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CHAPTER 27 PROKARYOTES AND THE ORIGINS OF METABOLIC DIVERSITY

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1 CHAPTER 27 PROKARYOTES AND THE ORIGINS OF METABOLIC DIVERSITY
Section A: The World of Prokaryotes 張學偉 助理教授 生物系

2 1. They’re (almost) everywhere! An overview of prokaryotic life
Prokaryotes the earliest organisms on Earth still dominate the biosphere today. Some species cause serious illness. more bacteria are benign or beneficial.

3 2. Bacteria and archaea are the two main branches of prokaryote evolution (in the five-kingdom system) The archaea inhabit extreme environments. The archaea differ from bacteria in many key structural, biochemical, and physiological characteristics. Archaea = 太古時代

4 A domain is a taxonomic level about kingdom.
Current taxonomy recognizes two prokaryotic domains: domain Bacteria and domain Archaea.  because they diverged so early in life and are so fundamentally different. But they are structurally organized at the prokaryotic level. Taxonomy 分類學; phylum 門 Fig. 27.2

5 CHAPTER 27 PROKARYOTES AND THE ORIGINS OF METABOLIC DIVERSITY
Section B1: The Structure, Function, and Reproduction of Prokaryotes

6 Introduction Most prokaryotes are unicellular.
Some species may aggregate transiently or form true colonies Most prokaryotes are 1-5 um ( um for most eukaryotic cell). The most common shapes among prokaryotes Fig. 27.3

7 1. Nearly all prokaryotes have a cell wall external to the plasma membrane
 affords physical protection  safe in a hypotonic environment. Most bacterial cell walls contain peptidoglycan, a polymer of modified sugars cross-linked by short polypeptides. But The walls of archaea lack peptidoglycan.

8 Fig. 27.5a Gram + The Gram stain is a valuable tool for identifying specific bacteria, based on differences in their cell walls. Gram - Fig. 27.5b

9 Gram-positive bacteria have simpler cell walls, with large amounts of peptidoglycans.
Gram-negative bacteria have more complex cell walls and less peptidoglycan.  lipopolysaccharides, carbohydrates bonded to lipids.

10 參考用 Fig. 7.28

11 Extracellular matrix 參考用 Fig. 7.29

12 gram-negative species are generally more threatening than gram-positive species.
The lipopolysaccharides on the walls are often toxic the outer membrane protects the pathogens from the defenses of their hosts. commonly more resistant to antibiotics. Many antibiotics, including penicillins, inhibit the synthesis of cross-links in peptidoglycans, preventing the formation of a functional wall, particularly in gram-positive species.

13 Fig The prokaryotic cell is much simpler in structure, lacking a nucleus and the other membrane-enclosed organelles of the eukaryotic cell.

14 Many prokaryotes secrete another sticky protective layer, the capsule, outside the cell wall.
Capsules adhere the cells to their substratum. They may increase resistance to host defenses. They glue together the cells of those prokaryotes that live as colonies.

15 Another way for prokaryotes to adhere to one another or to the substratum is by surface appendages called pili. Pili can fasten pathogenic bacteria to the mucous membranes of its host. Some pili are specialized for transfer DNA during conjugation. Fig. 27.6

16 2. Many prokaryotes are motile
About half of all prokaryotes are capable of directional movement. flagella scattered over the entire surface or concentrated at one or both ends. The flagella of prokaryotes differ in structure and function from those of eukaryotes.

17 參考用 Eukaryotic flagellum or cillum Fig. 7.24

18 the hook protein and the basal apparatus.
Rotation of the filament is driven by the diffusion of protons into the cell through the basal apparatus after the protons have been actively transported by proton pumps in the plasma membrane. Fig. 27.7

19 motility mechanisms in prokaryotes
1. The action of flagella is the most common method of movement. 2. Two or more helical filaments under the cell wall are attached to a basal motor attached to the cell. [spirochetes, helical bacteria] 3. cells that secrete a jet of slimy threads that anchors the cells to the substratum.

