ISE Prescott's Principles of Microbiology

Höfundar: Joanne Willey; Christopher J. Woolverton; Linda Sherwood (Útgáfa: 2)
ISE Prescott's Principles of Microbiology

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Prescott's Principles of Microbiology provides a balanced, comprehensive introduction to all major areas of microbiology. Because of this balance, Prescott's Principles of Microbiology  is appropriate for microbiology majors and mixed majors courses. The authors have focused on readability, artwork, and the integration of several key themes, including evolution, ecology and diversity, throughout the text, making an already superior text even better.

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Útgefandi
McGraw-Hill Higher Education (International)
ISBN
9781260590456
Print ISBN
9781260575552
Format
ePub
Útgáfa
2
Höfundar
Joanne Willey; Christopher J. Woolverton; Linda Sherwood
Tungumál
English
Útgefið
2020-01-30
Prent takmörkun á líftíma
100
Prent takmörkun
2
Afritunar takmörkun
2

Kaflar

  • Title Page
  • Copyright Page
  • Brief Contents
  • About the Authors
  • Connect Page
  • A Modern Approach to Microbiology
  • Student-Friendly Organization
  • Chapter Highlights
  • Acknowledgements
  • Table of Contents
  • Chapter 1    The Evolution of Microorganisms and Microbiology
  • 1.1   Members of the Microbial World
  • 1.2   Microbes Have Evolved and Diversified for Billions of Years
  • 1.3   Microbiology Advanced as New Tools for Studying Microbes Were Developed
  • 1.4   Microbiology Encompasses Many Subdisciplines
  • Chapter 2    Microscopy
  • 2.1   Lenses Create Images by Bending Light
  • 2.2   There Are Several Types of Light Microscopes
  • 2.3   Staining Helps to Visualize and Identify Microbes
  • 2.4   Electron Microscopes Use Beams of Electrons to Create Highly Magnified Images
  • Chapter 3    Bacterial and Archaeal Cell Structure
  • 3.1   Use of the Term “Prokaryote” Is Controversial
  • 3.2   Bacteria and Archaea Are Diverse but Share Some Common Features
  • 3.3   The Plasma Membrane Controls What Enters and Leaves the Cell
  • 3.4   Cell Walls Have Many Functions
  • 3.5   The Cell Envelope Often Includes Layers Outside the Cell Wall
  • 3.6   The Cytoplasm Is More Complex than Once Thought
  • 3.7   External Structures Are Used for Motility and Attachment
  • 3.8   Cells Move in Response to Environmental Conditions
  • 3.9   Bacterial Endospores Are a Survival Strategy
  • Chapter 4    Eukaryotic Cell Structure
  • 4.1   Eukaryotic Cells Are Diverse but Share Some Common Features
  • 4.2   Eukaryotic Cell Envelopes
  • 4.3   The Eukaryotic Cytoplasm Contains a Cytoskeleton and Organelles
  • 4.4   Several Organelles Function in the Secretory and Endocytic Pathways
  • 4.5   The Nucleus and Ribosomes Are Involved in Genetic Control of the Cell
  • 4.6   Mitochondria, Related Organelles, and Chloroplasts Are Involved in Energy Conservation
  • 4.7   Many Eukaryotic Microbes Have External Structures Used for Motility
  • Chapter 5    Bacterial and Archaeal Growth
  • 5.1   Most Bacteria and Archaea Reproduce by Binary Fission
  • 5.2   Bacterial Cell Cycles Can Be Divided into Three Phases
  • 5.3   Archaeal Cell Cycles Are Unique
  • 5.4   Growth Curves Consist of Five Phases
  • 5.5   Environmental Factors Affect Microbial Growth
