bodies. ChemCatChem,

More information

ω-transaminase from Ochrobactrum anthropi Is Devoid of Substrate and Product Inhibitions

ω-transaminase from Ochrobactrum anthropi Is Devoid of Substrate and Product Inhibitions AEM Accepts, published online ahead of print on 12 April 2013 Appl. Environ. Microbiol. doi:10.1128/aem.03811-12 Copyright 2013, American Society for Microbiology. All Rights Reserved. (Enzymology and

More information

Properties of a molecule. Absolute configuration, Cahn-Ingold Prelog. Planar, axial, topological chirality and chirality at atoms other than carbon

Properties of a molecule. Absolute configuration, Cahn-Ingold Prelog. Planar, axial, topological chirality and chirality at atoms other than carbon Key stereochemical terminology Stereochemical terminology in organic chemistry can refer to structure of a molecule or to properties of a physical sample of the molecule. It is very important to recognize

More information

ENZYMES FOR BIOCATALYSIS

ENZYMES FOR BIOCATALYSIS ENZYMES FOR BIOCATALYSIS for smarter chemical synthesis Graphical representation of alcalase molecule Rethink Tomorrow Proteases Biocatalysis Biocatalysis involves the implementation of natural catalysts,

More information

Anabolic and Catabolic Reactions are Linked by ATP in Living Organisms

Anabolic and Catabolic Reactions are Linked by ATP in Living Organisms Chapter 5: Microbial Metabolism Microbial Metabolism Metabolism refers to all chemical reactions that occur within a living a living organism. These chemical reactions are generally of two types: Catabolic:

More information

The Citric Acid Cycle

The Citric Acid Cycle The itric Acid ycle February 14, 2003 Bryant Miles I. itrate Synthase + 3 SoA The first reaction of the citric acid cycle is the condensation of acetyloa and oxaloacetate to form citrate and oas. The enzyme

More information

UNIVERSITY OF PÉCS. Palladium-catalysed aminocarbonylation reactions of iodoarenes and iodoalkenes. Attila Takács

UNIVERSITY OF PÉCS. Palladium-catalysed aminocarbonylation reactions of iodoarenes and iodoalkenes. Attila Takács UNIVERSITY OF PÉCS Doctoral School of Chemistry Palladium-catalysed aminocarbonylation reactions of iodoarenes and iodoalkenes PhD Thesis Attila Takács Supervisor: Dr. László Kollár professor PÉCS, 2014

More information

Reactions of Fats and Fatty Acids

Reactions of Fats and Fatty Acids Reactions of Fats and Fatty Acids Outline Fats and Oils Fatty Acid Biosynthesis Biodiesel Homework We hear quite a lot about the place of fats and oils in human nutrition. Foods high in fat are at the

More information

CELLULAR RESPIRATION. Chapter 19 & 20. Biochemistry by Campbell and Farell (7 th Edition) By Prof M A Mogale

CELLULAR RESPIRATION. Chapter 19 & 20. Biochemistry by Campbell and Farell (7 th Edition) By Prof M A Mogale CELLULAR RESPIRATION Chapter 19 & 20 Biochemistry by Campbell and Farell (7 th Edition) By Prof M A Mogale 1. Cellular respiration (energy capture) The enzymatic breakdown of food stuffs in the presence

More information

Copyright 2000-2003 Mark Brandt, Ph.D. 54

Copyright 2000-2003 Mark Brandt, Ph.D. 54 Pyruvate Oxidation Overview of pyruvate metabolism Pyruvate can be produced in a variety of ways. It is an end product of glycolysis, and can be derived from lactate taken up from the environment (or,

More information

MULTIPLE CHOICE QUESTIONS

MULTIPLE CHOICE QUESTIONS MULTIPLE CHOICE QUESTIONS 1. Most components of energy conversion systems evolved very early; thus, the most fundamental aspects of energy metabolism tend to be: A. quite different among a diverse group

More information

Microbial Metabolism. Biochemical diversity

Microbial Metabolism. Biochemical diversity Microbial Metabolism Biochemical diversity Metabolism Define Requirements Energy Enzymes Rate Limiting step Reaction time Types Anabolic Endergonic Dehydration Catabolic Exergonic Hydrolytic Metabolism

More information

Introduction to Proteins and Enzymes

Introduction to Proteins and Enzymes Introduction to Proteins and Enzymes Basics of protein structure and composition The life of a protein Enzymes Theory of enzyme function Not all enzymes are proteins / not all proteins are enzymes Enzyme

More information

How To Learn Chemistry And Biochemistry

How To Learn Chemistry And Biochemistry SUBJECT OUTLINE Subject Name: Chemistry and Biochemistry SECTION 1 GENERAL INFORMATION Subject Code: BIOB111 Award/s: Total course credit points: Level: Bachelor of Health Science (Naturopathy) 128 Core

