{"product_id":"fundamental-bacterial-genetics-isbn-9780632044481","title":"Fundamental Bacterial Genetics","description":"\u003cp\u003e\u003cb\u003e\u003ci\u003eFundamental Bacterial Genetics\u003c\/i\u003e presents a concise introduction to microbial genetics. The text focuses on one bacterial species, \u003ci\u003eEscherichia coli\u003c\/i\u003e, but draws examples from other microbial systems at appropriate points to support the fundamental concepts of molecular genetics.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eA solid balance of concepts, techniques and applications makes this book an accessible, essential introduction to the theory and practice of fundamental microbial genetics.\u003c\/p\u003e \u003cul\u003e \u003cli\u003eFYI boxes - feature key experiments that lead to what we now know, biographies of key scientists, comparisons with other species and more.\u003c\/li\u003e \u003cli\u003eStudy questions - at the end of each chapter, review and test students' knowledge of key chapter concepts.\u003c\/li\u003e \u003cli\u003eKey references - included both at chapter end and in a full reference list at the end of the book.\u003c\/li\u003e \u003cli\u003eFull Chapter on Genomics, Bioinformatics and Proteomics - includes coverage of functional genomics and microarrays.\u003c\/li\u003e \u003cli\u003eDedicated website – animations, study resources, web research questions and illustrations downloadable for powerpoint files provide students and instructors with an enhanced, interactive experience.\u003c\/li\u003e \u003c\/ul\u003e  \u003cb\u003e1. Introduction To The Cell\u003c\/b\u003e. \u003cp\u003eThe Molecules That Make Up A Cell.\u003c\/p\u003e \u003cp\u003eThe Bacterial Cell: A Quick Overview.\u003c\/p\u003e \u003cp\u003eHow Do Cells Grow?.\u003c\/p\u003e \u003cp\u003eWhat Is Genetics?.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e2. The Bacterial Dna Molecule.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eThe Structure Of DNA And RNA.\u003c\/p\u003e \u003cp\u003eDeoxyribonucleosides And Deoxyribonucleotides.\u003c\/p\u003e \u003cp\u003eDNA Is Only Polymerized 5’ To 3’.\u003c\/p\u003e \u003cp\u003eDouble-Stranded Dna.\u003c\/p\u003e \u003cp\u003eSupercoiling Double-Stranded Dna.\u003c\/p\u003e \u003cp\u003eReplication Of The Escherichia Coli Chromosome.\u003c\/p\u003e \u003cp\u003eConstraints That Influence Dna Replication.\u003c\/p\u003e \u003cp\u003eThe Replication Machinery.\u003c\/p\u003e \u003cp\u003eDna Polymerases.\u003c\/p\u003e \u003cp\u003eDnag Primase.\u003c\/p\u003e \u003cp\u003eReplication Of Both Strands.\u003c\/p\u003e \u003cp\u003eTheta Mode Replication.\u003c\/p\u003e \u003cp\u003eMinimizing Mistakes In Dna Replication.\u003c\/p\u003e \u003cp\u003eThe Dna Replication Machinery As Molecular Tools.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e3. Mutations.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003ePhenotype And Genotype.\u003c\/p\u003e \u003cp\u003eClasses Of Mutations.\u003c\/p\u003e \u003cp\u003ePoint Mutations And Their Consequences.\u003c\/p\u003e \u003cp\u003eMeasuring Mutations: Rate And Frequency.\u003c\/p\u003e \u003cp\u003eSpontaneous And Induced Mutations.\u003c\/p\u003e \u003cp\u003eErrors During Dna Replication: Incorporation Errors.\u003c\/p\u003e \u003cp\u003eErrors Due To Tautomerism.\u003c\/p\u003e \u003cp\u003eSpontaneous Alteration By Depurination.\u003c\/p\u003e \u003cp\u003eSpontaneous Alteration By Deamination.\u003c\/p\u003e \u003cp\u003eAlterations By Spontaneous Genetic Rearrangement.\u003c\/p\u003e \u003cp\u003eAlterations Caused By Transposition.\u003c\/p\u003e \u003cp\u003eInduced Mutations.\u003c\/p\u003e \u003cp\u003eChemicals That Mimic Normal Dna Bases: Base Analogues.