Chapter 27 Bacteria and Archaea.

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Chapter 27 Bacteria and Archaea

Overview: Masters of Adaptation Prokaryotes thrive almost everywhere, including places too acidic, salty, cold, or hot for most other organisms Most prokaryotes are microscopic, but what they lack in size they make up for in numbers There are more in a handful of fertile soil than the number of people who have ever lived

They have an astonishing genetic diversity Prokaryotes are divided into two domains: bacteria and archaea Video: Tubeworms

Concept 27.1: Structural and functional adaptations contribute to prokaryotic success Most prokaryotes are unicellular, although some species form colonies Most prokaryotic cells are 0.5–5 µm, much smaller than the 10–100 µm of many eukaryotic cells Prokaryotic cells have a variety of shapes The three most common shapes are spheres (cocci), rods (bacilli), and spirals

(a) Spherical (cocci) (b) Rod-shaped (bacilli) (c) Spiral 1 µm 2 µm Fig. 27-2 Figure 27.2 The most common shapes of prokaryotes 1 µm 2 µm 5 µm (a) Spherical (cocci) (b) Rod-shaped (bacilli) (c) Spiral

Cell-Surface Structures An important feature of nearly all prokaryotic cells is their cell wall, which maintains cell shape, provides physical protection, and prevents the cell from bursting in a hypotonic environment Eukaryote cell walls are made of cellulose or chitin Bacterial cell walls contain peptidoglycan, a network of sugar polymers cross-linked by polypeptides

Archaea contain polysaccharides and proteins but lack peptidoglycan Using the Gram stain, scientists classify many bacterial species into Gram-positive and Gram-negative groups based on cell wall composition Gram-negative bacteria have less peptidoglycan and an outer membrane that can be toxic, and they are more likely to be antibiotic resistant

Many antibiotics target peptidoglycan and damage bacterial cell walls

Fig. 27-3 layer Figure 27.3 Gram staining Carbohydrate portion of lipopolysaccharide Outer membrane Peptidoglycan layer Cell wall Cell wall Peptidoglycan layer Plasma membrane Plasma membrane Protein Protein Gram- positive bacteria Gram- negative bacteria Figure 27.3 Gram staining 20 µm (a) Gram-positive: peptidoglycan traps crystal violet. (b) Gram-negative: crystal violet is easily rinsed away, revealing red dye.

A polysaccharide or protein layer called a capsule covers many prokaryotes

Fig. 27-4 200 nm Figure 27.4 Capsule Capsule

Some prokaryotes have fimbriae (also called attachment pili), which allow them to stick to their substrate or other individuals in a colony Sex pili are longer than fimbriae and allow prokaryotes to exchange DNA

Fig. 27-5 Figure 27.5 Fimbriae Fimbriae 200 nm

Video: Prokaryotic Flagella (Salmonella typhimurium) Motility Most motile bacteria propel themselves by flagella that are structurally and functionally different from eukaryotic flagella In a heterogeneous environment, many bacteria exhibit taxis, the ability to move toward or away from certain stimuli Video: Prokaryotic Flagella (Salmonella typhimurium)

Flagellum Filament Cell wall Hook Basal apparatus Plasma membrane Fig. 27-6 Flagellum Filament 50 nm Cell wall Hook Basal apparatus Figure 27.6 Prokaryotic flagellum Plasma membrane

Filament Cell wall Hook Basal apparatus Plasma membrane Fig. 27-6a Figure 27.6 Prokaryotic flagellum Plasma membrane

Prokaryotic flagellum (TEM) Fig. 27-6b 50 nm Figure 27.6 Prokaryotic flagellum Prokaryotic flagellum (TEM)

Internal and Genomic Organization Prokaryotic cells usually lack complex compartmentalization Some prokaryotes do have specialized membranes that perform metabolic functions

(a) Aerobic prokaryote (b) Photosynthetic prokaryote Fig. 27-7 0.2 µm 1 µm Respiratory membrane Figure 27.7 Specialized membranes of prokaryotes Thylakoid membranes (a) Aerobic prokaryote (b) Photosynthetic prokaryote

(a) Aerobic prokaryote Fig. 27-7a 0.2 µm Respiratory membrane Figure 27.7 Specialized membranes of prokaryotes (a) Aerobic prokaryote