More information

Chemistry and Biochemistry

Chemistry and Biochemistry SUBJECT OUTLINE Subject Name: Chemistry and Biochemistry SECTION 1 GENERAL INFORMATION Subject Code: BIOB111 Award/s: Total course credit points: Level: Bachelor of Health Science (Naturopathy) 128 Core

More information

The Aerobic Fate of Pyruvate

The Aerobic Fate of Pyruvate The Aerobic Fate of yruvate February 12, 2003 Bryant Miles I could tell that some of you were not impressed by the mere 2 ATs produced per glucose by glycolysis. The 2 AT s produced are only a small fraction

More information

What affects an enzyme s activity? General environmental factors, such as temperature and ph. Chemicals that specifically influence the enzyme.

What affects an enzyme s activity? General environmental factors, such as temperature and ph. Chemicals that specifically influence the enzyme. CH s 8-9 Respiration & Metabolism Metabolism A catalyst is a chemical agent that speeds up a reaction without being consumed by the reaction. An enzyme is a catalytic protein. Hydrolysis of sucrose by

More information

Chapter 3 Molecules of Cells

Chapter 3 Molecules of Cells Bio 100 Molecules of cells 1 Chapter 3 Molecules of Cells Compounds containing carbon are called organic compounds Molecules such as methane that are only composed of carbon and hydrogen are called hydrocarbons

More information

Enzymes: Introduction

Enzymes: Introduction Enzymes: Introduction Firefly bioluminescence is produced by an oxidation reaction catalyzed by the enzyme firefly luciferase. The oxidized substrate (product of the reaction) is in an electronically excited

More information

Citric Acid Cycle. Cycle Overview. Metabolic Sources of Acetyl-Coenzyme A. Enzymes of the Citric Acid Cycle. Regulation of the Citric Acid Cycle

Citric Acid Cycle. Cycle Overview. Metabolic Sources of Acetyl-Coenzyme A. Enzymes of the Citric Acid Cycle. Regulation of the Citric Acid Cycle Citric Acid Cycle Cycle Overview Metabolic Sources of Acetyl-Coenzyme A Enzymes of the Citric Acid Cycle Regulation of the Citric Acid Cycle The Amphibolic Nature of the Citric Acid Cycle Cycle Overview

More information

Cellular Respiration and Fermentation

Cellular Respiration and Fermentation LECTURE PRESENTATIONS For CAMPBELL BIOLOGY, NINTH EDITION Jane B. Reece, Lisa A. Urry, Michael L. Cain, Steven A. Wasserman, Peter V. Minorsky, Robert B. Jackson Chapter 9 Cellular Respiration and Fermentation

More information

Bioenergetics. Free Energy Change

Bioenergetics. Free Energy Change Bioenergetics Energy is the capacity or ability to do work All organisms need a constant supply of energy for functions such as motion, transport across membrane barriers, synthesis of biomolecules, information

More information

Asymmetric Epoxidation of Pentadienols

Asymmetric Epoxidation of Pentadienols 10 Asymmetric Epoxidation of Pentadienols Asymmetric Epoxidation of Pentadienols Reinhard Brçckner, University of Freiburg, Germany Background The asymmetric epoxidation of allylic alcohols or Sharpless

More information

FHI Biotech Conference

FHI Biotech Conference Biocatalytic xidation of Alcohols FH Biotech Conference Leiden sabel Arends June 21, 2007 1 Biocatalysis Vermelding onderdeel and rganic organisatie Chemistry Catalytic xidations Using 2, H 2 2 (acl) Peroxidases

More information

Figure 5. Energy of activation with and without an enzyme.

Figure 5. Energy of activation with and without an enzyme. Biology 20 Laboratory ENZYMES & CELLULAR RESPIRATION OBJECTIVE To be able to list the general characteristics of enzymes. To study the effects of enzymes on the rate of chemical reactions. To demonstrate

More information

Fields of Application / Industry:

Fields of Application / Industry: = Fields of Application / Industry: Chemistry / Polymer Industry Clinical Chemistry / Medicine / Hygiene / Health Care Cosmetics Electronics Energy Environment / Water / Waste Food / Agriculture Geology

More information

How to build a comprehensive knowledge platform in Norway Opportunities through cooperation Potential for a "Norwegian BIC"

How to build a comprehensive knowledge platform in Norway Opportunities through cooperation Potential for a Norwegian BIC Biorefinery / Biobased Economy How to build a comprehensive knowledge platform in Norway Opportunities through cooperation Potential for a "Norwegian BIC" Realising the potential of Biorefinery related

More information

Chair of Chemistry of Biogenic Resources TU München - R&D activities -

Chair of Chemistry of Biogenic Resources TU München - R&D activities - Chair of Chemistry of Biogenic Resources TU München - R&D activities - Chair of Chemistry of Biogenic Resources Schulgasse 18, 94315 Straubing, Germany Sieber@tum.de www.rohstoffwandel.de Locations Freising