  • 5.6   Microbial Growth in Natural Environments
  • 5.7   Laboratory Culture of Microbes Requires Conditions That Mimic the Normal Habitat of a Microbe
  • 5.8   Microbial Population Size Can Be Measured Directly or Indirectly
  • 5.9   Chemostats and Turbidostats Are Used for Continuous Culture of Microorganisms
  • 5.10   Growing Microbes in Industrial Settings Presents Challenges
  • Chapter 6    Introduction to Metabolism
  • 6.1   Metabolism: Important Principles
  • 6.2   ATP: The Major Energy Currency of Cells
  • 6.3   Redox Reactions: Reactions of Central Importance in Metabolism
  • 6.4   Electron Transport Chains: Sets of Sequential Redox Reactions
  • 6.5   Biochemical Pathways: Sets of Linked Chemical Reactions
  • 6.6   Enzymes and Ribozymes Speed Up Cellular Chemical Reactions
  • 6.7   Metabolism Must Be Regulated to Maintain Homeostasis
  • Chapter 7    Catabolism: Energy Release and Conservation
  • 7.1   Metabolic Diversity and Nutritional Types
  • 7.2   There Are Three Chemoorganotrophic Fueling Processes
  • 7.3   Aerobic Respiration Can Be Divided into Three Steps
  • 7.4   Glucose to Pyruvate: The First Step
  • 7.5   Pyruvate to Carbon Dioxide (Step 2) Is Accomplished by the Tricarboxylic Acid Cycle
  • 7.6   Electron Transport and Oxidative Phosphorylation (Step 3) Generate the Most ATP
  • 7.7   Anaerobic Respiration Uses the Same Three Steps as Aerobic Respiration
  • 7.8   Fermentation Does Not Involve an Electron Transport Chain
  • 7.9   Catabolism of Organic Molecules Other Than Glucose
  • 7.10   Chemolithotrophy: “Eating Rocks”
  • 7.11   Flavin-Based Electron Bifurcation
  • 7.12   Phototrophy
  • Chapter 8    Anabolism: The Use of Energy in Biosynthesis
  • 8.1   Principles Governing Biosynthesis
  • 8.2   Precursor Metabolites: Starting Molecules for Biosynthesis
  • 8.3   CO2 Fixation: Reduction and Assimilation of CO2 Carbon
  • 8.4   Synthesis of Carbohydrates
  • 8.5   Synthesis of Amino Acids Consumes Many Precursor Metabolites
  • 8.6   Synthesis of Purines, Pyrimidines, and Nucleotides
  • 8.7   Lipid Synthesis
  • Chapter 9    Genome Replication
  • 9.1   Experiments Using Bacteria and Viruses Demonstrated that DNA Is the Genetic Material
  • 9.2   Nucleic Acid Structure
  • 9.3   DNA Replication in Bacteria
  • 9.4   DNA Replication in Eukaryotes and Archaea
  • Chapter 10    Gene Expression
  • 10.1   Proteins Are Polymers of Amino Acids
  • 10.2   Bacterial Genes Consist of Coding Regions and Other Sequences Important for Gene Function
  • 10.3   Transcription in Bacteria
  • 10.4   The Genetic Code Consists of Three-Letter “Words”
  • 10.5   Translation in Bacteria
  • 10.6   Protein Maturation and Secretion
  • 10.7   Gene Expression in Eukaryotes and Archaea
  • Chapter 11    Regulation of Cellular Processes
  • 11.1   Bacteria Use Many Regulatory Options
  • 11.2   Regulation of Transcription Initiation Saves Considerable Energy and Materials
  • 11.3   Attenuation and Riboswitches Stop Transcription Prematurely
  • 11.4   Riboswitches and Small RNAs Control Translation
  • 11.5   Mechanisms Used for Global Regulation
  • 11.6   Bacteria Combine Several Regulatory Mechanisms to Control Complex Cellular Processes
  • 11.7   Regulation of Cellular Processes in Eukaryotes and Archaea
  • Chapter 12    Mechanisms of Genetic Variation