\u003c\/p\u003e \u003cp\u003eChemicals That React With Dna Bases: Base Modifiers.\u003c\/p\u003e \u003cp\u003eChemicals That Bind Dna Bases: Intercalators.\u003c\/p\u003e \u003cp\u003eMutagens That Physically Damage The Dna: Ultraviolet Light And Ionizing.\u003c\/p\u003e \u003cp\u003eRadiation.\u003c\/p\u003e \u003cp\u003eMutator Strains.\u003c\/p\u003e \u003cp\u003eReverting Mutations.\u003c\/p\u003e \u003cp\u003eSuppression.\u003c\/p\u003e \u003cp\u003eAmes Test.\u003c\/p\u003e \u003cp\u003eHow Have We Exploited Bacterial Mutants.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e4. Dna Repair.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eLesions That Constitute Dna Damage.\u003c\/p\u003e \u003cp\u003eReverse, Excise Or Tolerate?.\u003c\/p\u003e \u003cp\u003eMechanisms That Reverse Dna Damage.\u003c\/p\u003e \u003cp\u003ePhotoreactivation.\u003c\/p\u003e \u003cp\u003eO6-Methylguanine Or O4-Methylthymine Methyltransferase.\u003c\/p\u003e \u003cp\u003eMechanisms That Excise Dna Damage.\u003c\/p\u003e \u003cp\u003eUvrabc Directed Nucleotide Excision Repair.\u003c\/p\u003e \u003cp\u003eMuthls Methyl Directed Mismatch Repair.\u003c\/p\u003e \u003cp\u003eVery Short Patch Repair.\u003c\/p\u003e \u003cp\u003eGlycosylases.\u003c\/p\u003e \u003cp\u003eUracil-N-Glycosylase Coupled With Ap Excision Repair.\u003c\/p\u003e \u003cp\u003eDeaminated Bases Removed By Dna Glycosylase.\u003c\/p\u003e \u003cp\u003eAlkylated Bases Removed By Dna Glycosylase.\u003c\/p\u003e \u003cp\u003eMutm\/Muty: Oxidative Damage.\u003c\/p\u003e \u003cp\u003eN-Glycosylases Specific For Pyrimidine Dimmers.\u003c\/p\u003e \u003cp\u003eMechanisms That Tolerate Dna Damage.\u003c\/p\u003e \u003cp\u003eTransdimer Synthesis.\u003c\/p\u003e \u003cp\u003ePost Replication\/Recombinational Repair (Prr).\u003c\/p\u003e \u003cp\u003eIntroduction To The Sos Regulon.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e5. Recombination:.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eHomologous Recombination.\u003c\/p\u003e \u003cp\u003eModels For Homologous Recombination.\u003c\/p\u003e \u003cp\u003eThe Holliday Or Double-Strand Invasion Model Of Recombination.\u003c\/p\u003e \u003cp\u003eAn Alternative To The Holliday Model: The Single Strand Invasion Model Of Meselson And Radding.\u003c\/p\u003e \u003cp\u003eFurther Enzymatic Considerations.\u003c\/p\u003e \u003cp\u003eSite-Specific Recombination.\u003c\/p\u003e \u003cp\u003eA Typical Site-Specific Recombinational Event.\u003c\/p\u003e \u003cp\u003eBacteriophage l:A Model For Site-Specific Recombination.\u003c\/p\u003e \u003cp\u003eOther Examples Of Site-Specific Recombination.\u003c\/p\u003e \u003cp\u003eIllegitimate Recombination.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e6. Transposition.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eThe Structure Of Transposons.\u003c\/p\u003e \u003cp\u003eThe Frequency Of Transposition.\u003c\/p\u003e \u003cp\u003eThe Two Types Of Transposition Reactions.\u003c\/p\u003e \u003cp\u003eThe Transposition Machinery.\u003c\/p\u003e \u003cp\u003eThe Transposition Machinery; Accessory Proteins Encoded By The Transposon.\u003c\/p\u003e \u003cp\u003eThe Transposition Machinery: Accessory Proteins Encoded By The Host.\u003c\/p\u003e \u003cp\u003eNon-Replicative Transposition.\u003c\/p\u003e \u003cp\u003eReplicative Transposition.\u003c\/p\u003e \u003cp\u003eDoes The Formation Of A Cointegrate Predict The Transposition Mechanism?.\u003c\/p\u003e \u003cp\u003eThe Fate Of The Donor Site.\u003c\/p\u003e \u003cp\u003eTarget Immunity.\u003c\/p\u003e \u003cp\u003eTransposons As Molecular Tools.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e7. Bacteriophage.