Redox Biocatalysis: Fundamentals and Applications

Table of Contents:
PREFACE ix 1. Enzymes Involved in Redox Reactions: Natural Sources and Mechanistic Overview 1 1.1 Motivation: Green Chemistry and Biocatalysis 1 1.2 Sources of Biocatalysts 2 1.2.1 Plants and Animals as Sources of Redox Biocatalysts 3 1.2.2 Wild-Type Microorganisms 7 1.2.2.1 Yeasts 7 1.2.2.2 Fungi 8 1.2.2.3 Bacteria 8 1.2.3 Metagenomic Assessments 9 1.3 Overview of Redox Enzymes 10 1.3.1 Dehydrogenases 13 1.3.1.1 Zn-Dependent Dehydrogenases 14 1.3.1.2 Flavin-Dependent Dehydrogenases 15 1.3.1.3 Pterin-Dependent Dehydrogenases 16 1.3.1.4 Quinoprotein Dehydrogenases 17 1.3.1.5 Dehydrogenases without Prosthetic Group 18 1.3.2 Oxygenases 19 1.3.2.1 Monooxygenases 20 1.3.2.2 Dioxygenases 38 1.3.3 Oxidases 50 1.3.3.1 Iron-Containing Oxidases 50 1.3.3.2 Copper-Containing Oxidases 51 1.3.3.3 Flavin-Dependent Oxidases 56 1.3.4 Peroxidases 61 1.4 Concluding Remarks 64 References 64 2. Natural Cofactors and Their Regeneration Strategies 86 2.1 Types of Natural Cofactors—Mechanisms 86 2.2 Cofactor Regeneration 88 2.2.1 Enzymatic Regeneration of Reduced Cofactors 88 2.2.1.1 Substrate-Assisted Method 88 2.2.1.2 Enzyme-Assisted Method 89 2.2.2 Enzymatic Regeneration of Oxidized Cofactors 92 2.2.3 Chemical Regeneration of Cofactors 94 2.2.4 Electrochemical Regeneration of Cofactors 95 2.2.5 Photochemical Regeneration of Cofactors 96 2.3 Concluding Remarks 97 References 98 3. Reactions Involving Dehydrogenases 101 3.1 General Considerations 101 3.2 Reduction of Carbonyl Groups 105 3.2.1 Reduction of Aliphatic and Aromatic Ketones 106 3.2.2 Reduction of α- and β-keto Esters and Derivatives 119 3.2.3 Reduction of Diketones 126 3.2.4 Reduction of Aldehydes 128 3.3 Racemization and Deracemization Reactions 130 3.4 Preparation of Amines 135 3.5 Reduction of C–C Double Bonds 142 3.6 Oxidation Reactions 152 3.7 Dehydrogenase-Catalyzed Redox Reactions in Natural Products 159 3.8 Concluding Remarks 164 References 165 4. Reactions Involving Oxygenases 180 4.1 Monooxygenase-Catalyzed Reactions 180 4.1.1 Hydroxylation of Aliphatic Compounds 181 4.1.2 Hydroxylation of Aromatic Compounds 187 4.1.3 Baeyer–Villiger Reactions 189 4.1.3.1 Classification and Metabolic Role of BVMOs 192 4.1.3.2 Isolated Enzymes versus Whole-Cell Systems (Wild-Type and Recombinant Microorganisms) 194 4.1.3.3 Substrate Profile of Available Baeyer–Villiger Monooxygenases 195 4.1.3.4 Synthetic Applications of BVMOs 201 4.1.4 Epoxidation of Alkenes 240 4.2 Dioxygenase-Catalyzed Reactions 251 4.2.1 Aromatic Dioxygenases 251 4.2.1.1 Dihydroxylation of Aromatic Compounds 251 4.2.1.2 Other Oxidation Reactions Performed by Aromatic Dioxygenases 274 4.2.2 Miscellaneous Dioxygenases 279 4.2.2.1 Lipoxygenase 279 4.3 Concluding Remarks 285 References 286 5. Reactions Involving Oxidases and Peroxidases 303 5.1 Oxidase-Catalyzed Reactions 304 5.1.1 Oxidases Acting on C–O Bonds 304 5.1.1.1 Galactose Oxidase 304 5.1.1.2 Pyranose Oxidase 308 5.1.1.3 Alcohol Oxidase 311 5.1.1.4 Glucose Oxidase 313 5.1.1.5 Glycolate Oxidase 313 5.1.2 Laccases and Tyrosinases (Phenol Oxidases) 315 5.1.2.1 Laccase 315 5.1.2.2 Tyrosinase and Other Polyphenol Oxidases 352 5.1.3 Oxidases Acting on C–N Bonds 361 5.1.3.1 d-Amino Acid Oxidase 361 5.1.3.2 l-Amino Acid Oxidase 368 5.1.3.3 Monoamine Oxidase 368 5.1.3.4 Copper Amine Oxidases 371 5.1.4 Miscellaneous 371 5.1.4.1 Cholesterol Oxidase 372 5.1.4.2 Vanillyl Alcohol Oxidase 373 5.1.4.3 Alditol Oxidase 373 5.2 Peroxidase-Catalyzed Reactions 375 5.2.1 