مشخصات کتاب

Molecular genetics of bacteria

ویرایش:  
نویسندگان: Jeremy Dale,  Simon Park  
سری:  
ISBN (شابک) : 9780470710340, 0470710349 
ناشر: Wiley-Blackwell 
سال نشر: 2010 
تعداد صفحات: 402 
زبان: English 
فرمت فایل : PDF (درصورت درخواست کاربر به PDF، EPUB یا AZW3 تبدیل می شود) 
حجم فایل: 9 مگابایت 

در صورت تبدیل فایل کتاب Molecular genetics of bacteria به فرمت های PDF، EPUB، AZW3، MOBI و یا DJVU می توانید به پشتیبان اطلاع دهید تا فایل مورد نظر را تبدیل نمایند.

توجه داشته باشید کتاب ژنتیک مولکولی باکتری ها نسخه زبان اصلی می باشد و کتاب ترجمه شده به فارسی نمی باشد. وبسایت اینترنشنال لایبرری ارائه دهنده کتاب های زبان اصلی می باشد و هیچ گونه کتاب ترجمه شده یا نوشته شده به فارسی را ارائه نمی دهد.

توضیحاتی درمورد کتاب به خارجی

Preface. 1 Nucleic Acid Structure and Function. 1.1 Structure of nucleic acids. 1.1.1 DNA. 1.1.2 RNA. 1.1.3 Hydrophobic interactions. 1.1.4 Different forms of the double helix. 1.1.5 Supercoiling. 1.1.6 Denaturation and hybridization. 1.1.7 Orientation of nucleic acid strands. 1.2 Replication of DNA. 1.2.1 Unwinding and rewinding. 1.2.2 Fidelity of replication; proofreading. 1.3 Chromosome replication and cell division. 1.4 DNA repair. 1.4.1 Mismatch repair. 1.4.2 Excision repair. 1.4.3 Recombination (post-replication) repair. 1.4.4 SOS repair. 1.5 Gene expression. 1.5.1 Transcription. 1.5.2 Translation. 1.5.3 Post-translational events. 1.6 Gene organization. 2 Mutation and Variation. 2.1 Variation and evolution. 2.1.1 Fluctuation test. 2.1.2 Replica plating. 2.1.3 Directed mutation in bacteria? 2.2 Types of mutation. 2.2.1 Point mutations. 2.2.2 Conditional mutants. 2.2.3 Variation due to larger-scale DNA alterations. 2.2.4 Extrachromosomal agents and horizontal gene transfer. 2.3 Recombination. 2.3.1 A model of the general (homologous) recombination process. 2.3.2 Enzymes involved in recombination. 2.4 Phenotypes. 2.4.1 Restoration of phenotype. 2.5 Mechanisms of mutation. 2.5.1 Spontaneous mutation. 2.5.2 Chemical mutagens. 2.5.3 Ultraviolet irradiation. 2.6 Isolation and identification of mutants. 2.6.1 Mutation and selection. 2.6.2 Replica plating. 2.6.3 Isolation of other mutants. 2.6.4 Molecular methods. 3 Regulation of Gene Expression. 3.1 Gene copy number. 3.2 Transcriptional control. 3.2.1 Promoters. 3.2.2 Terminators, attenuators and anti-terminators. 3.2.3 Induction and repression: regulatory proteins. 3.2.4 Two-component regulatory systems. 3.2.5 Global regulatory systems. 3.2.6 Quorum sensing. 3.3 Translational control. 3.3.1 Ribosome binding. 3.3.2 Codon usage. 3.3.3 Stringent response. 3.3.4 Regulatory RNA. 3.4 Phase variation. 4 Genetics of Bacteriophages. 4.1 Bacteriophage structure. 4.2 Single-strand DNA bacteriophages. 4.2.1 X174. 4.2.2 M13. 4.3 RNA-containing phages: MS2. 4.4 Double-stranded DNA phages. 4.4.1 Bacteriophage T4. 4.4.2 Bacteriophage lambda. 4.4.3 Lytic and lysogenic regulation of bacteriophage lambda. 4.5 Restriction and modification. 4.6 Bacterial resistance to phage attack. 4.7 Complementation and recombination. 4.8 Why are bacteriophages important? 4.8.1 Phage typing. 4.8.2 Phage therapy. 4.8.3 Phage display. 4.8.4 Phages in the natural environment. 4.8.5 Bacterial virulence and phage conversion. 5 Plasmids. 5.1 Some bacterial characteristics are determined by plasmids. 5.1.1 Antibiotic resistance. 5.1.2 Colicins and bacteriocins. 5.1.3 Virulence determinants. 5.1.4 Plasmids in plant-associated bacteria. 5.1.5 Metabolic activities. 5.2 Molecular properties of plasmids. 5.2.1 Plasmid replication and control. 5.2.2 Partitioning. 5.2.3 Host range. 5.2.4 Plasmid incompatibility. 5.3 Plasmid stability. 5.3.1 Plasmid integrity. 5.3.2 Partitioning. 5.3.3 Differential growth rate. 5.4 Associating a plasmid with a phenotype. 6 Gene Transfer. 6.1 Transformation. 6.2 Conjugation. 6.2.1 Mechanism of conjugation. 6.2.2 The F plasmid. 6.2.3 Conjugation in other bacteria. 6.3 Transduction. 