More information

Transition from Working Life into Retirement: Successful and Precarious Ways Associate HTProfessorTH Dr. Martin Brussig

Transition from Working Life into Retirement: Successful and Precarious Ways Associate HTProfessorTH Dr. Martin Brussig INDEX 2011 EDITORIAL LIST: UPOVERTY IN OLD AGE Areas of Research concerning Old-Age Poverty Dr. Jürgen Faik, Dr. Tim Köhler-Rama Old-Age Poverty in Germany Present Data Ulrich Bieber, Dr. Michael Stegmann

More information

Chemistry 20 Chapters 15 Enzymes

Chemistry 20 Chapters 15 Enzymes Chemistry 20 Chapters 15 Enzymes Enzymes: as a catalyst, an enzyme increases the rate of a reaction by changing the way a reaction takes place, but is itself not changed at the end of the reaction. An

More information

AP BIOLOGY CHAPTER 7 Cellular Respiration Outline

AP BIOLOGY CHAPTER 7 Cellular Respiration Outline AP BIOLOGY CHAPTER 7 Cellular Respiration Outline I. How cells get energy. A. Cellular Respiration 1. Cellular respiration includes the various metabolic pathways that break down carbohydrates and other

More information

Lecture 3: Biodegradable Polymers

Lecture 3: Biodegradable Polymers 4A3 Advanced Polymer Synthesis Lecture 3: Biodegradable Polymers 4A3 - Slide 40 Learning outcomes By the end of todays lecture you should be able to: (i) discuss what biodegradability means, and why it

More information

CHM333 LECTURE 13 14: 2/13 15/13 SPRING 2013 Professor Christine Hrycyna

CHM333 LECTURE 13 14: 2/13 15/13 SPRING 2013 Professor Christine Hrycyna INTRODUCTION TO ENZYMES Enzymes are usually proteins (some RNA) In general, names end with suffix ase Enzymes are catalysts increase the rate of a reaction not consumed by the reaction act repeatedly to

More information

Chapter 9 Mitochondrial Structure and Function

Chapter 9 Mitochondrial Structure and Function Chapter 9 Mitochondrial Structure and Function 1 2 3 Structure and function Oxidative phosphorylation and ATP Synthesis Peroxisome Overview 2 Mitochondria have characteristic morphologies despite variable

More information

Curriculum Vitae. Dr. Dilek Işık Taşgın

Curriculum Vitae. Dr. Dilek Işık Taşgın Curriculum Vitae Dr. Dilek Işık Taşgın Phone: +90-(312)-233 1405 E-mail: ditasgin@cankaya.edu.tr EDUCATION 2006-2013 Hacettepe University, Ankara, Turkey Ph.D. in organic chemistry Dissertation: Michael

More information

Chapter 16 The Citric Acid Cycle

Chapter 16 The Citric Acid Cycle Chapter 16 The Citric Acid Cycle Multiple Choice Questions 1. Which of the following is not true of the reaction catalyzed by the pyruvate dehydrogenase complex? A) Biotin participates in the decarboxylation.

More information

INDUSTRIAL BIOTECHNOLOGY. Production hosts for real-life feedstock utilization

INDUSTRIAL BIOTECHNOLOGY. Production hosts for real-life feedstock utilization Selection of production hosts for real-life feedstock utilization Karl Rumbold (karl.rumbold@tno.nl) INDUSTRIAL BIOTECHNOLOGY Industrial Biotechnology is the application of biotechnology for the processing

More information

CHEM 208(Organic Chemistry I) Instructor: Dr. Niranjan Goswami. Tel: (618)545-3361. Email: Ngoswami@kaskaskia.edu. Web: www.kc.cc.il.

CHEM 208(Organic Chemistry I) Instructor: Dr. Niranjan Goswami. Tel: (618)545-3361. Email: Ngoswami@kaskaskia.edu. Web: www.kc.cc.il. CHEM 208(Organic Chemistry I) Instructor: Dr. Niranjan Goswami Tel: (618)545-3361 Email: Ngoswami@kaskaskia.edu Web: www.kc.cc.il.us/ngoswami CHEM 208 COURSE SYLLABUS KASKASKIA COLLEGE NAME TERM YEAR TEXT:

More information

Aminocatalytic Asymmetric Diels-Alder Reactions: HOMO Activation and the Power of Many Pathways

Aminocatalytic Asymmetric Diels-Alder Reactions: HOMO Activation and the Power of Many Pathways Aminocatalytic Asymmetric Diels-Alder Reactions: HOMO Activation and the Power of Many Pathways Brought to you by: Li, J. -L.; Liu, T. -Y.; Chen, Y. -C. Acc. Chem. Res. 2012, 45, 1491 1500. and Barbra

