Fundamental Bacterial Genetics
1st Edition
Will be published approx. on 21. August 2003
Book
Paperback/Softback
302 pages
978-0-632-04448-1 (ISBN)
Description
Fundamental Bacterial Genetics presents a concise introduction to microbial genetics. The text focuses on one bacterial species, Escherichia coli, but draws examples from other microbial systems at appropriate points to support the fundamental concepts of molecular genetics.
A solid balance of concepts, techniques and applications makes this book an accessible, essential introduction to the theory and practice of fundamental microbial genetics.
FYI boxes - feature key experiments that lead to what we now know, biographies of key scientists, comparisons with other species and more.
Study questions - at the end of each chapter, review and test students' knowledge of key chapter concepts.
Key references - included both at chapter end and in a full reference list at the end of the book.
Full Chapter on Genomics, Bioinformatics and Proteomics - includes coverage of functional genomics and microarrays.
Dedicated website - animations, study resources, web research questions and illustrations downloadable for powerpoint files provide students and instructors with an enhanced, interactive experience.
A solid balance of concepts, techniques and applications makes this book an accessible, essential introduction to the theory and practice of fundamental microbial genetics.
FYI boxes - feature key experiments that lead to what we now know, biographies of key scientists, comparisons with other species and more.
Study questions - at the end of each chapter, review and test students' knowledge of key chapter concepts.
Key references - included both at chapter end and in a full reference list at the end of the book.
Full Chapter on Genomics, Bioinformatics and Proteomics - includes coverage of functional genomics and microarrays.
Dedicated website - animations, study resources, web research questions and illustrations downloadable for powerpoint files provide students and instructors with an enhanced, interactive experience.
More details
Language
English
Place of publication
Hoboken
United Kingdom
Publishing group
John Wiley and Sons Ltd
Target group
Professional and scholarly
Product notice
Paperback (trade)
Unsewn / adhesive bound
Dimensions
Height: 280 mm
Width: 220 mm
Thickness: 22 mm
Weight
848 gr
ISBN-13
978-0-632-04448-1 (9780632044481)
Copyright in bibliographic data and cover images is held by Nielsen Book Services Limited or by the publishers or by their respective licensors: all rights reserved.
Schweitzer Classification
Other editions
Additional editions
Nancy Trun | Janine Trempy
Fundamental Bacterial Genetics
E-Book
04/2009
Wiley-Blackwell
€87.99
Available for download
Persons
Janine E. Trempy, Ph.D., is an Associate Professor of Microbiology and the Associate Dean in the College of Science at Oregon State University. She has received numerous research and teaching awards from Oregon State University, and in 1996 she was named by the Carnegie Foundation/CASE as Oregon Professor of the Year for her development and use of innovative inquiry based cooperative learning environments. She was a Waksman/American Society for Microbiology Traveling Lecturer, presenting lectures focusing on science education reform. Her research focus is on bacterial crisis management systems, microbial applications (i.e. biosensor development; food safety) and developing inclusive learning environments that enhance science literacy.
Nancy Trun is an Assistant Professor in the Dept of Biological Sciences at Duquesne University where she teaches undergraduate and graduate level microbial genetics. She has taught microbial genetics courses at the University of Maryland and at Cold Spring Harbor Laboratory and received the National Institutes of Health Director's Award for science education at the elementary school level. Currently, her research focus is on chromosome folding in bacteria.
Nancy Trun is an Assistant Professor in the Dept of Biological Sciences at Duquesne University where she teaches undergraduate and graduate level microbial genetics. She has taught microbial genetics courses at the University of Maryland and at Cold Spring Harbor Laboratory and received the National Institutes of Health Director's Award for science education at the elementary school level. Currently, her research focus is on chromosome folding in bacteria.
Content
1. Introduction To The Cell. The Molecules That Make Up A Cell.
The Bacterial Cell: A Quick Overview.
How Do Cells Grow?.
What Is Genetics?.
Summary.
2. The Bacterial Dna Molecule.
The Structure Of DNA And RNA.
Deoxyribonucleosides And Deoxyribonucleotides.
DNA Is Only Polymerized 5' To 3'.
Double-Stranded Dna.
Supercoiling Double-Stranded Dna.
Replication Of The Escherichia Coli Chromosome.
Constraints That Influence Dna Replication.
The Replication Machinery.
Dna Polymerases.
Dnag Primase.
Replication Of Both Strands.
Theta Mode Replication.
Minimizing Mistakes In Dna Replication.
The Dna Replication Machinery As Molecular Tools.
Summary.
3. Mutations.
Phenotype And Genotype.
Classes Of Mutations.
