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Library | Item Barcode | Call Number | Material Type | Item Category 1 | Status |
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Searching... | 30000010121461 | QR92.B3 B32 2007 | Open Access Book | Book | Searching... |
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Summary
Summary
Microbes produce an extraordinary array of defense systems. These include bacteriocins, a class of antimicrobial molecules with narrow killing spectra, produced by bacteria. The book describes the diversity and ecological role of bacteriocins of Gram-positive and Gram-negative bacteria, presenting a new classification scheme for the former and a state-of-the-art look at the role of bacteriocins in bacterial communication. It discusses the molecular evolution of colicins and colicin-like bacteriocins, and provides a contemporary overview of archaeocins, bacteriocin-like antimicrobials produced by archaebacteria. Furthermore, various modeling (in silico) studies elucidate the role of bacteriocins in microbial community dynamics and fitness, delving into rock-paper-scissors competition and the counter-intuitive survival of the weakest. The book makes compelling reading for a multi-faceted scientific audience, including those working in the fields of biodiversity and biotechnology, notably in the human and animal health domain.
Table of Contents
1 Introduction | p. 1 |
2 The Diversity of Bacteriocins in Gram-Negative Bacteria | p. 5 |
Summary | p. 5 |
2.1 Introduction | p. 5 |
2.2 The Frequency of Bacteriocin Production | p. 7 |
2.2.1 Colicins | p. 7 |
2.2.2 Microcins | p. 8 |
2.3 Bacteriocin Diversity | p. 9 |
2.3.1 Colicins | p. 9 |
2.3.2 Microcins | p. 10 |
2.4 Multiple Bacteriocin Production | p. 11 |
2.5 Overview | p. 12 |
References | p. 17 |
3 Molecular Evolution of Bacteriocins in Gram-Negative Bacteria | p. 19 |
Summary | p. 19 |
3.1 Introduction | p. 19 |
3.2 Bacteriocins of Gram-Negative Bacteria | p. 20 |
3.3 Colicins and Colicin-like Bacteriocins | p. 21 |
3.3.1 Colicin Gene Organization | p. 21 |
3.3.2 Functional Domains in Colicin and CLB Proteins | p. 23 |
3.4 Models of Colicin Evolution | p. 25 |
3.4.1 Diversifying Selection | p. 25 |
3.4.2 Diversifying Recombination | p. 27 |
3.4.3 Evolution of Colicin-like Bacteriocins | p. 27 |
3.5 Evolution of Colicin Killing Domains | p. 29 |
3.6 Evolution of the Translocation and Receptor-Binding Domains | p. 36 |
3.7 Evolution of Colicin Regulatory Sequences | p. 37 |
3.8 Colicin D: A Possible Intermediate Between Pyocins and Colicins | p. 38 |
3.9 Conclusions | p. 40 |
References | p. 41 |
4 The Diversity of Bacteriocins in Gram-Positive Bacteria | p. 45 |
Summary | p. 45 |
4.1 Introduction | p. 45 |
4.1.1 Bacteriocins: A Historical Perspective | p. 45 |
4.1.2 Bacteriocins of Gram-Positive Bacteria | p. 46 |
4.1.3 Why Produce Bacteriocins? | p. 47 |
4.1.4 Detection of Bacteriocins of Gram-Positive Bacteria | p. 48 |
4.1.5 Nomenclature of Bacteriocins of Gram-Positive Bacteria | p. 49 |
4.1.6 Classification of Bacteriocins of Gram-Positive Bacteria | p. 50 |
4.2 Class I: The Lanthionine-Containing (Lantibiotic) Bacteriocins | p. 53 |
4.2.1 Type AI Lantibiotics | p. 53 |
4.2.2 Type AII Lantibiotics | p. 58 |
4.2.3 Type B (Globular) Lantibiotics | p. 61 |
4.2.4 Type C (Multi-Component) Lantibiotics | p. 62 |
4.3 Class II: The Unmodified Peptide Bacteriocins | p. 64 |
4.3.1 Type IIa: The Pediocin-like Peptides | p. 64 |
4.3.2 Type IIb: Multi-Component Bacteriocins | p. 66 |
4.3.3 Type IIc: Miscellaneous Unmodified Bacteriocins | p. 61 |
4.4 Class III: The Large (> 10 kDa) Bacteriocins | p. 74 |
4.4.1 Type IIIa: The Bacteriolysins (Bacteriolytic Enzymes) | p. 74 |
4.4.2 Type IIIb: The Non-Lytic Bacteriocins | p. 78 |
4.5 Class IV: The Cyclic Bacteriocins | p. 79 |
4.5.1 Enterocin AS-48 | p. 81 |
4.5.2 Gassericin A and Reutericin 6 | p. 82 |
4.5.3 Uberolysin | p. 82 |
4.6 Concluding Remarks | p. 83 |
References | p. 83 |
5 Peptide and Protein Antibiotics from the Domain Archaea: Halocins and Sulfolobicins | p. 93 |
Summary | p. 93 |
5.1 Introduction | p. 93 |
5.2 Halocins | p. 94 |
5.2.1 The Ubiquity of Halocin Production | p. 94 |
5.2.2 The Role of Halocins in the Environment and the Inability to Detect Halocin Activity in Hypersaline Crystallizer Ponds | p. 98 |
5.2.3 Activity Spectra | p. 99 |
5.2.4 Common Features of Halocins | p. 101 |
5.2.5 Microhalocins ([less than or equal] 10 kDa) | p. 102 |
5.2.6 Protein Halocins (> 10 kDa) | p. 104 |
5.3 Biotechnology of Halocins | p. 106 |
5.4 Sulfolobicins | p. 106 |
References | p. 107 |
6 The Ecological and Evolutionary Dynamics of Model Bacteriocin Communities | p. 111 |
Summary | p. 111 |
6.1 Introduction | p. 111 |
6.2 Dynamics in Two-Strain Communities: Getting over the Hump | p. 113 |
6.3 Dynamics in Three-Strain Communities: Playing Rock-Paper-Scissors | p. 119 |
6.4 Evolution in Three-Strain Communities: Survival of the Weakest | p. 125 |
6.5 Dynamics with many Strains: Universal Chemical Warfare | p. 128 |
6.6 Discussion | p. 129 |
Appendix Sensitivity is an ESS in the Well-Mixed RPS Game | p. 131 |
References | p. 132 |
7 Bacteriocins' Role in Bacterial Communication | p. 135 |
Summary | p. 135 |
7.1 Introduction | p. 135 |
7.2 Bacteriocin-Mediated Intercellular Communication | p. 137 |
7.2.1 Autoregulation of Class I Bacteriocins | p. 138 |
7.2.2 Quorum Sensing Regulation of Class II Bacteriocins | p. 138 |
7.3 Bacteriocin-Coordinated Multicellular Communication | p. 139 |
7.3.1 Oral Biofilms | p. 140 |
7.3.2 Gastrointestinal Biofilms | p. 141 |
7.4 Conclusions | p. 142 |
References | p. 143 |
Subject Index | p. 147 |