Freshly Printed - allow 7 days lead
Couldn't load pickup availability
Microbial Sensing in Fermentation
Satinder K. Brar (Edited by), S Brar (Author), Ratul K. Das (Edited by), Saurabh J. Sarma (Edited by)
9781119247968, Wiley
Hardback, published 21 December 2018
344 pages
24.1 x 16.3 x 2 cm, 0.794 kg
A comprehensive review of the fundamental molecular mechanisms in fermentation and explores the microbiology of fermentation technology and industrial applications Microbial Sensing in Fermentation presents the fundamental molecular mechanisms involved in the process of fermentation and explores the applied art of microbiology and fermentation technology. The text contains descriptions regarding the extraordinary sensing ability of microorganisms towards small physicochemical changes in their surroundings. The contributors — noted experts in the field — cover a wide range of topics such as microbial metabolism and production (fungi, bacteria, yeast etc); refined and non-refined carbon sources; bioprocessing; microbial synthesis, responses and performance; and biochemical, molecular and extra/intracellular controlling. This resource contains a compilation of literature on biochemical and cellular level mechanisms for microbial controlled production and includes the most significant recent advances in industrial fermentation. The text offers a balanced approach between theory and practical application, and helps readers gain a clear understanding of microbial physiological adaptation during fermentation and its cumulative effect on productivity. This important book: Written for researchers, graduate and undergraduate students from diverse backgrounds, such as biochemistry and applied microbiology, Microbial Sensing in Fermentation offers a review of the fundamental molecular mechanisms involved in the process of fermentation.
List of Contributors xi 1 Biochemical Aspects of Microbial Product Synthesis: a Relook 1 1.1 Introduction 1 1.2 History of Industrial Production of Microbial Products 2 1.2.1 Advances of Biochemical Engineering and Their Effects on Global Market of Microbial Products 3 1.2.2 Importance of Microbial Sensing in Product Formation 6 1.3 Conclusion 7 Acknowledgments 8 References 8 2 Cellular Events of Microbial Production: Important Findings So Far 11 2.1 Introduction 11 2.2 Microbial Metabolism and Evolution of Metabolic Pathways 12 2.3 Microbial Fermentation 12 2.4 The Microbial Cellular Events 15 2.5 Cell Signalling in Microorganisms 19 2.6 Microbial Performance Under Stress Conditions 21 Acknowledgment 24 References 24 3 Microbial Metabolism in a Refined Carbon Source: Generalities 27 3.1 Introduction 27 3.2 Microbial Metabolism in Presence of Pure and Crude Substrate 29 3.3 Microbial Metabolism in Presence of Pure and Mixed Cultures 31 3.4 Microbial Metabolism in the Presence of Co‐Substrate 33 3.5 Microbial Metabolism in the Presence of Input Parameters 35 3.6 Microbial Metabolism in the Presence of Varying Fermentation Conditions 37 3.7 Pros and Cons of Refined Substrate for Metabolic Metabolisms 38 3.8 Conclusions 39 Acknowledgment 40 References 40 4 Non‐refined Carbon Sources and Microbial Performance 43 4.1 Introduction 43 4.2 Non‐refined Carbon Sources: a Brief Account 43 4.3 Microbial Assimilation of Non‐Refined Carbon Sources 45 4.4 Microbial Sensing to Non‐Refined Carbon Sources 48 4.4.1 Microbial Metabolism and Regulatory Circuits 48 4.4.2 CCR Regulation of Carbon Uptake and Metabolism 51 4.5 Guiding Product Outcomes via Rewiring of Cellular Regulatory Circuit 53 4.5.1 Cellular Engineering in E. Coli for Bioprocessing of Non‐Refined Carbon Sources 54 4.5.2 Rewiring S. cerevisiae for Accumulation and Conversion of Non‐refined Carbon Sources 55 4.6 Conclusions 56 References 57 5 Cellular versus Biochemical Control over Microbial Products 61 5.1 Introduction 61 5.2 3 Hydroxy‐propionic Acid 62 5.3 Fumaric Acid 64 5.4 Itaconic Acid 65 5.5 Glucaric Acid 67 5.6 Butanol 68 5.7 Malic Acid 69 5.8 Gluconic Acid 71 5.9 Aminovalaric Acid 71 5.10 Glutamic Acid 73 5.11 Cadaverine (1,5‐diaminopentane) 74 5.12 Conclusion 76 Acknowledgment 76 References 76 6 Pre‐Treatment of Alternative Carbon Source: How Does it Make Sense to Microorganism at Cellular Level? 