More information

How To Understand The Chemistry Of An Enzyme

How To Understand The Chemistry Of An Enzyme Chapt. 8 Enzymes as catalysts Ch. 8 Enzymes as catalysts Student Learning Outcomes: Explain general features of enzymes as catalysts: Substrate -> Product Describe nature of catalytic sites general mechanisms

More information

SPRIN CALB Kit. Content Code Description Application. B from Candida antarctica on Polystyrene Resin. Acrylic Resin

SPRIN CALB Kit. Content Code Description Application. B from Candida antarctica on Polystyrene Resin. Acrylic Resin SPRIN CALB Kit SPRIN CALB Kit (20 g each) Product code: SCAK Kit content: Content Code Description Application SPRIN actisorb CALB LCAHNHE Adsorbed preparation of Lipase B from Candida antarctica on Polystyrene

More information

Lecture 10 Enzymes: Introduction

Lecture 10 Enzymes: Introduction Lecture 10 Enzymes: Introduction Reading: Berg, Tymoczko & Stryer, 6th ed., Chapter 8, pp. 205-217 (These pages in textbook are very important -- concepts of thermodynamics are fundamental to all of biochemistry.)

More information

1. A covalent bond between two atoms represents what kind of energy? a. Kinetic energy b. Potential energy c. Mechanical energy d.

1. A covalent bond between two atoms represents what kind of energy? a. Kinetic energy b. Potential energy c. Mechanical energy d. 1. A covalent bond between two atoms represents what kind of energy? a. Kinetic energy b. Potential energy c. Mechanical energy d. Solar energy A. Answer a is incorrect. Kinetic energy is the energy of

More information

Cleavage of Cyclobutanols and Cyclobutanones

Cleavage of Cyclobutanols and Cyclobutanones Literature Report VII Transition Metal-Catalyzed Enantioselective C-C C Bond Cleavage of Cyclobutanols and Cyclobutanones Huang, W.-X. checker: Yu, C.-B. 2014-04-2904 29 1 Contents 1. Background Information

More information

Prof. Dr. Burkhard König, Institut für Organische Chemie, Uni Regensburg 1. Enolate Chemistry

Prof. Dr. Burkhard König, Institut für Organische Chemie, Uni Regensburg 1. Enolate Chemistry Prof. Dr. Burkhard König, Institut für rganische Chemie, Uni Regensburg 1 1. Some Basics Enolate Chemistry In most cases the equilibrium lies almost completely on the side of the ketone. The ketone tautomer

More information

Chapter 16 The Citric Acid Cycle

Chapter 16 The Citric Acid Cycle Chapter 16 The Citric Acid Cycle Multiple Choice Questions 1. Production of acetyl-coa (activated acetate) Page: 603 Difficulty: 2 Ans: A Which of the following is not true of the reaction catalyzed by

More information

Disaccharides consist of two monosaccharide monomers covalently linked by a glycosidic bond. They function in sugar transport.

Disaccharides consist of two monosaccharide monomers covalently linked by a glycosidic bond. They function in sugar transport. 1. The fundamental life processes of plants and animals depend on a variety of chemical reactions that occur in specialized areas of the organism s cells. As a basis for understanding this concept: 1.

More information

Chapter 22 Carbonyl Alpha-Substitution Reactions

Chapter 22 Carbonyl Alpha-Substitution Reactions John E. McMurry www.cengage.com/chemistry/mcmurry Chapter 22 Carbonyl Alpha-Substitution Reactions The α Position The carbon next to the carbonyl group is designated as being in the α position Electrophilic

More information

Summary of Metabolism. Mechanism of Enzyme Action

Summary of Metabolism. Mechanism of Enzyme Action Summary of Metabolism Mechanism of Enzyme Action 1. The substrate contacts the active site 2. The enzyme-substrate complex is formed. 3. The substrate molecule is altered (atoms are rearranged, or the

More information

Enzyme Response Profiling: Integrating proteomics and genomics with xenobiotic metabolism and cytotoxicity

Enzyme Response Profiling: Integrating proteomics and genomics with xenobiotic metabolism and cytotoxicity Enzyme Response Profiling: Integrating proteomics and genomics with xenobiotic metabolism and cytotoxicity Proteomics high throughput separation and characterization of expressed proteins in tissue and

More information

Carbohydrates, proteins and lipids

Carbohydrates, proteins and lipids Carbohydrates, proteins and lipids Chapter 3 MACROMOLECULES Macromolecules: polymers with molecular weights >1,000 Functional groups THE FOUR MACROMOLECULES IN LIFE Molecules in living organisms: proteins,

More information

BIOCHEMICAL TECHNOLOGY PROGRAM

BIOCHEMICAL TECHNOLOGY PROGRAM BIOCHEMICAL TECHNOLOGY PROGRAM The division of biochemical technology offers graduate program leading to a Master of Science in Biochemical Technology and a Doctor of Philosophy in Biochemical Technology.

