Bioprocess engineering: basis concepts
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| Main Author: | |
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| Format: | Book |
| Language: | English |
| Published: |
Upper Saddle River, NJ
Prentice Hall PTR
2002
|
| Edition: | 2. ed. |
| Series: | Prentice Hall international series in the physical and chemical engineering sciences
|
| Subjects: | |
| Online Access: | Inhaltsverzeichnis |
| Item Description: | Includes bibliographical references and index |
| Physical Description: | XX, 553 S. graph. Darst. |
| ISBN: | 0130819085 |
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| adam_text | Titel: Bioprocess engineering
Autor: Shuler, Michael L
Jahr: 2002
Contents
PREFACE TO THE SECOND EDITION xvii
PREFACE TO THE FIRST EDITION xix
Part 1 Introduction 1
1 WHAT ISA BIOPROCESS ENGINEER? 1
1.1. Introductory Remarks 1
1.2. Biotechnology and Bioprocess Engineering 2
1.3. Biologists and Engineers Differ in Their Approach to Research 3
1.4. The Story of Penicillin: How Biologists and Engineers
Work Together 3
1.5. Bioprocesses: Regulatory Constraints 8
Suggestions for Further Reading 10
Problems • 10
Part 2 The Basics of Biology: An Engineer s Perspective 11
2 AN OVERVIEW OF BIOLOGICAL BASICS 11
2.1 Are All Cells the Same? 11
2.1.1. Microbial Diversity. 11
2.7.2. Naming Cells, 12
2.1.3. Viruses, 14
2.1.4. Procaryotes, 15
2.1.5. Eucaryotes, 19
2.2. Cell Construction 25
2.2.1. Introduction, 25
2.2.2. Amino Acids and Proteins, 26
2.2.3. Carbohydrates: Mono- and Polysaccharides, 34
2.2.4. Lipids, Fats, and Steroids, 38
2.2.5. Nucleic Acids, RNA, and DNA, 40
2.3. Cell Nutrients 46
2.3.1. Introduction, 46
2.3.2. Macronutrients, 49
2.3.3. Micronutrients, 50
2.3.4. Growth Media, 52
2.4. Summary 53
Suggestions for Further Reading 54
Problems 54
3 ENZYMES 57
3.1. Introduction 57
3.2. How Enzymes Work 58
3.3. Enzyme Kinetics 60
3.3.1. Introduction, 60
3.3.2. Mechanistic Models for Simple Enzyme Kinetics, 61
3.3.3. Experimentally Determining Rate Parameters
for Michaelis—Menten Type Kinetics, 64
3.3.4. Models for More Complex Enzyme Kinetics, 67
3.3.5. Effects of pH and Temperature, 75
3.3.6. Insoluble Substrates, 78
3.4. Immobilized Enzyme Systems 79
3.4.1. Methods of Immobilization, 79
3.4.2. Diffusional Limitations in Immobilized Enzyme Systems, 84
3.4.3. Electrostatic and Steric Effects in Immobilized
Enzyme Systems, 91
3.5. Large-scale Production of Enzymes 91
3.6. Medical and Industrial Utilization of Enzymes 92
3.7. Summary 96
Suggestions for Further Reading 97
Problems 97
4 HOW CELLS WORK 105
4.1. Introduction 105
4.2. The Central Dogma 105
4.3. DNA Replication: Preserving and Propagating the Cellular
Message 107
4.4. Transcription: Sending the Message 110
4.5. Translation: Message to Product 113
4.5.1. Genetic Code: Universal Message, 113
4.5.2. Translation: How the Machinery Works, 113
4.5.3. Posttranslational Processing: Making the Product Useful, 115
4.6. Metabolic Regulation 119
4.6.1. Genetic-level Control: Which Proteins Are Synthesized?, 119
4.6.2. Metabolic Pathway Control, 123
4.7. How the Cell Senses Its Extracellular Environment 124
4.7.1 Mechanisms to Transport Small Molecules across Cellular
Membranes, 124
4.7.2. Role of Cell Receptors in Metabolism and Cellular
Differentiation, 127
4.8. Summary 128
4.9. Appendix: Examples of Regulation of Complex Pathways 129
Suggestions for Further Reading 131
Problems 131