Point Mutations And Their Consequences.
Measuring Mutations: Rate And Frequency.
Spontaneous And Induced Mutations.
Errors During Dna Replication: Incorporation Errors.
Errors Due To Tautomerism.
Spontaneous Alteration By Depurination.
Spontaneous Alteration By Deamination.
Alterations By Spontaneous Genetic Rearrangement.
Alterations Caused By Transposition.
Induced Mutations.
Chemicals That Mimic Normal Dna Bases: Base Analogues.
Chemicals That React With Dna Bases: Base Modifiers.
Chemicals That Bind Dna Bases: Intercalators.
Mutagens That Physically Damage The Dna: Ultraviolet Light And Ionizing.
Radiation.
Mutator Strains.
Reverting Mutations.
Suppression.
Ames Test.
How Have We Exploited Bacterial Mutants.
Summary.
4. Dna Repair.
Lesions That Constitute Dna Damage.
Reverse, Excise Or Tolerate?.
Mechanisms That Reverse Dna Damage.
Photoreactivation.
O6-Methylguanine Or O4-Methylthymine Methyltransferase.
Mechanisms That Excise Dna Damage.
Uvrabc Directed Nucleotide Excision Repair.
Muthls Methyl Directed Mismatch Repair.
Very Short Patch Repair.
Glycosylases.
Uracil-N-Glycosylase Coupled With Ap Excision Repair.
Deaminated Bases Removed By Dna Glycosylase.
Alkylated Bases Removed By Dna Glycosylase.
Mutm/Muty: Oxidative Damage.
N-Glycosylases Specific For Pyrimidine Dimmers.
Mechanisms That Tolerate Dna Damage.
Transdimer Synthesis.
Post Replication/Recombinational Repair (Prr).
Introduction To The Sos Regulon.
Summary.
5. Recombination:.
Homologous Recombination.
Models For Homologous Recombination.
The Holliday Or Double-Strand Invasion Model Of Recombination.
An Alternative To The Holliday Model: The Single Strand Invasion Model Of Meselson And Radding.
Further Enzymatic Considerations.
Site-Specific Recombination.
A Typical Site-Specific Recombinational Event.
Bacteriophage l:A Model For Site-Specific Recombination.
Other Examples Of Site-Specific Recombination.
Illegitimate Recombination.
Summary.
6. Transposition.
The Structure Of Transposons.
The Frequency Of Transposition.
The Two Types Of Transposition Reactions.
The Transposition Machinery.
The Transposition Machinery; Accessory Proteins Encoded By The Transposon.
The Transposition Machinery: Accessory Proteins Encoded By The Host.
Non-Replicative Transposition.
Replicative Transposition.
Does The Formation Of A Cointegrate Predict The Transposition Mechanism?.
The Fate Of The Donor Site.
Target Immunity.
Transposons As Molecular Tools.
Summary.
7. Bacteriophage.
The Structure Of Phage.
The Life Cycle Of A Bacteriophage.
Lytic-Lysogenic Options.
The l Lifecycle.
l Adsorption.
l Dna Injection.
Protecting The l Genome In The Bacterial Cytoplasm.
What Happens To The l Genome After It Is Stabilized?.
l And The Lytic-Lysogenic Decision.
The l Lysogenic Pathway.
The l Lytic Pathway.
Dna Replication During The l Lytic Pathway.
Making l Phage.
Getting Out Of The Cell-The l S And R Proteins.
Induction Of By The Sos System.
Superinfection.
Restriction And Modification Of Dna.
The Lifecycle Of M13-M13 Adsorption And Injection.
Protection Of The M13 Genome.
M13 Dna Replication.
M13 Phage Production And Release From The Cell.
The Lifecycle Of P1.
Adsorption, Injection And Protection Of The Genome.
P1 Dna Replication And Phage Assembly.
The Location Of The P1 Prophage In A Lysogen.
P1 Transducing Particles.
The Lifecycle Of T4-T4 Adsorption And Injection.
T4rii Mutations And The Nature Of The Genetic Code.
Summary.
8. Transduction.
Generalized Transduction Vs Specialized Transduction.
P1 As A Model For Generalized Transducing Phage.
Packaging The Chromosome.
Moving Pieces Of The Chromosome From One Cell To Another.
Identifying Transduced Bacteria: Selection Vs Screen.
Carrying Out A Transduction.
Uses For Transduciton.
Two Factor Crosses To Determine Gene Linkage.
Mapping The Order Of Genes- Three Factor Crosses.
Uses For Transduction-Strain Construction.
Uses For Transduction-Localized Mutagenesis.