89 6.1 Introduction 89 6.2 Pre‐ Treated Carbon Source and Microbial Assimilation: Cellular and Biochemical Aspects 91 6.2.1 Alcohols 94 6.2.1.1 Bioethanol 94 6.2.1.2 Butanol and Acetone 96 6.2.2 Hydrogen 98 6.2.3 Methane/biogas 101 6.2.4 Organic Acids 103 6.3 Challenges of Inhibitory Hydrolysis Products and Strategic Solution 106 6.3.1 Inhibitory Products: Pretreatment Metabolites or By‐products 106 6.3.1.1 Aliphatic Compounds 106 6.3.1.2 Aromatic Compounds 107 6.3.1.3 Furan Aldehydes 108 6.3.2 Strategies to Control Inhibitory Effects 109 6.3.2.1 Biological Detoxification Strategy for the Inhibitors 110 6.3.2.2 Understanding the Mechanism of Microorganism Adaptation for The Detoxification of Inhibitory Compounds 110 6.3.2.2.1 Homeostasis 110 6.3.2.2.2 Enzymatic Detoxification 111 6.3.2.3 Physical and Chemical Detoxification Strategy for Inhibitors 112 6.3.3 Correlation (Synergistic Effects) of Inhibitory Compounds and their Detoxification 118 6.4 Conclusion 126 Acknowledgments 127 References 127 7 Microbial Metabolic Pathways in the Production of Valued‐added Products 137 7.1 Introduction 137 7.2 Microbial Molecular Structure 138 7.3 Biomass Production 140 7.3.1 Single Cell Oil 140 7.3.2 Single Cell Protein 142 7.4 Enzymes 148 7.5 Biofuels 150 7.6 Alkaloids, Terpenoids, Polyketides and Flavonoids 153 7.7 Organic Acids 155 7.8 Rare Sugars 156 7.9 Conclusions 157 References 158 8 Communication for a Collective Response to Environmental Stress: Bacterial and Fungal Perspectives 169 8.1 Introduction 169 8.2 Quorum Sensing in Bacteria and the Related Phenotypes 172 8.3 Fermentation and Quorum Sensing in Bacteria 177 8.4 Quorum Sensing in Fungi and the Related Phenotypes 183 8.5 Fermentation and Quorum Sensing in Fungi 186 8.6 Quorum Sensing in Bacteria and Fungi: Similarities and Differences 188 Acknowledgment 189 References 189 9 Biochemical and Cellular Events in Controlling Microbial Performance: A Comparative Account 201 9.1 Biochemical vs. Molecular Cues for Microbial Performances 201 9.1.1 Nutritional Parameters Optimization 201 9.1.2 Process Condition Optimization 202 9.1.3 Process Improvement by Using Batch and Fed‐Batch via Process and Modeling 203 9.1.4 Metabolic Engineering for Improving Microbial Performance 203 9.1.4.1 Metabolic Flux Balance Analysis 203 9.1.4.1.1 Constraint Based Flux Balance Analysis 203 9.1.4.1.2 Defining Biological Objective to Optimize a Phenotype 204 9.1.4.1.3 Applications of Flux Analysis 204 9.1.5 Strain Improvement for Microbial Performance 205 9.1.5.1 Mutagenesis for Strain Improvement 205 9.1.5.1.1 Physical Mutagenesis 205 9.1.5.1.2 Chemical Mutagenesis 206 9.1.5.1.3 Biological Mutagenesis 206 9.2 Sequential Evidences of Biochemical and Molecular Controlling Over Microbial Performances 206 9.3 Biochemically Influenced Molecular Events and Vice Versa 208 9.4 Facts at the Interface of Biochemical and Molecular Controlling: Products vs Applied Parameters 208 9.4.1 Sulfur‐Delivery into Biosynthetic Pathway 208 9.4.2 Synthetic Biochemistry Platform for Production of Glucose 212 9.4.3 Biochemical and Molecular Aspects of Metabolic Engineering Approaches 212 9.4.3.1 Engineering Regulatory Network 212 9.4.3.2 Heterologous Expression of Entire Gene Cluster 213 9.4.3.3 Rerouting Metabolic Pathway 213 9.4.3.4 Integration of Metabolic Engineering and Process Engineering 213 9.5 Conclusions 214 References 214 