More information

Services and their Composition

Services and their Composition Andreas Schönberger, Oliver Kopp, Niels Lohmann (eds.) Services and their Composition 4th Central European Workshop on Services and their Composition 4. Zentral-europäischer Workshop über Services und

More information

Syllabus for General Organic Chemistry M07A- Fall 2013 Prof. Robert Keil

Syllabus for General Organic Chemistry M07A- Fall 2013 Prof. Robert Keil Syllabus for General Organic Chemistry M07A- Fall 2013 Prof. Robert Keil Textbook and Materials What you must buy: Organic Chemistry 4 th Ed. Janice G. Smith, McGraw Hill. (Older edition is fine) Chem

More information

Chapter 3. Protein Structure and Function

Chapter 3. Protein Structure and Function Chapter 3 Protein Structure and Function Broad functional classes So Proteins have structure and function... Fine! -Why do we care to know more???? Understanding functional architechture gives us POWER

More information

The Molecules of Life - Overview. The Molecules of Life. The Molecules of Life. The Molecules of Life

The Molecules of Life - Overview. The Molecules of Life. The Molecules of Life. The Molecules of Life The Molecules of Life - Overview The Molecules of Life The Importance of Carbon Organic Polymers / Monomers Functions of Organic Molecules Origin of Organic Molecules The Molecules of Life Water is the

More information

Chapter 11 Homework and practice questions Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations

Chapter 11 Homework and practice questions Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations Chapter 11 Homework and practice questions Reactions of Alkyl Halides: Nucleophilic Substitutions and Eliminations SHORT ANSWER Exhibit 11-1 Circle your response in each set below. 1. Circle the least

More information

"Small and large molecules bioproduction by mammalian and microbial fermentation"

Small and large molecules bioproduction by mammalian and microbial fermentation "Small and large molecules bioproduction by mammalian and microbial fermentation" H.-P. Meyer Bio/PharMOS 2004-23-25 March 2004 Symposium B Business Diversification in Life Science "Small and large molecules

More information

Chapter 5 Classification of Organic Compounds by Solubility

Chapter 5 Classification of Organic Compounds by Solubility Chapter 5 Classification of Organic Compounds by Solubility Deductions based upon interpretation of simple solubility tests can be extremely useful in organic structure determination. Both solubility and

More information

Table of contents. Bibliografische Informationen http://d-nb.info/1006571213. digitalisiert durch

Table of contents. Bibliografische Informationen http://d-nb.info/1006571213. digitalisiert durch 1. Research scope: The role of structure rigid'tf'ication in nature and chemistry 1 2. Establishing a Dha=Tap backbone scan in order to elucidate structural properties of the N-terminusofNPY 5 2.1 Introduction.

More information

Course Prerequisite: Chemistry 141 or 143.

Course Prerequisite: Chemistry 141 or 143. Instructor: Matthias Brewer; Office: Cook A316; email: Matthias.Brewer@uvm.edu BlackBoard Site: bb.uvm.edu Lecture: 10:40am 11:30am MWF, Angell B106 Review Sessions: 5:30pm Thur., Angell B106 Laboratory

More information

Van batch naar flow: paradigmaverschuiving in de organische synthese

Van batch naar flow: paradigmaverschuiving in de organische synthese Van batch naar flow: paradigmaverschuiving in de organische synthese Floris Rutjes Instituut voor Moleculen en Materialen Radboud Universiteit Nijmegen F.Rutjes@science.ru.nl Labanalyse 2009 8 oktober

More information

SYNTHETIC STUDIES ON TULEARIN MACROLIDES. M.Montserrat Martínez, Luis A. Sarandeses, José Pérez Sestelo

SYNTHETIC STUDIES ON TULEARIN MACROLIDES. M.Montserrat Martínez, Luis A. Sarandeses, José Pérez Sestelo SYNTHETIC STUDIES N TULEARIN MACRLIDES M.Montserrat Martínez, Luis A. Sarandeses, José Pérez Sestelo Departamento de Química Fundamental, Universidade da Coruña, E-15071 A Coruña, Spain E-mail: mmartinezc@udc.es

More information

Curriculum for Structured Doctoral Candidate Training at the Heinrich Pette Institute Leibniz Institute for Experimental Virology

Curriculum for Structured Doctoral Candidate Training at the Heinrich Pette Institute Leibniz Institute for Experimental Virology Curriculum for Structured Doctoral Candidate Training at the Heinrich Pette Institute Leibniz Institute for Experimental Virology Please choose lectures and courses according to your interests and requirements.