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eThe Structure Of Phage.\u003c\/p\u003e \u003cp\u003eThe Life Cycle Of A Bacteriophage.\u003c\/p\u003e \u003cp\u003eLytic-Lysogenic Options.\u003c\/p\u003e \u003cp\u003eThe l Lifecycle.\u003c\/p\u003e \u003cp\u003el Adsorption.\u003c\/p\u003e \u003cp\u003el Dna Injection.\u003c\/p\u003e \u003cp\u003eProtecting The l Genome In The Bacterial Cytoplasm.\u003c\/p\u003e \u003cp\u003eWhat Happens To The l Genome After It Is Stabilized?.\u003c\/p\u003e \u003cp\u003el And The Lytic-Lysogenic Decision.\u003c\/p\u003e \u003cp\u003eThe l Lysogenic Pathway.\u003c\/p\u003e \u003cp\u003eThe l Lytic Pathway.\u003c\/p\u003e \u003cp\u003eDna Replication During The l Lytic Pathway.\u003c\/p\u003e \u003cp\u003eMaking l Phage.\u003c\/p\u003e \u003cp\u003eGetting Out Of The Cell-The l S And R Proteins.\u003c\/p\u003e \u003cp\u003eInduction Of By The Sos System.\u003c\/p\u003e \u003cp\u003eSuperinfection.\u003c\/p\u003e \u003cp\u003eRestriction And Modification Of Dna.\u003c\/p\u003e \u003cp\u003eThe Lifecycle Of M13-M13 Adsorption And Injection.\u003c\/p\u003e \u003cp\u003eProtection Of The M13 Genome.\u003c\/p\u003e \u003cp\u003eM13 Dna Replication.\u003c\/p\u003e \u003cp\u003eM13 Phage Production And Release From The Cell.\u003c\/p\u003e \u003cp\u003eThe Lifecycle Of P1.\u003c\/p\u003e \u003cp\u003eAdsorption, Injection And Protection Of The Genome.\u003c\/p\u003e \u003cp\u003eP1 Dna Replication And Phage Assembly.\u003c\/p\u003e \u003cp\u003eThe Location Of The P1 Prophage In A Lysogen.\u003c\/p\u003e \u003cp\u003eP1 Transducing Particles.\u003c\/p\u003e \u003cp\u003eThe Lifecycle Of T4-T4 Adsorption And Injection.\u003c\/p\u003e \u003cp\u003eT4rii Mutations And The Nature Of The Genetic Code.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e8. Transduction.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eGeneralized Transduction Vs Specialized Transduction.\u003c\/p\u003e \u003cp\u003eP1 As A Model For Generalized Transducing Phage.\u003c\/p\u003e \u003cp\u003ePackaging The Chromosome.\u003c\/p\u003e \u003cp\u003eMoving Pieces Of The Chromosome From One Cell To Another.\u003c\/p\u003e \u003cp\u003eIdentifying Transduced Bacteria: Selection Vs Screen.\u003c\/p\u003e \u003cp\u003eCarrying Out A Transduction.\u003c\/p\u003e \u003cp\u003eUses For Transduciton.\u003c\/p\u003e \u003cp\u003eTwo Factor Crosses To Determine Gene Linkage.\u003c\/p\u003e \u003cp\u003eMapping The Order Of Genes- Three Factor Crosses.\u003c\/p\u003e \u003cp\u003eUses For Transduction-Strain Construction.\u003c\/p\u003e \u003cp\u003eUses For Transduction-Localized Mutagenesis.\u003c\/p\u003e \u003cp\u003eSpecialized Transducing Phage.\u003c\/p\u003e \u003cp\u003eMaking Merodiploids With Specialized Transducing Phage.\u003c\/p\u003e \u003cp\u003eMoving Mutations From Plasmids To Specialized Transducing Phage To The.\u003c\/p\u003e \u003cp\u003eChromosome.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e9. Natural Plasmids.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eOrigins Of Replication.\u003c\/p\u003e \u003cp\u003ePlasmid Copy Number.\u003c\/p\u003e \u003cp\u003eSetting The Copy Number.\u003c\/p\u003e \u003cp\u003ePlasmid Incompatibility.\u003c\/p\u003e \u003cp\u003ePlasmid Amplification.\u003c\/p\u003e \u003cp\u003eOther Genes That Can Be Carried By Plasmids.\u003c\/p\u003e \u003cp\u003ePlasmids Can Be Circular Or Linear Dna.\u003c\/p\u003e \u003cp\u003eBroad Host Range Plasmids.\u003c\/p\u003e \u003cp\u003eMoving Plasmids From Cell To Cell.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e10. Conjugation:.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eThe F Factor.