Lecture 3 Flashcards

1
Q

Explain what limits prokaryotic cell size.

A

lack compartmentalization, limited by the distance that molecules can diffuse within the cell

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2
Q

describe 4 different prokaryotice cell shapes

A

cocci (spheres) - O
bacilli (rods)
spherical (spirals)
viberious (comma shaped)

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3
Q

cell wall

A
Cell wall 
• Function? 
• Helps to maintain shape, provides physical protection, and prevents cell from bursting in hypotonic environment. 
• What are plant cell walls made of? 
• Cellulose 
• Fungi? 
• Chitin 
• Bacteria? 
• Peptidoglycan 
• Archaea 
• Lack peptidoglycan; variety of other polysaccharides and proteins.
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4
Q

Capsule

A

Capsule
• Sticky protective layer of polysaccharide and protein secreted outside the cell wall.
• Function:
• Adhesion to substrate or other individuals in a colony.
• Protection against dehydration and/or resistance to attack from host’s immune system

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5
Q

Fimbriae

A

Fimbriae (attachment pili)
• Hair-like surface protein appendages.
• Function: adhesion to one another or to substrate (or host).

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6
Q

Sex pili

A

Sex pili: longer than attachment fimbriae - used to

pull two cells together during conjugation

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7
Q

Endospore

A

some species can produce a tough thick-walled cells that can survive unfavourable conditions for long periods of time

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8
Q

Distinguish between the structure and staining properties of gram positive and gram negative cells

A
  • Gram positive bacteria
  • Simpler cell wall with large amount of peptidoglycan
  • Thick peptidoglycan layer traps the stain crystal violet within the cytoplasm.

Gram negative bacteria
• More complex, with less peptidoglycan.
• Cell wall sandwiched between the plasma
membrane and an outer membrane.
• Outer membrane contains lipopolysaccharides.

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9
Q

Explain why gram staining is useful in medicine

A

can be used to quickly determine if an infection is due to gram negative or gram positive bacterium

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10
Q

Explain why Pathogenic gram negative bacteria are generally more resistant to antibiotics AND more deadly than pathogenic gram-positive bacteria.

A

Gram negative are more resistance because outer membrane impedes entry of drugs. Deadly because more resistance to antibiotics lipopolysaccarides are toxic and outer membrane resists host immune system

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11
Q

List 5 ways in which prokaryotes differ from eukaryotes in their internal and genomic structure.

A

1) lack compartmentalization
2) smaller genome 1/1000th as much DNA
3) lack nucleus
4) have singular circular chromosome with few associated proteins
5) have ribosomes that are smaller and differ in protein and RNA content

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12
Q

Describe pasmids

A

Some prokaryotes may have smaller rings of DNA called plasmids.
• Contain only a few genes for specialized functions; are not required under normal conditions.
• Replicate independently of main cellular chromosome

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13
Q

List 3 ways in which prokaryotes move.

A

1) flagella
2) Twitching and gliding by extending and retracting pili.
3) Cyanobacteria and other aquatic prokaryotes have gas vesicles to control buoyancy.

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14
Q

Define taxis

A

movement away or towards a stimulus

• e.g., moving towards oxygen and nutrients or away from toxic substances.

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15
Q

briefly explain how prokaryotic flagella differ from eukaryotiv flagella

A

Eukaryoes—> wip-like motor protein

Prokaryotes—> works like propeller

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16
Q

Differentiate between the following modes of nutrition discussed in this lecture and state which modes are exclusive to prokaryotes.

A

Photoautotrophs- organisms that use light energy to the synthesis of organic compounds from CO2

Chemoautotrophs: Organisms that use energy obtained from the oxidation of inorganic substances to drive the synthesis or organic compounds from CO2 (EXCLUSIVE PROKARYOTES)

Photoherterotrophs- use light energy to generate ATP, but obtain their carbon in organic form
(EXCLUSIVE TO PROKARYOTES)

Chemoheterotrophs- must consume organic molecules for both energy and as carbon source

17
Q

Differentiate between obligate aerobes, obligate anaerobes, facultative anaerobes, and aerotolerant anaerobes.