More information

CHM333 LECTURE 13 14: 2/13 15/12 SPRING 2012 Professor Christine Hrycyna

CHM333 LECTURE 13 14: 2/13 15/12 SPRING 2012 Professor Christine Hrycyna INTRODUCTION TO ENZYMES Enzymes are usually proteins (some RNA) In general, names end with suffix ase Enzymes are catalysts increase the rate of a reaction not consumed by the reaction act repeatedly to

More information

Alcohols An alcohol contains a hydroxyl group ( OH) attached to a carbon chain. A phenol contains a hydroxyl group ( OH) attached to a benzene ring.

Alcohols An alcohol contains a hydroxyl group ( OH) attached to a carbon chain. A phenol contains a hydroxyl group ( OH) attached to a benzene ring. Chapter : rganic Compounds with xygen Alcohols, Ethers Alcohols An alcohol contains a hydroxyl group ( H) attached to a carbon chain. A phenol contains a hydroxyl group ( H) attached to a benzene ring.

More information

Regulation of enzyme activity

Regulation of enzyme activity 1 Regulation of enzyme activity Regulation of enzyme activity is important to coordinate the different metabolic processes. It is also important for homeostasis i.e. to maintain the internal environment

More information

CURRICULUM VITAE. Yong-Cheol Park, Ph.D.

CURRICULUM VITAE. Yong-Cheol Park, Ph.D. CURRICULUM VITAE Yong-Cheol Park, Ph.D. Postdoctoral Research Associate Department of Biochemistry and Cell Biology, Rice University, Houston, TX 77005-1892, U.S.A. Tel) 1-713-348-3304, Fax) 1-713-348-5154,

More information

BERGEN COMMUNITY COLLEGE DIVISION OF MATHEMATICS, SCIENCE AND TECHNOLOGY DEPARTMENT OF PHYSICAL SCIENCES STUDENT COURSE OUTLINE

BERGEN COMMUNITY COLLEGE DIVISION OF MATHEMATICS, SCIENCE AND TECHNOLOGY DEPARTMENT OF PHYSICAL SCIENCES STUDENT COURSE OUTLINE BERGEN COMMUNITY COLLEGE DIVISION OF MATHEMATICS, SCIENCE AND TECHNOLOGY DEPARTMENT OF PHYSICAL SCIENCES STUDENT COURSE OUTLINE Course Title: Prerequisites: Course Description: Textbook: CHM 212 Organic

More information

Chem 306 Chapter 21 Bioenergetics Lecture Outline III

Chem 306 Chapter 21 Bioenergetics Lecture Outline III Chem 306 Chapter 21 Bioenergetics Lecture Outline III I. HOW IS ATP GENERATED IN THE FINAL STAGE CATABOLISM? A. OVERVIEW 1. At the end of the citric acid cycle, all six carbons of glucose have been oxidized

More information

Preliminary MFM Quiz

Preliminary MFM Quiz Preliminary MFM Quiz 1. The major carrier of chemical energy in all cells is: A) adenosine monophosphate B) adenosine diphosphate C) adenosine trisphosphate D) guanosine trisphosphate E) carbamoyl phosphate

More information

Publikationsliste Claudia Götz

Publikationsliste Claudia Götz Publikationsliste Claudia Götz 1. Reinhard,B., Götz, C., and Faillard, H.: Synthesis of N-Acetyl-9-Oacetylneuraminic acid α-p-aminophenylthioketoside and its application as ligand in the affinity chromatography

More information

Methods of Grading S/N Style of grading Percentage Score 1 Attendance, class work and assignment 10 2 Test 20 3 Examination 70 Total 100

Methods of Grading S/N Style of grading Percentage Score 1 Attendance, class work and assignment 10 2 Test 20 3 Examination 70 Total 100 COURSE: MIB 303 Microbial Physiology and Metabolism (3 Units- Compulsory) Course Duration: Three hours per week for 15 weeks (45 hours). Lecturer: Jimoh, S.O. B.Sc., M.Sc, Ph.D Microbiology (ABU, Zaria)

More information

Catalysis by Enzymes. Enzyme A protein that acts as a catalyst for a biochemical reaction.

Catalysis by Enzymes. Enzyme A protein that acts as a catalyst for a biochemical reaction. Catalysis by Enzymes Enzyme A protein that acts as a catalyst for a biochemical reaction. Enzymatic Reaction Specificity Enzyme Cofactors Many enzymes are conjugated proteins that require nonprotein portions

More information

Chapter 14- RESPIRATION IN PLANTS

Chapter 14- RESPIRATION IN PLANTS Chapter 14- RESPIRATION IN PLANTS Living cells require a continuous supply of energy for maintaining various life activities. This energy is obtained by oxidizing the organic compounds (carbohydrates,

More information

NO CALCULATORS OR CELL PHONES ALLOWED

NO CALCULATORS OR CELL PHONES ALLOWED Biol 205 Exam 1 TEST FORM A Spring 2008 NAME Fill out both sides of the Scantron Sheet. On Side 2 be sure to indicate that you have TEST FORM A The answers to Part I should be placed on the SCANTRON SHEET.