Specialized Transducing Phage.
Making Merodiploids With Specialized Transducing Phage.
Moving Mutations From Plasmids To Specialized Transducing Phage To The.
Chromosome.
Summary.
9. Natural Plasmids.
Origins Of Replication.
Plasmid Copy Number.
Setting The Copy Number.
Plasmid Incompatibility.
Plasmid Amplification.
Other Genes That Can Be Carried By Plasmids.
Plasmids Can Be Circular Or Linear Dna.
Broad Host Range Plasmids.
Moving Plasmids From Cell To Cell.
Summary.
10. Conjugation:.
The F Factor.
The R Factors.
The Conjugation Machinery.
Transfer Of The Dna.
Surface Exclusion.
F, Hfr Or F-Prime.
Formation Of The Hfr.
Transfer Of Dna From An Hfr To Another Cell.
Formation Of F-Primes.
Transfer Of F-Primes From One Cell To Another.
Genetic Uses Of F-Primes.
Genetic Uses Of Hfr Strains-Mapping Genes On The E. Coli Chromosome Using Hfr.
Crosses.
The 50% Rule.
Using Several Hfr Strains To Cover The Chromosome.
Mobilization Of Non-Conjugatible Plasmids By R And F.
Conjugation From Prokaryotes To Eukaryotes.
Summary.
11. Transformation:.
Natural Competency.
The Process Of Natural Transformation.
The Machinery Of Naturally Transformable Cells.
Artificial Transformation.
Transformation As A Genetic Tool: Gene Mapping.
Transformation As A Molecular Tool.
Summary.
12. Gene Expression And Regulation.
The Players In The Regulation Game.
Operons And Regulons.
Repression Of The Lac Operon.
Activation Of The Lac Operon By Cyclic Amp And The Cap Protein.
Regulation Of The Tryptophan Biosynthesis Operon By Attenuation.
Regulation Of The Heat Shock Regulon By An Alternative Sigma Factor, Mrna Stability And Proteolysis.
Regulation Of The Sos Regulon By Proteolytic Cleavage Of The Repressor.
Two Component Regulatory Systems, Signal Transduction And The Cps Regulon.
Summary.
13. Plasmids, Bacteriophage And Transposons As Tools.
What Is A Cloning Vector?.
Why Not Use Naturally Occurring Plasmids As Vectors?.
The Importance Of Copy Number.
An Example Of How A Cloning Vector Works-Pbr322.
Multiple Cloning Sites.
Determining Which Plasmids Contain An Insert.
Expression Vectors.
Vectors For Purifying The Cloned Gene Product.
Vectors For Localizing The Gene Product.
Vectors For Studying Gene Expression.
Shuttle Vectors.
Artificial Chromosomes.
Constructing Phage Vectors.
Suicide Vectors.
Phage Display Vectors.
Combining Phage Vectors And Transposons.
Summary.
14. DNA Cloning:.
Isolating DNA From Cells - Plasmid DNA Isolation.
Isolating DNA From Cells - Chromosomal DNA Isolation.
Cutting DNA Molecules.
Type I Restriction-Modification Systems.
Type II Restriction-Modification Systems.
Type III Restriction-Modification Systems.
Restriction-Modification As A Molecular Tool.
Generate Double Stranded Breaks In DNA By Shearing The Dna.
Joining DNA Molecules.
Manipulating The Ends Of Molecules.
Visualizing The Cloning Process.
Constructing Libraries Of Clones.
DNA Detection - Southern Blotting.
DNA Amplification: Polymerase Chain Reaction.
Adding Novel Dna Sequences To The Ends Of A Pcr Amplified Sequence.
Site Directed Mutagenesis Using Pcr.
Cloning And Expressing A Gene.
Dna Sequencing Using Dideoxy Sequencing.
Dna Sequence Searches.
Summary.
15. Bioinformatics And Proteomics.
Bioinformatics.
Strategies For Sequencing Genomes.
Bacterial Genomes.
Analyzing Genomes.
The E. Coli K-12 Genome.
Proteomics.
Techniques For Examining The Proteome-Sds-Page And 2-Dimensional Sds-Page.
Techniques For Examining The Proteome-Microarray Technology.
Summary.
Glossary.
Additional References.
The Bacterial Cell: A Quick Overview.
How Do Cells Grow?.
What Is Genetics?.
Summary.
2. The Bacterial Dna Molecule.
The Structure Of DNA And RNA.
Deoxyribonucleosides And Deoxyribonucleotides.
DNA Is Only Polymerized 5' To 3'.
Double-Stranded Dna.
Supercoiling Double-Stranded Dna.