\u003c\/p\u003e \u003cp\u003eThe R Factors.\u003c\/p\u003e \u003cp\u003eThe Conjugation Machinery.\u003c\/p\u003e \u003cp\u003eTransfer Of The Dna.\u003c\/p\u003e \u003cp\u003eSurface Exclusion.\u003c\/p\u003e \u003cp\u003eF, Hfr Or F-Prime.\u003c\/p\u003e \u003cp\u003eFormation Of The Hfr.\u003c\/p\u003e \u003cp\u003eTransfer Of Dna From An Hfr To Another Cell.\u003c\/p\u003e \u003cp\u003eFormation Of F-Primes.\u003c\/p\u003e \u003cp\u003eTransfer Of F-Primes From One Cell To Another.\u003c\/p\u003e \u003cp\u003eGenetic Uses Of F-Primes.\u003c\/p\u003e \u003cp\u003eGenetic Uses Of Hfr Strains-Mapping Genes On The E. Coli Chromosome Using Hfr.\u003c\/p\u003e \u003cp\u003eCrosses.\u003c\/p\u003e \u003cp\u003eThe 50% Rule.\u003c\/p\u003e \u003cp\u003eUsing Several Hfr Strains To Cover The Chromosome.\u003c\/p\u003e \u003cp\u003eMobilization Of Non-Conjugatible Plasmids By R And F.\u003c\/p\u003e \u003cp\u003eConjugation From Prokaryotes To Eukaryotes.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e11. Transformation:.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eNatural Competency.\u003c\/p\u003e \u003cp\u003eThe Process Of Natural Transformation.\u003c\/p\u003e \u003cp\u003eThe Machinery Of Naturally Transformable Cells.\u003c\/p\u003e \u003cp\u003eArtificial Transformation.\u003c\/p\u003e \u003cp\u003eTransformation As A Genetic Tool: Gene Mapping.\u003c\/p\u003e \u003cp\u003eTransformation As A Molecular Tool.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e12. Gene Expression And Regulation.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eThe Players In The Regulation Game.\u003c\/p\u003e \u003cp\u003eOperons And Regulons.\u003c\/p\u003e \u003cp\u003eRepression Of The Lac Operon.\u003c\/p\u003e \u003cp\u003eActivation Of The Lac Operon By Cyclic Amp And The Cap Protein.\u003c\/p\u003e \u003cp\u003eRegulation Of The Tryptophan Biosynthesis Operon By Attenuation.\u003c\/p\u003e \u003cp\u003eRegulation Of The Heat Shock Regulon By An Alternative Sigma Factor, Mrna Stability And Proteolysis.\u003c\/p\u003e \u003cp\u003eRegulation Of The Sos Regulon By Proteolytic Cleavage Of The Repressor.\u003c\/p\u003e \u003cp\u003eTwo Component Regulatory Systems, Signal Transduction And The Cps Regulon.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e13. Plasmids, Bacteriophage And Transposons As Tools.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eWhat Is A Cloning Vector?.\u003c\/p\u003e \u003cp\u003eWhy Not Use Naturally Occurring Plasmids As Vectors?.\u003c\/p\u003e \u003cp\u003eThe Importance Of Copy Number.\u003c\/p\u003e \u003cp\u003eAn Example Of How A Cloning Vector Works-Pbr322.\u003c\/p\u003e \u003cp\u003eMultiple Cloning Sites.\u003c\/p\u003e \u003cp\u003eDetermining Which Plasmids Contain An Insert.\u003c\/p\u003e \u003cp\u003eExpression Vectors.\u003c\/p\u003e \u003cp\u003eVectors For Purifying The Cloned Gene Product.\u003c\/p\u003e \u003cp\u003eVectors For Localizing The Gene Product.\u003c\/p\u003e \u003cp\u003eVectors For Studying Gene Expression.\u003c\/p\u003e \u003cp\u003eShuttle Vectors.\u003c\/p\u003e \u003cp\u003eArtificial Chromosomes.\u003c\/p\u003e \u003cp\u003eConstructing Phage Vectors.\u003c\/p\u003e \u003cp\u003eSuicide Vectors.\u003c\/p\u003e \u003cp\u003ePhage Display Vectors.\u003c\/p\u003e \u003cp\u003eCombining Phage Vectors And Transposons.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e14. DNA Cloning:.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eIsolating DNA From Cells - Plasmid DNA Isolation.\u003c\/p\u003e \u003cp\u003eIsolating DNA From Cells - Chromosomal DNA Isolation.\u003c\/p\u003e \u003cp\u003eCutting DNA Molecules.