(b) Photosynthetic prokaryote Fig. 27-7b 1 µm Figure 27.7 Specialized membranes of prokaryotes Thylakoid membranes (b) Photosynthetic prokaryote

The prokaryotic genome has less DNA than the eukaryotic genome Most of the genome consists of a circular chromosome Some species of bacteria also have smaller rings of DNA called plasmids

Chromosome Plasmids 1 µm Fig. 27-8 Figure 27.8 A prokaryotic chromosome and plasmids 1 µm

The typical prokaryotic genome is a ring of DNA that is not surrounded by a membrane and that is located in a nucleoid region

Reproduction and Adaptation Prokaryotes reproduce quickly by binary fission and can divide every 1–3 hours Many prokaryotes form metabolically inactive endospores, which can remain viable in harsh conditions for centuries

Fig. 27-9 Endospore Figure 27.9 An endospore 0.3 µm

Prokaryotes can evolve rapidly because of their short generation times

0.1 mL (population sample) Fitness relative to ancestor Fig. 27-10 EXPERIMENT Daily serial transfer 0.1 mL (population sample) Old tube (discarded after transfer) New tube (9.9 mL growth medium) RESULTS 1.8 1.6 Figure 27.10 Can prokaryotes evolve rapidly in response to environmental change? Fitness relative to ancestor 1.4 1.2 1.0 5,000 10,000 15,000 20,000 Generation

0.1 mL (population sample) Fig. 27-10a EXPERIMENT Daily serial transfer 0.1 mL (population sample) Old tube (discarded after transfer) New tube (9.9 mL growth medium) Figure 27.10 Can prokaryotes evolve rapidly in response to environmental change?

Fitness relative to ancestor Fig. 27-10b RESULTS 1.8 1.6 Fitness relative to ancestor 1.4 1.2 Figure 27.10 Can prokaryotes evolve rapidly in response to environmental change? 1.0 5,000 10,000 15,000 20,000 Generation

Prokaryotes have considerable genetic variation Concept 27.2: Rapid reproduction, mutation, and genetic recombination promote genetic diversity in prokaryotes Prokaryotes have considerable genetic variation Three factors contribute to this genetic diversity: Rapid reproduction Mutation Genetic recombination

Rapid Reproduction and Mutation Prokaryotes reproduce by binary fission, and offspring cells are generally identical Mutation rates during binary fission are low, but because of rapid reproduction, mutations can accumulate rapidly in a population High diversity from mutations allows for rapid evolution

Genetic Recombination Additional diversity arises from genetic recombination Prokaryotic DNA from different individuals can be brought together by transformation, transduction, and conjugation

Transformation and Transduction A prokaryotic cell can take up and incorporate foreign DNA from the surrounding environment in a process called transformation Transduction is the movement of genes between bacteria by bacteriophages (viruses that infect bacteria)

Fig. 27-11-1 Phage DNA A+ B+ A+ B+ Donor cell Figure 27.11 Transduction

Fig. 27-11-2 Phage DNA A+ B+ A+ B+ Donor cell A+ Figure 27.11 Transduction

Fig. 27-11-3 Phage DNA A+ B+ A+ B+ Donor cell A+ Recombination Figure 27.11 Transduction A+ A– B– Recipient cell

Fig. 27-11-4 Phage DNA A+ B+ A+ B+ Donor cell A+ Recombination Figure 27.11 Transduction A+ A– B– Recipient cell A+ B– Recombinant cell

Conjugation and Plasmids Conjugation is the process where genetic material is transferred between bacterial cells Sex pili allow cells to connect and pull together for DNA transfer A piece of DNA called the F factor is required for the production of sex pili The F factor can exist as a separate plasmid or as DNA within the bacterial chromosome

Fig. 27-12 Figure 27.12 Bacterial conjugation 1 µm Sex pilus

The F Factor as a Plasmid Cells containing the F plasmid function as DNA donors during conjugation Cells without the F factor function as DNA recipients during conjugation The F factor is transferable during conjugation

Fig. 27-13 F plasmid Bacterial chromosome F+ cell F+ cell Mating bridge F– cell F+ cell Bacterial chromosome (a) Conjugation and transfer of an F plasmid Recombinant F– bacterium Hfr cell A+ A+ A+ F factor Figure 27.13 Conjugation and recombination in E. coli A+ A– A+ A– A– A+ A– F– cell (b) Conjugation and transfer of part of an Hfr bacterial chromosome

