27 prokaryotes and the origins of metabolic diversity

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27 Prokaryotes and the Origins of Metabolic Diversity

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Page 1: 27 Prokaryotes and the Origins of Metabolic Diversity

27 Prokaryotes and the Origins of Metabolic Diversity

Page 2: 27 Prokaryotes and the Origins of Metabolic Diversity

Archaea live in extreme environments and have cell walls with no peptidoglycan, have histone and methionine for initial amino acid.

Archaea live in extreme environments and have cell walls with no peptidoglycan, have histone and methionine for initial amino acid.

Formerly

eubacteriaFormerly

eubacteria

Page 3: 27 Prokaryotes and the Origins of Metabolic Diversity

Most bacteria range from 1-5 um while eukaryotes range from 10-100 um

Most bacteria range from 1-5 um while eukaryotes range from 10-100 um

Page 4: 27 Prokaryotes and the Origins of Metabolic Diversity

Coccus shapeCoccus shape

Page 5: 27 Prokaryotes and the Origins of Metabolic Diversity

Bacillus shapeBacillus shape

Page 6: 27 Prokaryotes and the Origins of Metabolic Diversity

Helical or spiral shape

eg. Spirochetes

Helical or spiral shape

eg. Spirochetes

Page 7: 27 Prokaryotes and the Origins of Metabolic Diversity
Page 8: 27 Prokaryotes and the Origins of Metabolic Diversity

Simple cell wall with relatively large amounts of peptidoglycan

Penicillin prevents crosslinking in the peptidoglycan and prevents the formation of a functional cell wall in gram positive bacteria

Simple cell wall with relatively large amounts of peptidoglycan

Penicillin prevents crosslinking in the peptidoglycan and prevents the formation of a functional cell wall in gram positive bacteria

More complex cell wall with less peptidoglycan AND with an outer membrane with lipopolysaccharides -carbohydrates bonded to lipids -often toxic

More complex cell wall with less peptidoglycan AND with an outer membrane with lipopolysaccharides -carbohydrates bonded to lipids -often toxic

Page 9: 27 Prokaryotes and the Origins of Metabolic Diversity
Page 10: 27 Prokaryotes and the Origins of Metabolic Diversity

gonorrhea bacterium

gonorrhea bacterium

Sticky capsules found on the outside of bacteria will provide protection and glue together the cells

Sticky capsules found on the outside of bacteria will provide protection and glue together the cells

Pilli can be used for adhesion or conjugation

Pilli can be used for adhesion or conjugation

Page 11: 27 Prokaryotes and the Origins of Metabolic Diversity

Flagellin is wound in a tight spiral to form a helical filament, which is attached to another protein which forms a curved hook. The basal apparatus rotates the filament - it is powered by protons that have been pumped toward the plasma membrane

Flagellin is wound in a tight spiral to form a helical filament, which is attached to another protein which forms a curved hook. The basal apparatus rotates the filament - it is powered by protons that have been pumped toward the plasma membrane

In contrast Eukaryotic flagella have a 9+2 microtubular structure

Page 12: 27 Prokaryotes and the Origins of Metabolic Diversity

Bacteria can show taxis

- the movement towards or away from a stimulus

eg. Chemotaxis

Bacteria can show taxis

- the movement towards or away from a stimulus

eg. Chemotaxis

Page 13: 27 Prokaryotes and the Origins of Metabolic Diversity

Nucleoid region containing genophore

-prokaryotic DNA

Nucleoid region containing genophore

-prokaryotic DNA

Prokaryotes have smaller ribosomes that respond to different antibiotics that prevent them from doing protein synthesis

Prokaryotes have smaller ribosomes that respond to different antibiotics that prevent them from doing protein synthesis

Page 14: 27 Prokaryotes and the Origins of Metabolic Diversity

Reproduction by binary fission is a form of asexual reproduction

Reproduction by binary fission is a form of asexual reproduction

However genetic recombination can occur by transformation, conjugation and transduction

However genetic recombination can occur by transformation, conjugation and transduction

Page 15: 27 Prokaryotes and the Origins of Metabolic Diversity

4 Categories of Prokaryotes

• Photoautotrophs - cyanobacteria

• Chemoautotrophs - extracts energy by oxidizing inorganic substances

• Photoheterotrophs - can use light to generate ATP, but must eat for carbon

• Chemoheterotroph - consumer

P 508P 508

Page 16: 27 Prokaryotes and the Origins of Metabolic Diversity

Nutritional Diversity

• Most are chemoheterotrophs

• some are saprovores obtaining their energy from dead organic matter - a key feature ecologically in that it recycles material