  • 12.1   Mutations: Heritable Changes in a Genome
  • 12.2   Detection and Isolation of Mutants
  • 12.3   DNA Repair Maintains Genome Stability
  • 12.4   Microbes Use Mechanisms Other than Mutation to Create Genetic Variability
  • 12.5   Transposable Elements Move Genes Within and Between DNA Molecules
  • 12.6   Bacterial Conjugation Requires Cell-Cell Contact
  • 12.7   Bacterial Transformation Is the Uptake of Free DNA from the Environment
  • 12.8   Transduction Is Virus-Mediated DNA Transfer
  • 12.9   Evolution in Action: The Development of Antibiotic Resistance in Bacteria
  • Chapter 13    Gram-Positive Bacteria
  • 13.1   Class Actinobacteria
  • 13.2   Class Bacilli: Aerobic Endospore-­Forming Bacteria
  • 13.3   Class Clostridia: Anaerobic Endospore-Forming Bacteria
  • 13.4   Class Negativicutes: Gram-Positive Bacteria with Outer Membranes
  • 13.5   Firmicutes and Dental Disease
  • Chapter 14    Proteobacteria
  • 14.1   Class Alphaproteobacteria Includes Many Oligotrophs
  • 14.2   Class Betaproteobacteria Includes Chemoheterotrophs and Chemolithotrophs
  • 14.3   Class Gammaproteobacteria Is the Largest Bacterial Class
  • 14.4   Class Deltaproteobacteria Includes Chemoheterotrophic Anaerobes and Predators
  • 14.5   Class Epsilonproteobacteria Ranges from Pathogens to Deep-Sea Bacteria
  • Chapter 15    Nonproteobacterial Gram-Negative Bacteria
  • 15.1   Aquificae and Thermotogae Are Ancient Bacterial Lineages
  • 15.2   Deinococcus-Thermus Includes ­ Radiation-Resistant Bacteria
  • 15.3   Class Mollicutes, Phylum Tenericutes: Bacteria That Lack Cell Walls
  • 15.4   Photosynthetic Bacteria Are Diverse
  • 15.5   Superphylum Planctomycetes-Verrucomicrobia-Chlamydiae: Atypical Cell Division
  • 15.6   Phylum Spirochaetes: Bacteria with a Corkscrew Morphology
  • 15.7   Phylum Bacteroidetes Includes Important Gut Microbiota
  • 15.8   Phylum Fusobacteria: Commensal Anaerobes
  • Chapter 16    Archaea
  • 16.1   Overview of Archaea
  • 16.2   Proteoarchaeota, or TACK Superphylum
  • 16.3   Phylum Euryarchaeota: Methanogens, Haloarchaea, and Others
  • Chapter 17    Eukaryotic Microbes
  • 17.1   Protist Diversity Reflects Broad Phylogeny
  • 17.2   Supergroup Excavata: Primitive Eukaryotes
  • 17.3   Supergroup Amoebozoa Includes Protists with Pseudopodia
  • 17.4   Supergroup SAR: Protists of Global Importance
  • 17.5   Supergroup Archaeplastida Includes Green Algae
  • 17.6   Fungal Biology Reflects Vast Diversity
  • 17.7   Chytridiomycetes Produce Motile Spores
  • 17.8   Zygomycetes: Fungi with Coenocytic Hyphae
  • 17.9   Glomeromycota Are Mycorrhizal Symbionts
  • 17.10   Ascomycota Includes Yeasts and Molds
  • 17.11   Basidiomycota Includes Mushrooms and Plant Pathogens
  • 17.12   Microsporidia Are Intracellular Parasites
  • Chapter 18    Viruses and Other Acellular Infectious Agents
  • 18.1   Viruses Are Acellular
  • 18.2   Virion Structure Is Defined by Capsid Symmetry and Presence or Absence of an Envelope
  • 18.3   Viral Life Cycles Have Five Steps
  • 18.4   There Are Several Types of Viral Infections
  • 18.5   Cultivation and Enumeration of Viruses
  • 18.6   Virus Phylogeny Is Difficult to Establish
  • 18.7   Double-Stranded DNA Viruses Infect All Cell Types