Fig. 27-13-1 F plasmid Bacterial chromosome F+ cell Mating bridge F– cell Bacterial chromosome (a) Conjugation and transfer of an F plasmid Figure 27.13a Conjugation and recombination in E. coli

Fig. 27-13-2 F plasmid Bacterial chromosome F+ cell Mating bridge F– cell Bacterial chromosome (a) Conjugation and transfer of an F plasmid Figure 27.13a Conjugation and recombination in E. coli

Fig. 27-13-3 F plasmid Bacterial chromosome F+ cell F+ cell Mating bridge F– cell F+ cell Bacterial chromosome (a) Conjugation and transfer of an F plasmid Figure 27.13a Conjugation and recombination in E. coli

The F Factor in the Chromosome A cell with the F factor built into its chromosomes functions as a donor during conjugation The recipient becomes a recombinant bacterium, with DNA from two different cells It is assumed that horizontal gene transfer is also important in archaea

Fig. 27-13-4 Hfr cell A+ A+ A+ F factor A– A– F– cell (b) Conjugation and transfer of part of an Hfr bacterial chromosome Figure 27.13b Conjugation and recombination in E. coli

Fig. 27-13-5 Hfr cell A+ A+ A+ A+ F factor A– A– A+ A– F– cell (b) Conjugation and transfer of part of an Hfr bacterial chromosome Figure 27.13b Conjugation and recombination in E. coli

Fig. 27-13-6 Recombinant F– bacterium Hfr cell A+ A+ A+ A+ F factor A– A+ A– A– A+ A– F– cell (b) Conjugation and transfer of part of an Hfr bacterial chromosome Figure 27.13b Conjugation and recombination in E. coli

R Plasmids and Antibiotic Resistance R plasmids carry genes for antibiotic resistance Antibiotics select for bacteria with genes that are resistant to the antibiotics Antibiotic resistant strains of bacteria are becoming more common

Concept 27.3: Diverse nutritional and metabolic adaptations have evolved in prokaryotes Phototrophs obtain energy from light Chemotrophs obtain energy from chemicals Autotrophs require CO2 as a carbon source Heterotrophs require an organic nutrient to make organic compounds These factors can be combined to give the four major modes of nutrition: photoautotrophy, chemoautotrophy, photoheterotrophy, and chemoheterotrophy

Table 27-1 Table 27-1

The Role of Oxygen in Metabolism Prokaryotic metabolism varies with respect to O2: Obligate aerobes require O2 for cellular respiration Obligate anaerobes are poisoned by O2 and use fermentation or anaerobic respiration Facultative anaerobes can survive with or without O2

Nitrogen Metabolism Prokaryotes can metabolize nitrogen in a variety of ways In nitrogen fixation, some prokaryotes convert atmospheric nitrogen (N2) to ammonia (NH3)

Metabolic Cooperation Cooperation between prokaryotes allows them to use environmental resources they could not use as individual cells In the cyanobacterium Anabaena, photosynthetic cells and nitrogen-fixing cells called heterocytes exchange metabolic products Video: Cyanobacteria (Oscillatoria)

Photosynthetic cells Heterocyte 20 µm Fig. 27-14 Figure 27.14 Metabolic cooperation in a colonial prokaryote 20 µm

In some prokaryotic species, metabolic cooperation occurs in surface-coating colonies called biofilms

Fig. 27-15 Figure 27.15 A biofilm 1 µm

Concept 27.4: Molecular systematics is illuminating prokaryotic phylogeny Until the late 20th century, systematists based prokaryotic taxonomy on phenotypic criteria Applying molecular systematics to the investigation of prokaryotic phylogeny has produced dramatic results

Lessons from Molecular Systematics Molecular systematics is leading to a phylogenetic classification of prokaryotes It allows systematists to identify major new clades

Domain Eukarya Eukaryotes Korarcheotes Euryarchaeotes Domain Archaea Fig. 27-16 Domain Eukarya Eukaryotes Korarcheotes Euryarchaeotes Domain Archaea Crenarchaeotes UNIVERSAL ANCESTOR Nanoarchaeotes Proteobacteria Chlamydias Figure 27.16 A simplified phylogeny of prokaryotes Spirochetes Domain Bacteria Cyanobacteria Gram-positive bacteria