• some are parasites

Page 17: 27 Prokaryotes and the Origins of Metabolic Diversity

Nitrogen Metabolism

• Nitrogen is a key component of proteins and nucleic acids

• Nitrogen gas is unusable by most organisms

Page 18: 27 Prokaryotes and the Origins of Metabolic Diversity

Nitrogen Fixation

• Many prokaryotes including cyanobacteria can take N2 and change it to NH3 in a process called nitrogen fixation

cyanobacteriacyanobacteria

Page 19: 27 Prokaryotes and the Origins of Metabolic Diversity

Nitrogen Fixation

• Nitrogen fixation must occur in an anaerobic environment

• Hetrocyst are sealed cells were nitrogen fixation occurs

Page 20: 27 Prokaryotes and the Origins of Metabolic Diversity

Nitrogen Metabolism

• Chemoautotrophic bacteria such as Nitrosomonas can convert NH3 into NO2

+

• Pseudomonas can denitrify NO2+ and

NO3+ back to N2.

Page 21: 27 Prokaryotes and the Origins of Metabolic Diversity

Nitrosomonas

Pseudomonas

Rhizobia

Azotobacter

Page 22: 27 Prokaryotes and the Origins of Metabolic Diversity

Metabolic Relationships to Oxygen

• Obligate aerobes must have O2 to live

• Facultative aerobes will use O2 if present but can live anaerobically.

• Obligate anaerobes will be poisoned by O2.

Page 23: 27 Prokaryotes and the Origins of Metabolic Diversity

Possible sources of ATP for early cells

Possible sources of ATP for early cells

ATP available in the primordial soup

ATP available in the primordial soup

FeS and H2S are used by chemoautotrophs to produce ATP

FeS and H2S are used by chemoautotrophs to produce ATP

Page 24: 27 Prokaryotes and the Origins of Metabolic Diversity

Origin of Photosynthesis

• Photosensitive pigments embedded in the plasma membrane ex. Bacteriorhodopsin found in some archea pumps H+ outside of cell and that is used to generate ATP.

• Some others used light to drive electrons from H2S (hydrogen sulfide) to NADP+.

• First photosynthetic organisms could only make ATP not carbon compounds (Photosystem I).

Page 25: 27 Prokaryotes and the Origins of Metabolic Diversity

Cyanobacteria

• Many prokaryotes including cyanobacteria can make ATP and carbohydrates. Using photosystem II they could generate oxygen

• Mats of these fossilized into stramatolites

• Oxidizing atmosphere forms about 2.1 – 2.7 billion years ago

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• Carl Woese used signature sequences, regions of SSU-rRNA that are unique, to establish a phylogeny of prokaryotes. This is a line of evidence which separates Archaea into its own domain.

Fig. 27.13

Page 27: 27 Prokaryotes and the Origins of Metabolic Diversity

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

Essay Question:What are the lines of evidence that allowed scientist to place Archaea into its own DomainEX:Specific SSU rRNA sequences are found in archaea and not bacteria

PMRIIAHTSPRIMA THIS

Page 28: 27 Prokaryotes and the Origins of Metabolic Diversity

• 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.– Methanogens are important decomposers in

sewage treatment.

• 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.

Page 29: 27 Prokaryotes and the Origins of Metabolic Diversity

• 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.– Colonies of halophiles form

a purple-red scum from bacteriorhodopsin, a photosynthetic pigment very similar to the visual pigment in the human retina.

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

Fig. 27.14

Page 30: 27 Prokaryotes and the Origins of Metabolic Diversity

• 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.

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

Page 31: 27 Prokaryotes and the Origins of Metabolic Diversity

• Ongoing life depends on the recycling of chemical elements between the biological and chemical components of ecosystems.– If it were not for decomposers, especially

prokaryotes, carbon, nitrogen, and other elements essential for life would become locked in the organic molecules of corpses and waste products.

– Prokaryotes also mediate the return of elements from the nonliving components of the environment to the pool of organic compounds.

1. Prokaryotes are indispensable links in the recycling of

chemical elements in ecosystems

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

Page 32: 27 Prokaryotes and the Origins of Metabolic Diversity

• Prokaryotes have many unique metabolic capabilities.– They are the only organisms able to metabolize

inorganic molecules containing elements such as iron, sulfur, nitrogen, and hydrogen.