5 MAJOR METABOLIC PATHWAYS 133
5.1. Introduction 133
5.2. Bioenergetics 134
5.3. Glucose Metabolism: Glycolysis and the TCA Cycle 137
5.4. Respiration 141
5.5. Control Sites in Aerobic Glucose Metabolism 142
5.6. Metabolism of Nitrogenous Compounds 143
5.7. Nitrogen Fixation 144
5.8. Metabolism of Hydrocarbons 144
5.9. Overview of Biosynthesis 145
5.10. Overview of Anaerobic Metabolism 148
5.11. Overview of Autotrophic Metabolism 150
5.12. Summary 152
Suggestions for Further Reading 154
Problems 154
6 HOW CELLS GROW 155
6.1. Introduction 155
6.2. Batch Growth 156
6.2.1. Quantifying Cell Concentration, 156
6.2.2. Growth Patterns and Kinetics in Batch Culture, 160
6.2.3. How Environmental Conditions Affect Growth Kinetics, 169
6.2.4.- Heat Generation by Microbial Growth, 173
6.3. Quantifying Growth Kinetics 175
6.3.1. Introduction, 175
6.3.2. Using Unstructured Nonsegregated Models to Predict Specific
Growth Rate, 176
6.3.3. Models for Transient Behavior, 183
6.3.4. Cybernetic Models, 189
6.4. How Cells Grow in Continuous Culture 189
6.4.1. Introduction, 189
6.4.2. Some Specific Devices for Continuous Culture, 190
6.4.3. The Ideal Chemostat, 191
6.4.4. The Chemostat as a Tool, 198
6.4.5. Deviations from Ideality, 198
6.5. Summary 199
Suggestions for Further Reading 200
Problems 200
7 STOICHIOMETRY OF MICROBIAL GROWTH AND PRODUCT
FORMATION 207
7.1. Introduction 207
7.2. Some Other Definitions 207
7.3. Stoichiometric Calculations 209
7.3.1. Elemental Balances, 209
7.3.2. Degree of Reduction, 211
7.4. Theoretical Predictions of Yield Coefficients 215
7.5. Summary 216
Suggestions for Further Reading 216
Problems 216
8 HOW CELLULAR INFORMATION IS ALTERED 219
8.1. Introduction 219
8.2. Evolving Desirable Biochemical Activities through Mutation
and Selection 219
8.2.1. How Mutations Occur, 220
8.2.2. Selecting for Desirable Mutants, 221
8.3. Natural Mechanisms for Gene Transfer and Rearrangement 225
8.3.1. Genetic Recombination, 225
8.3.2. Transformation, 227
8.3.3. Transduction, 227
8.3.4. Episomes and Conjugation, 228
8.3.5. Transposons: Internal Gene Transfer, 230
8.4. Genetically Engineering Cells 230
8.4.1. Basic Elements of Genetic Engineering, 230
8.4.2. Genetic Engineering of Higher Organisms, 235
8.5. Genomics 236
8.5.1. Experimental Techniques, 237
8.5.2. Computational Techniques, 240
8.6. Summary 241
Suggestions for Further Reading 241
Problems 242
Part 3 Engineering Principles for Bioprocesses 245
9 OPERATING CONSIDERATIONS FOR BIOREACTORS
FOR SUSPENSION AND IMMOBILIZED CULTURES 245
9.1. Introduction 245
9.2. Choosing the Cultivation Method 246
9.3. Modifying Batch and Continuous Reactors 248
9.3.1. Chemostat with Recycle, 248
9.3.2. Multistage Chemostat Systems, 250
9.3.3. Fed-batch Operation, 256
9.3.4. Perfusion Systems, 262
9.4. Immobolized Cell Systems 263
9.4.1. Introduction, 263
9.4.2. Active Immobilization of Cells, 263
9.4.3. Passive Immobilization: Biological Films, 266
9.4.4. Diffusional Limitations in Immobilized Cell Systems, 268
9.4.5. Bioreactor Considerations in Immobilized Cell
Systems, 273
9.5. Solid-state Fermentations 276
9.6. Summary 278
Suggestions for Further Reading 280
Problems 280
10 SELECTION, SCALE-UP, OPERATION, AND CONTROL
OF BIOREACTORS 285
10.1. Introduction 285
10.2. Scale-up and Its Difficulties 286
10.2.1. Introduction, 286
10.2.2. Overview of Reactor Types, 286
10.2.3. Some Considerations on Aeration, Agitation, and Heat