Peroxidase Mediated Transformations 379 5.2.1.1 Oxidative Dehydrogenation (2 RH + H2O2 → 2 R• + 2 H2O→R-R) 379 5.2.1.2 Oxidative Halogenation (RH + H2O2 +X− + H+→RX + 2 H2O) 385 5.2.1.3 Oxygen-Transfer Reactions (RH + H2O2 → ROH + H2O) 390 5.3 Concluding Remarks 403 References 404 6. Hydrolase-Mediated Oxidations 433 6.1 Hydrolase Promiscuity and in situ Peracid Formation. Perhydrolases vs. Hydrolases. Other Promiscuous Hydrolase-Mediated Oxidations 433 6.2 Hydrolase-Mediated Bulk Oxidations in Aqueous Media (e.g., Bleaching, Disinfection, etc.) 436 6.3 Lipase-Mediated Oxidations: Prileshajev Epoxidations and Baeyer–Villiger Reactions 439 6.4 Hydrolase-Mediated Oxidation and Processing of Lignocellulosic Materials 445 6.5 Concluding Remarks 448 References 448 7. Bridging Gaps: From Enzyme Discovery to Bioprocesses 453 7.1 Context 453 7.2 Enzyme Directed Evolution and High-Throughput-Screening of Biocatalysts 454 7.3 Successful Case: Baker’s Yeast Redox Enzymes, Their Cloning, and Separate Overexpression 467 7.4 Whole-Cells vs. Isolated Enzymes: Medium Engineering 473 7.5 Beyond: Multistep Domino Biocatalytic Processes 477 7.6 Concluding Remarks 482 References 483 8. Industrial Applications of Biocatalytic Redox Reactions: From Academic Curiosities to Robust Processes 487 8.1 Motivation: Drivers for Industrial Biocatalytic Processes 487 8.2 Key Aspects in Industrial Biocatalytic Processes 488 8.3 Industrial Biocatalytic Redox Processes: Free Enzymes 492 8.4 Industrial Biocatalytic Redox Processes—Whole-Cells: The “Designer Bug” Concept and Beyond (Metabolic Engineering) 500 8.5 Concluding Remarks and Future Perspectives 511 References 516 INDEX 521

About the Author :
Daniela Gamenara, PhD, is Assistant Professor in the Organic Chemistry Department of the Faculty of Chemistry of Universidad de la República, Uruguay. After two short postdoctoral internships, her current scientific interest is the development of enzymatic methodologies for the synthesis of high added-value compounds and natural products as well, together with the use of new trends in organocatalysis for the same purposes. Gustavo A. Seoane, PhD, is Full Professor and Head of the Organic Chemistry Department of the Faculty of Chemistry of Universidad de la República, Uruguay. His main scientific interest is the use of green procedures for the synthesis of bioactive natural products and analogs, in particular, intensive use of biotransformations to prepare polyoxygenated targets. He works actively to promote the development of biocatalysis in South America. Patricia Saenz-Méndez, PhD, is Assistant Professor of Physical Organic Chemistry in the Faculty of Chemistry of Universidad de la República, Uruguay. She was previously appointed as postdoctoral fellow at the Örebro University, Sweden, and the National University of Ireland, Galway. Her work is devoted to the experimental and in silico development of biotechnological and organocatalytic tools for the preparation of high added-value chemicals and natural products. Pablo Domínguez de María, PhD, is Group Leader at the Institute for Technical and Macromolecular Chemistry (ITMC), RWTH Aachen University, Germany. He was previously affiliated with AkzoNobel BV in the Netherlands and Degussa AG in Germany. Dr. Domínguez de María has also worked as a technical freelance advisor on emerging technologies (e.g., catalysis) applied to sustainable chemistry (www.sustainablemomentum.net). He was awarded the Young Scientist Prize by the Iberoamerican Academy of Pharmacy.