– Cyanobacteria not only synthesize food and restore oxygen to the atmosphere, but they also fix nitrogen.• This stocks the soil and water with nitrogenous

compounds that other organisms can use to make proteins.

– When plants and animals die, other prokaryotes return the nitrogen to the atmosphere.

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

Page 33: 27 Prokaryotes and the Origins of Metabolic Diversity

• 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.• For example, while the fish

provides bioluminescentbacteria under its eye withorganic materials, the fishuses its living flashlightto lure prey and to signalpotential mates. Bacteria in our intestine produces Vitamin K.

Fig. 27.15

Page 34: 27 Prokaryotes and the Origins of Metabolic Diversity

• Prokaryotes are involved in all three categories of symbiosis with eukaryotes.– Legumes (peas, beans, alfalfa, and others) have

lumps in their roots which are the homes of mutualistic prokaryotes (Rhizobium) that fix nitrogen that is used by the host.• The plant provides sugars and other organic nutrients to

the prokaryote.

– Fermenting bacteria in the human vagina produce acids that maintain a pH between 4.0 and 4.5, suppressing the growth of yeast and other potentially harmful microorganisms.• Other bacteria are pathogens.

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

Page 35: 27 Prokaryotes and the Origins of Metabolic Diversity

• Some pathogens produce symptoms of disease by invading the tissues of the host.– The actinomycete that causes tuberculosis is an

example of this source of symptoms.

• More commonly, pathogens cause illness by producing poisons, called exotoxins and endotoxins.

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

Page 36: 27 Prokaryotes and the Origins of Metabolic Diversity

• 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, a serious disease characterized by severe diarrhea.

– Even strains of E. coli can be a source of exotoxins, causing traveler’s diarrhea.

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

Page 37: 27 Prokaryotes and the Origins of Metabolic Diversity

• Endotoxins are components of the outer membranes of some gram-negative bacteria.– The endotoxin-producing bacteria in the genus

Salmonella are not normally present in healthy animals.

– Salmonella typhi causes typhoid fever.– Other Salmonella species, including some that are

common in poultry, cause food poisoning.

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

Page 38: 27 Prokaryotes and the Origins of Metabolic Diversity

• Since the discovery that “germs” cause disease, improved sanitation and improved treatments have reduced mortality and extended life expectancy in developed countries.– More than half of our antibiotics (such as

streptomycin and tetracycline) come from the soil bacteria Streptomyces.• This genus uses to prevent encroachment by competing

microbes.

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

Page 39: 27 Prokaryotes and the Origins of Metabolic Diversity

• The decline (but not removal) of bacteria as threats to health may be due more to public-health policies and education than to “wonder-drugs.”

• For example, Lyme disease, caused by a spirochete spread by ticks that live on deer, field mice, and occasionally humans, can be cured if antibiotics are administered within a month after exposure.

• If untreated, Lyme disease causes arthritis, heart disease, and nervous disorders.

• The best defense is avoiding tick bites and seeking treatment if bit and a character-istic rash develops.

Copyright © 2002 Pearson Education, Inc., publishing as Benjamin CummingsFig. 27.17

Page 40: 27 Prokaryotes and the Origins of Metabolic Diversity

• The application of organisms to remove pollutants from air, water, and soil is bioremediation.– The most familiar example is the use of prokaryote

decomposers to treat human sewage.– Anaerobic bacteria

decompose theorganic matterinto sludge(solid matterin sewage), whileaerobic microbesdo the same toliquid wastes.

Copyright © 2002 Pearson Education, Inc., publishing as Benjamin CummingsFig. 27.18

Page 41: 27 Prokaryotes and the Origins of Metabolic Diversity

– Soil bacteria, called pseudomonads, have been developed to decompose petroleum products at the site of oil spills or to decompose pesticides.

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

Fig. 27.19

Page 42: 27 Prokaryotes and the Origins of Metabolic Diversity

• Humans also use bacteria as metabolic “factories” for commercial products.– The chemical industry produces acetone, butanol,

and other products from bacteria.– The pharmaceutical industry cultures bacteria to

produce vitamins and antibiotics.– The food industry used bacteria to convert milk to

yogurt and various kinds of cheese.

• The development of DNA technology has allowed genetic engineers to modify prokaryotes to achieve specific research and commercial outcomes.

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