10 Qualitative vs. Quantitative Control Over Microbial Products 223 10.1 Introduction 223 10.2 Qualitative vs. Quantitative Control Over Microbial Products/Fungal Products 224 10.2.1 Qualitative Control and Fungal Product 225 10.2.1.1 Diffusion Techniques 226 10.2.1.2 Thin Layer Chromatography (TLC) 229 10.2.1.3 Chromatography‐bioautography for Screening of Antimicrobial Activity 231 10.2.1.4 High‐performance Liquid Chromatography (HPLC) 232 10.2.2 Quantitative Control of Fungal Products 232 10.2.3 Speeding Up Fungal Product 234 10.3 Fungal Morphology and Product Spectrum: a Representative Theme 237 10.4 Effectiveness of Qualitative Domain for Different Microorganisms 241 10.5 Emphasizing the Need: Qualitative and Quantitative Importance 245 10.6 Conclusions 246 References 247 11 Microbes and Their Products as Sensors in Industrially Important Fermentations 253 11.1 Introduction 253 11.2 Sensors 254 11.3 Transducers in Conjunction With Microbe Sensors 254 11.3.1 Dissolved Oxygen (DO) Electrode 254 11.3.2 Electron Transfer Measuring Systems 255 11.4 Metabolite Measuring Systems 256 11.5 Other Measuring Systems 257 11.5.1 Bioluminescence Biosensor 257 11.6 Applications of Microbe Sensors in Some Commercially Important Products 258 11.6.1 Red Wine 260 11.6.2 Fermentation of Cereal Products 260 11.6.3 Mevalonate Production 261 11.6.4 Bioaerosols 261 11.6.5 Aptamers 262 11.7 Conclusions 263 References 263 12 Practical Aspects and Case Studies of Industrial Scale Fermentation 267 12.1 Introduction 267 12.2 Scale Up Challenges 269 12.2.1 Agitation 269 12.2.2 Mass Transfer of Oxygen (Mass Transfer, Morphology, and Rheology) 270 12.2.3 “Shear Damage” 271 12.2.4 Measurements for Control 273 12.2.5 Other Aspects 273 12.3 Microbial Tolerance 274 12.4 Phage Invasion 274 12.5 Process Failures 277 12.6 Potent Inhibitors (e.g. Substrate Inhibition) 278 12.7 Case Studies: Biofuels (Biodiesel, Ethanol) Enzymes (Novozymes), Antibiotics, Platform Chemicals 281 12.7.1 Biofuels (Biodiesel, Ethanol) 281 12.7.2 Enzymes (Novozymes) 283 12.7.3 Antibiotics 286 12.7.4 Platform Chemicals 288 12.8 Conclusions 289 Acknowledgments 290 References 290 13 Future Market and Policy Initiatives of New High Value Products 299 13.1 Introduction 299 13.2 Market Analysis, Market Trends and Statistics 299 13.2.1 Biofuels 299 13.2.2 Bio‐surfactants 302 13.2.3 Enzymes 305 13.3 Public Mobilization Initiatives and Government Policies 306 13.3.1 Public Mobilization Initiatives 306 13.3.2 Government Policies 307 13.3.3 Regional Policy Development for Growing Bio‐based Production 307 13.4 Regulations and Conformity – Case of Biofuels 307 13.5 Global Marketing and Competitiveness in Biofuel Sector 309 References 309 Index 311
G. Gallastegui, A. Larrañaga, Antonio Avalos Ramirez, and Thi Than Ha Pham
Devangana Bhuyan and Ratul Kumar Das
Vinayak Laxman Pachapur, Preetika Rajeev Kuknur, Satinder Kaur Brar, and Rosa Galvez-Cloutier
Guneet Kaur
Carlos S. Osorio-González, Krishnamoorthy Hegde, and Satinder Kaur Brar
Joseph Sebastian, Pratik Kumar, Krishnamoorthy Hegde, Satinder Kaur Brar, Mausam Verma, and Ratul Kumar Das
Gilberto V. de Melo Pereira, Ana M. Finco, Luiz A. J. Letti, Susan Grace Karp, Maria G. B. Pagnoncelli, Juliana de Oliveira, Vanete Thomaz Soccol, Satinder Kaur Brar, and Carlos Ricardo Soccol
Azadeh Kermanshahi Pour
Shadab Ahmed, Shreyas Niphadkar, Somnath Nandi, Satya Eswari, Vishal Pandey, Aishwarya Shankapal, and Aishvarya Agrawal
Rachna Goswami, Vijay Kumar Mishra, and Radhika Pilli
Ritu Raval and Keyur Raval
Sara Magdouli, Thana Saffar, Tayssir Guedri, Rouissi Tarek, Satinder Kaur Brar, and Jean François Blais
Ha Thi Thanh Pham, Maria Puig‐Gamero, Luz Sanchez‐Silva, Paula Sánchez, José Luis Valverde, Michele Heitz, and Antonio Avalos Ramirez
Subject Areas: Biology, life sciences [PS]