20 Environment and movement direction
In a relatively uniform environment, a flagellated cell may wander randomly. In a heterogenous environment, many prokaryotes are capable of taxis (趨性), movement toward (+) or away (-) from a stimulus. stimulus is chemicals  chemotaxis stimulus is light phototaxis

21 CHAPTER 27 PROKARYOTES AND THE ORIGINS OF METABOLIC DIVERSITY
Section B2: The Structure, Function, and Reproduction of Prokaryotes (continued) Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

22 3. The cellular and genomic organization of prokaryotes is fundamentally different from that of eukaryotes Prokaryotic cells lack a nucleus enclosed by membranes Prokaryotic cells lack the other internal compartments bounded by membranes.

23 Photosynthetic prokaryote
Instead, prokaryotes used infolded regions of the plasma membrane to perform many metabolic functions. Aerobic prokaryote Photosynthetic prokaryote Respiratory membrane Thylakoid membrane Fig. 27.8

24 Genome of prokaryote and eukaryote
Prokaryotes have smaller, simpler genomes than eukaryotes. (~1/1000). Typically, the DNA is concentrated as a snarl of fibers in the nucleoid region. The mass of fibers is actually the single prokaryotic chromosome, a double-stranded DNA molecule in the form of a ring. There is very little protein associated with the DNA.

25 Prokaryotes may also have smaller rings of DNA, plasmids, that consist of only a few genes.
Prokaryotes can survive in most environments without their plasmids because essential functions are programmed by the chromosomes. However, plasmids provide the cell genes for resistance to antibiotics. Plasmids replicate independently of the chromosome can be transferred between partners during conjugation.

26 the general processes for DNA replication and translation are alike for eukaryotes and prokaryotes, but of some differ. the prokaryotic ribosomes are slightly smaller than the eukaryotic version and differs in its protein and RNA content. Antibiotics, e.g., tetracycline and chloramphenicol, can block protein synthesis in many prokaryotes but not in eukaryotes.

27 4. Populations of prokaryotes grow and adapt rapidly
Prokaryotes reproduce only asexually via binary fission, synthesizing DNA almost continuously. A single cell in favorable conditions will produce a colony of offspring. Fig. 27.9

28 While lacking meiosis and sex as seen in eukarotes, prokaryotes have several mechanisms to combine genes between individuals. In transformation, a cell can absorb and integrate fragments of DNA from their environment. In conjugation, one cell directly transfers genes (e.g., plasmid) to another cell. In transduction, viruses transfer genes between prokaryotes.

29 DNA bacterial viruses = bacteriophages transduction

30 Conjugation = plasmid-directed transfer of DNA from one cell to another.

31 Lacking meiotic sex, mutation is the major source of genetic variation in prokaryotes.

32 The word growth as applied to prokaryotes refers to population or cell number increases, rather than enlargement of individual cells. Typical generation times range from 1-3 hours, but some species can double every 20 minutes.

33 Prokaryote can also withstand harsh conditions.
Some bacteria form resistant cells, endospores. In an endospore, a cell replicates its chromosome and surrounds one chromosome with a durable wall. Fig

34 Resistance and Weakness of endospore
Endospores can survive lack of nutrients and water, extreme heat or cold, and most poisons. Endospores may be dormant for centuries or more. When the environment becomes more hospitable, the endospore absorbs water and resumes growth. Sterilization in an autoclave kills even endospores by heating them to 120oC.

35 In most environments, prokaryotes compete with other prokaryotes (and other microorganisms) for space and nutrients. by release antibiotics, chemicals that inhibit the growth of other microorganisms

36 CHAPTER 27 PROKARYOTES AND THE ORIGINS OF METABOLIC DIVERSITY
Section C: Nutrition and Metabolic Diversity 1. Prokaryotes can be grouped into four categories according to how they obtain energy and carbon 2. Photosynthesis evolved early in prokaryotic life

37 1. Prokaryotes can be grouped into four categories according to how they obtain energy and carbon
Species that use light energy are phototrophs. Species that obtain energy from chemicals in their environment are chemotrophs. Organisms that need only CO2 as a carbon source are autotrophs. [自營] Organisms that require at least one organic nutrient as a carbon source are heterotrophs. [異營] These categories of energy source and carbon source can be combined.

38 Photoautotrophs are photosynthetic organisms that harness light energy to drive the synthesis of organic compounds from carbon dioxide. Among the photoautotrophic prokaryotes are the cyanobacteria. Among the photosynthetic eukaryotes are plants and algae.