A

Obligate aerobes- use O2 for cellular respiration and cannot grow without it… no other options

Obligate anaerobes- poisoned by O2 live exclusively by fermentation or anaerobic respiration, substances other then O2 as final electron acceptor

Facultative anaerobes- Use O2 when present, but are capable of switching to fermentation or anaerobic respiration in absence of O2

Aerotolerant anaerobes- do not use O2 but are not poisoned by it, obtain energy via anaerobic respiration, using final e- acceptor other than O2 at end of ETC

18
Q

Differentiate between oxygenic photosynthesis and anoxygenic photosynthesis

A

What is the ultimate source of electrons in photosynthesis by plants?
• Water –> produces oxygen as by-product
= Oxygenic photosynthesis
 Example prokaryote that carries out this type of photosynthesis?
(hint: history of life…crucial event…) cyanobacteria

• Some prokaryotes use molecules other than water as the source of electrons for photosynthesis.
• e.g., H2S, Fe2+
–> by-products are sulfur and ferric iron.
= Anoxygenic photosynthesis

19
Q

Explain the importance of nitrogen fixation by prokaryotes to life on Earth.

A
  • Eukaryotes are very limited in the forms of nitrogen that they can use; cannot use N2
  • Prokaryotes can obtain nitrogen in a wide variety of forms, including N2
  • Cyanobacteria and some archaea (methanogens) can convert N2to NH3 via nitrogen fixation.
  • The “fixed” nitrogen can then be incorporated into amino acids and other organic molecules.
20
Q

Explain how the cyanobacterium Anabaena cooperates to use environmental resources.

A

Anabaena (cyanobacterium)
• Can carry out photosynthesis and nitrogen fixation, but not both in a single cell.
• Forms colonies - majority of cells carry out photosynthesis; a few specialized cells (heterocysts or heterocytes) carry out nitrogen fixation.

21
Q

Describe “biofilm” and provide an example of a beneficial and harmful consequence of biofilm.

A

Biofilms
• Surface-coating colonies.
• Secrete proteins that glue adjacent cells together and to substrate.
• Helps community of cells to remain in favorable location for growth.
• -ve: Contribute to tooth decay, accumulate in
pipelines —> damage
• +ve : Help stabilize and enrich sand and soil

22
Q

Explain how pathogenic bacteria communicate and the advantage of communicating (what does it allow them to do?)

A

Bacteria “talk” to each other via a chemical
language = “quorum sensing.”
• In infectious bacteria: is used to coordinate attacks on host and evade immune system.
• Upon entering host, bacterial cells “sit and wait” – release chemical communication molecules into environment.
• Chemical binds to specific receptor on bacterial cell’s surface.
• Allows bacteria to count how many other bacterial cells are present in population.
• Once amount of molecule in environment reaches a certain amount, indicating a certain population size, the cells all launch an attack on the host together!
• Increases success of bacteria against host.
• Each species produces a very specific molecule, allowing for intraspecies communication….but bacteria are also multilingual!
• Also have a generic system - a universal language “spoken” by all bacteria.
• Allows bacteria to count how many of other species are present, and behave accordingly.

23
Q

Very briefly describe the process by which a prokaryotic cell reproduces

A

• Prokaryotes are highly successful because they
have the potential to reproduce VERY quickly in
favorable environments.
• Reproduce via binary
fission.

24
Q

Explain the connection between botulism and endospores.