More information

Mitsunobu Reaction (1934-2003)

Mitsunobu Reaction (1934-2003) Mitsunobu eaction (1934-2003) utline General Information: Who discovered this? What is the basic reaction? The Mechanism: What exactly happens and how? Applications: i) Variations of the method- where

More information

Enzymes and Metabolism

Enzymes and Metabolism Enzymes and Metabolism Enzymes and Metabolism Metabolism: Exergonic and Endergonic Reactions Chemical Reactions: Activation Every chemical reaction involves bond breaking and bond forming A chemical reaction

More information

Analysis of structural dynamics by H/D-exchange coupled to mass spectrometry HDX-MS

Analysis of structural dynamics by H/D-exchange coupled to mass spectrometry HDX-MS Analysis of structural dynamics by H/D-exchange coupled to mass spectrometry () New Approaches in Drug Design & Discovery 2014 25 th of March 2014 Introduction What are the challenges in structure-based

More information

Change Management in Tourism

Change Management in Tourism Change Management in Tourism From Old to New Tourism Edited by Christopher Kronenberg, Sabine Müller, Prof. Dr. Mike Peters, Dr. Birgit Pikkemaat and Prof. Dr. Klaus Weiermair With Contributions by Gerald

More information

Enzymes. Enzyme Structure. Enzyme Classification. CHEM464/Medh, J.D. Reaction Rate and Enzyme Activity

Enzymes. Enzyme Structure. Enzyme Classification. CHEM464/Medh, J.D. Reaction Rate and Enzyme Activity Enzymes Enzymes are biological catalysts They are not consumed or altered during the reaction They do not change the equilibrium, just reduce the time required to reach equilibrium. They increase the rate

More information

Descendants of Friedrich Ohlhausen Sr. Family History

Descendants of Friedrich Ohlhausen Sr. Family History Descendants of Friedrich Ohlhausen Sr. Family History Generation One 1. Friedrich OHLHAUSEN Sr. was born on 5 Apr 1863 in Belz, Bessarabia. He was confirmed on 9 Jun 1878 in Bortscheag, Bessarabia. Friedrich

More information

CHAPTER 6: RECOMBINANT DNA TECHNOLOGY YEAR III PHARM.D DR. V. CHITRA

CHAPTER 6: RECOMBINANT DNA TECHNOLOGY YEAR III PHARM.D DR. V. CHITRA CHAPTER 6: RECOMBINANT DNA TECHNOLOGY YEAR III PHARM.D DR. V. CHITRA INTRODUCTION DNA : DNA is deoxyribose nucleic acid. It is made up of a base consisting of sugar, phosphate and one nitrogen base.the

More information

for excitation to occur, there must be an exact match between the frequency of the applied radiation and the frequency of the vibration

for excitation to occur, there must be an exact match between the frequency of the applied radiation and the frequency of the vibration ! = 1 2"c k (m + M) m M wavenumbers! =!/c = 1/" wavelength frequency! units: cm 1 for excitation to occur, there must be an exact match between the frequency of the applied radiation and the frequency

More information

Biological molecules:

Biological molecules: Biological molecules: All are organic (based on carbon). Monomers vs. polymers: Monomers refer to the subunits that, when polymerized, make up a larger polymer. Monomers may function on their own in some

More information

Lecture 15: Enzymes & Kinetics Mechanisms

Lecture 15: Enzymes & Kinetics Mechanisms ROLE OF THE TRANSITION STATE Lecture 15: Enzymes & Kinetics Mechanisms Consider the reaction: H-O-H + Cl - H-O δ- H Cl δ- HO - + H-Cl Reactants Transition state Products Margaret A. Daugherty Fall 2004

More information

6,011,024 Jan. 4, 2000

6,011,024 Jan. 4, 2000 United States Patent [19] Reed et al. US006011024A [11] Patent Number: [45] Date of Patent: 6,011,024 Jan. 4, 2000 [54] STEROID SULPHATASE INHIBITORS [75] Inventors: Michael John Reed, London; Barry Victor

More information

4/18/2011. 9.8 Substituent Effects in Electrophilic Substitutions. Substituent Effects in Electrophilic Substitutions

4/18/2011. 9.8 Substituent Effects in Electrophilic Substitutions. Substituent Effects in Electrophilic Substitutions 9.8 Substituent effects in the electrophilic substitution of an aromatic ring Substituents affect the reactivity of the aromatic ring Some substituents activate the ring, making it more reactive than benzene