39 Chemoautotrophs need only CO2 as a carbon source, but they obtain energy by oxidizing inorganic substances, rather than light. These substances include hydrogen sulfide (H2S), ammonia (NH3), and ferrous ions (Fe2+) among others. This nutritional mode is unique to prokaryotes.

40 Photoheterotrophs use light to generate ATP but obtain their carbon in organic form.
This mode is restricted to prokaryotes. Chemoheterotrophs must consume organic molecules for both energy and carbon. This nutritional mode is found widely in prokaryotes, protists, fungi, animals, and even some parasitic plants.

41 The majority of known prokaryotes are chemoheterotrophs.

42 diverse prokaryotes can metabolize most nitrogenous compounds, but eukaryotes just for limited kinds. Prokaryotes are responsible for the key steps in the cycling of nitrogen through ecosystems.

43 oxygen impact on the growth of prokaryotes.
Obligate aerobes require O2 for cellular respiration. Facultative anaerobes will use O2 if present but can also grow by fermentation in an anaerobic environment. Obligate anaerobes are poisoned by O2 and use either fermentation or anaerobic respiration. In anaerobic respiration, inorganic molecules other than O2 accept electrons from electron transport chains.

44 2. Photosynthesis evolved early in prokaryotic life
anaerobic Glycolysis was probably one of the first metabolic pathways. Natural selection would have favored harness the energy of sunlight to drive the synthesis of ATP generate reducing power to synthesize organic compounds from CO2.

45 Photosynthetic groups are scattered.
Fig The most reasonable hypothesis is that photosynthesis evolved just once. Heterotrophic groups represent a loss of photosynthetic ability during evolution.

46 The early evolution of cyanobacteria is also consistent with an early origin of photosynthesis.
Cyanobacteria are the only autotrophic prokaryotes that release O2 by splitting water during the light reaction.

47 Oxygenic photosynthesis is especially complex because it requires two cooperative photosystems.
Some modern groups of prokaryotes use a single photosystem to extract electrons from compounds such as H2S instead of splitting water. A logical inference is that cyanobacteria evolved from ancestors with simpler, nonoxygenic photosystems.

48 CHAPTER 27 PROKARYOTES AND THE ORIGINS OF METABOLIC DIVERSITY
Section D: A Survey of Prokaryotic Diversity 1. Molecular systematics is leading to a phylogenetic classification of prokaryotes 2. Researchers are identifying a great diversity of archaea in extreme environments and in the oceans 3. Most known prokaryotes are bacteria Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

49 1. Molecular systematics is leading to phylogenetic classification of prokaryotes
The limited fossil record and structural simplicity of prokaryotes created great difficulties in developing a classification of prokaryotes. Carl Woese et al. cluster prokarotes into taxonomic groups by comparisons of DNA sequences. Especially useful was the small-subunit ribosomal RNA (SSU-rRNA) because all organisms have ribosomes.

50 Woese used signature sequences, regions of SSU-rRNA that are unique, to establish a phylogeny of prokarotes. Fig

51 Before molecular phylogeny, phenotypic characters were used to establish prokaryotic phylogeny but are poor guides to phylogeny. More recently, researchers have sequenced the complete genomes of several prokaryotes.  supported most of the taxonomic conclusions based on SSU-rRNA comparisons, but produced some surprises.

52 2. Researchers are identifying a great diversity of archaea in extreme environments and in the oceans Early on prokaryotes diverged into two lineages, the domains Archaea and Bacteria.

53 Copyright © 2002 Pearson Education, Inc
Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

54 Archaea are extremophiles, “lovers” of extreme environments. [ecology]
Most species of archaea sorted into the kingdom Euryarchaeota or the kingdom Crenarchaeota [phylogeny]. Archaea are extremophiles, “lovers” of extreme environments. [ecology] classified into: 1. methanogens, 2. extreme halophiles, 3. extreme thermophilies.

55 Methanogens are among the strictest anaerobes.
Methanogens obtain energy by using CO2 to oxidize H2 replacing methane as a waste. Methanogens are among the strictest anaerobes. They live in swamps and marshes where other microbes have consumed all the oxygen. Other methanogens live in the anaerobic guts of herbivorous animals, playing an important role in their nutrition. They may contribute to the greenhouse effect, through the production of methane.