Replication Of The Escherichia Coli Chromosome.
Constraints That Influence Dna Replication.
The Replication Machinery.
Dna Polymerases.
Dnag Primase.
Replication Of Both Strands.
Theta Mode Replication.
Minimizing Mistakes In Dna Replication.
The Dna Replication Machinery As Molecular Tools.
Summary.
3. Mutations.
Phenotype And Genotype.
Classes Of Mutations.
Point Mutations And Their Consequences.
Measuring Mutations: Rate And Frequency.
Spontaneous And Induced Mutations.
Errors During Dna Replication: Incorporation Errors.
Errors Due To Tautomerism.
Spontaneous Alteration By Depurination.
Spontaneous Alteration By Deamination.
Alterations By Spontaneous Genetic Rearrangement.
Alterations Caused By Transposition.
Induced Mutations.
Chemicals That Mimic Normal Dna Bases: Base Analogues.
Chemicals That React With Dna Bases: Base Modifiers.
Chemicals That Bind Dna Bases: Intercalators.
Mutagens That Physically Damage The Dna: Ultraviolet Light And Ionizing.
Radiation.
Mutator Strains.
Reverting Mutations.
Suppression.
Ames Test.
How Have We Exploited Bacterial Mutants.
Summary.
4. Dna Repair.
Lesions That Constitute Dna Damage.
Reverse, Excise Or Tolerate?.
Mechanisms That Reverse Dna Damage.
Photoreactivation.
O6-Methylguanine Or O4-Methylthymine Methyltransferase.
Mechanisms That Excise Dna Damage.
Uvrabc Directed Nucleotide Excision Repair.
Muthls Methyl Directed Mismatch Repair.
Very Short Patch Repair.
Glycosylases.
Uracil-N-Glycosylase Coupled With Ap Excision Repair.
Deaminated Bases Removed By Dna Glycosylase.
Alkylated Bases Removed By Dna Glycosylase.
Mutm/Muty: Oxidative Damage.
N-Glycosylases Specific For Pyrimidine Dimmers.
Mechanisms That Tolerate Dna Damage.
Transdimer Synthesis.
Post Replication/Recombinational Repair (Prr).
Introduction To The Sos Regulon.
Summary.
5. Recombination:.
Homologous Recombination.
Models For Homologous Recombination.
The Holliday Or Double-Strand Invasion Model Of Recombination.
An Alternative To The Holliday Model: The Single Strand Invasion Model Of Meselson And Radding.
Further Enzymatic Considerations.
Site-Specific Recombination.
A Typical Site-Specific Recombinational Event.
Bacteriophage l:A Model For Site-Specific Recombination.
Other Examples Of Site-Specific Recombination.
Illegitimate Recombination.
Summary.
6. Transposition.
The Structure Of Transposons.
The Frequency Of Transposition.
The Two Types Of Transposition Reactions.
The Transposition Machinery.
The Transposition Machinery; Accessory Proteins Encoded By The Transposon.
The Transposition Machinery: Accessory Proteins Encoded By The Host.
Non-Replicative Transposition.
Replicative Transposition.
Does The Formation Of A Cointegrate Predict The Transposition Mechanism?.
The Fate Of The Donor Site.
Target Immunity.
Transposons As Molecular Tools.
Summary.
7. Bacteriophage.
The Structure Of Phage.
The Life Cycle Of A Bacteriophage.
Lytic-Lysogenic Options.
The l Lifecycle.
l Adsorption.
l Dna Injection.
Protecting The l Genome In The Bacterial Cytoplasm.
What Happens To The l Genome After It Is Stabilized?.
l And The Lytic-Lysogenic Decision.
The l Lysogenic Pathway.
The l Lytic Pathway.
Dna Replication During The l Lytic Pathway.
Making l Phage.
Getting Out Of The Cell-The l S And R Proteins.
Induction Of By The Sos System.
Superinfection.
Restriction And Modification Of Dna.
The Lifecycle Of M13-M13 Adsorption And Injection.
Protection Of The M13 Genome.
M13 Dna Replication.
M13 Phage Production And Release From The Cell.
The Lifecycle Of P1.
Adsorption, Injection And Protection Of The Genome.
P1 Dna Replication And Phage Assembly.
The Location Of The P1 Prophage In A Lysogen.
P1 Transducing Particles.
The Lifecycle Of T4-T4 Adsorption And Injection.
T4rii Mutations And The Nature Of The Genetic Code.
Summary.
8. Transduction.
Generalized Transduction Vs Specialized Transduction.
P1 As A Model For Generalized Transducing Phage.
Packaging The Chromosome.