The use of polymerase chain reaction (PCR) has allowed for more rapid sequencing of prokaryote genomes A handful of soil many contain 10,000 prokaryotic species Horizontal gene transfer between prokaryotes obscures the root of the tree of life

Archaea Archaea share certain traits with bacteria and other traits with eukaryotes

Fig. 27-UN1 Eukarya Archaea Bacteria

Table 27-2 Table 27.2

Some archaea live in extreme environments and are called extremophiles Extreme halophiles live in highly saline environments Extreme thermophiles thrive in very hot environments

Fig. 27-17 Figure 27.17 Extreme thermophiles

Methanogens live in swamps and marshes and produce methane as a waste product Methanogens are strict anaerobes and are poisoned by O2 In recent years, genetic prospecting has revealed many new groups of archaea Some of these may offer clues to the early evolution of life on Earth

Bacteria Bacteria include the vast majority of prokaryotes of which most people are aware Diverse nutritional types are scattered among the major groups of bacteria

Fig. 27-UN2 Eukarya Archaea Bacteria

Proteobacteria These gram-negative bacteria include photoautotrophs, chemoautotrophs, and heterotrophs Some are anaerobic, and others aerobic

Subgroup: Alpha Proteobacteria Fig. 27-18a Subgroup: Alpha Proteobacteria Alpha Beta Gamma Proteobacteria Delta Epsilon 2.5 µm Rhizobium (arrows) inside a root cell of a legume (TEM) Subgroup: Beta Proteobacteria Subgroup: Gamma Proteobacteria 1 µm 0.5 µm Nitrosomonas (colorized TEM) Thiomargarita namibiensis containing sulfur wastes (LM) Figure 27.18 Major groups of bacteria For the Discovery Video Bacteria, go to Animation and Video Files. Subgroup: Delta Proteobacteria Subgroup: Epsilon Proteobacteria B. bacteriophorus 10 µm 5 µm 2 µm Fruiting bodies of Chondromyces crocatus, a myxobacterium (SEM) Bdellovibrio bacteriophorus attacking a larger bacterium (colorized TEM) Helicobacter pylori (colorized TEM)

Alpha Beta Gamma Proteobacteria Delta Epsilon Fig. 27-18b Figure 27.18 Major groups of bacteria—proteobacteria Epsilon

Subgroup: Alpha Proteobacteria Many species are closely associated with eukaryotic hosts Scientists hypothesize that mitochondria evolved from aerobic alpha proteobacteria through endosymbiosis

Example: Rhizobium, which forms root nodules in legumes and fixes atmospheric N2 Example: Agrobacterium, which produces tumors in plants and is used in genetic engineering

Rhizobium (arrows) inside a root cell of a legume (TEM) Fig. 27-18c 2.5 µm Figure 27.18 Major groups of bacteria—alpha proteobacteria Rhizobium (arrows) inside a root cell of a legume (TEM)

Subgroup: Beta Proteobacteria Example: the soil bacterium Nitrosomonas, which converts NH4+ to NO2–

Nitrosomonas (colorized TEM) Fig. 27-18d 1 µm Figure 27.18 Major groups of bacteria—beta proteobacteria Nitrosomonas (colorized TEM)

Subgroup: Gamma Proteobacteria Examples include sulfur bacteria such as Chromatium and pathogens such as Legionella, Salmonella, and Vibrio cholerae Escherichia coli resides in the intestines of many mammals and is not normally pathogenic

Thiomargarita namibiensis containing sulfur wastes (LM) Fig. 27-18e 0.5 µm Figure 27.18 Major groups of bacteria—gamma proteobacteria Thiomargarita namibiensis containing sulfur wastes (LM)

Subgroup: Delta Proteobacteria Example: the slime-secreting myxobacteria

Chondromyces crocatus, a myxobacterium (SEM) Fig. 27-18f 10 µm Figure 27.18 Major groups of bacteria—delta proteobacteria Fruiting bodies of Chondromyces crocatus, a myxobacterium (SEM)