More information

Copyright 2010 Pearson Education, Inc. Chapter Fourteen 1

Copyright 2010 Pearson Education, Inc. Chapter Fourteen 1 An alcohol has an OH bonded to an alkyl group; a phenol has an OH bonded directly to an aromatic ring; and an ether has an O bonded to two organic groups. Chapter Fourteen 1 Ethyl alcohol, dimethyl ether,

More information

Strategies for optimized biotechnological production of rhamnolipids:

Strategies for optimized biotechnological production of rhamnolipids: : Forum Life Science 2013 March 13-14, 2013, Technische Universität München - Garching Marius Henkel, Anke Schmidberger, Christian Kühnert, Janina Beuker, Thomas Schwartz, Thomas Bernard, Christoph Syldatk

More information

Chemical Bonds and Groups - Part 1

Chemical Bonds and Groups - Part 1 hemical Bonds and Groups - Part 1 ARB SKELETS arbon has a unique role in the cell because of its ability to form strong covalent bonds with other carbon atoms. Thus carbon atoms can join to form chains.

More information

Tetrabutylammoniumbromide mediated Knoevenagel condensation in water: synthesis of cinnamic acids

Tetrabutylammoniumbromide mediated Knoevenagel condensation in water: synthesis of cinnamic acids Tetrabutylammoniumbromide mediated Knoevenagel condensation in water: synthesis of cinnamic acids Monika Gupta a * and Basant Purnima Wakhloo b a Department of Chemistry, University of Jammu, Jammu-180

More information

Biocatalysis INTRODUCTION THE SCOPE OF BIOCATALYSIS. Advantages and Disadvantages of Biocatalysis vs. Chemical Catalysis

Biocatalysis INTRODUCTION THE SCOPE OF BIOCATALYSIS. Advantages and Disadvantages of Biocatalysis vs. Chemical Catalysis Biocatalysis Tyler Johannes Michael R. Simurdiak Huimin Zhao Department of Chemical and Biomolecular Engineering, University of Illinois, Urbana, Illinois, U.S.A. INTRODUCTION Biocatalysis may be broadly

More information

Lecture Overview. Hydrogen Bonds. Special Properties of Water Molecules. Universal Solvent. ph Scale Illustrated. special properties of water

Lecture Overview. Hydrogen Bonds. Special Properties of Water Molecules. Universal Solvent. ph Scale Illustrated. special properties of water Lecture Overview special properties of water > water as a solvent > ph molecules of the cell > properties of carbon > carbohydrates > lipids > proteins > nucleic acids Hydrogen Bonds polarity of water

More information

Chemotaxonomische Identifikation einzelner Bakterienzellen mit Hilfe der Mikro-Raman- Spektroskopie Online-Monitoring von Bioaerosolen (OMIB)

Chemotaxonomische Identifikation einzelner Bakterienzellen mit Hilfe der Mikro-Raman- Spektroskopie Online-Monitoring von Bioaerosolen (OMIB) 1. Jenaer Workshop Spektralsensorik 0. September 00 Chemotaxonomische Identifikation einzelner Bakterienzellen mit Hilfe der Mikro-Raman- Spektroskopie Online-Monitoring von Bioaerosolen (OMIB) P. Rösch

More information

A disaccharide is formed when a dehydration reaction joins two monosaccharides. This covalent bond is called a glycosidic linkage.

A disaccharide is formed when a dehydration reaction joins two monosaccharides. This covalent bond is called a glycosidic linkage. CH 5 Structure & Function of Large Molecules: Macromolecules Molecules of Life All living things are made up of four classes of large biological molecules: carbohydrates, lipids, proteins, and nucleic

More information

Bioremediation. Biodegradation

Bioremediation. Biodegradation Bioremediation A technology that encourages growth and reproduction of indigenous microorganisms (bacteria and fungi) to enhance biodegradation of organic constituents in the saturated zone Can effectively

More information

Chemical Basis of Life Module A Anchor 2

Chemical Basis of Life Module A Anchor 2 Chemical Basis of Life Module A Anchor 2 Key Concepts: - Water is a polar molecule. Therefore, it is able to form multiple hydrogen bonds, which account for many of its special properties. - Water s polarity

More information

I N V E S T I C E D O R O Z V O J E V Z D Ě L Á V Á N Í ENZYMES

I N V E S T I C E D O R O Z V O J E V Z D Ě L Á V Á N Í ENZYMES = substances that... biological reactions 1. Provide an alternative reaction route which has a lower... energy 2. Reactions catalysed by enzymes occur under mild conditions + good yield + fast 3. Enzymes

More information

Chapter 8: Energy and Metabolism

Chapter 8: Energy and Metabolism Chapter 8: Energy and Metabolism 1. Discuss energy conversions and the 1 st and 2 nd law of thermodynamics. Be sure to use the terms work, potential energy, kinetic energy, and entropy. 2. What are Joules

More information