A

endospores allow cells to survive unfavorable conditions so botulism occurs when endospores allow bacteria to remain on food despite heat or other conditions that would normally eliminate them

25
Name 2 processes that contribute to genetic diversity in prokaryotes
1) mutations | 2) gene transfer
26
Define gene transfer and distinguish between conjugation, transformation, and transduction.
Genetic material is transferred from one bacterial cell to another. • Conjugation: involves direct contact between bacterial cells (see next slide). • Transformation: DNA that is released into the environment when a bacterium dies is taken up by another bacterial cell, which incorporates the DNA into its own chromosome. • Transduction: a virus infects a bacterial cell and then transfers some of the cell’s DNA to another bacterium.
27
Distinguish between vertical and horizontal gene transfer.
* Vertical gene transfer: occurs when genes are passed from one generation to the next (i.e. from parents to offspring). * Horizontal gene transfer: process by which organisms acquire genes from another organism, without being the offspring of that organism (i.e. conjugation, transformation, and transduction)
28
Explain why horizontal gene transfer makes it difficult to classify prokaryotes into monophyletic groups.
Because it mixes up the DNA making it impossible to distinguish lineages Conjugation, transformation, and transduction can occasionally occur between cells of different bacterial species!
29
Briefly describe the role of prokaryotes in the recycling of chemical elements in ecosystems.
* Ecosystems depend on continual recycling of chemical elements between living and nonliving components of the environment. * Chemoheterotrophic prokaryotes play a major role. * Breakdown dead animals, dead vegetation, and waste products. * Release carbon, nitrogen, and other “supplies” within these resources. * Prokaryotes also convert inorganic compounds into organic compounds. * Carbon fixation * Nitrogen fixation * And don’t forget oxygen production!
30
Define symbiosis, and distinguish between mutualism, commensalism, and parasitism. Provide an example involving a prokaryote for each type of symbiosis.
• Symbiosis: an ecological relationship in which two species live in close contact with one another • Mutualism: both the host and the symbiont benefit from their association with each other. • Bacteria that live in our intestines • Flashlight fish + bioluminescent bacteria • Commensalism: one species benefits, while the other is neither harmed nor helped. • Species of bacteria that live on the surface of your body • Parasitism: one species, the parasite, benefits, while the other is harmed, but not killed – at least not immediately… pylori: which causes ulcers from living in stomach wall
31
Provide 3 examples of pathogenic bacteria and the disease they cause
1) TUberculosis- myobacterium tuberculosis 2) Tetanus- clostridium tetani 3) Botulism- clostridium botulism
32
Distinguish between exotoxins and endotoxins and give an example of each.
• Exotoxins: proteins that are secreted by bacteria and other organisms. • e.g., Exotoxin secreted by Vibrio cholerae stimulates the intestinal cells to release chloride ions into the intestine – which will cause what to happen? • Endotoxins: lipopolysaccharide components of the outer membrane of gram negative bacteria; are only released when the bacteria die and their cell walls break down. • e.g., Produced by Salmonella typhi and other Salmonella species
33
State two ways via which pathogenic bacteria may acquire antibiotic resistance.
1) a change in the bacterias own genome (mutation) | 2) Horizontal transfer of resistant gens from a resistant stain
34
Provide 3 examples of how resistant strains of bacteria may counteract the action of antibiotics.
* breaks down the drug * pumps the drug out of the cell * prevents the drug from inhibiting cellular processes.
35
Provide 3 examples of how prokaryotes have benefitted humans and/or human society.
1) yogert and cheese 2) bio-remediation --Decompose organic matter in sewage; metabolize oils after a spill. 3) bacteria used to make natural durable biodegradable plastics 4) vitamins
36
State three ways in which bacteria and archaea differ
Archea have DNA associated with histone proteins bacteria does not Organelles are present in Bacteria and not in Archea Almost all bacteria are unicellular and all archea are unicellular
37
Explain why some archaea are known as extremophiles. Describe the distinguishing features of methanogens, extreme halophiles, and extreme thermophiles.
• Extremophiles: “lovers” of extreme environments. • Extreme thermophiles: live in very hot environments. • Volcanic springs ~ 90C • Deep sea hydrothermal vents - up to 121C!! Most organisms die at temperatures this high – why?? -- enzymes loose shape • Extreme halophiles: live in very salty environments. • Dead sea, Great Salt Lake, Owens Lake • Not all Archaea live in extreme environments. • Methanogens • Produce methane (CH4) as a by-product of cellular respiration. • Obligate anaerobe. • Live in swamps and marshes where all oxygen has been consumed by other microbes. • “Marsh gas” = methane produced by methanogens.