\u003c\/p\u003e \u003cp\u003eType I Restriction-Modification Systems.\u003c\/p\u003e \u003cp\u003eType II Restriction-Modification Systems.\u003c\/p\u003e \u003cp\u003eType III Restriction-Modification Systems.\u003c\/p\u003e \u003cp\u003eRestriction-Modification As A Molecular Tool.\u003c\/p\u003e \u003cp\u003eGenerate Double Stranded Breaks In DNA By Shearing The Dna.\u003c\/p\u003e \u003cp\u003eJoining DNA Molecules.\u003c\/p\u003e \u003cp\u003eManipulating The Ends Of Molecules.\u003c\/p\u003e \u003cp\u003eVisualizing The Cloning Process.\u003c\/p\u003e \u003cp\u003eConstructing Libraries Of Clones.\u003c\/p\u003e \u003cp\u003eDNA Detection – Southern Blotting.\u003c\/p\u003e \u003cp\u003eDNA Amplification: Polymerase Chain Reaction.\u003c\/p\u003e \u003cp\u003eAdding Novel Dna Sequences To The Ends Of A Pcr Amplified Sequence.\u003c\/p\u003e \u003cp\u003eSite Directed Mutagenesis Using Pcr.\u003c\/p\u003e \u003cp\u003eCloning And Expressing A Gene.\u003c\/p\u003e \u003cp\u003eDna Sequencing Using Dideoxy Sequencing.\u003c\/p\u003e \u003cp\u003eDna Sequence Searches.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003e\u003cb\u003e15. Bioinformatics And Proteomics.\u003c\/b\u003e\u003c\/p\u003e \u003cp\u003eBioinformatics.\u003c\/p\u003e \u003cp\u003eStrategies For Sequencing Genomes.\u003c\/p\u003e \u003cp\u003eBacterial Genomes.\u003c\/p\u003e \u003cp\u003eAnalyzing Genomes.\u003c\/p\u003e \u003cp\u003eThe E. Coli K-12 Genome.\u003c\/p\u003e \u003cp\u003eProteomics.\u003c\/p\u003e \u003cp\u003eTechniques For Examining The Proteome-Sds-Page And 2-Dimensional Sds-Page.\u003c\/p\u003e \u003cp\u003eTechniques For Examining The Proteome-Microarray Technology.\u003c\/p\u003e \u003cp\u003eSummary.\u003c\/p\u003e \u003cp\u003eGlossary.\u003c\/p\u003e \u003cp\u003eAdditional References.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eJanine E. Trempy\u003c\/b\u003e, 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.\u003c\/p\u003e \u003cp\u003e\u003cb\u003eNancy Trun\u003c\/b\u003e 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.\u003c\/p\u003e \u003cp\u003e\u003ci\u003eFundamental Bacterial Genetics\u003c\/i\u003e presents a concise introduction to microbial genetics. The text focuses on one bacterial species, \u003ci\u003eEscherichia coli\u003c\/i\u003e, 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.\u003c\/p\u003e \u003cp\u003e\u003ci\u003eFundamental Bacterial Genetics\u003c\/i\u003e features:\u003c\/p\u003e \u003cul\u003e \u003cli\u003eFYI boxes – feature key experiments that lead to what we now know, comparisons with other species and more.\u003c\/li\u003e \u003cli\u003eStudy questions – at the end of each chapter, review and test students' knowledge of key chapter concepts.\u003c\/li\u003e \u003cli\u003eKey references – included both at chapter end and in a full reference list at the end of the book.\u003c\/li\u003e \u003cli\u003eFull chapter on bioinformatics and proteomics - includes coverage of functional genomics and microarrays.\u003c\/li\u003e \u003cli\u003eDedicated website – www.blackwellpublishing.com\/trun – animations, study resources, web research questions, and illustrations downloadable for PowerPoint files provide students and instructors with an enhanced, interactive experience.\u003c\/li\u003e \u003c\/ul\u003e","brand":"Wiley-Blackwell","offers":[{"title":"Default Title","offer_id":47989254684901,"sku":"NP9780632044481","price":109.95,"currency_code":"USD","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/1842\/7735\/files\/9780632044481.jpg?v=1761783394","url":"https:\/\/k12savings.com\/es\/products\/fundamental-bacterial-genetics-isbn-9780632044481","provider":"K12savings","version":"1.0","type":"link"}