B. bacteriophorus 5 µm Bdellovibrio bacteriophorus Fig. 27-18g B. bacteriophorus 5 µm Figure 27.18 Major groups of bacteria—delta proteobacteria Bdellovibrio bacteriophorus attacking a larger bacterium (colorized TEM)

Subgroup: Epsilon Proteobacteria This group contains many pathogens including Campylobacter, which causes blood poisoning, and Helicobacter pylori, which causes stomach ulcers

Helicobacter pylori (colorized TEM) Fig. 27-18h 2 µm Figure 27.18 Major groups of bacteria—epsilon proteobacteria Helicobacter pylori (colorized TEM)

Chlamydias These bacteria are parasites that live within animal cells Chlamydia trachomatis causes blindness and nongonococcal urethritis by sexual transmission

GRAM-POSITIVE BACTERIA Fig. 27-18i CHLAMYDIAS SPIROCHETES 2.5 µm 5 µm Chlamydia (arrows) inside an animal cell (colorized TEM) Leptospira, a spirochete (colorized TEM) CYANOBACTERIA GRAM-POSITIVE BACTERIA Figure 27.18 Major groups of bacteria 50 µm 1 µm 5 µm Two species of Oscillatoria, filamentous cyanobacteria (LM) Streptomyces, the source of many antibiotics (colorized SEM) Hundreds of mycoplasmas covering a human fibroblast cell (colorized SEM)

Spirochetes These bacteria are helical heterotrophs Some, such as Treponema pallidum, which causes syphilis, and Borrelia burgdorferi, which causes Lyme disease, are parasites

Cyanobacteria These are photoautotrophs that generate O2 Plant chloroplasts likely evolved from cyanobacteria by the process of endosymbiosis

Gram-Positive Bacteria Gram-positive bacteria include Actinomycetes, which decompose soil Bacillus anthracis, the cause of anthrax Clostridium botulinum, the cause of botulism Some Staphylococcus and Streptococcus, which can be pathogenic Mycoplasms, the smallest known cells

Concept 27.5: Prokaryotes play crucial roles in the biosphere Prokaryotes are so important to the biosphere that if they were to disappear the prospects for any other life surviving would be dim

Chemical Cycling Prokaryotes play a major role in the recycling of chemical elements between the living and nonliving components of ecosystems Chemoheterotrophic prokaryotes function as decomposers, breaking down corpses, dead vegetation, and waste products Nitrogen-fixing prokaryotes add usable nitrogen to the environment

Prokaryotes can sometimes increase the availability of nitrogen, phosphorus, and potassium for plant growth Prokaryotes can also “immobilize” or decrease the availability of nutrients

Uptake of K by plants (mg) Fig. 27-19 1.0 0.8 0.6 Uptake of K by plants (mg) 0.4 0.2 Figure 27.19 Impact of bacteria on soil nutrient availability No bacteria Strain 1 Strain 2 Strain 3 Soil treatment

Ecological Interactions Symbiosis is an ecological relationship in which two species live in close contact: a larger host and smaller symbiont Prokaryotes often form symbiotic relationships with larger organisms

In mutualism, both symbiotic organisms benefit In commensalism, one organism benefits while neither harming nor helping the other in any significant way In parasitism, an organism called a parasite harms but does not kill its host Parasites that cause disease are called pathogens

Fig. 27-20 Figure 27.20 Mutualism: bacterial “headlights”

Concept 27.6: Prokaryotes have both harmful and beneficial impacts on humans Some prokaryotes are human pathogens, but others have positive interactions with humans

Pathogenic Prokaryotes Prokaryotes cause about half of all human diseases Lyme disease is an example

5 µm Fig. 27-21 Figure 27.21 Lyme disease For the Discovery Video Antibiotics, go to Animation and Video Files.

Pathogenic prokaryotes typically cause disease by releasing exotoxins or endotoxins Exotoxins cause disease even if the prokaryotes that produce them are not present Endotoxins are released only when bacteria die and their cell walls break down Many pathogenic bacteria are potential weapons of bioterrorism

Prokaryotes in Research and Technology Experiments using prokaryotes have led to important advances in DNA technology Prokaryotes are the principal agents in bioremediation, the use of organisms to remove pollutants from the environment

Some other uses of prokaryotes: Recovery of metals from ores Synthesis of vitamins Production of antibiotics, hormones, and other products