  • 18.8   Single-Stranded DNA Viruses Use a Double-Stranded Intermediate in Their Life Cycles
  • 18.9   Double-Stranded RNA Viruses: RNA-Dependent RNA Polymerase Replicates the Genome and Synthesizes mRNA
  • 18.10   Positive-Strand RNA Viruses: Genomes That Can Be Translated upon Entry
  • 18.11   Negative-Strand RNA Viruses: RNA-Dependent RNA Polymerase Is Part of the Virion
  • 18.12   Retroviruses: Positive-Strand Viruses That Use Reverse Transcriptase in Their Life Cycles
  • 18.13   Reverse Transcribing DNA Viruses
  • 18.14   Viroids and Satellites: Nucleic Acid-Based Subviral Agents
  • 18.15   Prions Are Composed Only of Protein
  • Chapter 19    Microbial Interactions
  • 19.1   Many Types of Microbial Interactions Exist
  • 19.2   Mutualism and Cooperation Are Two-Way Interactions
  • 19.3   Commensalism and Amensalism Are One-Way Interactions
  • 19.4   Antagonistic Interactions Characterize Predation, Parasitism, and Competition
  • Chapter 20    Biogeochemical Cycling and Global Climate Change
  • 20.1   Biogeochemical Cycling Sustains Life on Earth
  • 20.2   Global Climate Change: Biogeochemical Cycling Out of Balance
  • Chapter 21    Microorganisms in Natural Ecosystems
  • 21.1   Water Is the Largest Microbial Habitat
  • 21.2   Microorganisms in Marine Ecosystems
  • 21.3   Microorganisms in Freshwater Ecosystems
  • 21.4   Soils Are an Important Microbial Habitat
  • 21.5   Diverse Microorganisms Inhabit Soil
  • 21.6   Microbe-Plant Interactions Can Be Positive, Negative, or Neutral
  • Chapter 22    Innate Host Resistance
  • 22.1   Immunity Arises from Innate Resistance and Adaptive Defenses
  • 22.2   Innate Resistance Starts with Barriers
  • 22.3   Innate Resistance Relies on Chemical Mediators
  • 22.4   Each Type of Innate Immune Cell Has a Specific Function
  • 22.5   Secondary Lymphoid Tissues and Organs Connect Innate and Adaptive Immunity
  • 22.6   Phagocytosis Destroys Invaders
  • 22.7   Inflammation Unites All Components of Immunity
  • Chapter 23    Adaptive Immunity
  • 23.1   Adaptive Immunity Relies on Recognition and Memory
  • 23.2   Antigens Elicit Immunity
  • 23.3   Adaptive Immunity Can Be Earned or Borrowed
  • 23.4   Recognition of Foreignness Is Critical for a Strong Defense
  • 23.5   T Cells Are Critical for Immune Function
  • 23.6   B Cells Make Antibodies
  • 23.7   Antibodies Bind Specific 3-D Antigens
  • 23.8   Antibodies Doom Antigens
  • 23.9   Immune Tolerance Is a Must
  • 23.10   The Immune System Can Malfunction
  • Chapter 24    The Human Microbiome and Host Interactions
  • 24.1   Humans Are Holobionts
  • 24.2   The Microbiome Develops from Birth to Adulthood
  • 24.3   A Functional Core Microbiome Is Required for Human Homeostasis
  • 24.4   Many Diseases Are Linked to Dysbiosis
  • 24.5   Microbiome Manipulation Can Be Therapeutic
  • Chapter 25    Infection and Pathogenicity
  • 25.1   The Process of Infection
  • 25.2   Transmission and Entry into the Host
  • 25.3   Surviving the Host Defenses
  • 25.4   Damage to the Host
  • Chapter 26    Epidemiology and Public Health Microbiology
  • 26.1   Epidemiology Is an Evidence-Based Science
  • 26.2   Epidemiology Is Rooted in Well-Tested Methods
  • 26.3   Infectious Disease Is Revealed Through Patterns Within a Population
  • 26.4   Infectious Diseases and Pathogens Are Emerging and Reemerging