56 Extreme halophiles live in such saline places as the Great Salt Lake and the Dead Sea.
Some species merely tolerate elevated salinity; others require an extremely salty environment to grow. Fig

57 Extreme thermophiles thrive in hot environments.
The optimum temperatures for most thermophiles are 60oC-80oC. Sulfolobus oxidizes sulfur in hot sulfur springs in Yellowstone National Park. Another sulfur-metabolizing thermophile lives at 105oC water near deep-sea hydrothermal vents.

58 All the methanogens and halophiles fit into Euryarchaeota.
Most thermophilic species belong to the Crenarchaeota.

59 3. Most known prokaryotes are bacteria
The name bacteria was once synonymous with “prokaryotes,” but it now applies to just one of the two distinct prokaryotic domains. Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

60 Table 27.3, continued Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

61 CHAPTER 27 PROKARYOTES AND THE ORIGINS OF METABOLIC DIVERSITY
Section E: The Ecological Impact of Prokaryotes 1. Prokaryotes are indispensable links in the recycling of chemical elements in ecosystems 2. Many prokaryotes are symbiotic 3. Pathogenic prokaryotes cause many human diseases 4. Humans use prokaryotes in research and technology Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

62 1. Prokaryotes are indispensable links in the recycling of chemical elements in ecosystems
Ongoing life depends on the recycling of chemical elements between the biological and chemical components of ecosystems. decomposers, especially prokaryotes, can recycle.

63 Prokaryotes have many unique metabolic capabilities.
They are the only organisms able to metabolize inorganic molecules (such as iron, sulfur, nitrogen, and hydrogen). Cyanobacteria not only synthesize food and restore oxygen to the atmosphere, but they also fix nitrogen. When plants and animals die, other prokaryotes return the nitrogen to the atmosphere.

64 2. Many prokaryotes are symbiotic
Prokaryotes often interact with other species of prokaryotes or eukaryotes with complementary metabolisms. Organisms involved in an ecological relationship with direct contact (symbiosis) are known as symbionts. If one symbiont is larger than the other, it is also termed the host.

65 In mutualism, both symbionts benefit.
In commensalism, one symbiont receives benefits while the other is not harmed or helped by the relationship. In parasitism, one symbiont, the parasite, benefits at the expense of the host. In mutualism, both symbionts benefit. Legumes roots are the homes of mutualistic prokaryotes (Rhizobium) that fix nitrogen that is used by the host. Prokaryotes are involved in all three categories of symbiosis with eukaryotes.

66 Some pathogens are opportunistic.
3. Pathogenic prokaryotes cause many human diseases about half of all human disease Some pathogens are opportunistic. These are normal residents of the host, but only cause illness when the host’s defenses are weakened. Robert Koch was the first to connect certain diseases to specific bacteria. He identified the bacteria responsible for anthrax and the bacteria that cause tuberculosis.

67 These postulates work for most pathogens, but exceptions do occur.
Koch’s postulates guide medical microbiology. (1) The researcher must find the same pathogen in each diseased individual investigated, (2) Isolate the pathogen form the diseased subject and grow the microbe in pure culture, (3) Induce the disease in experimental animals by transferring the pathogen from culture, and (4) Isolate the same pathogen from experimental animals after the disease develops. These postulates work for most pathogens, but exceptions do occur.

68 Some pathogens produce symptoms of disease by invading the tissues of the host
E.g., actinomycete causes tuberculosis More commonly, pathogens cause illness by producing poisons, called exotoxins and endotoxins. Actinomycete = 放射菌類

69 Exotoxins are proteins secreted by prokaryotes.
Exotoxins can produce disease symptoms even if the prokaryote is not present. Clostridium botulinum, which grows anaerobically in improperly canned foods, produces an exotoxin that causes botulism. An exotoxin produced by Vibrio cholerae causes cholera. strains of E. coli can be a source of exotoxins, causing traveler’s diarrhea. Botulism =類桿菌中毒

70 Endotoxins are components of the outer membranes of some gram-negative bacteria.
Salmonella typhi, which are not normally present in healthy animals, causes typhoid fever. Other Salmonella species, including some that are common in poultry, cause food poisoning. Typhoid = 傷寒症 Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings

71 biological weapons remains a threat to world peace.
Today, the rapid evolution of antibiotic- resistant strains of pathogenic bacteria is a serious health threat. biological weapons remains a threat to world peace. Copyright © 2002 Pearson Education, Inc., publishing as Benjamin Cummings


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