Editor-in-Chief <\/p>\n
Volume Editors <\/p>\n
Section Editors <\/p>\n
General Preface <\/p>\n
Nomenclature Guidelines <\/p>\n
Permission Acknowledgments <\/p>\n
1.01. Introduction <\/p>\n
1.02. Amino Acid Metabolism <\/p>\n
Glossary <\/p>\n
1.02.1. Introduction <\/p>\n
1.02.2. General Properties, Classification, and Structure of Amino Acids <\/p>\n
1.02.3. Biosynthesis of Amino Acids <\/p>\n
1.02.4. Catabolism of Amino Acids <\/p>\n
1.02.5. Important Biomolecules Synthesized from Amino Acids <\/p>\n
1.03. Enzyme Biocatalysis <\/p>\n
Glossary <\/p>\n
1.03.1. Introduction to Enzymes <\/p>\n
1.03.2. Enzyme Kinetics <\/p>\n
1.03.3. Enzyme Engineering <\/p>\n
1.03.4. Enzyme Production <\/p>\n
1.03.5. Immobilized Enzymes <\/p>\n
1.03.6. Enzyme Applications <\/p>\n
1.03.7. Conclusions <\/p>\n
1.04. Immobilized Biocatalysts <\/p>\n
1.04.1. Introduction: Definitions and Scope <\/p>\n
1.04.2. Applications of Immobilized Enzymes <\/p>\n
1.04.3. Methods of Enzyme Immobilization <\/p>\n
1.04.4. Properties of Immobilized Enzymes <\/p>\n
1.04.5. Evaluation of Enzyme Immobilization <\/p>\n
1.04.6. Heterogeneous Biocatalysis <\/p>\n
1.04.7. Future Prospects for Immobilized Biocatalysts <\/p>\n
1.05. Lipids, Fatty Acids <\/p>\n
Glossary <\/p>\n
1.05.1. Introduction <\/p>\n
1.05.2. Structure of Fatty Acids <\/p>\n
1.05.3. Nomenclature <\/p>\n
1.05.4. Form in the Cell <\/p>\n
1.05.5. What Do Lipids Do? <\/p>\n
1.05.6. Biosynthesis of Fatty Acids and Lipids <\/p>\n
1.05.7. Biochemistry of Lipid Accumulation <\/p>\n
1.06. DNA Cloning in Plasmid Vectors <\/p>\n
Glossary <\/p>\n
1.06.1. Introduction <\/p>\n
1.06.2. Cloning Vectors: Replication Origins and Partition Regions <\/p>\n
1.06.3. Cloning Vectors: Selection Markers <\/p>\n
1.06.4. Preparing DNA Fragments for Ligation <\/p>\n
1.06.5. Ligation Systems <\/p>\n
1.06.6. Methods of Bacterial and Yeast Transformation <\/p>\n
1.06.7. Exploitation of Bacteriophage Packaging for DNA Cloning in Plasmid Vectors <\/p>\n
1.06.8. Screening of Plasmid Clones in Bacteria for the Desired Recombinant Plasmids <\/p>\n
1.06.9. Vector-Implemented Systems for the Direct Selection of Recombinant Plasmids <\/p>\n
1.06.10. Direct Selection of Recombinant Plasmids Involving Restriction Enzyme Digestion of the Ligation Mixture <\/p>\n
1.06.11. Particular Features of Oligonucleotides Cloning <\/p>\n
1.06.12. Particular Features of Cloning of PCR Amplicons <\/p>\n
1.06.13. Introduction of Deletions into Plasmids <\/p>\n
1.06.14. Instability of Recombinant Plasmids <\/p>\n
1.06.15. DNA Cloning Using Site-Specific Recombination <\/p>\n
1.06.16. DNA Cloning Using Homologous (General) Recombination <\/p>\n
1.06.17. Employment of Transposons for In Vivo Cloning and Manipulation of Large Plasmids <\/p>\n
1.06.18. Conclusion <\/p>\n
1.07. Structure and Biosynthesis of Glycoprotein Carbohydrates <\/p>\n
Glossary <\/p>\n
Acknowledgments <\/p>\n
1.07.1. Introduction <\/p>\n
1.07.2. Monosaccharide Structure <\/p>\n
1.07.3. Oligosaccharide Structure <\/p>\n
1.07.4. Biosynthesis of Glycoproteins <\/p>\n
1.07.5. Glycosylation of Therapeutic Glycoproteins <\/p>\n
1.08. Nucleotide Metabolism <\/p>\n
Glossary <\/p>\n
1.08.1. Introduction <\/p>\n
1.08.2. Synthesis of Phosphoribosyl Diphosphate (PRPP) <\/p>\n
1.08.3. Purine Biosynthesis <\/p>\n
1.08.4. Pyrimidine Biosynthesis <\/p>\n
1.08.5. Nucleoside Triphosphate Formation <\/p>\n
1.08.6. Deoxyribonucleotide Biosynthesis <\/p>\n
1.08.7. Nucleotide Salvage <\/p>\n
1.08.8. Purine and Pyrimidine Catabolism <\/p>\n
1.08.9. Regulation of Gene Expression in Bacterial Nucleotide Synthesis <\/p>\n
1.08.10. Exploitation of the Knowledge of Nucleotide Metabolism in Biotechnology <\/p>\n
1.09. Organic Acids <\/p>\n
Glossary <\/p>\n
1.09.1. Introduction <\/p>\n
1.09.2. Citric Acid <\/p>\n
1.09.3. Gluconic Acid <\/p>\n
1.09.4. Lactic Acid <\/p>\n
1.09.5. Itaconic Acid <\/p>\n
1.09.6. Other Acids <\/p>\n
1.10. Peptides and Glycopeptides <\/p>\n
Glossary <\/p>\n
1.10.1. Introduction <\/p>\n
1.10.2. Peptide Hormones <\/p>\n
1.10.3. Neuropeptides <\/p>\n
1.10.4. Antibacterial Peptides <\/p>\n
1.10.5. Glycosylation Is a Common and Important Post-Translational Modification of Peptides <\/p>\n
1.10.6. Common Glycosidic Linkages <\/p>\n
1.10.7. Peptide Synthesis <\/p>\n
1.10.8. Glycopeptide Synthesis <\/p>\n
1.10.9. Peptides and Glycopeptides as Models of Proteins and Glycoproteins <\/p>\n
1.10.10. Application of Synthetic Peptides and Glycopeptides for the Treatment of Disease <\/p>\n
<\/p>\n
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\nComprehensive Biotechnology - 2nd Edition<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"