Transfer, 292
10.2.4. Scale-up, 297
10.2.5. Scale-down, 301
10.3. Bioreactor Instrumentation and Control 307
10.3.1. Introduction, 307
10.3.2. Instrumentation for Measurements of Active
Fermentation, 307
10.3.3. Using the Information Obtained, 311
10.4. Sterilization of Process Fluids 314
10.4.1. Introduction and the Kinetics of Death, 314
10.4.2. Sterilization of Liquids, 315
10.4.3. Sterilization of Gases, 320
10.5. Summary 323
Suggestions for Further Reading 324
Problems 325
11 RECOVERY AND PURIFICATION OF PRODUCTS 329
11.1. Strategies to Recover and Purify Products 329
11.2. Separation of Insoluble Products 331
11.2.1. Filtration, 332
11.2.2. Centrifugation, 336
11.2.3. Coagulation and Flocculation, 340
11.3. Cell Disruption 341
11.3.1. Mechanical Methods, 341
11.3.2. Nonmechanical Methods, 342
11.4. Separation of Soluble Products 343
11.4.1. Liquid-Liquid Extraction, 343
11.4.2. Aqueous Two-phase Extraction, 348
11.4.3. Precipitation, 349
11.4.4. Adsorption, 351
11.4.5. Dialysis, 355
11.4.6. Reverse Osmosis, 356
11.4.7. Ultrafiltration andMicrofiltration, 358
11.4.8. Cross-flow Ultrafiltration and Microfiltration, 360
11.4.9. Chromatography, 365
11.4.10. Electrophoresis, 375
11.4.11. Electrodialysis, 376
11.5. Finishing Steps for Purification 378
11.5.1. Crystallization, 378
11.5.2. Drying, 378
11.6. Integration of Reaction and Separation 379
11.7. Summary 380
Suggestions for Further Reading 381
Problems 382
Part 4 Applications to Nonconventional Biological Systems 385
12 BIOPROCESS CONSIDERATIONS IN USING ANIMAL
CELL CULTURES 385
12.1. Structure and Biochemistry of Animal Cells 385
12.2. Methods Used for the Cultivation of Animal Cells 387
12.3. Bioreactor Considerations for Animal Cell Culture 396
12.4. Products of Animal Cell Cultures 400
12.4.1. Monoclonal Antibodies, 400
12.4.2. Immunobiological Regulators, 401
12.4.3. Virus Vaccines, 401
12.4.4. Hormones, 401
12.4.5. Enzymes, 401
12.4.6. Insecticides, 402
12.4.7. Whole Cells and Tissue Culture, 402
12.5. Summary 402
Suggestions for Further Reading 403
Problems 403
13 BIOPROCESS CONSIDERATIONS IN USING PLANT
CELL CULTURES 405
13.1. Why Plant Cell Cultures? 405
13.2. Plant Cells in Culture Compared to Microbes 407
13.3. Bioreactor Considerations 411
13.3.1. Bioreactors for Suspension Cultures, 411
.13.3.2. Reactors Using Cell Immobilization, 413
13.3.3. Bioreactors for Organized Tissues, 414
13.4. Economics of Plant Cell Tissue Cultures 417
13.5. Summary 417
Suggestions for Further Reading 418
Problems 418
14 UTILIZING GENETICALLY ENGINEERED ORGANISMS 421
14.1. Introduction 421
14.2. How the Product Influences Process Decisions 421
14.3. Guidelines for Choosing Host-Vector Systems 424
14.3.1. Overview, 424
14.3.2. Escherichia coli, 424
14.3.3. Gram-positive Bacteria, 426
14.3.4. Lower Eucaryotic Cells, 427
14.3.5. Mammalian Cells, 428
14.3.6. Insect Cell-Baculovirus System, 429
14.3.7. Transgenic Animals, 430
14.3.8. Transgenic Plants and Plant Cell Culture, 432
14.3.9. Comparison of Strategies, 432
14.4. Process Constraints: Genetic Instability 433
14.4.1. Segregational Loss, 434
14.4.2. Plasmid Structural Instability, 436
14.4.3. Host Cell Mutations, 436
14.4.4. Growth-rate-dominated Instability, 437
14.5. Considerations in Plasmid Design to Avoid Process Problems 438
14.6. Predicting Host-Vector Interactions and Genetic Instability 441
14.7. Regulatory Constraints on Genetic Processes 451
14.8. Metabolic Engineering 452