  • 26.5   Health-Care Facilities Harbor Infectious Agents
  • 26.6   Coordinated Efforts Are Required to Prevent and Control Epidemics
  • 26.7   Bioterrorism Readiness Is an Integral Component of Public Health Microbiology
  • Chapter 27    Control of Microorganisms in the Environment
  • 27.1   Microbial Growth and Replication: Targets for Control
  • 27.2   Physical Control Methods Isolate or Kill Microorganisms
  • 27.3   Microorganisms Are Controlled with Chemical Agents
  • 27.4   Antimicrobial Agents Must Be Evaluated for Effectiveness
  • 27.5   Microorganisms Can Be Controlled by Biological Methods
  • Chapter 28    Antimicrobial Chemotherapy
  • 28.1   Antimicrobial Chemotherapy Evolved from Antisepsis Efforts
  • 28.2   Antimicrobial Drugs Have Selective Toxicity
  • 28.3   Antimicrobial Activity Can Be Measured by Specific Tests
  • 28.4   Antibacterial Drugs
  • 28.5   Antiviral Drugs
  • 28.6   Antifungal Drugs
  • 28.7   Antiprotozoan Drugs
  • 28.8   Antimicrobial Drug Resistance Is a Public Health Threat
  • Chapter 29    Microbiology of Food
  • 29.1   Microbial Growth Can Cause Food Spoilage
  • 29.2   Various Methods Are Used to Control Food Spoilage
  • 29.3   Food-Borne Disease Outbreaks
  • 29.4   Detection of Food-Borne Pathogens Requires Government-Industry Cooperation
  • 29.5   Microbiology of Fermented Foods: Beer, Cheese, and Much More
  • Chapter 30    Industrial and Environmental Microbiology
  • 30.1   Microbes Are the Source of Many Products of Industrial Importance
  • 30.2   Biofuel Production Is a Dynamic Field
  • 30.3   Microbial Fuel Cells: Batteries Powered by Microbes
  • 30.4   Agricultural Biotechnology Relies on a Plant Pathogen
  • 30.5   Purification and Sanitary Analysis Ensure Safe Drinking Water
  • 30.6   Wastewater Treatment Maintains Human and Environmental Health
  • 30.7   Biodegradation and Bioremediation Harness Microbes to Clean the Environment
  • Chapter 31    Microbial DNA Technologies
  • 31.1   Key Discoveries Led to the Development of DNA Cloning Technology
  • 31.2   Polymerase Chain Reaction Amplifies Targeted DNA
  • 31.3   Genomic and Metagenomic Libraries: Cloning Genomes in Pieces
  • 31.4   Expressing Foreign Genes in Host Cells
  • 31.5   Cas9 Nuclease Is a Precise Tool for Genome Editing
  • 31.6   Biotechnology Develops Custom Microbes for Industrial Use
  • Chapter 32    Microbial Genomics
  • 32.1   DNA Sequencing Methods
  • 32.2   Genome Sequencing
  • 32.3   Metagenomics Provides Access to Uncultured Microbes
  • 32.4   Bioinformatics: What Does the Sequence Mean?
  • 32.5   Functional Genomics Links Genes to Phenotype
  • 32.6   Systems Biology: Making and Testing Complex Predictions
  • Chapter 33    Methods in Microbial Biology
  • 33.1   Microbial Biology Relies on Cultures
  • 33.2   Microbial Identification Is Largely Based on Molecular Characterization
  • 33.3   Assessing Microbial Diversity
  • 33.4   Assessing Microbial Community Activity
  • Chapter 34    Clinical Microbiology and Immunology
  • 34.1   The Clinical Microbiology Laboratory Detects Infectious Agents and Protects Its Workers
  • 34.2   Identification of Microorganisms from Specimens
  • 34.3   Immune Responses Can Be Exploited to Detect Infections
  • Appendix I
  • Appendix II
  • Appendix III
  • Glossary
  • Index