6.3.1 Specialized transduction. 6.4 Recombination. 6.4.1 Consequences of recombination. 6.4.2 Site-specific and non-homologous (illegitimate) recombination. 6.5 Mosaic genes and chromosome plasticity. 7 Genomic Plasticity: Movable Genes and Phase Variation. 7.1 Insertion sequences. 7.1.1 Structure of insertion sequences. 7.1.2 Occurrence of insertion sequences. 7.2 Transposons. 7.2.1 Structure of transposons. 7.2.2 Integrons. 7.2.3 IS CR elements. 7.3 Mechanisms of transposition. 7.3.1 Replicative transposition. 7.3.2 Non-replicative (conservative) transposition. 7.3.3 Regulation of transposition. 7.3.4 Activation of genes by transposable elements. 7.3.5 Mu: A transposable bacteriophage. 7.3.6 Conjugative transposons. 7.4 Phase variation. 7.4.1 Variation mediated by simple DNA inversion. 7.4.2 Variation mediated by nested DNA inversion. 7.4.3 Antigenic variation in the gonococcus. 7.4.4 Phase variation by slipped-strand mispairing. 7.4.5 Phase variation mediated by differential DNA methylation. 7.5 Clustered regularly interspersed short palindromic repeats. 8 Genetic Modification: Exploiting the Potential of Bacteria. 8.1 Strain development. 8.1.1 Generation of variation. 8.1.2 Selection of desired variants. 8.2 Overproduction of primary metabolites. 8.2.1 Simple pathways. 8.2.2 Branched pathways. 8.3 Overproduction of secondary metabolites. 8.4 Gene cloning. 8.4.1 Cutting and joining DNA. 8.4.2 Plasmid vectors. 8.4.3 Bacteriophage lambda vectors. 8.4.4 Cloning larger fragments. 8.4.5 Bacteriophage M13 vectors. 8.5 Gene libraries. 8.5.1 Construction of genomic libraries. 8.5.2 Screening a gene library. 8.5.3 Cloning PCR products. 8.5.4 Construction of a cDNA library. 8.6 Products from cloned genes. 8.6.1 Expression vectors. 8.6.2 Making new genes. 8.6.3 Other bacterial hosts. 8.6.4 Novel vaccines. 8.7 Other uses of gene technology. 9 Genetic Methods for Investigating Bacteria. 9.1 Metabolic pathways. 9.1.1 Complementation. 9.1.2 Cross-feeding. 9.2 Microbial physiology. 9.2.1 Reporter genes. 9.2.2 Chromatin immunoprecipitation. 9.2.3 Cell division. 9.2.4 Motility and chemotaxis. 9.2.5 Cell differentiation. 9.3 Bacterial virulence. 9.3.1 Wide-range mechanisms of bacterial pathogenesis. 9.3.2 Detection of virulence genes. 9.4 Specific mutagenesis. 9.4.1 Gene replacement. 9.4.2 Antisense RNA. 9.5 Taxonomy, evolution and epidemiology. 9.5.1 Molecular taxonomy. 9.5.2 GC content. 9.5.3 16 S rRNA. 9.5.4 Denaturing-gradient gel electrophoresis and temperature-gradient gel electrophoresis. 9.5.5 Diagnostic use of PCR. 9.5.6 Molecular epidemiology. 10 Gene Mapping to Genomics and Beyond. 10.1 Gene mapping. 10.1.1 Conjugational analysis. 10.1.2 Gene libraries. 10.1.3 Restriction mapping and pulsed-field gel electrophoresis. 10.2 DNA sequence determination. 10.2.1 Sanger sequencing. 10.2.2 Dye terminator sequencing. 10.2.3 Pyrosequencing. 10.2.4 Massively parallel sequencing. 10.3 Genome sequencing. 10.3.1 Genome-sequencing strategies. 10.3.2 Relating sequence to function. 10.3.3 Metagenomics. 10.4 Comparative genomics. 10.4.1 Microarrays. 10.5 Analysis of gene expression. 10.5.1 Transcriptional analysis. 10.5.2 Translational analysis. 10.6 Metabolomics. 10.7 Systems biology and synthetic genomics. 10.7.1 Systems biology. 10.7.2 Synthetic genomics. 10.8 Conclusion. Appendix A Further Reading. Appendix B Abbreviations Used. Appendix C Glossary. Appendix D Enzymes and other Proteins. Appendix E Genes. Appendix F Standard Genetic Code. Appendix G Bacterial Species. Index

نظرات کاربران

کتاب های تصادفی

دانلود کتاب Comment is free ; & Start swimming: two plays

دانلود کتاب Qualities of food

دانلود کتاب English Idioms in Use Advanced Keys

دانلود کتاب Tools and Algorithms for the Construction and Analysis of Systems: First International Workshop, TACAS '95 Aarhus, Denmark, May 19–20, 1995 Selected Papers

دانلود کتاب Lonely Planet Hiking & Tramping in New Zealand