Moving Pieces Of The Chromosome From One Cell To Another.
Identifying Transduced Bacteria: Selection Vs Screen.
Carrying Out A Transduction.
Uses For Transduciton.
Two Factor Crosses To Determine Gene Linkage.
Mapping The Order Of Genes- Three Factor Crosses.
Uses For Transduction-Strain Construction.
Uses For Transduction-Localized Mutagenesis.
Specialized Transducing Phage.
Making Merodiploids With Specialized Transducing Phage.
Moving Mutations From Plasmids To Specialized Transducing Phage To The.
Chromosome.
Summary.
9. Natural Plasmids.
Origins Of Replication.
Plasmid Copy Number.
Setting The Copy Number.
Plasmid Incompatibility.
Plasmid Amplification.
Other Genes That Can Be Carried By Plasmids.
Plasmids Can Be Circular Or Linear Dna.
Broad Host Range Plasmids.
Moving Plasmids From Cell To Cell.
Summary.
10. Conjugation:.
The F Factor.
The R Factors.
The Conjugation Machinery.
Transfer Of The Dna.
Surface Exclusion.
F, Hfr Or F-Prime.
Formation Of The Hfr.
Transfer Of Dna From An Hfr To Another Cell.
Formation Of F-Primes.
Transfer Of F-Primes From One Cell To Another.
Genetic Uses Of F-Primes.
Genetic Uses Of Hfr Strains-Mapping Genes On The E. Coli Chromosome Using Hfr.
Crosses.
The 50% Rule.
Using Several Hfr Strains To Cover The Chromosome.
Mobilization Of Non-Conjugatible Plasmids By R And F.
Conjugation From Prokaryotes To Eukaryotes.
Summary.
11. Transformation:.
Natural Competency.
The Process Of Natural Transformation.
The Machinery Of Naturally Transformable Cells.
Artificial Transformation.
Transformation As A Genetic Tool: Gene Mapping.
Transformation As A Molecular Tool.
Summary.
12. Gene Expression And Regulation.
The Players In The Regulation Game.
Operons And Regulons.
Repression Of The Lac Operon.
Activation Of The Lac Operon By Cyclic Amp And The Cap Protein.
Regulation Of The Tryptophan Biosynthesis Operon By Attenuation.
Regulation Of The Heat Shock Regulon By An Alternative Sigma Factor, Mrna Stability And Proteolysis.
Regulation Of The Sos Regulon By Proteolytic Cleavage Of The Repressor.
Two Component Regulatory Systems, Signal Transduction And The Cps Regulon.
Summary.
13. Plasmids, Bacteriophage And Transposons As Tools.
What Is A Cloning Vector?.
Why Not Use Naturally Occurring Plasmids As Vectors?.
The Importance Of Copy Number.
An Example Of How A Cloning Vector Works-Pbr322.
Multiple Cloning Sites.
Determining Which Plasmids Contain An Insert.
Expression Vectors.
Vectors For Purifying The Cloned Gene Product.
Vectors For Localizing The Gene Product.
Vectors For Studying Gene Expression.
Shuttle Vectors.
Artificial Chromosomes.
Constructing Phage Vectors.
Suicide Vectors.
Phage Display Vectors.
Combining Phage Vectors And Transposons.
Summary.
14. DNA Cloning:.
Isolating DNA From Cells - Plasmid DNA Isolation.
Isolating DNA From Cells - Chromosomal DNA Isolation.
Cutting DNA Molecules.
Type I Restriction-Modification Systems.
Type II Restriction-Modification Systems.
Type III Restriction-Modification Systems.
Restriction-Modification As A Molecular Tool.
Generate Double Stranded Breaks In DNA By Shearing The Dna.
Joining DNA Molecules.
Manipulating The Ends Of Molecules.
Visualizing The Cloning Process.
Constructing Libraries Of Clones.
DNA Detection - Southern Blotting.
DNA Amplification: Polymerase Chain Reaction.
Adding Novel Dna Sequences To The Ends Of A Pcr Amplified Sequence.
Site Directed Mutagenesis Using Pcr.
Cloning And Expressing A Gene.
Dna Sequencing Using Dideoxy Sequencing.
Dna Sequence Searches.
Summary.
15. Bioinformatics And Proteomics.
Bioinformatics.
Strategies For Sequencing Genomes.
Bacterial Genomes.
Analyzing Genomes.
The E. Coli K-12 Genome.
Proteomics.
Techniques For Examining The Proteome-Sds-Page And 2-Dimensional Sds-Page.
Techniques For Examining The Proteome-Microarray Technology.
Summary.
Glossary.
Additional References.