14.9. Protein Engineering 456
14.10. Summary 457
Suggestions for Further Reading 458
Problems 460
15 MEDICAL APPLICATIONS OF BIOPROCESS ENGINEERING 463
15.1. Introduction 463
15.2. Tissue Engineering 463
15.2.1. What Is Tissue Engineering?, 463
15.2.2. Commercial Tissue Culture Processes, 465
15.3. Gene Therapy Using Viral Vectors 467
15.3.1. Models of Viral Infection, 467
15.3.2. Mass Production of Retrovirus, 470
15.4. Bioreactors 471
15.4.1. Stem Cells and Hematopoiesis, 471
15.4.2. Extracorporeal Artificial Liver, 472
15.5. Summary 473
Suggestions for Further Reading 473
Problems 473
16 MIXED CULTURES 475
16.1. Introduction 475
16.2. Major Classes of Interactions in Mixed Cultures 476
16.3. Simple Models Describing Mixed-culture Interactions 479
16.4. Mixed Cultures in Nature 485
16.5. Industrial Utilization of Mixed Cultures 487
16.6. Biological Waste Treatment: An Example of the Industrial
Utilization of Mixed Cultures 488
16.6.1. Overview, 488
16.6.2. Biological Waste Treatment Processes, 491
16.6.3. Advanced Waste-water Treatment Systems, 501
16.6.4. Conversion of Waste Water to Useful Products, 506
16.7. Summary 508
Suggestions for Further Reading 508
Problems 509
17 EPILOGUE 513
APPENDIX TRADITIONAL INDUSTRIAL BIOPROCESSES 515
A. 1. Anaerobic Bioprocesses 515
A. 1.1. Ethanol Production, 515
A.1.2. Lactic Acid Production, 519
A.1.3. Acetone-Butanol Production, 521
A.2. Aerobic Processes 524
A.2.1. Citric Acid Production, 524
A.2.2. Production of Bakers Yeast, 526
A.2.3. Production of Penicillins, 527
A.2.4. Production of High-Fructose Corn Syrup (HFCS), 530
Suggestions for Further Reading 533
INDEX 535
|
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| spelling | Shuler, Michael L. Verfasser aut Bioprocess engineering basis concepts Michael L. Shuler ; Fikret Kargi 2. ed. Upper Saddle River, NJ Prentice Hall PTR 2002 XX, 553 S. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Prentice Hall international series in the physical and chemical engineering sciences Includes bibliographical references and index Génie biochimique Ingeniería bioquímica Biochemical engineering Biotechnologie (DE-588)4069491-4 gnd rswk-swf 1\p (DE-588)4151278-9 Einführung gnd-content Biotechnologie (DE-588)4069491-4 s DE-604 Kargi, Fikret Sonstige oth HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=009844324&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
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| title_auth | Bioprocess engineering basis concepts |
| title_exact_search | Bioprocess engineering basis concepts |
| title_full | Bioprocess engineering basis concepts Michael L. Shuler ; Fikret Kargi |
| title_fullStr | Bioprocess engineering basis concepts Michael L. Shuler ; Fikret Kargi |
| title_full_unstemmed | Bioprocess engineering basis concepts Michael L. Shuler ; Fikret Kargi |
| title_short | Bioprocess engineering |
| title_sort | bioprocess engineering basis concepts |
| title_sub | basis concepts |
| topic | Génie biochimique Ingeniería bioquímica Biochemical engineering Biotechnologie (DE-588)4069491-4 gnd |
| topic_facet | Génie biochimique Ingeniería bioquímica Biochemical engineering Biotechnologie Einführung |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=009844324&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT shulermichaell bioprocessengineeringbasisconcepts AT kargifikret bioprocessengineeringbasisconcepts |